Skip to main content

Varestrongylus eleguneniensis sp. n. (Nematoda: Protostrongylidae): a widespread, multi-host lungworm of wild North American ungulates, with an emended diagnosis for the genus and explorations of biogeography



A putative new species of Varestrongylus has been recently recognized in wild North American ungulates based on the ITS-2 sequences of larvae isolated from feces during a wide geographic survey. No taxonomic description was provided, as adult specimens were not examined.


Lungworm specimens were collected in the terminal bronchioles of muskoxen from Quebec, and a woodland caribou from central Alberta, Canada. The L3 stage was recovered from experimentally infected slugs (Deroceras spp.). Description of specimens was based on comparative morphology and integrated approaches. Molecular identity was determined by PCR and sequencing of the ITS-2 region of the nuclear ribosomal DNA, and compared to other protostrongylids.


Varestrongylus eleguneniensis sp. n. is established for a recently discovered protostrongylid nematode found in caribou (Rangifer tarandus), muskoxen (Ovibos moschatus) and moose (Alces americanus); hosts that collectively occupy an extensive geographic range across northern North America. Adults of Varestrongylus eleguneniensis are distinguished from congeners by a combination of characters in males (distally bifurcate gubernaculum, relatively short equal spicules not split distally, a strongly elongate and bifurcate dorsal ray, and an undivided copulatory bursa) and females (reduced provagina with hood-like fold extending ventrally across prominent genital protuberance). Third-stage larvae resemble those found among other species in the genus. The genus Varestrongylus is emended to account for the structure of the dorsal ray characteristic of V. eleguneniensis, V. alpenae, V. alces and V. longispiculatus.


Herein we describe and name V. eleguneniensis, a pulmonary protostrongylid with Rangifer tarandus as a primary definitive host, and which secondarily infects muskoxen and moose in areas of sympatry. Biogeographic history for V. eleguneniensis and V. alpenae, the only two endemic species of Varestrongylus known from North America, appears consistent with independent events of geographic expansion with cervid hosts from Eurasia into North America during the late Pliocene and Quaternary.


Nematodes of the Family Protostrongylidae Leiper, 1926 are characteristic and often pathogenic parasites among Bovidae, particularly Caprinae, and Cervidae (Artiodactyla) across the Holarctic (comprised by the Palaearctic and Nearctic regions) [1]-[3], and less frequently in tropical regions of the southern hemisphere [4],[5]. The Nearctic protostrongylid fauna includes genera and species, partitioned among four subfamilies, occurring in domestic and free-ranging ungulates and lagomorphs: Protostrongylinae Kamensky, 1905; Muelleriinae Skrjabin, 1933; Elaphostrongylinae Boev & Shulz, 1950; and Varestrongylinae Boev, 1968, e.g. [2]. Species within the Protostrongylinae, Muelleriinae, and Varestrongylinae are strictly pulmonary parasites, with adult nematodes residing in the bronchi, bronchioles, or lung parenchyma, whereas those of the Elaphostrongylinae are found in the skeletal musculature or central nervous system of their hosts. Although the protostrongylid assemblage of Nearctic ungulates was thought to be well defined, there is a growing body of knowledge regarding their biodiversity with new insights about historical processes, host range, geographic distribution and faunal structure, e.g. [6]-[15].

Within the Varestrongylinae, the genus Varestrongylus Bhalerao, 1932 is of special interest due to its complex taxonomic history [1],[16],[17]. Currently, there are nine nominal species considered valid within the genus, with free-ranging cervids and wild and domestic caprine bovids as the main hosts [1],[18]-[20]. The center of diversity for the genus is Eurasia [13], where eight species have been described.

Until recently, Varestrongylus alpenae (Dikmans, 1935) a lungworm in the white-tailed deer, Odocoileus virginianus (Zimmermann), occurring at temperate and subtropical regions of southern, eastern and central North America [12],[21]-[26], was recognized as the sole species of Varestrongylus endemic in North America. However, during the last decade molecular-based survey of high latitude protostrongylids in North America resulted in the detection of a putative second Nearctic species of Varestrongylus[12]. This parasite was distinguished from other protostrongylids based on sequences of the internal transcribed spacer region-2 (ITS-2) of the nuclear ribosomal DNA (rDNA) derived from first-stage dorsal-spined larvae (DSL) extracted from ungulates feces [12]. Although sequence data suggested its placement within the genus Varestrongylus, considerable divergence was demonstrated relative to V. alpenae see [12].

At the time of the original discovery [12], field collections indicated a broad geographic range, extending throughout the northern Nearctic, encompassing five Canadian provinces and territories: mainland Labrador and Newfoundland, Quebec (QC), Nunavut (NU), Northwest Territories and the Yukon, as well as Alaska, USA [12]. More recently, this undescribed species was found on Victoria Island in the Canadian Arctic, demonstrating that its distribution is not restricted to mainland North America [15]. The host range of this new species is remarkably broad, with natural infections detected in caribou of three subspecies: the woodland caribou, Rangifer tarandus caribou (Gmelin), the barrenground caribou, Rangifer tarandus groenlandicus (Borowski), and the Grant’s caribou, Rangifer tarandus granti; muskoxen of two subspecies, Ovibos moschatus moschatus (Zimmermann) and Ovibos moschatus wardi Lyddeker; and one subspecies of moose, A. americanus gigas Miller [12],[15],[27]; Verocai, Kutz, unpublished data.

Protostrongylids have an indirect life-cycle, requiring gastropods as intermediate hosts (IH) [1],[3],[28]. To date, the only known naturally infected IH is the meadow slug Deroceras laeve (Müller, 1774) [12]. This species is widely distributed across northern North America [29] and is believed to be the main intermediate host for several protostrongylids [27].

Recent collections of adult nematodes from the bronchioles of caribou and muskoxen now allow a complete description and series of comparisons to characterize this previously unknown species. In this study we propose the establishment of Varestrongylus eleguneniensis sp. n. for this geographically wide-spread, multi-host protostrongylid lungworm occurring across northern North America. Further, we provide an emended diagnosis for the genus Varestrongylus, and explore the historical biogeography of these nematodes in the Nearctic.


Taxonomic criteria

Host taxonomic classification follows Grubb [30] and Hernández-Fernández and Vrba [31]. Parasite taxonomy is largely consistent with the latest revision [1] and the most recent phylogenetic hypothesis for the family Protostrongylidae [2].


Muskoxen: Muskoxen were harvested from a free-ranging population in Nunavik, QC. These animals were introduced in 1967 from Ellesmere Island, NU to Old Fort Chimo located across the Koksoak River, near Kuujjuaq, for farming purposes, mainly for qiviut production (muskox wool). The farm was shut down and animals were released between 1973 and 1983, and their descendants are currently distributed throughout much of the Ungava Peninsula in northern QC extending eastwards into Labrador [32],[33]. All muskoxen examined in this study were harvested through either subsistence or sport hunting regulated by the Ministry of Natural Resources and Fauna of Quebec (Ministère des Ressources Naturelles et de la Faune du Québec). Hunters submitted selected samples of harvested muskoxen to the Nunavik Research Centre (NRC), Makivik Corporation, located in Kuujjuaq, for general health and food safety assessment (zoonotic diseases and contaminants). Nematodes were isolated from the lungs of two muskoxen harvested near the town of Tasiujaq, QC in late March, 2010: an adult female (Om-01-2010, March 20th, 58°44′51″N, 70°02′06″W) and an adult male (Om-02-2010, March 28th, 58°44′10″N, 69°34′18″W). Another adult female (Om-10-2010) found dead on 31 December, 2009 near Kuujjuaq (58°06′24″N, 68°23′55″W) was collected by NRC personal and kept frozen until necropsy. Additionally, a single female nematode, collected from an adult male muskox (Om-10-2007) hunted near Kuujjuaq (58°45′00″N, 68°33′29″W) on March 21st, 2007, was preserved in 70% ethanol by M. Simard, and later identified as Varestrongylus, and also used for the species description.


Additional adult nematodes were collected from the lungs of an adult male woodland caribou belonging to the Cold Lake herd, Alberta, Canada. The animal was found dead, likely killed by collision with motor vehicle, at 55°2′25″N, 110°34′5″W, near the border with Saskatchewan. The carcass was collected by the Fish and Wildlife Division (FWD) of the Alberta Sustainable Resource Development under the Alberta Wildlife Research Permit no. 48549.

Fecal analyses

Fecal samples of the three muskoxen and the woodland caribou were collected and kept frozen at −20°C until analyses. Samples were analyzed for the presence of protostrongylid DSL using the modified beaker Baermann technique [34] at the NRC and the University of Calgary, prior to lung dissection.

Lung dissection

Lungs were thawed and individually processed. Briefly, they were first grossly examined for pathology and presence of nematodes. A first wash was done with the lungs still intact by flushing tap water into the trachea and then pouring the fluid from the lungs back through a 75 μm mesh sieve. Material retained on the sieve was put in Petri dishes and examined under a stereomicroscope for the presence of nematodes. The entire bronchial tree was then dissected with repeated washing of the exposed airways and pulmonary tissue through the sieve. Material retained in the sieve was examined as described above. All intact nematodes or fragments were collected, identified by gender, and stored in 70% ethanol.

Morphological identification

Nematodes examined

Adults. Specimens and fragments of adult nematodes were mounted and cleared in either lactophenol or phenol-alcohol, and examined under light microscopy with differential interference optics. Photomicrographs were prepared with a Nikon DX 1200 digital camera and a Zeiss Axiophot microscope. Line drawings were prepared with the use of a drawing tube. Throughout the descriptions, measurements are given in micrometres (μm) unless specified otherwise, and are presented with the numbers of adult male, female or larval (DSL and third-stage larvae, L3) nematodes examined (n=), and the range is followed by the mean ± 1 SD within parentheses. First-stage larvae. DSL from feces were recovered from muskox Om-02-10 using the modified beaker Baermann technique [34]. Isolated live DSL were killed in steaming 70% ethanol/glycerine solution (19:1), and held for further evaluation. Species identity was confirmed by molecular sequencing prior to the use of DSL to establish experimental infections in slug intermediate hosts (see below). Third-stage larvae. DSL for infection of slugs D. laeve and Deroceras reticulatum were isolated from feces of the same muskox population at Nunavik, QC (UC-133, representative DSL ITS-2 sequence in Table 1). The slugs were experimentally exposed to 300 DSL/slug as per [35]. Gastropods were maintained in Petri dishes for a day and transferred to plastic containers with an autoclaved soil/vermiculite mix kept at 20°C, making sure that there was constant moisture, and provided with food (lettuce and carrot). Slugs were killed between 18–21 or 50–60 days post exposure (D. laeve and D. reticulatum, respectively), cut into small pieces, and digested in HCl/pepsin solution [6],[36]. Material was analyzed under a dissecting microscope, and all L3 recovered were preserved in 70% ethanol.

Table 1 Summary of collected specimens of Varestrongylus eleguneniensis sp. n. from muskoxen ( Ovibos moschatus wardi ) from Nunavik Region, Quebec, Canada, and woodland caribou ( Rangifer tarandus caribou ) from Alberta, Canada

Molecular analyses

DNA extraction and amplification

Adult nematode fragments were recovered and subsampled from each of the three muskoxen and the caribou. These fragments were individually transferred into wells prior to DNA extraction. Of these, eight fragments (6 from the 3 muskoxen, and 2 from the caribou) had matching caudal extremities or caudal and cephalic extremities used in the morphological description of the species, and, therefore, are part of the type-series (holotype and paratypes) deposited in the United States National Parasite Collection (USNPC), Agricultural Research Service, USDA, Beltsville, MD, USA (see Table 1). In accordance with section 8.5 of the ICZN’s International Code of Zoological Nomenclature, details of the new species have been submitted to the ZooBank under the life science identifier (LSID)

Genomic DNA (gDNA) was extracted from 2–4 mm nematode fragments in 2 mL tubes containing 5 μL of deionized water. To each tube was added 25 μL of lysis buffer (0.5 mg/mL of proteinase K, 10× PCR buffer). DNA extraction followed the following protocol: tubes containing adult worm fragments were incubated at 60°C for 60 min, 65°C for 60 min, then at 95°C for 15 min. The lysis was repeated, after the addition of 1 μL of proteinase K (20 mg/mL) in each well, following the same protocol. Extracted DNA was diluted 1:10. For species identification, a PCR modified from [12] was performed using primers NC1 (5′-ACG TCT GGT TCA GGG TTG TT-3′) and NC2 (5′- TTA GTT TCT TTT CCT CCG CT-3′) targeting the ITS-2 region of rDNA. PCR amplification was performed in 40 μL reactions containing: 20.4 μL of water, 8 μL of 10× PCR buffer + MgCl2, 0.8 μL of 10 mmol dNTPs, 4 μL (10 μM) of each primer, 0.4 μL of bovine serum albumin, 0.4 μL of Taq Phusion HF DNA polymerase, and 2 μL of DNA template. The amplification conditions used were an initial 2 min denaturation at 98°C, followed by 35 cycles of 98°C for 10 s, 52.5°C for 30 s, and 72°C for 30 s, annealing. A final extension phase of 72°C for 5 min was followed by cooling to 10°C.

PCR products were cleaned using ExoSAP-it® and sequenced directly using NC1 and NC2 primers using BigDye Terminator Cycle Sequencing (Applied Biosystems).

Molecular identification of larvae

Specific identity of first-stage larvae used for gastropod infection (L3 description) and from the woodland caribou (UC178-2) was also based on PCR and sequencing of the ITS-2 region of the nuclear ribosomal DNA. DNA lysis was performed as described above, and PCR was done using the same NC1 and NC2 primers. Each in 20 μL reactions contained 10.2 μL of water, 4 μL of 5× PCR buffer + Mg, 0.4 μL of 10 mmol dNTPs, 2 μL (10 μM) of each primer, 0.2 μL of Taq Phusion HF DNA polymerase, 0.2 μL of bovine serum albumine (20 mg/mL), and 1 μL of DNA template. The amplification conditions used were the same as described above. PCR products were also cleaned and sequenced as previously described, and sequences analyzed accordingly. Representative sequences were deposited in GenBank.

Sequence analyses

Direct sequences at the ITS-2 locus of adults and larvae of V. eleguneniensis produced in the present study were edited using FinchTV 1.4.0 (Geospiza Inc.) and MEGA version 5 [37]. ITS-2 sequences were compared with those of putative V. eleguneniensis sequences [12],[15], and those for other protostrongylids from eight genera and 13 species represented in the original finding of this new species [12] and available from GenBank: Varestrongylus alpenae (AY648407), Parelaphostrongylus andersoni (AF504030), Parelaphostrongylus odocoilei (AF504031), Parelaphostrongylus tenuis (Dougherty, 1945) (AF504029), Elaphostrongylus rangiferi (Mitskevitch, 1960) (EU018482, AF504033), Elaphostrongylus alces Stéen, Chabaud & Rehbinder, 1989 (AF504034), Elaphostrongylus cervi Cameron, 1931 (AF504026), Umingmakstrongylus pallikuukensis Hoberg, Polley, Gunn & Nishi, 1995 (AY648409), Muellerius capillaris (Mueller, 1889) (AY679527), Cystocaulus ocreatus (Railliet & Henry, 1908) (EU018481), Orthostrongylus macrotis (Dikmans, 1931) (EU018483), Protostrongylus stilesi Dikmans, 1931 (EU018484), and Protostrongylus rufescens (Leuckart, 1965) (EU018485). Sequences were then aligned using PRANK, a probabilistic multiple alignment program available through the European Bioinformatics Institute (

The maximum identity of the V. eleguneniensis ITS-2 sequences (including range, average and SD) obtained in this study and those previously produced for this species [12],[15] was calculated using the pairwise distance matrix produced by Geneious [38]. In order to test the hypothesis of conspecificity of isolates, including the holotype and paratypes for V. eleguneniensis, and selected sequences from [12] (n = 8) and [15] (n = 2), an unrooted neighbour-joining tree was designed in Geneious [38], using the substitution model HKY, with gaps treated as complete deletion, and 5,000 bootstrap replicates, including also the sequences of all protostrongylid species mentioned above.

Other specimens examined

Specimens of Varestrongylus alces Demidova & Naumitscheva, 1953, V. alpenae, Varestrongylus pneumonicus Bhalerao, 1932, Varestrongylus sagittatus (Mueller, 1890), and specimens attributable to Varestrongylus capreoli (Stroh & Schmid, 1938) (referred as Varestrongylus cf. capreoli in [20]) available in the USNPC were examined and compared to those of the undescribed species during the development of the morphological description (see Table one from [20]). Representative specimens of other species were not immediately available for comparison.

Community consultation

The first DSL confirmed as belonging to this novel protostrongylid species were isolated from feces of a barrenground caribou belonging to the Bluenose East herd that ranges in the Sahtu Settlement Area (SSA), NT [12] and vicinities. Therefore, we returned to three communities in the SSA: Deline (Délînê), Fort Good Hope (Rádeyîlîkóé), and Colville Lake (K’áhbamį́túé), where Sahtu Dene elders and hunters were consulted on naming the parasite species in their language. The name proposed was based on the North Slavey (Sahtúot’ı̨nę Yatį́) language, which belongs to the northwestern Canada group of the Northern Athabaskan language family [39].


Lung and fecal analyses, and specimens examined

No gross pulmonary lesions indicative of parasite infection were observed in the three muskoxen and one caribou. Nine entire male and four entire female nematodes and four male fragments and five female fragments containing relevant morphological characteristics were recovered from four muskoxen and the woodland caribou (Table 1). Also, numerous DSL and eggs containing different developmental stages (from morula to fully developed DSL) were found in lung washes. Results for larvae per gram (LPG) of feces for the muskoxen and the woodland caribou are provided in Table 1.

Molecular findings

Genetic identity (similarity) based on ITS-2 sequences from 10 adult nematodes from this study and DSL belonging to the putative species of Varestrongylus discovered and reported by Kutz et al. [12],[15] was 95–100% (98.7 ± 1.4). The neighbor-joining tree supports the conspecificity of these widespread populations of Varestrongylus represented by adults and larval parasites (Figure 1). Further, reciprocal monophyly is demonstrated relative to the putative sister species within Varestrongylus (99.3 bootstrap support), and homologous sequences are distinct among other species of Varestrongylus where molecular data are available (see [20]; present study). The independent nature of Varestrongylus among related protostongylids and within the subfamilies Elaphostrongylinae, Muelleriinae, and Protostrongylinae is confirmed. Sequences from adult nematodes were deposited in the GenBank under accession numbers: JQ478644–49 for muskox isolates and for JX115006–07 for caribou isolates; all of these are linked to vouchers in the type series in the USNPC (see Table 1). Representative ITS-2 sequences were deposited for DSL used for gastropod infection and from the same caribou (JQ478650 and JQ478651, respectively).

Figure 1

Unrooted neighbor-joining tree of the ITS-2 region, demonstrating reciprocal monophyly of Varestrongylus eleguneniensis . Unrooted neighbor-joining tree based on HKY distances at the ITS-2 region of the nuclear ribosomal DNA, demonstrating the identity of adult and larval specimens of V. eleguneniensis produced in the current study and those previously attributed to an unknown species of Varestrongylus at high altitudes of North America. Selected sequences shown in this tree represent adults, L1 and L3 of V. eleguneniensis from the current study, L1 ‘Protostrongylid’ from [12] and L1 of ‘Varestrongylus sp.’ from [15]. Sequences at the ITS-2 locus for other genera and species of protostrongylids included those used in the original comparisons by [12]; GenBank accession numbers in Methods). Bootstraps (5,000) values are only shown for branches with over 95% support. Superscript (*) refers to the holotype and (**) to paratypes of V. eleguneniensis deposited at the United States National Parasite Collection (see Table 1).


Varestrongylus eleguneniensis sp. n.

General description: (Figures 2, 3, 4, 5, 6, 7 and 8). Protostrongylidae, Varestrongylinae, minuscule, thread-like nematodes, reddish-brown prior to fixation, with delicate cuticle marked by transverse striations. Cephalic extremity bluntly rounded. Buccal aperture surrounded by four papillae. Esophagus cylindrical, clavate, broadening at base, poorly demarcated into muscular and glandular regions. Nervering indistinct, located in anterior third or mid-third of esophagus; minuscule cervical papillae and excretory pore usually situated posterior to nerve ring, in middle or posterior third of esophagus.

Figure 2

Varestrongylus eleguneniensis sp. n. female. 2. Cephalic extremity at ventral view. 3. Caudal extremity at lateral view, note poorly developed provagina.

Figure 3

Varestrongylus eleguneniensis sp. n. male, caudal extremity. 4. Ventral view, note the dorsally notched copulatory bursa and the disposition of bursal rays, and bifurcate gubernaculum. 5. Ventro-lateral view, note the denticulate plate of crura, and genital protuberances. 6. Lateral view: spicule, partially covering gubernaculum, denticulate plates of crura. 7. Ventral view, detail on the elongate, bifurcate dorsal ray, and genital protuberances.

Figure 4

Varestrongylus eleguneniensis sp. n. male. 8. Ventral view of gubernaculum and denticulate plates of crura. 9. Lateral view of gubernaculum and denticulate plates of crura, and poorly developed telamon plate. 10. Lateral view of spicule; 11. Lateral view of spicule tip, non-split and ending in a finger-like projection.

Figure 5

Varestrongylus eleguneniensis sp. n. larval stages. 12. First-stage larva (L1 or dorsal spined-larva, DSL) at lateral view. 13. Detail on caudal extremity of the First-stage larva (dorsal spined-larva) at lateral view. 14. Third-stage larva (L3) at lateral view.

Figure 6

Varestrongylus eleguneniensis sp. n. female. 15. Cephalic extremity of a female specimen at ventral view, note the claviform esophagus, nerve-ring (nr), and cervical papillae (cp), excretory pore (ep) located at posterior third of esophagus (40×).16. Caudal extremity of a female specimen at lateral view, note the poorly developed provagina, genital protuberance (gp) and vaginal opening (v), (40×).17. Caudal extremity of a female specimen at lateral view, showing the anus (a), and the conical tail (40×).

Figure 7

Varestrongylus eleguneniensis sp. n. male. 18. Caudal extremity ventral view: cuticular striations, denticulate plates of crura (dc), (40×). 19. Caudal extremity at lateral view showing disposition of the bursal rays: ventral (v), externo-lateral (el), medio-lateral (ml), postero-lateral (pl), externo-dorsal (ed), dorsal (d) (40×). 20. Caudal extremity at lateral view: distal portion of spicule and gubernaculum, and gubernaculum (dashed arrows) and denticulate plates of crura (dc), (100×). 21. Detail on caudal extremity of a male specimen: crura (c), and genital protuberances (arrows) (160×). 22. Lateral view of the tip of protruded spicule, non-split and ending in a finger-like projection (100×).

Figure 8

Varestrongylus eleguneniensis sp. n. third-stage larva (L3). 23. Cephalic extremity of L3 at dorsal view: buccal structures, stylets (arrows), and anterior part of esophagus (100×). 24. Caudal extremity of L3 at lateral view: detail on the cuticular striations, anus (a), and tail spike (ts) or caudal protuberance (64×).

Males: Based on specimens in muskoxen (8 intact males, including holotype, and two posterior end fragments) and caribou (one intact male, one anterior end, and one posterior end). Total length (n = 10) 8.8–14.7 mm (11.2 ± 1.64); maximum width (n = 10) 78–147 (102.7 ± 18.08) attained approximately at mid-body. Esophagus (n = 9) 247–395 (325.7 ± 51.23) long, 44–62 (50.9 ± 6.35) wide, (n = 8) 2.8–3.5% (2.9 ± 0.46%) of body length. Nerve-ring (n = 7) 87–196 (142.1 ± 37.11), cervical papillae (n = 4) 151–215 (187.5 ± 27.43), excretory pore (n = 7) 147–242 (202.3 ± 37.27) from cephalic extremity. Copulatory bursa rounded, lacking distinct lobes, slightly notched at posterior margin. Bursal rays approaching, but rarely attaining margin of bursa. Body width at bursa (n = 12) 50–75 (59.2 ± 6.90), bursa length (n = 11) 65–91 (79.5 ± 7.27), bursa width (n = 11) 95–135 (110.2 ± 9.77). Ventroventral and lateroventral rays equal, arising from common stalk, parallel to one another, tips of rays distally separate, and directed anteriad and isolated from others. Lateral rays arising from common base; externo-lateral elongate, reaching margin and isolated from medio- and postero-lateral rays. Medio-lateral ray long and postero-lateral ray reduced, tips separate from near middle or less than half of common stalk. Externo-dorsal rays long, origins independent from base of dorsal ray. Dorsal ray elongate (n = 9) 23–39 (29.2 ± 6.10) long, (n = 8) 21–31 (26.8 ± 3.11) wide at base. Dorsal ray bifurcated near middle or posterior third (n = 9) 11–26 (17.9 ± 5.67) from base, representing (n = 9) 47–78% (60.6 ± 13%) of dorsal ray length; bifurcation with a single papilla, each of two branches containing two pedunculate papillae, disposed on postero-ventral margin. Spicules equal, symmetrical, yellowish brown (n = 12) 105–148 (126.8 ± 12.62) in length; prominent paired alae arising in anterior third (determined from capitulum) extending to near distal spicule tip; alae strongly trabeculate through most of length, with trabeculae becoming indistinct distally. Shaft of spicule not split, tip blunt rounded at extremity, claw-like at lateral-view. Gubernaculum lacking capitulum, composed of bifurcate corpus with paired legs and paired denticulate plates of crura. Corpus thin, arched, elongate (n = 11) 60–86 (73.4 ± 6.95) in total length; composed unpaired anterior portion (body) (n = 11) 32–57 (42.1 ± 6.66) long, bifurcating in two lateral legs (n = 11) 23–36 (31.3 ± 4.27) long, near mid-length; distal tips of legs of gubernaculum situated slightly ventral and medial between denticulate plates of crura. Crurae plates (n = 11) 15–25 (19.5 ± 2.91) long, each with 4–5 denticulate processes (usually five), often not equally distributed in individual specimens; axis of plates slightly twisted. Denticulate crurae with delicate wing-like expansions extending anteriad from proximal end; appear joined ventrally (across corpus split/legs) by relatively narrow hyaline band of tissue. Post-cloacal papilliform protuberances situated antero-ventral to cloaca, disposed ventrally to base of dorsal ray. Telamon present, bar-like at lateral view and poorly developed.

Females: Based on specimens from muskoxen (allotype, three additional entire females, and cephalic or caudal extremities). Total length (n = 3) 18.4–21.3 mm (19.4 ± 1.63); maximum width (n = 4) 108–195 (147.3 ± 36.09). Esophagus (n = 4) 265–332 (313.8 ± 28.89) long and 39–64 (49.8 ± 9.04) wide, (n = 3) 1.2–1.8% (1.6 ± 0.32) of body length. Nerve-ring (n = 3) 63–156 (118.7 ± 49.14), cervical papillae (n = 2) 189–217, excretory pore (n = 2) 154–237 from cephalic extremity. Uteri paired, prodelphic; sphincter at termination of uterine limbs (n = 4) 52–57 (54.5 ± 2.89) long. Vagina uterina voluminous, (n = 4) 260–598 (468.8 ± 154.39) long, extending posteriad from sphincter (n = 4) 52–57 (54.5 ± 2.89), vagina vera (n = 4) 62–117 (99 ± 25.26) in length. Vulvar aperture on solid knob-like protuberance; body width at vulva (n = 7) 57–78 (68.4 ± 11.86). Provagina reduced with hood-like fold extending from anterior lip of vulva ventrally across prominent genital protuberance. Perivulval pores situated bilaterally at level of vulva and genital protuberance. Anus in middle to distal third between vulva and tail tip; distance vulva-anus (n = 7) 99–166 (131.3 ± 22.38); vulva-tail (n = 7) 143–215 (178.6 ± 24.76). Tail conical (n = 8) 39–55 (46.3 ± 6.39) long, with lateral phasmids near apex.

Ova: Eggs, as determined in lung washes from caribou UC-178-2, spherical to ovoid with delicate, smooth shell (n = 20) 60–78 (68.4 ± 5.39) long by 57–74 (64.9 ± 5.06) wide.

First-stage larvae: Body slender, often coiled in life, with paired lateral alae extending from near cephalic extremity to near anus. Tail composed of three segments defined by prominent folds; dorsal spine at level of insertion of the proximal tail fold; tail tip with acutely pointed terminal spike. Meristic data provided in Kutz’s original findings [12], and compared in Table five of [20].

Second-stage larvae: Transitional larval stage, non-diagnostic, characterized by variation in developmental attributes relative to age of infection in intermediate host. Usually cuticle of L1 retained; interior of body often appearing vacuolated.

Third-stage larvae: Based on 21 fully developed L3 recovered from digested D. laeve. Total length (n = 21) 453–540 (497 ± 25.95). Cephalic extremity with papillae surrounding oral aperture. Buccal cavity with prominent, paired stylet-like structures (n = 5) 7.5–8.5 (7.9 ± 0.42). Esophagus claviform (n = 20) 151–210 (178 ± 14.12) long and 14–21 (16.4 ± 2.14) wide, with bulbous formation in anterior; (n = 20) 30–42% (35.9 ± 3.1) of body length. Body width at esophageal base (n = 20) 23–40 (29.8 ± 4.5). Nerve-ring (n = 20) 71–94 (83.8 ± 5.66) in anterior half of esophagus, excretory pore (n = 19) 92–119 (105.5 ± 6.6), and genital primordium (n = 7) 288–400 (349.4 ± 46.7), from cephalic extremity. Tail (n = 21) 25–34 (29.4 ± 3.5) in length, with spike-like protuberance located ventrally on tip (n = 21) 2–5 (3 ± 0.88), structurally variable, ranging from bluntly rounded to slightly elongate and acute.

Additional data based on four fully developed L3 recovered from digested D. reticulatum. Total length (n = 4) 451–541 (491 ± 37.34). Esophagus (n = 4) 163–187 (180.3 ± 11.53) long and 15–18 (16.3 ± 1.26) wide, (n = 4) 35–38% (36.8 ± 1.5) of body length. Body width at oesophageal base (n = 4) 31–34 (31.8 ± 1.5). Nerve-ring (n = 2) 72–85 (78.5 ± 9.19), excretory pore (n = 4) 90–108 (101.8 ± 8.5), and genital primordium (n = 3) 301–384 (336.6 ± 42.85), from cephalic extremity. Tail (n = 4) 26–31 (29.8 ± 2.5) in length, with spike-like protuberance located ventrally on tip (n = 4) 2.5–4 (3.3 ± 0.61).

Taxonomic summary

Type-host: Muskox, Ovibos moschatus wardi (Lyddeker, 1900).

Additional hosts: Woodland caribou, Rangifer tarandus caribou (Gmelin, 1788). Also known in Rangifer tarandus groenlandicus (Borowski, 1780), Rangifer tarandus grantii (Allen, 1902), Alces americanus gigas Miller 1899, and Ovibos moschatus moschatus (Zimmermann, 1780) (in part based on sequence comparisons from Kutz’s original findings [12]).

Intermediate hosts: Natural gastropod intermediate host: Deroceras laeve (Müller, 1774) [12]. Experimental intermediate host: Deroceras reticulatum (Müller, 1774).

Predilection site: Adult males and females occur in terminal bronchioles and alveoli of lungs based on recovery of few intact worms from repeated tracheal washes, and dissection of minute bronchi.

Type-locality: Tasiujaq, Nunavik Region, Quebec, Canada (58°44′51″N, 70° 02′ 06″W).

Additional localities: Near Tasiujaq and type locality (58° 44′ 10″N; 69° 34′ 18″W); near Kuujjuaq, Nunavik Region, Quebec (58° 45′ 00″N; 68° 33′29″W); and the Cold Lake Air Weapons Range, Alberta, Canada (55° 2′ 25″N; 110° 34′5″W) (type series). Also known to be widely distributed across high latitudes of North America based on prior sampling of DSL (see Table two in [12]).

Type-specimens: Adult specimens: Holotype male from type-host and locality on 7 April 2010 collected by G. Verocai, S. Kutz and M. Simard, USNPC 103740 (GenBank JQ478646). Allotype female on 8 April 2010 collected by G. Verocai, S. Kutz and M. Simard from O. m. wardi near type-locality adjacent to Tasiujaq, Quebec, USNPC 103741. Paratypes include males and females in host Om-10-2007 (1 vial), USNPC 103743 collected by M. Simard on 21 March 2007 at Kuujjuaq, Quebec; Om-02-2010 (9 vials), USNPC 103742 (GenBank JQ478649), 103748 (GenBank JQ478647), and 103749 (GenBank JQ478648); and Om-10-2010 (7 vials), USNPC 103744 (GenBank JQ478644-5), collected by G. Verocai, S. Kutz and M. Simard in O. m. wardi in Kuujjuaq in animals from Tasiujaq and Kuujjuaq (Table 1), respectively, Nunavik Region, Quebec, on April 7th and 8th , 2010. Additional paratypes from woodland caribou (UC178-2) from the Cold Lake herd, Alberta, found road killed in November 23rd 2010 (Bob McClymont, Alberta FWD), collected by G. Verocai on October, 2011, USNPC 105697 (GenBank JX115006), 105698, and 105699 (GenBank J115007). First-stage larvae: Paratypes in Om-02-2010 under accession number USNPC 103742. Additional paratypes used for DSL morphometric and molecular data in [12] are available under the following accession numbers: O. m. wardi, Nunavik, QC, USNPC 98648–98652 (GenBank EU018464, 018465, 018479); and R. t. granti, North Alaska Peninsula, AK, USNPC 10585, 10586, and 10589 (GenBank EU018478). Third-stage larvae: L3 paratypes recovered from experimentally infected terrestrial slug D. reticulatum, in September 2008 by J. Ouellet, USNPC 103745 (matching DSL: USNPC103747), and March 2010 by G. Verocai, USNPC 103746 (GenBank JQ478650); and experimentally infected terrestrial slug D. laeve by G. Verocai in September 2011, USNPC 107784.

Etymology: The specific name, “eleguneniensis” denotes the extensive geographic distribution across northern North America for this protostrongylid. The derivation is from the North Slavey language spoken by the Dene people from the Sahtu Settlement Area, NT, Canada, in which “elegu” means cold and “nene” means land. The term “elegunene” is used by them to refer to the northern lands. This specific name is in recognition of over a decade of collaboration with the Sahtu Dene supporting wildlife health and parasitology research in northern Canada [40].

Differential diagnosis

In the context of our studies, we accept the validity of the Varestrongylinae and placement of the genus Varestrongylus within this restricted group of protostrongylids see [1],[2]. Following the characterization of V. eleguneniensis the genus now contains ten valid species of lungworms typical of caprine bovids and cervids across the Holarctic [1],[12],[18]-[20]. Species are mainly diagnosed by the structure of the copulatory bursa and its rays, and configuration of the spicules and gubernaculum (corpus and plate-like paired crurae) in males and by the structure of provagina in females [1],[16],[17]. Varestrongylus eleguneniensi s is established based on an integration of comparative morphological and molecular criteria for adults and larval parasites.

Adult nematodes: Consistent with the current generic diagnosis, males of V. eleguneniensis possess prominent, paired denticulate plates of the crurae disposed slightly lateral, dorsal and distal to the legs of the gubernaculum, and a configuration of bursal rays typical to the genus. In females there is a reduced provagina.

Males: Among males (Table 2), V. eleguneniensis is immediately distinguished by the dimensions of its miniscule spicules from: V. alpenae; Varestrongylus capricola Sarwar, 1944; Varestrongylus longispiculatus Liu, 1989; V. pneumonicus; Varestrongylus qinghaiensis Liu, 1984; V. sagittatus; and Varestrongylus tuvae (Boev & Sulimov, 1963); we refer to these seven species as ‘long-spicule forms’ [20]. In contrast, spicules of V. eleguneniensis are small (105–148 μm) compared to > 200 μm for all of the above species. Further, the diminutive, split gubernaculum (60–86 μm) of V. eleguneniensis contrasts with the solid, rod-like corpus typical of V. capricola, V. longispiculatus, V. pneumonicus and V. tuvae. The split gubernaculum in other long-spicule forms of Varestrongylus (V. alpenae, V. qinghaiensis and V. sagittatus), has legs that are usually fused by a poorly cuticularized membrane. Varestrongylus eleguneniensis is distinguished from all others by the configuration of the denticulate plates of crurae e.g., [1],[18],[19].

Table 2 Comparative morphometry of males of all valid species within the genus Varestrongylus

Specimens of V. eleguneniensis are further characterized and distinct from congeners based on a combination of attributes of the male genital system and copulatory bursa. The conformation of the gubernaculum allows recognition of two groups in the genus: (i) species in which the corpus is distally bifurcate with an evident separation of anterior (corpus) and posterior (legs) regions (V. eleguneniensis, V. alces, V. alpenae, V. capreoli and V. qinghaiensis); or (ii) where the corpus is entire, and usually rod-like, without distal legs (V. pneumonicus, V. sagittatus, V. capricola, V. tuvae and V. longispiculatus). Further, the distal extremity of the spicules can be either: (i) entire (V. eleguneniensis, V. capreoli, V. alces, V. longispiculatus and V. qinghaiensis); or (ii) branched (V. pneumonicus, V. sagittatus, V. alpenae, V. capricola andV. tuvae). In general, in species of Varestrongylus spicules are equal in length, except for those in V. qinghaiensis and V. longispiculatus, whose spicules are sub-equal. Species can also be divided in two groups based on length of the dorsal ray: (i) where the dorsal ray is short, rounded and often indistinct (V. pneumonicus, V. sagittatus, V. capreoli, V. capricola, V. tuvae and V. qinghaiensis); or (ii) where the dorsal ray is elongate with prominent papilliform structures (V. eleguneniensis, V. alces, V. alpenae and V. longispiculatus).

Although males of V. eleguneniensis are immediately distinguished from seven congeneric species based on spicule length, specimens are most similar to those of V. alces and V. capreoli in the overall dimensions of the spicules, and structure and dimensions of the gubernaculum. Collectively, these three species characterize the small-spicule forms within the genus. Although equivalent in length, the morphology of the spicule tips and alae effectively distinguish V. eleguneniensis from V. capreoli and V. alces. Spicules are distally entire in the three species, but for V. eleguneniensis the paired spicule alae taper distally, are not inflated, and do not reach the apex of the spicule tip; in V. alces, a somewhat spatulate condition is apparent distally [20]. The form of the denticulate plates of the crurae is an additional diagnostic feature among these three species. In V. eleguneniensis and V. alces the relatively “stocky” plates are twisted on the longitudinal axis and have a similar number of denticulate processes, 4–5 in the former and always 5 in the latter; plates in V. alces contrast with V. eleguneniensis in being strongly arched in dorso-ventral view. In contrast to these species, V. capreoli (and specimens identified as V. cf. capreoli) has strongly triangular plates armed with four acute, prominent teeth. Telamon plates of V. eleguneniensis and V. capreoli are bar-like and poorly developed, whereas in V. alces, these are slightly more developed and triangular in lateral view. The bursa of V. eleguneniensis and V. alces is dorsally notched with an indistinct dorsal lobe, differing from V. capreoli, in which it is weakly bi-lobed. Also, the relative disposition of bursal rays in V. eleguneniensis is comparable to that of V. alces, but differs from that of V. capreoli: the dorsal ray in V. alces is slightly elongate and bifurcate instead of short and rounded and the externo-dorsal lateral rays originate independently from each other. Ventral rays in the three species originate from a common stalk, but are distally split in V. eleguneniensis and V. alces, and basally split in V. capreoli.

Females: Females of V. elegunieniensis differ from V. capreoli and V. alces, and all other valid species of Varestrongylus, by having a strongly reduced provagina (Table 3). The only other species with a reduced provagina is V. capricola, although the relative degree of development exceeds that observed in V. eleguneniensis. Among other members of Varestrongylus, the well-developed provagina (at different degrees) is a membranous, tubular structure extending posterior from the vulva along the ventral aspect of the tail anterior to the anus. Eggs are expelled from the vulva after and are released posterior to the genital protuberance through this series of tubular membranes.

Table 3 Comparative morphometry of females of all valid species within the genus Varestrongylus

Identification of DSL and L3 stages: Attributes of DSL and L3 stages, but not the L2, were considered because these are the larval stages of diagnostic relevance. We compared morphometric features of both stages to these of other protostrongylids that may occur in a similar spectrum of hosts, or which potentially may be sympatric with V. eleguneniensis in North America.

The characteristic dorsal-spine readily separates V. eleguneniensis DSL from L1 of species within the Subfamily Protostrongylinae (including known or potentially sympatric Pr. stilesi, Protostrongylus rushi Dikmans, 1937, and O. macrotis), but it is shared among all genera/species within the Subfamilies Elaphostrongylinae and Muelleriinae [2],[12]. The morphometry of DSL of V. eleguneniensis may overlap not only with other Varestrongylus species as previously mentioned, but also with those of other genera within Elaphostrongylinae and Muelleriinae, although larvae of V. eleguneniesis are generally shorter than those of the sympatric Parelaphostrongylus spp., and U. pallikuukensis[3],[12],[15]. DSL of V. eleguneniensis are also shorter than those of Elaphostrongylus spp. [3],[20],[44]. The importance of differentiating these two is uncertain as it is unclear if the new species occurs in sympatry with E. rangiferi in Newfoundland, Eastern Canada, where this Eurasian protostrongylid has been introduced [45],[46].

The L3 stage of V. eleguneniensis appears to be similar to those of species within Varestrongylus and Elaphostrongylinae, in which all have a caudal protuberance. Despite this similarity, L3 of elaphostrongylines that geographically co-occur with V. eleguneniensis (Parelaphostrongylus spp. and, potentially, E. rangiferi) are generally double the size of these of V. eleguneniensis, and larval total length may be useful for identification at the generic level (i.e., Varestrongylus) (see Table 4; [3],[47],[48]. L3 of V. eleguneniensis can easily be distinguished from those of species within Muelleriinae, in particular the sympatric U. pallikuukensis, in which the rounded tail lacks a caudal protuberance [6],[35]. Further, L3 of V. eleguneniensis appear undistinguishable from those of V. alpenae, although the geographic range of this latter is not well characterized, and it is not certain if these congeners may occur in sympatry or are characterized by parapatric ranges in North America. Morphometric data of L3’s should be cautiously interpreted since intra-specific variation exists mainly related to age of larva (i.e., early, intermediate, or late stage, e.g. [36]), but also may reflect variation related to development in different gastropod species.

Table 4 Comparative morphometrics of L3 of Varestrongylus eleguneniensis and selected Protostrongylidae species (Varestrongylinae, Elaphostrongylinae, Muellerinae)

Emended diagnosis of Varestrongylus Bhalerao, 1932

Details from the current study and description of V. eleguneniensis along with the recent resurrection of V. alces[20] have made it necessary to propose an emended diagnosis for the genus in order to accommodate adequate recognition of some morphological attributes typical of Varestrongylus. The need for an emended diagnosis reflects inconsistency in prior descriptions and the names applied to designate some structural features (e.g. [1],[20],[28],[42]). We, hereby, emend the generic diagnosis of Varestrongylus as follows:

Varestrongylus Bhalerao, 1932 (syn. Strongylus Müller, 1780 (in part., sensu Mueller 1891)); Protostrongylus Kamensky, 1905 (in part.); Synthetocaulus Railliet & Henry, 1907 (in part.); Bicaulus Schulz & Boev, 1940; Leptostrongylus Dougherty & Goble, 1946; Capreocaulus Schulz & Kadenazy, 1948, Cystocaulus Boev, 1950 (in part.).

Metastrongyloidea: Protostrongylidae: Varestrongylinae. Male: dorsal ray of copulatory bursa short or elongate, sometimes almost reduced (V. capreoli, V. tuvae); apex sometimes bifurcate (V. alpenae, V. longispiculatus, V. eleguneniensis) with variable number of small papillae. Postero-lateral rays of bursa considerably shorter than medio-lateral rays. Telamon plates variable: complex structure (V. tuvae), poorly developed, or absent (V. qinghaiensis). Spicules of filamentous composition, distally entire or bifurcate, provided with alae and lacking manubrium. Capitulum of gubernaculum present (V. capreoli sensu stricto) or absent. Body of gubernaculum in form of long, narrow, and usually colorless structure, entire or distally bifurcate as distinct legs. Paired plates of crurae of gubernaculum (sometimes referred as feet) independent of body or fused by hyaline membrane and in form of two structures with odontoid processes on their edges (denticules) (except in V. tuvae, which has smooth feet). Female: provagina always present; reduced (V. eleguneniensis, V. capricola) or well-developed; tail conical, pointed, often acute. First-stage larva with dorsal spine on tail insertion (DSL), tip of tail kinked and composed by three segments defined by transverse folds. Third-stage larvae possess morphologically variable caudal protuberance. Parasites of lungs in Cervidae: Cervus and Dama (Cervinae), and Capreolus, Alces, Rangifer, Odocoileus (Odocoileinae); and Bovidae (Caprinae): Ovis, Pseudois, Capra, Ovibos, and Budorcas. Valid species: V. sagittatus (Mueller, 1890) Dougherty, 1945; V. pneumonicus Bhalerao, 1932; V. alpenae (Dikmans, 1935) Dougherty, 1945; V. capreoli (Stroh & Schmid, 1938) Dougherty, 1945; V. capricola Sarwar, 1944; Varestrongylus alces Demidova & Naumitscheva, 1953; V. tuvae (Boev & Sulimov, 1963) Boev, 1968; Varestrongylus qinghaiensis Liu, 1984; Varestrongylus longispiculatus Liu, 1989; V. eleguneniensis (present study).


Varestrongylus eleguneniensis sp. n. is the first protostrongylid ‘true lungworm’ to be described in caribou and is also found in muskoxen and, less often, moose from boreal to Arctic environs of North America, with exception of High Arctic islands of the Canadian Archipelago and Greenland. The description of this species corroborates the discovery of a previously unknown protostrongylid circulating in ungulates across high latitudes of North America [12]. This new taxon is clearly distinct from other protostrongylids, varestrongylines, and species of Varestrongylus on the basis of morphological attributes of adult males and females. Molecular sequence data confirm the conspecificity of adult and larval parasites, and provide further differentiation among the small-spicule forms known in the genus [12],[15],[20]. Current knowledge of geographic distribution and host associations across an extensive range in the northern Nearctic, combined with phylogenetic analysis based on morphological characters (G. Verocai, E.P. Hoberg, unpublished), suggests that caribou (i.e., subspecies of R. tarandus native to North America) may be the primary host for V. eleguneniensis, as cervids are considered the ancestral hosts for the genus Varestrongylus[13].

Host distribution

Varestrongylus eleguneniensis is the only known protostrongylid lungworm associated with subspecies of Rangifer, and appears to be restricted to the Nearctic. Previous studies have reported only elaphostrongyline protostrongylids in Eurasian reindeer, e.g. [1],[49],[50], and subspecies of caribou or introduced semi-domesticated reindeer from North America [1],[14],[17],[45],[46],[48],[51]-[53]. Prior to the advent of molecular-based diagnostics it is likely that DSL of V. eleguneniensis were identified as P. andersoni in caribou herds across Canada [12],[45],[46],[48]. These two protostrongylids occur in sympatry and cases of mixed infections have been reported [12],[27].

In muskoxen, lung-dwelling protostrongylids were unknown until relatively recently [6],[8]. Muskoxen at high latitudes of North America are infected with U. pallikuukensis and Pr. stilesi, the latter of which is considered to be a result of independent events of host-switching from Dall’s sheep (Ovis dalli dalli Nelson) in areas of sympatry in Northwest Territories, Yukon and Alaska ([8]; Verocai, Adams, Kutz, unpublished observations). All confirmed records of V. eleguneniensis in muskoxen come from populations sympatric to caribou, either through: (i) long-term sympatry as it occurs in the core of muskox range in mainland central Canadian Arctic [12],[15]; (ii) recent translocation events in the 20th century with traceable origins (i.e. Ellesmere Island and Greenland, where protostrongylids have not been detected in caribou nor muskoxen) ([12],[27]; present study); or (iii) occur in areas that lungworms until recent years, due to environmental conditions, could not complete their life cycle, and establish [15]. These findings reinforce the hypothesis that this previously unrecognized species has the caribou as its ancestral host. However, given the high prevalence of V. eleguneniensis found in some muskox populations sympatric with infected caribou ([12],[15]; G. Verocai, M. Simard and S. Kutz, unpublished obs.), we predict that this parasite could be maintained in muskoxen in the absence of caribou.

In contrast to caribou and muskoxen, until now, the Yukon-Alaska moose (Alces americanus gigas Miller, 1899) had never been reported as host of protostrongylid lungworms. Pulmonary protostrongylid parasites appear to be rare in other moose subspecies from the Nearctic, although, in southern latitudes, there has been an isolated report of O. macrotis in naturally infected Alces americanus andersoni Peterson 1952 ([54]; G. Verocai, C. Kashivakura and S. Kutz, unpublished obs.). Moose in Newfoundland are believed to be infected with P. andersoni[46],[53], along with E. rangiferi, but larval identity was not confirmed by molecular techniques and nor were adult worms recovered. Similar to other lungworms, we consider the findings of V. eleguneniensis in moose to be relatively isolated and indicative of incidental infections [12].

Available survey data suggest that V. eleguneniensis is restricted to the Nearctic, and records for protostrongylids in reindeer, Eurasian moose (Alces alces L.), or introduced muskoxen in Eurasia, involve other genera and species. In the Palearctic, only the tissue-dwelling E. rangiferi has been recognized in populations of reindeer (R. t. tarandus L., R. t. fennicus Lönnberg, R. t. platyrhynchus Vrolik) [1]. For instance, there have been reports of E. rangiferi as far east as Buryatia, near Lake Baikal [50]. Yet, studies on reindeer in the Russian Far East are scarce. The irrefutable veterinary importance of E. rangiferi may have led researchers to overlook the potential presence of a small and obscure, pulmonary protostrongylid species such as V. eleguneniensis that are associated with significant gross pathology. However, lesions apparently characteristic of infections by Varestrongylus sp. have recently been observed in semi-domesticated reindeer (R. t. tarandus) from north-central Finland, but the parasite species involved has not been identified (A. Oksanen and S. Laaksonen, Pers. comm., 2010).

The Eurasian moose, congeneric with the North American moose, is recognized as a primary and potentially the only host for V. alces, in Russia, Poland, and Fennoscandia [55]-[61]. Presence of V. eleguneniensis in this host is unlikely, as the parasite seems to only incidentally infect moose in Alaska, and has not been found in assessed moose populations in northern Canada [12]. For introduced muskoxen in Norway and Sweden it is also unlikely that V. eleguneniensis is present. These animals were originally introduced from Greenland, a location where protostrongylids have not previously been detected in caribou or muskoxen [27]. Dorsal-spined larvae have been reported in muskoxen from Norway and Sweden but are most certainly acquired locally [62], and DSL and adult specimens from the Norwegian population were identified as M. capillaris[63]. More extensive field collections are required to completely resolve faunal diversity and host associations for protostrongylids in the northern Palearctic.

Pathology and significance

Varestrongylus eleguneniensis does not appear to cause substantial pulmonary pathology in infected hosts. No gross lesions were observed in any of the muskox and caribou lungs examined in the present study. Also, previously, despite careful examination, our group failed to find lesions in over 50 caribou lungs and over 100 muskoxen lungs from areas that we now know are in the geographic range of V. eleguneniensis[12]. Little is known about its pathology and impact on infected ungulates, although light parasitic pneumonia was histologically demonstrated in muskoxen from the same source population (M. Simard, S. Lair, A. Dallaire, Pers. comm.). Further investigations and histological examination of infected lungs are warranted. In contrast, other species of Varestrongylus, such as V. alces[20],[56], V. capreoli[41], V. alpenae[22],[23], and V. pneumonicus[43], are known to cause gross lesions, and histopathologic changes.

Co-infections of V. eleguneniensis with P. andersoni in caribou (G. Verocai, S. Kutz, unpublished data) and U. pallikuukensis in muskoxen [15] occur, and could have additive effects on the hosts. Co-infections with other protostrongylids that overlap in host and geographic range, such as P. odocoilei in caribou and Pr. stilesi in muskoxen have not been reported. Additionally, another lungworm, Dictyocaulus eckerti Skrjabin, 1931, occurs in caribou and muskox populations across the distribution of V. eleguneniensis[12], and at least one muskox evaluated in this study was co-infected (G. Verocai, M. Simard, S. Kutz, unpublished obs.).

Explorations on historical biogeography

Species of Varestrongylus are known from ungulates of the families Cervidae (six species in Cervinae and Odocoileinae (=Capreolinae)) and Bovidae (four species in Caprinae) in Eurasia and North America ([1],[20],[28]; present study). Eurasia is the center of diversity for both these ungulate groups. The modern tribes of Caprinae and Cervinae originated in Central Asia near 14.7-14.5 Ma (millions of years ago) during the middle Miocene; and Odocoileinae diversified between 11.0-10.0 Ma around the middle and late Miocene boundary [31],[64]. Coincidentally, Eurasia is the center of diversity for species within Varestrongylus, as well as for other members of Protostrongylidae and a substantially broader strongylate nematode fauna in artiodactyls [6],[13],[65],[66]. As a generality, Eurasian biodiversity or species richness among ungulate nematodes considerably exceeds that observed in the Nearctic [13]. Geographically, Varestrongylus is characterized by eight species endemic to Eurasia and the western Palearctic [1],[20] in contrast to V. alpenae and V. eleguneniensis which have distributions restricted to North America ([21]; present study).

The formation of the contemporary North American fauna involved expansion from Eurasia, with successive waves of invasion and geographic colonization during the late Pliocene and Quaternary across the Bering Land Bridge [13],[64],[67]-[69]. A consequence of these episodic processes has been the development of an extensive faunal mosaic coinciding with asynchronous arrival and recurrent establishment of particular ungulate groups and their associated parasite faunas [13],[65],[66],[70]. During these independent events of geographic colonization, the hosts of the two Nearctic species of Varestrongylus entered North America and expanded across much of the continent. The ancestors of O. virginianus, the only known host of V. alpenae, reached the Nearctic around 4 Ma, whereas the three known hosts of V. eleguneniensis invaded and became established in North America in more recent times. Current evidence based on field surveys including collections of adult parasites, fecal examination and sequencing, and studies documenting the distribution of P. andersoni, P. tenuis, P. odocoilei, Protostrongylus coburni Dikmans, 1935, O. macrotis and V. alpenae among species of Odocoileus have not revealed the presence of V. eleguneniensis in relatively southern host populations [3],[10],[11],[13],[21],[28].

Rangifer is a Beringian endemic, and first arrived to North America approximately 2 Ma, but multiple events of expansion and retraction followed during glacial-interglacial cycles of the Pleistocene, with secondary isolation of Rangifer north and south of the Nearctic continental glaciers [71]-[73]. From Beringia, Rangifer also expanded westwards through the Palearctic, resulting in its present Holarctic distribution [71]-[74]. In contrast, the other two hosts of V. eleguneniensis only became established in North America in shallower time. Ovibos (as Ovibos moschatus) expanded into Beringia around 900–700 Ka (thousands of years ago) and, similarly to Rangifer, occurred in isolated populations both in Beringia and environs south of the ice-sheets during the Pleistocene. Currently, natural muskox populations only occur in North America. The species became extinct in the Palearctic in the Holocene [13],[64],[75]. Alces, as a late Pleistocene migrant to the Nearctic, entered the Nearctic only 14–11 Ka, with subsequent eastwards and southwards expansion after the recession of the continental ice [64],[76],[77].

Historical biogeography of these host-parasite assemblages and development of associations of these parasites with cervids and caprines is complex and can be initially considered in the context of phylogenetic inference among the protostrongylids and species of Varestrongylus. An ancestral association with cervids has been proposed for Varestrongylus[13], which is supported by the host-associations of the Elaphostrongylinae, the sister group of Varestrongylinae [2], also primarily parasites of cervids [1],[3],[4],[78]. Concurrently, this supports a primary association of V. eleguneniensis with caribou and secondary host switching to muskoxen and moose in zones of relatively recent to very recent contact, proposed by Hoberg et al. [13]. This primary association is further supported by the current geographic distribution of V. eleguneniensis, which virtually mirrors that of caribou in North America Further, an ancient association with Rangifer may indicate that V. eleguneniensis may also have been a Beringian endemic during the late Pliocene, but since subsequently multiple expansion events of Rangifer have occurred it is impossible to estimate with precision when V. eleguneniensis first arrived in the continent [13],[68].

A limited phylogenetic analysis (based on ITS-2) among five species of Varestrongylus suggests that V. eleguneniesis is genetically closer to V. alces and V. capreoli[20]. This putative association of V. eleguneniensis with these Eurasian species, as opposed to the only other Nearctic species, V. alpenae, appears consistent with at least two independent events of host-parasite invasion from Eurasia, involving Beringia, to the Nearctic during the late Pliocene and Quaternary. The morphological similarities of the two Eurasian species and V. eleguneniensis, which collectively form the ‘short-spicule’ group within Varestrongylus, further support their relationship (see also [20]). Therefore, we hypothesize that two distinct Varestrongylus species crossed Beringia and reached the Nearctic from Eurasia: with V. alpenae and V. eleguneniensis, or their ancestors, invading North America along with Odocoileus and Rangifer hosts, respectively. Based on these empirical data, a primary association of V. eleguneniensis with muskoxen, a caprine host would not be predicted; its presence in muskoxen is likely the result of several independent host switching events in areas of sympatry with infected caribou, including recent events linked to translocations and introductions (see Host Distribution section above). Also, a primary association with muskoxen would be considerably shallow in time; and perhaps, more difficult considering the strong population bottlenecks and extinctions across its range [75],[79]. Contrasting with this distribution, muskoxen are the only recognized hosts for an otherwise relictual protostrongylid species, U. pallikuukensis[6],[80]. Besides its very recent invasion of the Nearctic, infection of moose with V. eleguneniensis is rare and incidental, and is only reported in areas of sympatry with caribou [12].

Considering finer scale geographic and host associations, genetic studies on Rangifer distinguish two main lineages of caribou in the Nearctic, the North-American Rangifer lineage (NAL), which ranged during glacial maxima south of the Laurentide and Cordilleran ice-sheets, isolated from the Beringian-Eurasian lineage (BEL) vastly distributed from Europe to Beringia [71]-[74],[81].The ancient association of V. eleguneniensis with Rangifer and this host’s intricate historical biogeography allow us to articulate testable hypotheses on the historical biogeography and phylogeography of this novel lungworm species: (i) the parasite was maintained within BEL caribou and restricted to Beringia, and expanded along with caribou eastwards and southwards, colonizing NAL populations; (ii) the parasite was maintained both within BEL in Beringia and within NAL south of ice sheets, and expanded geographically with both lineages; (iii) the parasite was maintained within NAL, solely south of the ice sheets in one or multiple refugia and expanded northwards with NAL caribou and, later, colonized and expanded with BEL populations. Future studies on the population genetics of V. eleguneniensis, involving geographically extensive sampling across its vast range in North America, may reveal genetic signatures compatible to such events of expansion and/or isolation within a single or multiple refugia.


Herein we have described and named V. eleguneniensis, a pulmonary protostrongylid with Rangifer as a primary definitive host; that secondarily infects muskoxen and moose in areas of sympatry. The parasite appears to be geographically restricted to North America; however there is a lack of surveys for pulmonary protostrongylids in Rangifer from Eurasia, including western Beringia. Detailed investigations for the presence of V. eleguneniensis, its close relative V. alces, or another Varestrongylus in reindeer from the Palearctic remain necessary. The biogeographic history for two endemic species of Varestrongylus known from North America appears consistent with events of parasite invasion with cervid hosts from Eurasia into North America during the late Pliocene and Quaternary. The putative ancient association with Rangifer hosts could be investigated through the phylogeography of V. eleguneniensis, which may provide new insights on caribou historical biogeography and the history of colonization of the Nearctic by host-parasite assemblages.


  1. 1.

    Boev SN: Protostrongylids. Fundamentals of Nematology, Vol. 25. Edited by: Ryzhikov KM. 1975, Helminthological Laboratory, Academy of Sciences of the USSR, Moscow, [English translation by the U.S. Department of Agriculture, Washington, D.C., and Amerind Publishing Co., New Delhi, 1984]

    Google Scholar 

  2. 2.

    Carreno RA, Hoberg EP: Evolutionary relationships among the Protostrongylidae (Nematoda: Metastrongyloidea) as inferred from morphological characters, with consideration of parasite-host coevolution. J Parasitol. 1999, 85: 638-648. 10.2307/3285736.

    CAS  Article  PubMed  Google Scholar 

  3. 3.

    Lankester MW: Extrapulmonary Lungworms of Cervids. Parasitic Diseases of Wild Mammals. Edited by: Samuel WMP, Pybus MJ, Kocan AA. 2001, Iowa State University Press, Ames, 576-2

    Google Scholar 

  4. 4.

    Carreno RA, Caporossi D, Beade MS, Marull CA, Uhart MM, Markwardt DD, Nadler SA: Discovery of an undescribed protostrongylid nematode from the endangered Pampas deer (Ozotoceros bezoarticus celer) in Argentina. J Wildl Dis. 2012, 48: 724-731. 10.7589/0090-3558-48.3.724.

    Article  PubMed  Google Scholar 

  5. 5.

    Canaris A, Gardner SL: Bibliography of Helminth Species Described from African Vertebrates 1800–1967. Bibliography of Helminth Species Described from African Vertebrates 1800–1967 (eds). 2003, The Harold W. Manter Laboratory of Parasitology, Lincoln

    Google Scholar 

  6. 6.

    Hoberg EP, Polley L, Gunn A, Nishi JS:Umingmakstrongylus pallikuukensis gen. nov. et sp. nov. (Nematoda: Protostrongylidae) from muskoxen, Ovibos moschatus, in the central Canadian Arctic, with comments on biology and biogeography. Can J Zool. 1995, 73: 2266-2282. 10.1139/z95-269.

    Article  Google Scholar 

  7. 7.

    Kutz SJ, Veitch AM, Hoberg EP, Elkin BT, Jenkins EJ, Polley L: New host and geographic records for two protostrongylids in Dall’s sheep. J Wildl Dis. 2001, 37: 761-774. 10.7589/0090-3558-37.4.761.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Hoberg EP, Kutz S, Nagy J, Jenkins EJ, Elkin B, Branigan M, Cooley D:Protostrongylus stilesi (Nematoda: Protostrongylidae): ecological isolation and putative host-switching between Dall’s sheep and muskoxen in a contact zone. Comp Parasitol. 2002, 69: 1-9. 10.1654/1525-2647(2002)069[0001:PSNPEI]2.0.CO;2.

    Article  Google Scholar 

  9. 9.

    Jenkins EJ, Appleyard GD, Hoberg EP, Rosenthal BM, Kutz SJ, Veitch AM, Schwantje HM, Elkin BT, Polley L: Geographic distribution of the muscle-dwelling nematode Parelaphostrongylus odocoilei in North America, using molecular identification of first-stage larvae. J Parasitol. 2005, 91: 574-584. 10.1645/GE-413R.

    Article  PubMed  Google Scholar 

  10. 10.

    Asmundsson IM, Mortenson JA, Hoberg EP: Muscleworms, Parelaphostrongylus andersoni (Nematoda: Protostrongylidae), discovered in Columbia white-tailed deer from Oregon and Washington: implications for biogeography and host associations. J Wildl Dis. 2008, 44: 16-27. 10.7589/0090-3558-44.1.16.

    CAS  Article  PubMed  Google Scholar 

  11. 11.

    Mortenson JA, Abrams A, Rosenthal BM, Dunams D, Hoberg EP, Bildfel RJ, Green RL:Parelaphostrongylus odocoilei in Columbian black-tailed deer from Oregon. J Wildl Dis. 2006, 42: 527-535. 10.7589/0090-3558-42.3.527.

    Article  PubMed  Google Scholar 

  12. 12.

    Kutz SJ, Asmundsson I, Hoberg EP, Appleyard GD, Jenkins EJ, Beckmen K, Branigan M, Butler L, Chilton NB, Cooley D, Elkin B, Huby-Chilton F, Johnson D, Kuchboev A, Nagy J, Oakley M, Polley L, Popko R, Scheer A, Simard M, Veitch A: Serendipitous discovery of a novel protostrongylid (Nematoda: Metastrongyloidea) in caribou, muskoxen, and moose from high latitudes of North America based on DNA sequence comparisons. Can J Zool. 2007, 85: 1143-1156. 10.1139/Z07-091.

    CAS  Article  Google Scholar 

  13. 13.

    Hoberg EP, Galbreath KE, Cook JA, Kutz SJ, Polley L: Northern host-parasite assemblages: history and biogeography on the borderlands of episodic climate and environmental transition. Adv Parasitol. 2012, 79: 1-97.

    Article  PubMed  Google Scholar 

  14. 14.

    Verocai GG, Lejeune M, Finstad GL, Kutz SJ: A Nearctic parasite in a Palearctic host: Parelaphostrongylus andersoni (Nematoda; Protostrongylidae) infecting semi-domesticated reindeer in Alaska. Int J Parasitol: Parasit Wildl. 2013, 2: 119-123.

    Google Scholar 

  15. 15.

    Kutz SJ, Checkley S, Verocai GG, Dumond M, Hoberg E, Peacock R, Wu J, Orsel K, Seegers K, Warren A, Abrams A: Invasion, establishment, and range expansion of two protostrongylid nematodes in the Canadian Arctic. Glob Change Biol. 2013, 19: 3254-3262.

    Google Scholar 

  16. 16.

    Dougherty EC, Goble FC: The genus Protostrongylus Kamenskii, 1905 (Nematoda: Metastrongylidae), and its relatives: preliminary note. J Parasitol. 1946, 32: 7-16. 10.2307/3272696.

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Dougherty EC: The nematode lungworms (Suborder Strongylina) of North American deer of the genus Odocoileus. Parasitol. 1945, 36: 199-208. 10.1017/S003118200001218X.

    Article  Google Scholar 

  18. 18.

    Liu S-X: A new species of protostrongylid lungworm from Takin. Acta Zootax Sinica. 1989, 14: 269-272.

    Google Scholar 

  19. 19.

    Liu W-D: A new species of nematode in the family Protostrongylidae. Acta Zootax Sinica. 1984, 9: 8-11.

    Google Scholar 

  20. 20.

    Verocai GG, Hoberg EP, Vikøren T, Handeland K, Ytrehus B, Rezansoff AM, Davidson RK, Gilleard JS, Kutz SJ: Resurrection and redescription of Varestrongylus alces (Nematoda; Protostrongylidae), a lungworm of the Eurasian moose ( Alces alces ), with report on associated pathology.Parasit Vectors 2014, 7:557.,

  21. 21.

    Dikmans G: Two New Lungworms, Protostrongylus coburni n. sp., and Pneumostrongylus alpenae, n. sp. from the Deer, Odocoileus virginianus, in Michigan. T Am Microsc Soc. 1935, 54: 138-144. 10.2307/3222121.

    Article  Google Scholar 

  22. 22.

    Cheatum EL: Disease in relation to winter mortality of deer in New York. J Wildl Manage. 1951, 15: 216-220. 10.2307/3796614.

    Article  Google Scholar 

  23. 23.

    Cheatum EL: A contribution to the life-history of the deer lungworm, Leptostrongylus alpenae (Nematoda: Metastrongylidae), with observations on its incidence and biology. PhD thesis. University of Michigan; 1949.

  24. 24.

    O’Roke EC, Cheatum EL: Experimental transmission of the deer lungworm Leptostrongylus alpenae. Cornell Vet. 1952, 40: 315-323.

    Google Scholar 

  25. 25.

    Prestwood AK, Pursglove SR:Leptostrongylus alpenae in White-Tailed Deer (Odocoileus virginianus) of Georgia and Louisiana. J Parasitol. 1974, 60: 573-10.2307/3278708.

    CAS  Article  PubMed  Google Scholar 

  26. 26.

    Gray JB, Samuel WM, Shostak AW, Pybus MJ:Varestrongylus alpenae (Nematoda, Metastrongyloidea) in white-tailed deer (Odocoileus virginianus) of Saskatchewan. Can J Zool. 1985, 63: 1449-1454. 10.1139/z85-216.

    Article  Google Scholar 

  27. 27.

    Kutz SJ, Ducrocq J, Verocai GG, Hoar BM, Colwell DD, Beckmen K, Polley L, Elkin BT, Hoberg EP: Parasites of ungulates of arctic North America and Greenland: a view of contemporary diversity, ecology, and impact in a world under change. Adv Parasitol. 2012, 79: 99-252.

    Article  PubMed  Google Scholar 

  28. 28.

    Anderson RC: Nematode Parasites of Vertebrates. Their Development and Transmission. 2000, CAB Publishing, Oxford

    Google Scholar 

  29. 29.

    Pilsbry HA: Land Mollusca of North America (north of Mexico). 1946, George W. Carpenter Fund for the Encouragement of Original Scientific Research, Philadelphia

    Google Scholar 

  30. 30.

    Grubb P: Order Artiodactyla. Manual Species of the World: A Taxonomic and Geographic Reference. Edited by: Wilson DE, Reeder DM. 2005, The Johns Hopkins University Press, Baltimore, 652-722.

    Google Scholar 

  31. 31.

    Hernández-Fernández M, Vrba ES: A complete estimate of the phylogenetic relationships in Ruminantia: a date species-level supertree of the extant ruminants. Biol Rev. 2005, 80: 269-302. 10.1017/S1464793104006670.

    Article  PubMed  Google Scholar 

  32. 32.

    Le Hénaff D, Crête M: Introduction of muskoxen in northern Quebec: the demographic explosion of a colonizing herbivore. Can J Zool. 1989, 67: 1102-1105. 10.1139/z89-156.

    Article  Google Scholar 

  33. 33.

    Chubbs TE, Brazil J: The occurrence of muskoxen, Ovibos moschatus in Labrador. Can Field-Nat. 2007, 121: 81-84.

    Google Scholar 

  34. 34.

    Forrester SG, Lankester MW: Extracting protostrongylid nematode larvae from ungulate feces. J Wildl Dis. 1997, 33: 511-516. 10.7589/0090-3558-33.3.511.

    CAS  Article  PubMed  Google Scholar 

  35. 35.

    Kutz S, Hoberg EP, Polley L: Experimental infections of muskoxen (Ovibos moschatus) and domestic sheep with Umingmakstrongylus pallikuukensis (Nematoda: Protostrongylidae): parasite development, population structure, and pathology. Can J Zool. 1999, 77: 1562-1572. 10.1139/cjz-77-10-1562.

    Article  Google Scholar 

  36. 36.

    Kutz SJ, Hoberg EP, Polley L:Umingmakstrongylus pallikuukensis (Nematoda: Protostrongylidae) in gastropods: Larval morphology, morphometrics, and development rates. J Parasitol. 2001, 87: 527-535. 10.1645/0022-3395(2001)087[0527:UPNPIG]2.0.CO;2.

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S: MEGA5: Molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011, 28: 2731-2739. 10.1093/molbev/msr121.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  38. 38.

    Drummond AJ, Ashton B, Buxton S, Cheung M, Cooper A, Duran C, Field M, Heled J, Kearse M, Markowitz S, Moir R, Stones-Havas S, Sturrock S, Thierer T, Wilson A: Geneious v5.5 []

  39. 39.

    Cook E-D, Flynn D: Aboriginal Languages of Canada. Contemporary Linguistic Analysis: An Introduction. Edited by: O’ Grady W, Archibald D. 2008, Pearson Longman, Toronto, 318-333. 6

    Google Scholar 

  40. 40.

    Brook RK, Kutz SJ, Veitch AM, Popko RA, Elkin BT, Guthrie G: Fostering community-based wildlife health monitoring and research in the Canadian North. EcoHealth. 2009, 6: 266-278. 10.1007/s10393-009-0256-7.

    Article  PubMed  Google Scholar 

  41. 41.

    Stroh G, Schmid G:Protostrongylus capreoli nov. sp. der haufigste lungewurm des reher. Berl Tierarztl Wochenschr. 1938, 9: 121-123.

    Google Scholar 

  42. 42.

    Bhalerao GD: On some nematodes of goat and sheep of Mutkesar. Ind J Vet Sci. 1932, 2: 242-254.

    Google Scholar 

  43. 43.

    Bhatia BB, Pande BP: Studies on lungworms (Metastrongylidae Leiper, 1908) parasitising Indian livestock II. Observations of natural infestations with species of Dictyocaulus Railliet and Henry, 1907 and Varestrongylus Bhalerao, 1932 in the sheep of hills of Uttar Pradesh. Proc Nat Acad Sci, India B. 1960, 30: 217-233.

    Google Scholar 

  44. 44.

    Lankester MW, Olsson IMC, Steen M, Gajadhar AA: Extra-mammalian larval stages of Elaphostrongylus alces (Nematoda : Protostrongylidae), a parasite of moose (Alces alces) in Fennoscandia. Can J Zool. 1998, 76: 33-38. 10.1139/z97-168.

    Article  Google Scholar 

  45. 45.

    Lankester MW, Fong D: Distribution of elaphostrongyline nematodes (Metastrongyloidea, Protostrongylidae) in Cervidae and possible effects of moving Rangifer spp. into and within North America. Alces. 1989, 25: 133-145.

    Google Scholar 

  46. 46.

    Lankester MW, Fong D: Protostrongylid nematodes from caribou (Rangifer tarandus caribou) and moose (Alces alces) in Newfoundland. Rangifer. 1998, 10: 73-83. 10.7557/

    Article  Google Scholar 

  47. 47.

    Ballantyne RJ, Samuel WM: Diagnostic morphology of the third-stage larvae of three species of Parelaphostrongylus (Nematoda, Metastrongyloidea). J Parasitol. 1984, 70: 3-10.2307/3281415.

    Article  Google Scholar 

  48. 48.

    Lankester MW, Hauta PL:Parelaphostrongylus andersoni (Nematoda, Protostrongylidae) in caribou (Rangifer tarandus) of Northern and Central Canada. Can J Zool. 1989, 67: 1966-1975. 10.1139/z89-281.

    Article  Google Scholar 

  49. 49.

    Halvorsen O: Epidemiology of reindeer parasites. Parasitol Today. 1986, 2: 334-339. 10.1016/0169-4758(86)90053-0.

    CAS  Article  PubMed  Google Scholar 

  50. 50.

    Kontrimavichus V, Delyamure SL, Boev SN: Metastrongyloids of domestic and wild animals. Fundamentals in Nematology. Vol 26. Edited by: Ryzhikov KM. 1976, Helminthological Laboratory, Academy of Sciences of the USSR, Moscow, 240-[English translation by the U.S. Department of Agriculture, Washington, D.C., and Amerind Publishing Co., New Delhi, 1984].

    Google Scholar 

  51. 51.

    Hadwen S: Society proceedings: the helminthological society of Washington. J Parasitol. 1922, 9: 38-39.

    Google Scholar 

  52. 52.

    Dikmans G: Helminth parasites North American semidomesticated and wild ruminants. Proc Helminth Soc Washington. 1939, 6: 97-101.

    Google Scholar 

  53. 53.

    Ball MC, Lankester MW, Mahoney SP: Factors affecting the distribution and transmission of Elaphostrongylus rangiferi (Protostrongylidae) in caribou (Rangifer tarandus caribou) of Newfoundland, Canada. Can J Zool. 2001, 79: 1265-1277.

    Google Scholar 

  54. 54.

    Samuel WM, Barrett MW, Lynch GM: Helminths in moose of Alberta. Can J Zool. 1976, 54: 307-312. 10.1139/z76-034.

    CAS  Article  PubMed  Google Scholar 

  55. 55.

    Demidova NV, Naumitscheva MI: A new nematode Varestrongylus alces sp. nov. in moose. Moskovskij Pushno-Mekhovoj Institut Trudy. 1953, 4: 303-306.

    Google Scholar 

  56. 56.

    Petrosyan SL: Pathomorphological changes in the lungs of elks caused by Varestrongylus alces. Helminthologia. 1963, 4: 390-396.

    Google Scholar 

  57. 57.

    Dróżdż J: Studies on helminths and helminthiases in Cervidae II. The helminth fauna of Cervidae in Poland. Acta Parasitol Pol. 1966, 14: 1-13.

    Google Scholar 

  58. 58.

    Nilsson O: The inter-relationship of endo-parasites in wild cervids (Capreolus capreolus L. and Alces alces L.) and domestic ruminants in Sweden. Acta Vet Scan. 1971, 12: 36-68.

    CAS  Google Scholar 

  59. 59.

    Stuve G:Elaphostrongylus cervi infection in moose (Alces alces). Prevalence and pathological changes in relation to age and season. Acta Vet Scan. 1987, 28: 157-164.

    CAS  Google Scholar 

  60. 60.

    Stuve G: The prevalence of Elaphostrongylus cervi infection in moose (Alces alces) in Southern Norway. Acta Vet Scan. 1986, 27: 397-409.

    CAS  Google Scholar 

  61. 61.

    Stéen M, Faber WE, Oksanen A: Disease and genetical investigations of Fennoscandian cervids: a review. Alces. 1998, 34: 287-310.

    Google Scholar 

  62. 62.

    Alendal E, Helle O: Helminth parasites of muskoxen Ovibos moschatus in Norway including Spitsbergen and in Sweden, with a synopsis of parasites reported from this host. Fauna Nor A. 1983, 4: 41-52.

    Google Scholar 

  63. 63.

    Davidson RK, Amundsen H, Lie NO, Luyckx K, Robertson LJ, Verocai GG, Kutz SJ, Ytrehus B: Sentinels in a climatic outpost: endoparasites in the introduced muskox (Ovibos moschatus) population of Dovrefjell, Norway. Int J Parasitol: Parasit Wildl. 2014, 3: 154-160.

    Google Scholar 

  64. 64.

    Kurtén B, Anderson E: Pleistocene Mammals of North America. 1980, Columbia University Press, New York

    Google Scholar 

  65. 65.

    Hoberg EP: Coevolution and biogeography among Nematodirinae (Nematoda: Trichostrongylina), Lagomorpha and Artiodactyla (Mammalia): Exploring determinants of history and structure for the northern fauna across the Holarctic. J Parasitol. 2005, 91: 358-369. 10.1645/GE-3466.

    Article  PubMed  Google Scholar 

  66. 66.

    Hoberg EP, Abrams A, Pilitt PA, Jenkins EJ: Discovery and description of a new trichostrongyloid species (Nematoda: Ostertagiinae), abomasal parasites in Mountain Goat, Oreamnos americanus, from the western Cordillera of North America. J Parasitol. 2012, 98: 817-846. 10.1645/GE-3047.1.

    Article  PubMed  Google Scholar 

  67. 67.

    Hoberg EP, Kutz SJ, Galbreath KE, Cook JA: Arctic biodiversity: from discovery to faunal baselines- revealing the history of a dynamic ecosystem. J Parasitol. 2003, 89: S84-S95. 10.1645/0022-3395(2003)089[0084:DOMPIO]2.0.CO;2.

    Article  Google Scholar 

  68. 68.

    Hoberg EP, Brooks DR: A macroevolutionary mosaic: episodic host-switching, geographical colonization and diversification in complex host-parasite systems. J Biogeogr. 2008, 35: 1533-1550. 10.1111/j.1365-2699.2008.01951.x.

    Article  Google Scholar 

  69. 69.

    Shafer ABA, Cullingham CI, Côté SD, Coltman DW: Of glaciers and refugia: a decade of study sheds new light on the phylogeography of northwestern North America. Mol Ecol. 2010, 19: 4589-4621. 10.1111/j.1365-294X.2010.04828.x.

    Article  PubMed  Google Scholar 

  70. 70.

    Hoberg EP: Invasive processes, mosaics and the structure of helminth parasite faunas. Rev Sci Tech OIE. 2010, 29: 255-272.

    CAS  Google Scholar 

  71. 71.

    Banfield AWF: A revision of the reindeer and caribou, genus Rangifer. Bull Nat Mus Can Biol Ser. 1961, 177: 1-137.

    Google Scholar 

  72. 72.

    Flagstad O, Røed KH: Refugial origins of Reindeer (Rangifer tarandus L.) inferred from mitochondrial DNA sequences. Evolution. 2003, 57: 658-670. 10.1111/j.0014-3820.2003.tb01557.x.

    CAS  Article  PubMed  Google Scholar 

  73. 73.

    Weckworth BV, Musiani M, McDevitt AD, Hebblewhite M, Mariani S: Reconstruction of caribou evolutionary history in Western North America and its implications for conservation. Mol Ecol. 2012, 12: 3610-3624. 10.1111/j.1365-294X.2012.05621.x.

    Article  Google Scholar 

  74. 74.

    McDevitt AD, Mariani S, Hebblewhite M, Decesare NJ, Morgantini L, Seip D, Weckworth BV, Musiani M: Survival in the Rockies of an endangered hybrid swarm from diverged caribou (Rangifer tarandus) lineages. Mol Ecol. 2009, 18: 665-679. 10.1111/j.1365-294X.2008.04050.x.

    CAS  Article  PubMed  Google Scholar 

  75. 75.

    Campos PF, Willerslev E, Sher A, Orlando L, Axelsson E, Tikohonov A, Aaris-Sørensen K, Greenwood AD, Kahlke R-D, Kosintsev P, Krakmalnaya T, Kuznetsova T, Lemey P, MacPhee R, Norris CA, Shepherd K, Suchard MA, Zazula GD, Shapiro B, Gilbert MT: Ancient DNA analyses exclude humans as the driving force behind late Pleistocene musk ox (Ovibos moschatus) population dynamics. Proc Natl Acad Sci U S A. 2010, 107: 5675-5680. 10.1073/pnas.0907189107.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  76. 76.

    Hundertmark KJ, Bowyer RT, Shields GF, Schwartz CC: Mitochondrial phylogeography of moose (Alces alces) in North America. J Mammal. 2003, 84: 718-728. 10.1644/1545-1542(2003)084<0718:MPOMAA>2.0.CO;2.

    Article  Google Scholar 

  77. 77.

    Hundertmark KJ, Shields GF, Udina IG, Bowyer RT, Danilkin AA, Schwartz CC: Mitochondrial phylogeography of moose (Alces alces): late Pleistocene divergence and population expansion. Mol Phylogenet Evol. 2002, 22: 375-387. 10.1006/mpev.2001.1058.

    CAS  Article  PubMed  Google Scholar 

  78. 78.

    Carreno RA, Lankester MW: A reevaluation of the phylogeny of Parelaphostrongylus Boev and Schulz, 1950 (Nematoda, Protostrongylidae). Syst Parasitol. 1994, 28: 145-151. 10.1007/BF00009592.

    Article  Google Scholar 

  79. 79.

    Gunn A, Adamczewski J: Muskoxen. Deer of the World: their Evolution, Behaviour and Ecology. Volume 1. Edited by: Geist V. 1998, Stackpoles Books, Mechanicsburg, Pennsylvania, USA, 1076-1094.

    Google Scholar 

  80. 80.

    Kutz SJ, Hoberg EP, Polley L: A new lungworm in muskoxen: an exploration in Arctic parasitology. Trends Parasitol. 2001, 17: 276-280. 10.1016/S1471-4922(01)01882-7.

    CAS  Article  PubMed  Google Scholar 

  81. 81.

    Klütsch CFC, Manseau M, Wilson PJ: Phylogeographical analysis of mtDNA data indicates postglacial expansion from multiple glacial refugia in Woodland Caribou (Rangifer tarandus caribou). PLoS ONE. 2012, 7: e52661-10.1371/journal.pone.0052661.

    PubMed Central  Article  PubMed  Google Scholar 

Download references


This research is part of G. Verocai’s PhD Thesis, and was supported by the Faculty of Veterinary Medicine of the University of Calgary, Alberta Innovates Health Solutions, Alberta Conservation Association – Grants in Biodiversity, The W. Garfield Weston/Wildlife Conservation Society Canada Fellowship for Northern Conservation, and the CircumArctic Rangifer Monitoring and Assessment Network (CARMA,, NSERC Canada International Polar Year Funding, and partially funded by Alberta Innovates and NSERC Discovery, Northern Supplement, and Research Tools and Instruments grants secured by S.J. Kutz; the Beringian Coevolution Project (DEB- Biotic Surveys and Inventory- 0415668) with funding from the National Science Foundation to J. A. Cook (University of New Mexico) and E. P. Hoberg (USNPC). Our study was completed through the Integrated Inventory of Biomes of the Arctic (NSF, DEB-Biodiversity Discovery and Analysis – 1258010) to J. A. Cook, E. P. Hoberg, K. E. Galbreath (Northern Michigan University) and E. Dechaine (Western Washington University). The authors thank the Nunavik Research Centre, Makivik Corporation, especially Bill Doidge, François Martin, Peter May, Mishal Naseer, and the hunters from Tasiujaq; Dr. Margo Pybus and Bob McClymont and, Alberta Fish and Wildlife Division; Patricia Pilitt and Art Abrams from the USNPC, USDA; Drs. Alexander Eberhardt, and John Gilleard (UCVM); the Kutz lab members: Jessica Ouellet, Jayninn Yue, Dean Brown, Jesse Invik, Manigandan Lejeune and James Wang. Likewise, we would like to acknowledge the crew involved in the trip to communities in the Sahtu Settlement Area, NT in search for the species name: Alasdair M. Veitch and Richard Popko, Department of Environment and Natural Resources, Government of the Northwest Territories, and Dr. Cyntia K. Kashivakura (UCVM). We specially acknowledge the communities in the Sahtu Settlement Area, NT: Bruce Kenny and Verna Firth, and the Kenny family from Déline; Rodger Boniface, Angus Shae, Wilfred Jackson, Michel Lafferty, and George Voudrak (Renewable Resources Committee) from Fort Good Hope; Joseph and Wilbert Kochon, Barry Gully (Behdzi Ahda First Nation), and the elders Mary Rose Drybones (translator), John Gully, Hyacinth, Marie and Antoine Kochon, and Johnny Blancho from Colville Lake, for providing input on naming of the parasite and Dora Grandjambe for assisting with enquiries on the North Slavey language.

Author information



Corresponding author

Correspondence to Guilherme G Verocai.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

GGV lead the study and preparation of the manuscript. GGV, SJK and MS collected the parasite specimens in the field and lab. SJK and EPH oversaw the study. GGV and EPH did morphological description of specimens. GGV carried out the molecular genetic study. All authors critically revised and approved the final manuscript.

Authors’ original submitted files for images

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Verocai, G.G., Kutz, S.J., Simard, M. et al. Varestrongylus eleguneniensis sp. n. (Nematoda: Protostrongylidae): a widespread, multi-host lungworm of wild North American ungulates, with an emended diagnosis for the genus and explorations of biogeography. Parasites Vectors 7, 556 (2014).

Download citation


  • Alces americanus
  • Cervidae
  • Nearctic
  • Rangifer tarandus
  • Ovibos moschatus
  • Taxonomy
  • Varestrongylinae
  • Verminous pneumonia