Skip to main content
Download PDF

Contributions to the phylogeny of Ixodes (Pholeoixodes) canisuga, I. (Ph.) kaiseri, I. (Ph.) hexagonus and a simple pictorial key for the identification of their females

Parasites & Vectors volume 10, Article number: 545 (2017) Cite this article

Abstract

Background

In Europe, hard ticks of the subgenus Pholeoixodes (Ixodidae: Ixodes) are usually associated with burrow-dwelling mammals and terrestrial birds. Reports of Pholeoixodes spp. from carnivores are frequently contradictory, and their identification is not based on key diagnostic characters. Therefore, the aims of the present study were to identify ticks collected from dogs, foxes and badgers in several European countries, and to reassess their systematic status with molecular analyses using two mitochondrial markers.

Results

Between 2003 and 2017, 144 Pholeoixodes spp. ticks were collected in nine European countries. From accurate descriptions and comparison with type-materials, a simple illustrated identification key was compiled for adult females, by focusing on the shape of the anterior surface of basis capituli. Based on this key, 71 female ticks were identified as I. canisuga, 21 as I. kaiseri and 21 as I. hexagonus. DNA was extracted from these 113 female ticks, and from further 31 specimens. Fragments of two mitochondrial genes, cox1 (cytochrome c oxidase subunit 1) and 16S rRNA, were amplified and sequenced. Ixodes kaiseri had nine unique cox1 haplotypes, which showed 99.2–100% sequence identity, whereas I. canisuga and I. hexagonus had eleven and five cox1 haplotypes, respectively, with 99.5–100% sequence identity. The distribution of cox1 haplotypes reflected a geographical pattern. Pholeoixodes spp. ticks had fewer 16S rRNA haplotypes, with a lower degree of intraspecific divergence (99.5–100% sequence identity) and no geographical clustering. Phylogenetic analyses were in agreement with morphology: I. kaiseri and I. hexagonus (with the similar shape of the anterior surface of basis capituli) were genetically more closely related to each other than to I. canisuga. Phylogenetic analyses also showed that the subgenus Eschatocephalus (bat ticks) clustered within the subgenus Pholeoixodes.

Conclusions

A simple, illustrated identification key is provided for female Pholeoixodes ticks of carnivores (including I. hexagonus and I. rugicollis) to prevent future misidentification of these species. It is also shown that I. kaiseri is more widespread in Europe than previously thought. Phylogenetic analyses suggest that the subgenus Pholeoixodes is not monophyletic: either the subgenus Eschatocephalus should be included in Pholeoixodes, or the latter subgenus should be divided, which is a task for future studies.

Background

Hard ticks (Acari: Ixodidae) are regarded as the most important vectors of pathogens [1]. Among them, the genus Ixodes Latreille, 1795 contains the highest number of species, exceeding 244 [2]. Traditionally, this genus was subdivided into subgenera, eight of which have representatives in the western Palaearctic [3]. The subgenus Pholeoixodes was erected [4] based on common morphological and ecological features of its members. For instance, the females of this subgenus have relatively short palps, there are no auriculae on the ventral basis capituli, and the first tarsi show a subapical dorsal hump [5]. Pholeoixodes species are usually associated with burrow-dwelling mammals, as well as terrestrial birds that nest in cavities (tree holes or burrows). Species of this subgenus usually feed on mammals, particularly carnivores (mainly Canidae, Mustelidae) and hedgehogs (Erinaceidae), in the western Palaearctic including I. canisuga Johnston, 1849, I. kaiseri Arthur, 1957, I. crenulatus Koch, 1844, I. hexagonus Leach, 1815 and I. rugicollis Schulze & Schlottke, 1929.

Revised extensively by Babos [6], the systematics of the subgenus Pholeoixodes has yet to be fully understood. In particular, problems with identification and nomenclature led to the incorrect definition of geographical ranges. For instance, I. crenulatus was considered to occur in western, central and eastern Europe [7]. However, recent studies on ticks from carnivores confirmed its presence in Romania [8], but not in central and western Europe [9,10,11]. Furthermore, the validity of I. crenulatus was questioned because of its uninformative description that often results in it being misidentified as I. hexagonus [12]. Also, based on the morphological similarities of I. crenulatus and I. kaiseri, their synonymization was proposed [13], and later rejected [14].

Ixodes hexagonus and I. canisuga are common species on carnivores in the western Palaearctic [3, 11, 15,16,17]. While I. hexagonus can also be found in eastern Europe [8, 9, 14], I. canisuga occurs predominantly in western and central Europe [9, 18, 19]. In regions where they are sympatric, the classical morphological approach to distinguishing females of these two species is the observation of the internal spur on the first coxae, which is present in I. hexagonus, but absent in I. canisuga [20]. However, I. hexagonus appears to be sometimes mistakenly identified as I. canisuga, as concluded from identical GenBank sequences (e.g. [21]: I. canisuga [JF928508], I. hexagonus [AF001400]). Furthermore, both species may be easily mistaken with I. crenulatus [12, 22].

Another controversy regarding the systematics and morphology of Pholeoixodes species is related to I. rugicollis. In the original drawing of the gnathosoma of I. rugicollis [23] (Fig. 1a), there was no indication of two frontal bumps on the anterior surface of basis capituli (between the basis of the hypostome and the palps). Later this species was even depicted without frontal bumps [7]. Furthermore, the drawings of the gnathosoma of I. rugicollis in its original description [23] and redescription [24] do not show broad separation of the porose areas, unlike what was reported in an electron microscopic study [25]. Ixodes rugicollis was also synonymized with I. cornutus [26], the porose areas of which are relatively close to each other [14].

Fig. 1
figure 1

Key features of Ixodes rugicollis females. a Original drawing of the gnathosoma by Schulze & Schlottke [23]). b-d Female syntype (USNTC): b scutum with “rugose” (wrinkled) surface, and basis capituli; c basis capituli, dorsal surface, enlarged; d basis capituli, ventral aspect. Numbered arrows indicate (in the order of presentation in the key): (1) pronounced, pointed frontal bump near the hypostome basis; (2) “stalked” palp; (3) curved (convex) lateral edge of palp; (4) broad space between inconspicuous, small porose areas

Full size image

In light of the above uncertainties, when contradictions arise with the traditional morphology-based identification of ticks, molecular comparison of representative specimens may provide additional and important clues to solve problems. Recently, North American members of the subgenus Pholeoixodes have been included in such molecular analyses [27]. However, no phylogenetic study has been performed on Pholeoixodes tick species collected from carnivores in Europe. Therefore, the aims of the present study were to morphologically identify female ticks collected from dogs, foxes and badgers in nine European countries, with subsequent molecular analyses using two mitochondrial markers. The study also aimed to clarify the taxonomic status and phylogenetic relationships of some Pholeoixodes species.

Methods

Sample collection and tick identification

Ticks were collected between 2003 and 2017. Specimens from Germany were stored frozen, and others were stored in 96% ethanol. Female ticks (except those from Serbia, from which the DNA was extracted previously) were examined morphologically with a VHX-5000 digital microscope (Keyence Co., Osaka, Japan). For species identification of females within Pholeoixodes, the following literature sources and type-materials were used: I. hexagonus [14], I. canisuga (neotypes loaned by the Natural History Museum, London, UK [NHM], accession numbers NHMUK 010305616–8: collected from dogs, UK), I. kaiseri ([14, 28]; paratype deposited in the United States National Ticks Collection [USNTC], accession number USNMENT00859298; and paratype loaned by NHM, accession number 1957.1.28.1: collected from fox, Egypt), I. crenulatus [14], I. rugicollis (syntype deposited in the USNTC, accession number USNMENT00865840: collected from pine marten, Germany). Adult ixodid ticks are usually easier to identify at the species level than immature stages, therefore morphological comparisons focused on adult female specimens. Nymphs were identified molecularly with PCR and sequencing two mitochondrial markers, which were compared to those of female ticks.

Molecular and phylogenetic analyses

DNA was extracted from the ticks (from part of the idiosoma and/or legs) individually with the QIAamp DNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s instructions, including an overnight digestion in tissue lysis buffer and Proteinase-K at 56 °C. The cytochrome c oxidase subunit I (cox1) gene was chosen as the primary target for molecular analysis, on account of its suitability as a DNA-barcode sequence for tick species identification [29]. The PCR (modified from [30]) amplifies an approximately 710 bp long fragment of the cox1 gene. The primers HCO2198 (5′-TAA ACT TCA GGG TGA CCA AAA AAT CA-3′) and LCO1490 (5′-GGT CAA CAA ATC ATA AAG ATA TTG G-3′) were used in a reaction volume of 25 μl, containing 1 U (0.2 μl) HotStarTaq Plus DNA polymerase (Qiagen), 2.5 μl 10× CoralLoad Reaction buffer (including 15 mM MgCl2), 0.5 μl PCR nucleotide Mix (0.2 mM each), 0.5 μl (1 μM final concentration) of each primer, 15.8 μl ddH2O and 5 μl template DNA. For amplification, an initial denaturation step at 95 °C for 5 min was followed by 40 cycles of denaturation at 94 °C for 40 s, annealing at 48 °C for 1 min and extension at 72 °C for 1 min. Final extension was performed at 72 °C for 10 min.

To complement the results obtained with the cox1 gene, all samples that showed different cox1 haplotype within a country, were also tested for another mitochondrial marker. This PCR amplifies an approximately 460 bp fragment of the 16S rRNA gene of Ixodidae [31], with the primers 16S + 1 (5′-CTG CTC AAT GAT TTT TTA AAT TGC TGT GG-3′) and 16S-1 (5′-CCG GTC TGA ACT CAG ATC AAG T-3′). Other reaction components and cycling conditions were the same as above, except for annealing at 51 °C.

PCR products were visualized in a 1.5% agarose gel. Purification and sequencing were done by Biomi Inc. (Gödöllő, Hungary). If identical sequences were found in a country, only one representative sequence was submitted to GenBank (accession numbers for the cox1 gene: KY962011–KY962051; for the 16S rRNA gene: KY962052–KY962077). Positions of nucleotide differences according to haplotypes are provided in Tables 1, 2.

Table 1 Data of samples used in this study, and results of cox1 sequence analyses
Full size table
Table 2 Haplotypes of 16S rRNA gene sequences according to the country of origin
Full size table

For comparison and phylogenetic analyses, the sequences were trimmed to the same length (cox1: 631 bp, 16S rRNA gene: 402 bp). Tick species from other studies were included in the phylogenetic analyses only if their sequence(s) available in GenBank had 99–100% coverage with the sequences in this study. This dataset was resampled 1000 times to generate bootstrap values. Phylogenetic analyses were conducted with the Maximum Likelihood method by using MEGA version 6.0. The MEGA model selection method was applied to choose the appropriate model (GTR and Jukes-Cantor model for cox1 and 16S rRNA genes, respectively). The ratio of haplotypes between different geographical regions was compared by Fisher’s exact test (condition of significance: P < 0.05).

Results

Morphological identification of female ticks

Altogether 113 female ticks (all Pholeoixodes spp.) were compared morphologically with adequate descriptions, and, when available, with type material. For their species identification, the following simplified keys were compiled, taking into account distinctive cardinal criteria observed in the present study.

Key to the females of Pholeoixodes spp. of carnivores in Europe

1a Basis capituli ending anteriorly as cone-like protuberance with lateral surface forming obtuse angles relative to longitudinal axis of hypostome ................................................................................................ 2

1b Basis capituli is not cone-like anteriorly ........................….................................................................... 4

2a Internal spur on coxa I long and pointed (Fig. 2) .......................................................................... Ixodes hexagonus

Fig. 2
figure 2

Key features of Ixodes hexagonus females. a Basis capituli, dorsal surface. b Basis capituli, ventral aspect. c Scutum and basis capituli. d Coxae I-IV. Numbered arrows indicate (in the order of presentation in the key): (1) cone-like anterior surface of basis capituli; (2) long and pointed internal spur on coxa I

Full size image

2b Internal spur on coxa I short and blunt ......................................................................................................... 3

3a Hypostome length to width ratio approx. 3:1; porose areas with ridge-like margins; surface of coxa I divided by a longitudinal line; external spurs as distinct small tuberosities present on all coxae (Fig. 3) ................................................................................. Ixodes kaiseri

Fig. 3
figure 3

Key features of Ixodes kaiseri females. a Basis capituli, dorsal surface with rounded porose areas. b Basis capituli of another morphotype, with triangular porose areas. c Scutum and basis capituli. d Basis capituli, ventral aspect with coxae I. Numbered arrows indicate (in the order of presentation in the key): (1) cone-like shape of the anterior surface of basis capituli; (2) ridge-like margin of porose area; (3) longitudinal line (starting medially to the basis of external spur), which divides the surface of coxa I; (4) external spur on coxa I

Full size image

3b Hypostome length to width ratio approx. 2:1; presence of double longitudinal ridges between the porose areas, diverging anteriorly towards anterolateral edges of basis capituli ........................................................................... Ixodes crenulatus

4a Anterior surface of basis capituli flat (plateau-like), perpendicular to longitudinal axis of hypostome, inconspicuous rounded bumps on anterior surface of basis capituli between hypostome and palps, palps laterally straight; separation of porose areas less than their diameter (Figs. 4, 5) ....................................................................................... Ixodes canisuga

Fig. 4
figure 4

Key features of Ixodes canisuga females. a Basis capituli, dorsal surface. b Basis capituli of another morphotype, with considerably smaller porose areas. c Basis capituli, ventral aspect. d Coxa I (short, blunt internal spur viewed from a proper angle). Numbered arrows indicate (in the order of presentation in the key): (1) flat “plateau-like” anterior surface of basis capituli around the hypostome basis; (2) inconspicuous, rounded bump, i.e. slightly forward projecting ridge of “plateau”; (3) relatively straight lateral edge of palp; (4) narrow space between porose areas (i.e. less than their diameter)

Full size image
Fig. 5
figure 5

The similarity of Ixodes canisuga females to I. crenulatus. Basis capituli with dorsal ridge (between arrows) in case of two identical haplotypes (“A”) of I. canisuga, which thus resemble I. crenulatus. a Female from Bosnia and Herzegovina. b Female from Hungary

Full size image

4b Pronounced and pointed bumps on anterior surface of basis capituli between hypostome and palps, palps “stalked” and laterally curved (convex); space between porose areas more than twice as wide as diameter of porose area (Fig. 1) .......................................................... Ixodes rugicollis

By using these morphological keys, the material collected and further analyzed consisted of 71 females identified as I. canisuga, 21 females as I. kaiseri and 21 females as I. hexagonus. Neither I. crenulatus nor I. rugicollis were found.

Molecular and phylogenetic analyses

DNA was extracted from 144 ticks (113 females, 30 nymphs, one male). Thus, 84 DNA samples of I. canisuga, 34 DNA samples of I. kaiseri and 26 DNA samples of I. hexagonus were analyzed. Ticks identified as I. canisuga had 11 (“A to K”) cox1 haplotypes: two of them were represented by seven and five individuals, respectively, while the remaining nine were found only once. These haplotypes showed up to three nucleotide differences from each other, corresponding to 99.5–100% sequence identity (628–631/631 bp). The distribution of some haplotypes reflected a clear geographical pattern (Table 1). Haplotype “H” was significantly more frequently identified in samples from western Europe than from central and south-eastern Europe (P < 0.0001). Several other haplotypes were identified only in one country (e.g. “B” in Hungary; “C”, “D” and “K” in Romania; “E”, “G” and “I” in Croatia; “F” in France; “J” in UK). However, haplotype “A” occurred in all evaluated regions of Europe (Table 1).

Ticks identified as I. kaiseri had nine (“L to T”) cox1 haplotypes, which showed a higher rate of polymorphism compared to I. canisuga, i.e. up to five nucleotide differences from each other (626–631/631 bp = 99.2–100% sequence identity). The occurrence of these haplotypes was restricted to central and south-eastern Europe (Table 1). Haplotypes “M” and “O” were unique to Germany, whereas the others occurred in Hungary and south-eastern Europe (Table 1). Ticks identified as I. hexagonus had five (“U to Y”) cox1 haplotypes, which showed up to three nucleotide differences from each other, i.e. 99.5–100% sequence identity (628–631/631 bp). Haplotype “X” was only identified in Germany and Austria, whereas all the others were present in south-eastern Europe (Table 1).

The 16S rRNA gene sequences of analyzed Pholeoixodes ticks had lower degree of intraspecific divergence compared to cox1 (i.e. 400–402/402 bp, i.e. 99.5–100% sequence identity) and fewer haplotypes (I–VII: Table 2). These haplotypes did not show geographical separation (e.g. haplotypes I-II occurred in western, central and south-eastern Europe).

The phylogenetic relationships of cox1 and 16S rRNA haplotypes are shown in Figs. 6 and 7, respectively. Morphological identification of the three species was supported by the phylogenetic analyses, because all morphologically a priori identified individuals of the three Pholeoixodes species grouped in the phylogenetic trees (Figs. 6, 7). The topologies of both phylogenetic trees reflect that (based on the investigated sequences) the subgenus Pholeoixodes is not monophyletic. Isolates of I. kaiseri and I. hexagonus formed two sister groups, whereas samples of I. canisuga were more closely related to the bat tick species I. vespertilionis, I. ariadnae and I. simplex (subgenus Eschatocephalus). Thus, the phylogenetic group of Pholeoixodes spp. also contained the clade of Eschatocephalus spp. (Figs. 6, 7).

Fig. 6
figure 6

Phylogenetic tree based on the cox1 gene, including sequences obtained in this study (indicated with bold characters) and representative sequences of other Ixodes spp. from the GenBank. Pholeoixodes spp. are marked with red color and dashed vertical lines connected to encircled #1; Eschatocephalus spp. are marked with purple color and dashed vertical line connected to encircled #2. Between the species name and the accession number, the country of origin is shown. Branch lengths represent the number of substitutions per site inferred according to the scale shown

Full size image
Fig. 7
figure 7

Phylogenetic tree based on the 16S rRNA gene, including sequences obtained in this study (indicated with bold characters) and representative sequences of other Ixodes spp. from the GenBank, as well as Rhipicephalus sanguineus as outgroup. Pholeoixodes spp. are marked with red color and dashed vertical lines connected to encircled #1; Eschatocephalus spp. are marked with purple color and dashed vertical line connected to encircled #2. Between the species name and the accession number, the country of origin is shown. Branch lengths represent the number of substitutions per site inferred according to the scale shown

Full size image

Discussion

This is the first comprehensive phylogenetic analysis involving three tick species from the subgenus Pholeoixodes collected from carnivores in Europe. In the present study, the morphological identification of I. canisuga and I. hexagonus was confirmed with molecular-phylogenetic methods, validating the morphological characters selected and described in the above taxonomic key. This identification key highlights differences among Pholeoixodes spp. in the shape of the anterior surface of basis capituli (between the hypostome and the palps). While the shape of the anterior surface of basis capituli has been reported to be a distinctive character between various Ixodes spp., including I. canisuga and I. hexagonus [32], this character has not been incorporated into the identification keys provided by other authors (e.g. [20]). These data suggest that the shape of the anterior surface of basis capituli should always be observed for the morphological differentiation of female Pholeoixodes ticks of carnivores (i.e. I. canisuga vs I. hexagonus and I. kaiseri).

The data presented here expand the known geographical range of I. kaiseri in Europe. Recently, ticks resembling I. kaiseri were reported in Poland [33]. Although I. kaiseri was previously reported from Romania [34], this was not confirmed by later studies involving or reporting ticks of carnivores [8, 35,36,37]. Here, the evidence is provided for the occurrence of I. kaiseri in Romania, as well as in three other countries, where it had not been reported yet (Germany, Hungary and Serbia). These new records are probably not a consequence of recent emergence of this tick species in new regions, but rather that its specimens have hitherto been misdiagnosed. Therefore, the keys presented here will be useful for future studies, which will help to define the geographical range of I. kaiseri.

Ixodes crenulatus was not found in the present study, not even in Romania, where it has been recently reported to occur [8]. On the other hand, reports of its occurrence in western Europe (Ireland, UK, Germany) are more than half a century old [7], and require verification. The diagnosis of this species is difficult, because the redescription (although adequate) is not easily accessible and is written in Russian [14], and no type-specimen is available [2]. The most important diagnostic feature of I. crenulatus females, the longitudinal ridges on the basis capituli [14] bear a resemblance to the ridge (rounded bumps) of the plateau seen in I. canisuga (Fig. 5), therefore further studies involving both species will be needed to reassess their synonymy, which was proposed by some authors [2].

Similarly, based on the inadequacy (and contradictions) of descriptions, illustrations in some former and recent reports on I. rugicollis, the relevant data should be interpreted with caution, taking into account the type specimens and key of females presented here (in Romania [7]: porose areas different, frontal bumps absent; in Poland [38]: porose areas not shown, frontal bumps are rounded). Also, I. rugicollis has recently been identified in Hungary [39] in part according to the description of I. cornutus [14], which was regarded as a synonym of I. rugicollis [26]. However, based on the type specimens investigated here and the identification criteria presented in the key, this synonymy cannot be maintained.

Phylogenetic analyses performed here suggest that the subgenus Pholeoixodes is not monophyletic. Taking into account that in both the cox1 and 16S rRNA gene phylogenetic analyses I. canisuga specimens (and I./Ph. lividus) formed one clade with bat ticks of the subgenus Eschatocephalus, it is necessary to test the parsimony of the inclusion of the latter subgenus in Pholeoixodes. Alternatively, Pholeoixodes should be divided into two subgenera. These data, on the other hand, confirm the phylogenetic relevance of morphological traits, because these bat tick species lack auriculae and long/pointed internal spur on coxa I, similarly to most Pholeoixodes spp.

The results presented here should also be considered in a geographical context. Although geographical structuring of several (but not all) cox1 mitochondrial lineages was observed, sequence and phylogenetic analyses of the 16S rRNA gene did not reflect the same pattern. These findings suggest that genetic exchange within each Pholeoixodes species is not limited between different European populations investigated here, i.e. these tick species are not subdivided into geographically distinct populations, but undergo constant gene flow. One underlying reason may be that populations of an important host species, the red fox (Vulpes vulpes) are apparently in contact and mix throughout Europe, allowing gene flow, with little spatial structuring [40]. The emergence of golden jackals (Canis aureus) towards western Europe [41] may have also contributed to the dispersal of tick species investigated here. This could also counterbalance genetic differences that would have otherwise resulted from separation of populations of the main hosts (hedgehog species) of I. hexagonus (i.e. Erinaceus europaeus in Germany vs E. roumanicus in Hungary and south-eastern Europe).

Conclusions

Reference sequences are provided for I. canisuga and I. kaiseri based on female specimens determined according to simple identification keys (including I. hexagonus and I. rugicollis), to prevent future misdiagnoses of these species. These results confirm that the shape and the morphological features of the anterior surface of basis capituli, the details of spurs on coxa I and the relative width of the scutum of females are important characters for species identification among Pholeoixodes ticks of carnivores. It is also demonstrated that I. kaiseri is more widespread in Europe than previously thought. Based on phylogenetic analyses, the subgenus Pholeoixodes is not monophyletic, as the subgenus Eschatocephalus clustered within its clade. This should be further elaborated by future taxonomic studies.

Abbreviations

NHM:

The Natural History Museum, London, UK

USNTC:

United States National Ticks Collection, Statesboro, USA

References

  1. Jongejan F, Uilenberg G. The global importance of ticks, 2004. Parasitology. 129(Suppl):S3–S14.

  2. Guglielmone AA, Robbins RG, Apanaskevich DA, Petney TN, Estrada-Peña A, Horak IG. The hard ticks of the world. Dordrecht: Springer; 2014. p. 738.

    Book  Google Scholar 

  3. Estrada-Peña A, Pfäffle M, Baneth G, Kleinerman G, Petney TN. Ixodoidea of the western Palaearctic: a review of available literature for identification of species. Ticks Tick Borne Dis. 2017:512–25.

  4. Schulze P. Die morphologische Bedeutung des Afters und seiner Umgebung bei den Zecken. Zschr Morphol Ökol Tiere. 1942;38:630–58.

    Google Scholar 

  5. Pérez-Eid C. Les tiques. Identification, biologie, importance médicale et vétérinaire. Paris: Monographie de microbiologie, Tec & Doc EMinter- Lavoisier; 2007. p. 314.

    Google Scholar 

  6. Babos S. Revision des subgenus Pholeoixodes Schulze, 1942 (Acaroidea: Ixodidae). Acta Zool Hung. 1964;10:269–307.

    Google Scholar 

  7. Feider Z. Fauna Republicii Populare Române. Arachnida, vol. 5, fasc. 2. Acaromorpha, Suprafamilie Ixodoidea (Capuse). Bucuresti: Editura Academiei Republicii Populare Române; 1965. 404 pp.

    Google Scholar 

  8. Mihalca AD, Dumitrache MO. Magdas C, Gherman CM, Doms a C, Mircean V, et al. Synopsis of the hard ticks (Acari: Ixodidae) of Romania with update on host associations and geographical distribution. Exp Appl Acarol. 2012;58:183–206.

  9. Petney TN, Pfäffle MP, Skuballa JD. An annotated checklist of the ticks (Acari: Ixodida) of Germany. System Appl Acarol. 2012;17:115–70.

    Article  Google Scholar 

  10. Najm NA, Meyer-Kayser E, Hoffmann L, Herb I, Fensterer V, Pfister K, Silaghi C. A molecular survey of Babesia spp. and Theileria spp. in red foxes (Vulpes vulpes) and their ticks from Thuringia, Germany. Ticks Tick Borne Dis. 2014;5:386–91.

    Article  PubMed  Google Scholar 

  11. Abdullah S, Helps C, Tasker S, Newbury H, Wall R. Ticks infesting domestic dogs in the UK: a large-scale surveillance programme. Parasit Vectors. 2016;9:391.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Černý V. About some systematic and nomenclature problems within the subgenus Pholeoixodes (Ixodidae). Folia Parasitol. 1969;16:348.

    Google Scholar 

  13. Sonenshine DE, Kohls GM, Clifford CM. Ixodes crenulatus Koch, 1844 synonymy with I. kaiseri Arthur, 1957 and re-descriptions of the male-female, nymph, and larva (Acarina: Ixodidae). Acarologia. 1969;11:193–206.

    CAS  PubMed  Google Scholar 

  14. Filippova NA. Ixodid ticks (Ixodinae). Fauna USSR New Ser. 1977;4:1–316. (In Russian)

    Google Scholar 

  15. Ogden NH, Cripps P, Davison CC, Owen G, Parry JM, Timms BJ, Forbes AB. The ixodid tick species attaching to domestic dogs and cats in Great Britain and Ireland. Med Vet Entomol. 2000;14:332–8.

  16. Smith F, Ballantyne R, Morgan E, Wall R. The incidence of tick infestation on domestic dogs in the UK. Med Vet Entomol. 2011;25:377–84.

    Article  CAS  PubMed  Google Scholar 

  17. Clarebout E, Losson B, Cochez C, Casaert S, Dalemans A-C, De Cat A, et al. Ticks and associated pathogens collected from dogs and cats in Belgium. Parasit Vectors. 2013;6:183.

    Article  Google Scholar 

  18. Manilla G. [Fauna d’Italia. Acari, Ixodida.] Bologna: Edizioni Calderini; 1998. p. 280. (In Italian).

  19. Földvári G, Farkas R. Ixodid tick species attaching to dogs in Hungary. Vet Parasitol. 2005;129:125–31.

    Article  PubMed  Google Scholar 

  20. Hillyard PD. Ticks of North-West Europe: keys and notes for identification of the species. Synopses of the British fauna (new series) (52). Shrewsbury: Field Studies Council; 1996. 178 pp.

  21. Karger A, Kampen H, Bettin B, Dautel H, Ziller M, Hoffmann B, et al. Species determination and characterization of developmental stages of ticks by whole-animal matrix-assisted laser desorption/ionization mass-spectrometry. Ticks Tick Borne Dis. 2012;3:78–89.

    Article  PubMed  Google Scholar 

  22. Gothe R, Stendel W, Holm R. Zum Vorkommen von Ixodes canisuga Johnston, 1848, in Deutschland, ein Beitrag zur Ixodes-Fauna. Zeitsch Parasitenk. 1977;53:123–8.

    Article  CAS  Google Scholar 

  23. Schulze P, Schlottke E. Kleinhohlenbewohnende deutsche Zecken mit Beschreibung dreiel neuer Bauhohlenbruter und einer Bestimmungstabelle der deutschen Ixodes. Sitz Bey Abhandl NafwJ Ges Rostock 1927–1929. 1929;2:95–110.

    Google Scholar 

  24. Morel PC, Aubert MFA. Contribution à la connaissance de Pholeoixodes rugicollis (Schulze et Schlottke, 1929) (Acariens, Ixodina). Cahiers ORSTOM Série Entomologie Médicale et Parasitologie. 1975;13:99–109.

    Google Scholar 

  25. Cordas T, Aeschlimann A, Morel PC. Étude morphologique des Ixodidae s. str. (Schulze: 1937) de Suisse au microscope électronique à balayage. Acarologia. 1993;34:21–46.

  26. Camicas JL, Hervy JP, Adam F, Morel PC. Catalogue les tiques du monde. Nomenclature, stades décrits, hôtes, répartition (Acarida, Ixodida). Paris: Orstom; 1998. p. 233.

    Google Scholar 

  27. Ondrejicka DA, Morey K¸ Hanner RH. DNA barcodes identify medically important tick species in Canada. Genome 2016;60:74–84.

  28. Arthur DR. Two north African Ixodes ticks. I. kaiseri sp. nov. from Egyptian desert fox cubs. A redescription of the female and a description of the male of I. festai, Rondelli, 1926 (Ixodoidea, Ixodidae). J Parasitol. 1957;43:578–85.

    Article  CAS  PubMed  Google Scholar 

  29. Lv J, Wu S, Zhang Y, Chen Y, Feng C, Yuan X, et al. Assessment of four DNA fragments (COI, 16S rDNA, ITS2, 12S rDNA) for species identification of the Ixodida (Acari: Ixodida). Parasit Vectors. 2014;7:93.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R. DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Mel Marine Biol Biot. 1994;3:294–9.

  31. Black WC, Piesman J. Phylogeny of hard and soft-tick taxa (Acari: Ixodida) based on mitochondrial 16s rDNA sequences. Proc Natl Acad Sci U S A. 1994;91:10034–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Arthur DR. The morphology of the British Prostriata with particular reference to Ixodes hexagonus Leach. II Parasitology. 1953;42:161–86.

  33. Wodecka B, Michalik J, Lane RS, Nowak-Chmura M, Wierzbicka A. Differential associations of Borrelia species with European badgers (Meles meles) and raccoon dogs (Nyctereutes procyonoides) in western Poland. Ticks Tick Borne Dis. 2016;7:1010–6.

    Article  PubMed  Google Scholar 

  34. Filippova NA, Uspenskaya IG. [Ixodes kaiseri Arthur 1957 (Ixodidae) species taxonomic status.] Parazitologiya. 1973;7:297–306. (In Russian).

  35. Coipan EC, Vladimirescu AF, Ciolpan O, Teodorescu I. Tick species (Acari: Ixodoidea) distribution, seasonality and host associations in Romania. Travaux du Muséum National d’Histoire Naturelle ‘Grigore Antipa’ 2011;54:301–17.

  36. D'Amico G, Dumitrache MO, Matei IA, Ionică AM, Gherman CM, Sándor AD, et al. Ixodid ticks parasitizing wild carnivores in Romania. Exp Appl Acarol. 2017;71:139–49.

    Article  PubMed  Google Scholar 

  37. Sándor AD, D'Amico G, Gherman CM, Dumitrache MO, Domșa C, Mihalca AD. Mesocarnivores and macroparasites: altitude and land use predict the ticks occurring on red foxes (Vulpes vulpes). Parasit Vectors. 2017;10:173.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Siuda K, Nowak M, Gierczak M. Confirmation of occurrence of Ixodes (Pholeoixodes) rugicollis Schulze et Schlottke, 1929 (Acari: Ixodidae) in Poland, including the morphological description and diagnostic features of this species. Wiad Parazytol. 2010;56:77–80.

    PubMed  Google Scholar 

  39. Hornok S, Trauttwein K, Takács N, Hodžić A, Duscher GG, Kontschán J. Molecular analysis of Ixodes rugicollis, Candidatus Neoehrlichia sp. (FU98) and a novel Babesia genotype from a European badger (Meles meles). Ticks Tick Borne Dis. 2017;8:41–4.

    Article  PubMed  Google Scholar 

  40. Teacher AG, Thomas JA, Barnes I. Modern and ancient red fox (Vulpes vulpes) in Europe show an unusual lack of geographical and temporal structuring, and differing responses within the carnivores to historical climatic change. BMC Evol Biol. 2011;11:214.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Arnold J, Humer A, Heltai M, Murariu D, Spassov N, Hackländer K. Current status and distribution of golden jackals (Canis aureus L., 1758) in Europe. Mammal Rev. 2012;42:1–11.

    Article  Google Scholar 

Download references

Acknowledgements

The survey was organized in the framework of the EurNegVec COST Action TD1303. The authors are grateful to Dr. Martin Hall and Mrs. Janet Beccaloni for help in accessing type specimens at NHML, to Dr. Laurence Vial for the loan of Ixodes rugicollis female collected by P. C. Morel, and to Gerald Umhang and Dr. Céline Richomme for providing four I. canisuga specimens from Nancy.

Availability of data and materials

The sequences obtained and/or analyzed during the current study are deposited in GenBank under accession numbers KY962011–KY962051 (cox1 gene) and KY962052–KY962077 (16S rRNA gene). All other relevant data are included in the manuscript and the references.

Funding

Molecular analyses were funded by OTKA 115854 (Hungary). The publication of this research was supported by the 12190–4/2017/FEKUTSTRAT grant of the Hungarian Ministry of Human Capacities. Sample collection was supported by the grants PN-II-RU-TE-2014-4-1389 (Romania), GENOTICKTRECK-1957 (Croatia) and OI173006 (Serbia). GF was supported by the János Bolyai Research Scholarship of the Hungarian Academy of Sciences.

Author information

Authors and Affiliations

  1. Department of Parasitology and Zoology, University of Veterinary Medicine, Budapest, Hungary

    Sándor Hornok, Róbert Farkas, Nóra Takács & Gábor Földvári

  2. Department of Parasitology and Parasitic Diseases, University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca, Romania

    Attila D. Sándor

  3. Department for Bacteriology and Parasitology, Croatian Veterinary Institute, Zagreb, Croatia

    Relja Beck

  4. U.S. National Tick Collection, Institute for Coastal Plain Science, Georgia Southern University, Statesboro, GA, USA

    Lorenza Beati

  5. Plant Protection Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, Budapest, Hungary

    Jenő Kontschán

  6. National Centre for Vector Entomology, Institute of Parasitology, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland

    Cornelia Silaghi

  7. State Office for Consumer Protection (TLV), Bad Langensalza, Germany

    Elisabeth Meyer-Kayser

  8. Department of Pathobiology, Institute of Parasitology, University of Veterinary Medicine Vienna, Vienna, Austria

    Adnan Hodžić & Georg Gerhard Duscher

  9. Department for Medical Entomology, Institute for Medical Research, University of Belgrade, Belgrade, Serbia

    Snežana Tomanović

  10. Veterinary Parasitology and Ecology Group, School of Biological Sciences, Life Sciences Building, University of Bristol, Bristol, UK

    Swaid Abdullah & Richard Wall

  11. Department of Animal Health, Faculty of Veterinary Medicine, Zaragoza, Spain

    Agustín Estrada-Peña

  12. BIOEPAR, INRA, Oniris, Nantes, France

    Olivier Plantard

Authors
  1. Sándor Hornok
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Attila D. Sándor
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Relja Beck
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Róbert Farkas
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Lorenza Beati
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Jenő Kontschán
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Nóra Takács
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Gábor Földvári
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Cornelia Silaghi
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Elisabeth Meyer-Kayser
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Adnan Hodžić
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Snežana Tomanović
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Swaid Abdullah
    View author publications

    You can also search for this author in PubMed Google Scholar

  14. Richard Wall
    View author publications

    You can also search for this author in PubMed Google Scholar

  15. Agustín Estrada-Peña
    View author publications

    You can also search for this author in PubMed Google Scholar

  16. Georg Gerhard Duscher
    View author publications

    You can also search for this author in PubMed Google Scholar

  17. Olivier Plantard
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

SH initiated and supervised the study, extracted the DNA, did part of the morphological and genetic comparisons, wrote the manuscript. ADS, RB, GF, CS, EMK, AH, ST, SA, RW, GGD and OP provided important samples for the study. RF and LB organized the availability of type material from NHML and USNTC, respectively. JK made the microscopic pictures and performed phylogenetic analyses. NT performed the PCRs. AEP and OP contributed significantly to the design of the study and several parts of the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Sándor Hornok.

Ethics declarations

Ethics approval and consent to participate

In Hungary and Romania pet dogs were sampled during regular veterinary care, therefore no ethical approval was needed. Other tick samples from Romania and those from Croatia, Germany were collected from corpses of red foxes. In France, ticks were collected from corpses of road-killed badgers. In the UK, tick collection from dogs was carried out with the approval of the University of Bristol ethics committee, UIN: UB/15/008. In Bosnia and Herzegovina, all ticks were collected from foxes legally shot under the frame of an oral antirabies vaccination campaign (BIH-PSD-G-EC 30, Subproject ID: CRIS Number: 2010/022–259). In Austria, the ticks were collected during a study approved by the institutional ethics committee (University of Veterinary Medicine Vienna) and the Austrian Ministry for Science and Research (GZ68.205/25-II/10b/2010).

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hornok, S., Sándor, A.D., Beck, R. et al. Contributions to the phylogeny of Ixodes (Pholeoixodes) canisuga, I. (Ph.) kaiseri, I. (Ph.) hexagonus and a simple pictorial key for the identification of their females. Parasites Vectors 10, 545 (2017). https://doi.org/10.1186/s13071-017-2424-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13071-017-2424-x

Keywords

Parasites & Vectors

ISSN: 1756-3305

Contact us