Skip to main content
Download PDF

Culicoides paolae and C. circumscriptus as potential vectors of avian haemosporidians in an arid ecosystem

Parasites & Vectors volume 11, Article number: 524 (2018) Cite this article

Abstract

Background

Haemosporidians are the most important vector-borne parasites due to their cosmopolitan distribution and their wide range of hosts, including humans. Identification of their vectors is critical to highlight ecologically and epidemiologically relevant features such as host specificity or transmission routes. Biting midges of the genus Culicoides are considered the main vectors of Haemoproteus spp., yet important information on aspects such as vector feeding preferences or vector-host specificity involving haemosporidian parasites is frequently missing.

Methods

We assessed the abundance of Culicoides circumscriptus and C. paolae and blood sources of the latter at the nests of cavity-nesting bird species (mainly the European roller Coracias garrulus) and in their surroundings. We also explored the prevalence and genetic diversity of avian haemosporidians in parous females of both species.

Results

Both C. circumscriptus and C. paolae were abundant in the study area and common at European roller nests. Culicoides paolae had a diverse ornithophilic diet, feeding on at least seven bird species. Human DNA was also detected in the blood meal of some individuals. Four Haemoproteus lineages, including a new one reported here for the first time, were isolated from parous females of both biting midges.

Conclusions

Culicoides circumscriptus and C. paolae can play a locally important role in the transmission dynamics of Haemoproteus parasites in a community of cavity-nesting bird species in an arid ecosystem.

Background

Biting midges of the genus Culicoides are small, cosmopolitan blood-sucking insects playing an important role as vectors of numerous viruses, filarial nematodes and protozoa affecting human, livestock and wildlife [1, 2]. Culicoides are regarded as the main vectors of Haemoproteus (class Aconoidasida, order Haemosporidia, subgenus Parahaemoproteus) [3]. Still, they are the least studied of the major dipteran vector groups and our knowledge of their vectorial role is biased. On one side, their participation in the transmission of livestock and human viruses has received much attention (e.g. bluetongue virus [4], African horse sickness virus [5], Oropouche virus [6]). On the other side, much less is known about their role in the transmission of avian haemosporidians. In particular, malaria-like parasites of the genus Haemoproteus are highly prevalent avian haemoparasites [7] with a relevant impact on the health status, longevity and fitness of their avian hosts [8,9,10,11,12,13,14]. Haemoproteus presents a high diversity in host-parasite associations [7] and it is unclear to what extent this diversity is due to host-parasite, host-vector or vector-parasite specificity [15,16,17,18,19,20]. Moreover, the vector identity and ecology of most Haemoproteus lineages is unknown [7, 21].

Tracing the feeding preferences (i.e. feeding patterns) of female Culicoides is critical to identify host-vector-parasite associations as well as ecologically and epidemiologically relevant features such as host specificity or transmission routes. Biting midges have a clear preference to feed mainly on either birds or mammals, with some species showing an opportunistic behaviour [22]. Traditionally, the feeding preferences of Culicoides have been assessed based on morphological characterization of the sensory structures (i.e. palps and antennae [23,24,25]). Other methods, such as the precipitin test [26,27,28], immunological assays [29, 30], and more recently, MALDI-TOF [31] and molecular tools [32, 33], have been applied to specifically identify the blood meal sources of female Culicoides and other insect vectors. Methods like the immunological assays are useful when the suitable hosts are suspected, which is commonly the case for the Culicoides surveys done in relation with livestock [34,35,36,37]. Yet, biting midges trapped in the wild may have a broad range of potential hosts, supporting the necessity to use approaches allowing the identification of a wide range of vertebrate species [22]. Studies on Culicoides feeding preferences in natural areas are especially scarce, although they provide a more complete view of the circulation of the blood parasites in the wild.

Here we studied the role of two common ornithophilic species of Culicoides in the transmission of avian haemosporidians in the driest European area, the Desert of Tabernas (south-eastern Spain). In this area, the prevalence of infection by Haemoproteus spp. varies between avian species, with a total absence of parasites found in adult Trumpeter finches (Bucanetes githagineus) while all the adult European rollers (Coracias garrulus) sampled showed evidence of infection [38, 39]. The haemosporidian species described for rollers in this area (Haemoproteus coraciae) was clustered, based on phylogenetic analysis, with other Haemoproteus spp. vectored by Culicoides [39], although the dipteran species involved in its transmission remains unidentified.

At least 81 species of the genus Culicoides are present in Spain [40]. In south-eastern Spain, different ornithophilic Culicoides species have been recorded including Culicoides paolae. This species, registered for first time in Spain in 2008 [41], has been frequently associated with livestock farms [34, 42, 43]. However, analysis of the sensory structures suggests an ornithophilic preference in this species [44], although the host sources of blood remain unidentified, and its role for the transmission of avian haemosporidians is completely unknown. This contrasts with other well-known, sympatric ornithophilic species such as C. circumscriptus, a common species in southern Spain which may be involved in the transmission of Haemoproteus parasites [18, 45, 46].

To assess the potential of C. paolae and C. circumscriptus as the vectors of blood parasites in a community of birds in south-eastern Spain we: (i) collected the specimens of the two species inside and in the surroundings of the nests of the European roller, one of the locally most abundant troglodytic species; (ii) identified the blood meal sources of engorged females; and (iii) studied the prevalence and genetic diversity of Haemoproteus parasites harboured by parous biting midge females.

Methods

Study area

This study was performed in an approximately 50 km2 area located in the Desert of Tabernas (Almería, SE Spain, 37°05'N, 2°21'W). The landscape mostly consists of open shrubland with olive and almond groves interspersed among numerous dry riverbeds (ramblas). Inhabited farms are scarce and scattered along the study area. The climate is temperate, semiarid Mediterranean with a strong water deficit during the long, hot summer months (June to September), when the absolute maximum monthly temperature is higher than 40 °C and the monthly average of the maximum daily temperatures remains above 30 °C [47]. The average annual temperature is 18 °C, with mild inter-annual oscillations of 3–4 °C and significant intra-annual fluctuations [47]. The mean annual rainfall is c.230 mm with high inter-annual and intra-annual variability [48].

The bird community comprises species that breed mainly in cavities in the study area (e.g. the little owl Athene noctua, scops owl Otus scops, Eurasian jackdaw Corvus monedula, common kestrel Falco tinnunculus and feral pigeon Columba livia), chiefly in natural holes in sandy cliffs but also in cavities in human constructions [49]. The European roller (hereafter roller) is a common breeding species in the study area where it is distributed patchily according to distinct geomorphological units [50]: (i) ramblas (dry stream channels with steep sandstone banks), which are linear, continuous geographical units separated from neighbouring ramblas by hills and human settlements; (ii) individual bridges with numerous, densely spaced cavities (c.2–3 m apart); and (iii) spatial aggregations of suitable nesting places, mostly trees with nest boxes but also small sandstone banks with natural cavities and isolated country houses with cavities. Wooden nest boxes have been placed in these habitat types and most rollers individuals are currently breeding in them (height × length × width: 310 × 232 × 230 mm, entrance diameter: 60 mm, with a removable upper lid to allow nest monitoring) installed on isolated eucalyptus trees, sandstone banks and isolated and deserted country houses [49, 50]. Rollers are migratory birds wintering in Africa and arriving at the breeding grounds in the study area when resident, secondary cavity-nesting birds are already settled. Eggs (mean clutch size = 4.23) [51] are incubated by both sexes [52] during c.21 days. Rollers rear a single brood per year [52] with fledglings leaving the nest approximately 20–22 days after hatching in the studied population [50].

Culicoides trapping

Culicoides spp. specimens were trapped using two methods: sticky traps and CDC light traps. Sticky traps were placed in nest boxes occupied by rollers during the 2016 and 2017 breeding seasons (from 18 May to 4 July in 2016 and from 2 June to 18 July in 2017). Specifically, sticky traps were fixed under the upper lid of 69 nest boxes (32 in 2016 and 37 in 2017). In 2016 we took advantage of a pair of kestrels breeding in a next box close to a breeding pair of rollers, thus resembling natural nesting conditions with different cavity nesting bird species breeding in close proximity [50]. We followed the method described by Tomás et al. [53] (i.e using Petri dishes smeared with body gel-oil as a non-attractant glue) but replacing Petri dishes by white vegetal papers that were fixed by thumbtacks on the inner side of the upper lid. In 2016, these sticky traps (size = 63.6 cm2) were kept for three days in two periods of the breeding cycle: (i) at the end of the incubation phase (18–20 days after the first egg was laid); and (ii) during the nestling phase, when all chicks had already hatched (13–15 days after the first egg hatched). In 2017, sticky traps were only placed during the nestling stage, because most vectors were captured during this stage in 2016, and the trap size was increased (size = 175.5 cm2). Thus, in 2017, a first trap was set 13 days after the first egg hatched and kept for four days. Then, it was replaced by a new trap that was kept for a second period of four days. Additionally, opportunistic catches of Culicoides at the nests were made by hand during routine visits.

Additionally, CDC traps were set throughout the study area during 2016 and 2017. We used traps with UV light as they are recommended to attract Culicoides [54]. Moreover, since this study is part of a broader one aimed at studying the community of dipteran vectors, we also used incandescent light traps. Both trap types were put together and were also baited with CO2 in order to use as many different stimuli as possible. Dry ice was used as source of CO2 (1 kg of dry ice per night and pair of traps to ensure the continued emission of CO2 until the collection of the traps at dawn). Thus, 20 pairs of CDC traps (each pair formed by one trap with incandescent light and one with UV light, c.50 cm apart from each other, both baited with CO2) were set all over the study area and in the main breeding habitats of the roller, namely trees, ramblas and bridges (see above), so that eight traps were located on ramblas, eight on trees and four on bridges during 2016 and 2017. The traps were powered by a 6 V battery of 12 Ah. The trapping sessions were adjusted according to the breeding season of rollers and the moon calendar, so that traps were active on the days during or close to the period of the new moon (reducing the effect of ambient light [55]), and avoiding windy nights. In 2016 we placed one group of 10 pairs of traps from 8 June to 10 June and a second group of 10 trap pairs from 7 July to 8 July. In 2017, all 20 trap pairs were set from 22 June to 1 July. Most traps (82.5%) were set before dusk or shortly after and were removed after sunrise. Captured insects were moved to the Estación Experimental de Zonas Áridas and frozen in 70% ethanol until identification.

Morphological identification

Biting midges were identified to the species level based on González & Goldarazena [56] and Mathieu et al. [57] taxonomic keys under a Zeiss Discovery V8 stereomicroscope. Culicoides circumscriptus and C. paolae were the most abundant biting midges at the nests (see Results), and individuals of these species collected at the nests and with CDC light traps were analysed for blood meal origin (engorged females) or Haemoproteus detection (parous females). Engorged females were identified based on the presence of blood remains in the abdomen. The abdomen of each C. paolae engorged female was separated from the head-thorax using sterile tips on chilly Petri dishes and, subsequently, maintained in individual vials. Diet analyses were restricted to C. paolae as only two engorged C. circumscriptus females were captured. Parous females were identified based on the presence of burgundy-red pigmented abdomen that develops during the first gonotrophic cycle [58]. As previous studies have reported a low prevalence of avian haemosporidians in Culicoides from southern Spain ([46], our unpublished observations], parous females were grouped in pools from 1 to 11 individuals according to species, date and site of capture.

DNA extraction and molecular analyses

Genomic DNA from the abdomen of each engorged C. paolae females and biting midge pools was extracted using the DNeasy Blood and Tissue® kit (Qiagen, Hilden, Germany) following company specifications. Negative controls (reagents without a template) were used to detect possible contaminations. DNA was stored at -20 °C until PCR amplification. To confirm the morphological identification of Culicoides species, we amplified a 658 base pair (bp) fragment of the mitochondrial cytochrome c oxidase 1 (cox1 gene, barcoding region) of four individuals following Gutiérrez-López et al. [59]. The vertebrate hosts of Culicoides females were identified by amplification of a fragment of 758 bp of the vertebrate cox1 gene following Alcaide et al. [32]. Finally, the presence and identity of Haemoproteus and Plasmodium spp. were assessed for the pools of parous female Culicoides specimens using the protocol by Hellgren et al. [60]. Parasite determination was conducted at least twice per sample to avoid false negative results [61]. The presence of amplicons was verified on 1.8% agarose gels. Positive amplifications were sequenced using the Macrogen laboratories sequencing service (Madrid, Spain) and sequences were edited using the software Sequencher™ v.4.9 (Gene Codes Corp, Ann Arbor, MI, USA).

The identity of Culicoides species and their vertebrate hosts were established by comparison with sequences deposited in GenBank DNA sequence database (National Center for Biotechnology Information BLAST) or the Barcode of Life Data Systems (BOLD). The molecular identification of two female C. paolae and two female C. circumscriptus confirmed the morphological identifications. Vertebrate species were confirmed if agreement was ≥ 98% with deposited sequences. Parasite lineages and morphospecies were identified by BLAST comparison with the sequences available in GenBank and MalAvi [62].

Statistical analyses

The abundance of parous C. paolae and C. circumscriptus captured in CDC traps were analysed with a generalized linear mixed model (GLMM) with the negative binomial distribution of errors. Year (2016 and 2017) and biting midge species were included as independent variables. Scaled and centred date of sampling was included in a GLMM as a covariate. The number (log-transformed, scaled and centred) of blood-feeding parasitic dipterans captured per pair of traps was included as an offset variable to correct for their abundance in each sampling point. Trap location, identical during both years, was included as a random factor. The interaction between sampling date and Culicoides species was introduced to explore a seasonal effect in the capture of the two species. One outlier due to the capture of 94 parous C. paoale was detected and the analyses were run with and without this datum. Given that the results obtained were qualitatively comparable, we report the analysis including this datapoint.

The prevalence of Haemoproteus spp. in Culicoides pools was estimated considering variable pool sizes and 100% test specificity and sensitivity following Sergeant [63]. Statistical analyses were performed using the R environment [64] with the lme4 and effects packages [65, 66].

Results

Abundance of Culicoides spp. in avian nests

Overall, 57 Culicoides spp. were collected in avian nest during both years (n = 42 in 2016 and n = 15 in 2017, Table 1). From the 57 captures, four individuals were collected opportunistically in the nest and 53 were collected by sticky traps. In addition, Simuliidae (n = 230) and Phlebotominae (n = 105) were other blood-feeding dipterans collected with the sticky traps at the nests.

Table 1 Abundance, mean ± SD, and range (in parentheses) for Culicoides spp. (overall data set) and for the subset of parous and engorged females of C. paolae and C. circumscriptus trapped in avian nests and their surroundings during 2016 and 2017
Full size table

The most abundant biting midges were C. paolae (57.9%, 33 out of 57) and C. circumscriptus (22.8%, 13 out of 57). Twenty-seven C. paolae specimens were parous and six were engorged, whereas 11 C. circumscriptus specimens were parous, two nulliparous (not included in Table 1) and no engorged individual was captured. Twenty-two out of the 32 C. paolae collected in 2016 were captured in a common kestrel nest.

Abundance of Culicoides spp. in CDC traps

Overall, 7764 Culicoides spp. were captured using CDC traps (Table 1). Of them, 341 were parous females of C. paolae and C. circumscriptus, representing 4.4% of the total Culicoides spp. specimens captured (Table 1). The average number of parous females per pair of traps was 3.8 of C. paolae and 1.7 of C. circumscriptus in 2016 and 9 of C. paolae and 2.5 of C. circumscriptus in 2017. Furthermore, 30 engorged females of C. paolae and two engorged females of C. circumscriptus were also captured (Table 1).

The abundance of parous biting midges (C. paolae and C. circumscriptus) was greater in 2017 and decreased through the breeding season. Culicoides paolae was significantly more abundant than C. circumscriptus (Table 2). The interaction between Culicoides species and sampling date was also significant (Table 2), because parous C. paolae was more abundant late in the roller breeding season and parous C. circumscriptus was more abundant early in the season (Fig. 1).

Table 2 Results of a generalised mixed model analysing the abundance of parous Culicoides paolae and C. circumscriptus collected using CDC traps in relation to year (2016, 2017), date of capture, and the interaction between date of capture and the species of Culicoides biting midges
Full size table
Fig. 1
figure1

Relationship between capture date and abundance of parous females of Culicoides circumscriptus (estimate ± SE = -0.63 ± 0.23, P < 0.01) and C. paolae (estimate ± SE = 0.48 ± 0.21, P = 0.022) captured with CDC traps in south-eastern Spain during 2016 and 2017. Date of capture was scaled and centred. Lines represent fitted values with shaded regions showing areas delimited by 95% confidence intervals

Full size image

Culicoides paolae feeding patterns

Blood meals of 21 (58.3%) out of the 36 engorged C. paolae were successfully identified. Of them, the six females captured in avian nests fed on the species breeding in these nest boxes (two on common kestrels and four on rollers) (Table 3). Culicoides paolae females captured with CDC traps (n = 15) fed mainly on birds (66.7% of the identified blood meals) corresponding to five different species including cavity-nesting and open-nesting species. Finally, human DNA was found in five (33.3%) out of 15 C. paolae collected with CDC traps (Table 3).

Table 3 Hosts of C. paolae based on the molecular identification of blood meal origin. The number of successfully identified blood meals is shown for each species
Full size table

Prevalence and identification of haemosporidian parasites

The prevalence of Haemoproteus spp. was 4.4% (95% CI: 1.39–9.95%, n = 95 individuals) and 0.7% (95% CI: 0.12–2.21%, n = 284 individuals) for C. circumscriptus and C. paolae pools, respectively. Overall, four Haemoproteus and one Plasmodium lineages were found. Of them, the three Hemoproteus lineages, TURDUS2, GAGLA03 (= GAGLA05, both sequences with equal coverage and identity) and AEFUN03, and the Plasmodium lineage SYAT05 (Plasmodium vaughani), were identified with 100% coverage and identity. The three Haemoproteus lineages, TURDUS2, GAGLA03 (=GAGLA05) and AEFUN03, were isolated from C. circumscriptus specimens (Table 4). The Haemoproteus lineage TURDUS2 and the Plasmodium lineage SYAT05 were isolated from C. paolae specimens (Table 4). In addition, a new lineage (CUPAO-01, GenBank: MH237967) was isolated from a C. paolae specimen. This lineage showed 93% overlap and 99% similarity with the Haemoproteus coraciae lineage H1CG.1 (GenBank: KU297278) (Table 4). In fact, six nucleotide bases differed between both lineages.

Table 4 Molecular identification of haemosporidians in pools of parous C. circumscriptus and C. paolae females trapped in avian nests and surroundings. Lineages and accession numbers from GenBank sequences showing the highest percentage of coverage and identity to those found in this study are shown. Previous information regarding these sequences is reported including the parasite morphospecies (when described), avian hosts and potential insect vectors (in bold) according to information of the reported sequences
Full size table

Discussion

This study reveals that C. circumscriptus and C. paolae are common endophagous insects at the nests of cavity-nesting species, with C. paolae being identified for the first time, using identification of blood meals, as a potential vector of avian haemosporidians. This assertion is supported by detecting a high diversity of avian hosts including cavity-nesting and open-nesting species and the identification of avian haemosporidian parasites for C. paolae.

Whereas C. circumscriptus is common in Spain [56, 67,68,69,70,71,72], C. paolae was detected for the first time in 2008 [41]. It has been proposed that the latter species was introduced into Europe by Columbus’s travels from America five centuries ago [44, 73]. In spite of some morphological differences, C. paolae is very similar to the American Culicoides jamaicensis [44] and a recent phylogenetic study related the former species with Culicoides from the New World [73]. Nowadays, in addition to Spain, where C. paolae is currently expanding its distribution range [41], this biting midge is the most widespread and abundant species of all Culicoides in Malta [34] and one of the most abundant species in central Tunisia [74] and Sardinia [75], where its importance on the local transmission of avian vector-borne pathogens should be considered. Culicoides paolae is commonly found near livestock farms [34, 74, 75], but according to our results, this species may also be widespread in the wild and, at least for the study period, it is even more abundant than C. circumscriptus (Tables 1, 2). Data from two breeding seasons suggest that the two species exhibit different phenologies, C. paolae being more abundant late in the roller breeding season whereas the opposite is true for C. circumscriptus. Furthermore, whereas the ability of some ornithophilic biting midges to feed inside enclosed places (endophagy) has been previously shown [39, 53, 69, 76], to our knowledge this is the first time that endophagy has been recorded for C. paolae.

Culicoides paolae is defined as ornithophilic according to its sensory structures [44]. Here we provide for the first time, unequivocal identification of its hosts, including seven different bird species within the study area. This broad spectrum of hosts has already been described for other ornithophilic Culicoides species [22, 77]. Interestingly, some of the host species are not particularly abundant in the study area, suggesting a remarkable feeding range of this biting midge and excellent host-searching abilities. Nonetheless, a greater effort in sampling engorged females C. paolae together with an analysis of the bird community composition around the traps is still necessary for a better knowledge of host selection by this dipteran. Our results also suggest that C. paolae could feed on humans. Even though we tried to minimize the risk of contamination, we did not type the human-positive samples with DNA samples of the experimenters (e.g. [78]). Thus, we cannot discard the possibility of sample contamination. Nonetheless, other ornithophilic species like C. kibunensis [79, 80], C. circumscriptus [81], or C. pictipennis [82], have previously been reported to feed on humans. The broad range of hosts could help biting midges to face environmental changes [79], and in our case, it could have facilitated the establishment of C. paolae in a new area.

DNA from four Haemoproteus lineages and one Plasmodium lineage was detected in parous C. paolae and C. circumscriptus. Even though multiple Plasmodium lineages have been molecularly detected in Culicoides [18, 46], this does not imply vector competence [83]. Plasmodium is mainly transmitted by Culex mosquitoes [7] and our result could simply reflect the presence of abortive stages of P. vaughani in C. paolae [84].

We isolated four different Haemoproteus lineages from six pools of Culicoides females. A lineage of H. minutus (TURDUS2) was detected both in C. paolae and C. circumscriptus. This is a geographically widespread lineage (northwest Africa, northwest Iberia, Transcaucasia and western Greater Caucasus) infecting different avian species, with Turdus merula probably playing a central role as reservoir [85]. Additionally, GAGLA03 (=GAGLA05) was previously isolated in Bulgaria from Garrulus glandarius [86], C. circumscriptus in Spain ([46], this study) and Turkey (GenBank: MF594402 and MF095639). The lineage AEFUN03 that had been only detected previously in Aegolious funereus [87] was found in C. circumscriptus in south-eastern Spain. This bird species is absent from the study area and probably this Haemoproteus lineage is infecting another locally abundant owl (e.g. little owl Athene noctua). Finally, we also detected a new Haemoproteus lineage highly similar (99% similarity) to the one corresponding to the haplotype H1CG.1 (identified as H. coraciae), which was detected previously in the same roller breeding population by Václav et al. [39]. Microscopic examination of smears suggested that this lineage might correspond to the species Haemoproteus coraciae [39], a parasite identified in rollers in Bulgaria [88] and Kazakhstan [89]. For the case of avian malaria parasites and related haemosporidians, different lineages are described with differences of a single nucleotide base in their sequences [62]. However, different lineages showing few differences may correspond to the same parasite morphospecies. Thus, it is likely that the new lineage reported here (H1CG.1) corresponds to the H. coraciae morphospecies. Further analyses are necessary to confirm this possibility. Haemoproteus coraciae were widely prevalent in adult rollers and also present in nestlings, suggesting the presence of a competent vector in the breeding area [39]. Václav et al. [39] pointed out that the detection of a Haemoproteus species only infecting adult rollers was intriguing because all the Culicoides species studied by Bobeva et al. [82] were feeding on a wide range of avian host. Our results suggest that C. paolae may be a competent vector for H. coraciae probably playing a role on the transmission of locally circulating parasites that could be amplified by the migratory behaviour of rollers. Further analyses are necessary to confirm the vector competence of this Culicoides species for the transmission of the lineages isolated here [83].

The prevalence of Haemoproteus in C. circumscriptus in the study area (4.4%) is slightly lower than the one observed in central Spain (16.7% [18]) and southwestern Spain (10.3% [46]), yet it is higher than the prevalence found in the sympatric C. paolae (0.7 vs 4.4%). On the other hand, C. paolae is seemingly locally more abundant than C. circumscriptus both at the nests and in their surroundings. Therefore, both species could play an important role in the transmission dynamics of haemosporidian parasites in the study area. Nevertheless, other factors such as the efficiency of parasite transmission or seasonality in vector abundance should be considered. Concerning the latter, our study reveals that differential exposure of the hosts to individual biting midge species along the season is worth studying to fully understand the risk of haemosporidian transmission by each species.

Conclusions

Vectors for most haemosporidians are unidentified [7, 90] and thus parasite-vector associations remain an enigmatic aspect of haemosporidian parasite ecology [17, 19, 91]. Here, we provide valuable information about the Haemoproteus lineages potentially transmitted by two biting midges species. Culicoides paolae and C. circumscriptus were abundant both at the nests of cavity bird species and in their surroundings, with seasonal differences in abundance during the study period. We assessed the ornithophilic diet of C. paolae that fed on at least seven bird species and possibly also on humans. Both biting midge species harboured several Haemoproteus lineages. These findings provide an important first step towards the identification of C. paolae and C. circumscriptus as potential vectors of avian haemosporidian parasites.

Abbreviations

MALDI-TOF:

matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

CDC:

Centers for Disease Control

GLMM:

Generalized linear mixed effects models

References

  1. 1.

    Borkent A. The biting midges, the Ceratopogonidae (Diptera). In: Marquardt WC, editor. Biology of Disease Vectors. 2nd ed. San Diego: Elsevier Academic Press; 2005. p. 113–26.

    Google Scholar 

  2. 2.

    Carpenter S, Groschup MH, Garros C, Felippe-Bauer ML, Purse BV. Culicoides biting midges, arboviruses and public health in Europe. Antiviral Res. 2013;100:102–13.

    CAS  Article  Google Scholar 

  3. 3.

    Atkinson CT, Van Riper C. Pathogenicity and epizootiology of avian haematozoa: Plasmodium, Leucocytozoon and Haemoproteus. In: Loye JE, Zuk M, editors. Bird-Parasite Interactions: Ecology, Evolution, and Behaviour. London: Oxford University Press; 1991. p. 19–48.

    Google Scholar 

  4. 4.

    Mellor PS, Boorman J, Baylis M. Culicoides biting midges: their role as arbovirus vectors. Annu Rev Entomol. 2000;45:307–40.

    CAS  Article  Google Scholar 

  5. 5.

    Mellor PS, Boorman J. The transmission and geographical spread of African horse sickness and bluetongue viruses. Ann Trop Med Parasitol. 1995;89:1–15.

    CAS  Article  Google Scholar 

  6. 6.

    Da Rosa JFT, de Souza WM, de Paula Pinheiro F, Figueiredo ML, Cardoso JF, Acrani GO, et al. Oropouche virus: clinical, epidemiological, and molecular aspects of a neglected Orthobunyavirus. Am J Trop Med Hyg. 2017;96:1019–30.

    Google Scholar 

  7. 7.

    Valkiūnas G. Avian Malaria Parasites and Other Haemosporidia. Boca Raton: CRC Press; 2005.

    Google Scholar 

  8. 8.

    Merino S, Moreno J, Sanz JJ, Arriero E. Are avian blood parasites pathogenic in the wild? A medication experiment in blue tits (Parus caeruleus). Proc R Soc Lond B Biol Sci. 2000;267:2507–10.

    CAS  Article  Google Scholar 

  9. 9.

    Marzal A, De Lope F, Navarro C, Møller AP. Malarial parasites decrease reproductive success: an experimental study in a passerine bird. Oecologia. 2005;142:541–5.

    Article  Google Scholar 

  10. 10.

    Valkiūnas G, Zickus T, Shapoval AP, Iezhova TA. Effect of Haemoproteus belopolskyi (Haemosporida: Haemoproteidae) on body mass of the blackcap Sylvia atricapilla. J Parasitol. 2006;92:1123–5.

    Article  Google Scholar 

  11. 11.

    Tomás G, Merino S, Moreno J, Morales J, Martínez-de la Puente J. Impact of blood parasites on immunoglobulin level and parental effort: a medication field experiment on a wild passerine. Funct Ecol. 2007;21:125–33.

  12. 12.

    Martínez-de la Puente J, Merino S, Tomás G, Moreno J, Morales J, Lobato E, et al. The blood parasite Haemoproteus reduces survival in a wild bird: a medication experiment. Biol Lett. 2010;6:663–5.

    Article  Google Scholar 

  13. 13.

    Asghar M, Hasselquist D, Bensch S. Are chronic avian haemosporidian infections costly in wild birds? J Avian Biol. 2011;42:530–7.

    Article  Google Scholar 

  14. 14.

    Asghar M, Hasselquist D, Hansson B, Zehtindjiev P, Westerdahl H, Bensch S. Hidden costs of infection: chronic malaria accelerates telomere degradation and senescence in wild birds. Science. 2015;347:436–8.

    CAS  Article  Google Scholar 

  15. 15.

    Hellgren O, Bensch S, Malmqvist B. Bird hosts, blood parasites and their vectors - associations uncovered by molecular analyses of blackfly blood meals. Mol Ecol. 2008;17:1605–13.

    CAS  Article  Google Scholar 

  16. 16.

    Ishtiaq F, Guillaumot L, Clegg SM, Phillimore AB, Black RA, Owens IPF, et al. Avian haematozoan parasites and their associations with mosquitoes across Southwest Pacific Islands. Mol Ecol. 2008;17:4545–55.

    CAS  Article  Google Scholar 

  17. 17.

    Kimura M, Darbro JM, Harrington LC. Avian malaria parasites share congeneric mosquito vectors. J Parasitol. 2010;96:144–51.

    CAS  Article  Google Scholar 

  18. 18.

    Martínez-de la Puente J, Martínez J, Rivero-de Aguilar J, Herrero J, Merino S. On the specificity of avian blood parasites: revealing specific and generalist relationships between haemosporidians and biting midges. Mol Ecol. 2011;20:3275–87.

    Article  Google Scholar 

  19. 19.

    Njabo KY, Cornel AJ, Bonneaud C, Toffelmier E, Sehgal RNM, Valkiūnas G, et al. Nonspecific patterns of vector, host and avian malaria parasite associations in a central African rainforest. Mol Ecol. 2011;20:1049–61.

    CAS  Article  Google Scholar 

  20. 20.

    Santiago-Alarcon D, Palinauskas V, Schaefer HM. Diptera vectors of avian haemosporidian parasites: untangling parasite life cycles and their taxonomy. Biol Rev. 2012;87:928–64.

    Article  Google Scholar 

  21. 21.

    Garnham PCC. Malaria Parasites and other Haemosporidia. Oxford: Blackwell Scientific Publications; 1966.

    Google Scholar 

  22. 22.

    Martínez-de la Puente J, Figuerola J, Soriguer R. Fur or feather? Feeding preferences of species of Culicoides biting midges in Europe. Trends Parasitol. 2015;3:16–22.

    Article  Google Scholar 

  23. 23.

    Jamnback H. The Culicoides of New York State (Diptera: Ceratopogonidae). NY State Mus Sci Serv Bull. 1965;399:1–154.

    Google Scholar 

  24. 24.

    Braverman Y, Hulley PE. The relationship between the numbers and distribution of some antennal and palpal sense organs and host preference in some Culicoides (Diptera: Ceratopogonidae) from southern Africa. J Med Entomol. 1979;15:419–24.

    Article  Google Scholar 

  25. 25.

    Augot D, Hadj-Henni L, Strutz SE, Slama D, Millot C, Depaquit J, et al. Association between host species choice and morphological characters of main sensory structures of Culicoides in the Palaeartic region. PeerJ. 2017;5:e3478.

    Article  Google Scholar 

  26. 26.

    Weitz B. Identification of blood meals of blood-sucking arthropods. Bull World Health Organ. 1956;15:473.

    CAS  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Braverman Y, Boreham PFL, Galum R. The origin of blood meals of female Culicoides pallidipennis trapped in a sheepfold in Israel. J Med Entomol. 1971;8:379–81.

    CAS  Article  Google Scholar 

  28. 28.

    Nevill EM, Anderson D. Host preferences of Culicoides midges (Diptera: Ceratopogonidae) in South Africa as determined by precipitin tests and light trap catches. Onderstepoort J Vet Res. 1972;39:147–52.

    CAS  PubMed  Google Scholar 

  29. 29.

    Blackwell A, Mordue W. Identification of bloodmeals of the Scottish biting midge, Culicoides impunctatus, by indirect enzyme-linked immunosorbent assay (ELISA). Med Vet Entomol. 1994;8:20–4.

    CAS  Article  Google Scholar 

  30. 30.

    Blackwell A, Brown M, Mordue W. The use of an enhanced ELISA method for the identification of Culicoides bloodmeals in host-preference studies. Med Vet Entomol. 1995;9:214–8.

    CAS  Article  Google Scholar 

  31. 31.

    Niare S, Berenger JM, Dieme C, Doumbo O, Raoult D, Parola P, et al. Identification of blood meal sources in the main African malaria mosquito vector by MALDI-TOF MS. Malar J. 2016;15:87.

    Article  Google Scholar 

  32. 32.

    Alcaide M, Rico C, Ruiz S, Soriguer R, Muñoz J, Figuerola J. Disentangling vector-borne transmission networks: a universal DNA barcoding method to identify vertebrate hosts from arthropod bloodmeals. PLoS One. 2009;4:e7092.

    Article  Google Scholar 

  33. 33.

    Van der Saag MR, Gu X, Ward MP, Kirkland PD. Development and evaluation of real-time PCR assays for bloodmeal identification in Culicoides midges. Med Vet Entomol. 2016;30:155–65.

    CAS  Article  Google Scholar 

  34. 34.

    Goffredo M, Buttigieg M, Meiswinkel R, Delécolle JC, Chircop S. Entomological surveillance for bluetongue on Malta: first report of Culicoides imicola Kieffer. Vet Ital. 2004;40:278–81.

    CAS  PubMed  Google Scholar 

  35. 35.

    Lysyk TJ. Abundance and species composition of Culicoides (Diptera: Ceratopogonidae) at cattle facilities in southern Alberta, Canada. J Med Entomol. 2006;43:840–9.

    CAS  Article  Google Scholar 

  36. 36.

    Casati S, Racloz V, Delécolle JC, Kuhn M, Mathis A, Griot C, et al. An investigation on the Culicoides species composition at seven sites in southern Switzerland. Med Vet Entomol. 2009;23:93–8.

    CAS  Article  Google Scholar 

  37. 37.

    Narladkar BW, Shivpuje PR. Prevalence, population dynamics and host preferences of Culicoides spp. (Diptera: Ceratopogonidae) of livestock in Marathwada region of Maharashtra State. Vet World. 2014;7:717–26.

    Article  Google Scholar 

  38. 38.

    Valera F, Carrillo CM, Barbosa A, Moreno E. Low prevalence of haematozoa in Trumpeter finches Bucanetes githagineus from south-eastern Spain: additional support for a restricted distribution of blood parasites in arid lands. J Arid Environ. 2003;55:209–13.

    Article  Google Scholar 

  39. 39.

    Václav R, Betáková T, Švančarová P, Pérez-Serrano J, Criado-Fornelio Á, Škorvanová L, et al. Nest ecology of blood parasites in the European roller and its ectoparasitic carnid fly. Exp Parasitol. 2016;165:71–80.

    Article  Google Scholar 

  40. 40.

    Alarcón-Elbal PM, Lucientes J. Actualización del catálogo de Culicoides Latreille, 1809 (Diptera, Ceratopogonidae) de España. Graellsia. 2012;68:353–62.

    Article  Google Scholar 

  41. 41.

    Estrada R, Carmona VJ, Alarcón-Elbal PM, Miranda MA, Borrás D, Roche ML, et al. Primera cita de Culicoides paolae Boorman, 1996 (Diptera, Ceratopogonidae) para la Península Ibérica. Bol SEA. 2011;49:217–21.

    Google Scholar 

  42. 42.

    Boorman J, Mellor PS, Scaramozzino P. A new species of Culicoides (Diptera, Ceratopogonidae) from southern Italy. Parassitologia. 1996;38:501–3.

    CAS  PubMed  Google Scholar 

  43. 43.

    Barceló C, Miranda MA. Bionomics of livestock-associated Culicoides (biting midge) bluetongue virus vectors under laboratory conditions. Med Vet Entomol. 2017; https://doi.org/10.1111/mve.12286.

  44. 44.

    Meiswinkel R, Labuschagne K, Goffredo M. Christopher Columbus and Culicoides: was C. jamaicensis Edwards, 1922 introduced into the Mediterranean 500 years ago and later re-named C. paolae Boorman 1996? Vet Ital. 2004;40:340–4.

    CAS  PubMed  Google Scholar 

  45. 45.

    Černý O, Votýpka J, Svobodová M. Spatial feeding preferences of ornithophilic mosquitoes, blackflies and biting midges. Med Vet Entomol. 2011;25:104–8.

    Article  Google Scholar 

  46. 46.

    Ferraguti M, Martínez-de la Puente J, Ruiz S, Soriguer R, Figuerola J. On the study of the transmission networks of blood parasites from SW Spain: diversity of avian haemosporidians in the biting midge Culicoides circumscriptus and wild birds. Parasit Vectors. 2013;6:208.

    Article  Google Scholar 

  47. 47.

    Lázaro R, Rodríguez-Tamayo ML, Ordiales R, Puigdefábregas J. El clima. In: Mota J, Cabello J, Cerrillo MI, Rodríguez-Tamayo ML, editors. Subdesiertos de Almería: naturaleza de cine. Murcia: Consejería de Medio Ambiente, Junta de Andalucía; 2004. p. 63–79.

    Google Scholar 

  48. 48.

    Lázaro R, Rodrigo FS, Gutiérrez L, Domingo F, Puigdefábregas J. Analysis of a thirty-year rainfall record (1967–1997) from semi-arid SE Spain: a plant ecological perspective. J Arid Environ. 2001;48:373–95.

    Article  Google Scholar 

  49. 49.

    Valera F, Václav R, Calero-Torralbo MA, Martínez T, Veiga J. Natural cavity restoration as an alternative to nest box supplementation. Restor Ecol. 2018; https://doi.org/10.1111/rec.12841.

  50. 50.

    Václav R, Valera F, Martínez T. Social information in nest colonisation and occupancy in a long-lived, solitary breeding bird. Oecologia. 2011;165:617–27.

    Article  Google Scholar 

  51. 51.

    Avilés JM, Sánchez JM, Sánchez A, Parejo D. Breeding biology of Roller Coracias garrulus L. 1758 in farming areas of the southwest of the Iberian Peninsula. Bird Study. 1999;46:217–23.

    Article  Google Scholar 

  52. 52.

    Cramp S. Handbook of the Birds of Europe the Middle East and North Africa: the Birds of the Western Palearctic, Vol. IV. Terns to Woodpeckers. Oxford: Oxford University Press; 1985.

  53. 53.

    Tomás G, Merino S, Martínez-de la Puente J, Moreno J, Morales J, Lobato E. A simple trapping method to estimate abundances of blood-sucking flying insects in avian nests. Anim Behav. 2008;75:723–9.

    Article  Google Scholar 

  54. 54.

    González M, Alarcón-Elbal PM, Valle-Mora J, Goldarazena A. Comparison of different light sources for trapping Culicoides biting midges, mosquitoes and other dipterans. Vet Parasitol. 2016;226:44–9.

    Article  Google Scholar 

  55. 55.

    McDermott EG, Mullens BA. The dark side of light traps. J Med Entomol. 2018;55:251–61.

    Article  Google Scholar 

  56. 56.

    González M, Goldarazena A. El género Culicoides en el País Vasco. Guía Práctica para su identificación y control. Vitoria-Gasteiz, España: Servicio Central de Publicaciones del Gobierno Vasco; 2011.

    Google Scholar 

  57. 57.

    Mathieu B, Cêtre-Sossah C, Garros C, Chavernac D, Balenghien T, Carpenter S, et al. Development and validation of IIKC: an interactive identification key for Culicoides (Diptera: Ceratopogonidae) females from the Western Palaearctic region. Parasit Vectors. 2012;5:137.

    Article  Google Scholar 

  58. 58.

    Dyce AL. The recognition of nulliparous and parous Culicoides (Diptera: Ceratopogonidae) without dissection. Aus J Ent. 1969;8:11–5.

    Article  Google Scholar 

  59. 59.

    Gutiérrez-López R, Martínez-de la Puente J, Gangoso L, Soriguer RC, Figuerola J. Comparison of manual and semi-automatic DNA extraction protocols for the barcoding characterization of hematophagous louse flies (Diptera: Hippoboscidae). J Vector Ecol. 2015;40:11–5.

    Article  Google Scholar 

  60. 60.

    Hellgren O, Waldenström J, Bensch S. A new PCR assay for simultaneous studies of Leucocytozoon, Plasmodium, and Haemoproteus from avian blood. J Parasitol. 2004;90:797–802.

    CAS  Article  Google Scholar 

  61. 61.

    McClintock BT, Nichols JD, Bailey LL, MacKenzie DI, Kendall W, Franklin AB. Seeking a second opinion: uncertainty in disease ecology. Ecol Lett. 2010;13:659–74.

    Article  Google Scholar 

  62. 62.

    Bensch S, Hellgren O, Pérez-Tris J. MalAvi: a public database of malaria parasites and related haemosporidians in avian hosts based on mitochondrial cytochrome b lineages. Mol Ecol Res. 2009;9:1353–8.

    Article  Google Scholar 

  63. 63.

    Sergeant ESG. Epitools epidemiological calculators. Ausvet Pty Ltd. 2018; http://epitools.ausvet.com.au. Accessed 18 Apr 2018

  64. 64.

    R Core Team. R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2015.

    Google Scholar 

  65. 65.

    Fox J. Effect displays in R for generalised linear models. J Stat Softw. 2003;8:1–27.

    Article  Google Scholar 

  66. 66.

    Bates D, Mächler M, Bolker B, Walker S. Fitting linear mixed-effects models using lme4. J Stat Softw. 2015;67:1–48.

    Article  Google Scholar 

  67. 67.

    Ortega MD, Mellor PS, Rawlings O, Pro MJ. The seasonal and geographical distribution of Culicoides imicola, C. pulicaris group and C. obsoletus group biting midges in central and southern Spain. Arch Virol. 1998;14:85–91.

    CAS  Google Scholar 

  68. 68.

    Ventura D, Pagès N, Sarto V. Citas nuevas e interesantes de Culicoides Latreille, 1809 para Cataluña y la Península Ibérica (Diptera, Nematocera, Ceratopogonidae). Bol Asoc Esp Entomol. 2005;29:75–86.

    Google Scholar 

  69. 69.

    Martínez-de la Puente J, Merino S, Tomás G, Moreno J, Morales J, Lobato E, et al. Factors affecting Culicoides species composition and abundance in avian nests. Parasitology. 2009;136:1033–41.

    Article  Google Scholar 

  70. 70.

    Del Río R. Estrategias de control y competencia vectorial de las especies de Culicoides vectores del virus de la lengua azul en península Ibérica y Baleares, PhD Thesis. Palma de Mallorca: Universitat de les Illes Balears; 2012.

  71. 71.

    Estrada R, Alarcón-Elbal PM, Carmona Salido VJ, Ruiz Arrondo I, Delacour S, Pinal R, et al. Culicoides (Diptera, Cerotopogonidae) de Aragón. Bol SEA. 2013;53:153–60.

    Google Scholar 

  72. 72.

    Alarcón-Elbal PM, Estrada R, Carmona-Salido VJ, Calvete C, Lucientes J. Composición faunística y dinámica poblacional de los Culicoides (Diptera: Ceratopogonidae) de Castilla-La Mancha. An Biol. 2016;28:37–61.

    Article  Google Scholar 

  73. 73.

    Augot D, Mathieu B, Hadj-Henni L, Barriel V, Mena SZ, Smolis S, et al. Molecular phylogeny of 42 species of Culicoides (Diptera, Ceratopogonidae) from three continents. Parasite. 2017;24:23.

    Article  Google Scholar 

  74. 74.

    Slama D, Haouas N, Mezhoud H, Babba H, Chaker E. Blood meal analysis of Culicoides (Diptera: Ceratopogonidae) in central Tunisia. PLoS One. 2015;10:e0120528.

    Article  Google Scholar 

  75. 75.

    Foxi C, Pinna M, Monteys VSI, Delrio G. An updated checklist of the Culicoides Latreille (Diptera: Ceratopogonidae) of Sardinia (Italy), and seasonality in proven and potential vectors for bluetongue virus (BTV). Proc Entomol Soc Wash. 2011;113:403–16.

    Article  Google Scholar 

  76. 76.

    Votýpka J, Synek P, Svobodova M. Endophagy of biting midges attacking cavity-nesting birds. Med Vet Entomol. 2009;23:277–80.

    Article  Google Scholar 

  77. 77.

    Pettersson E, Bensch S, Ander M, Chirico J, Sigvald R, Ignell R. Molecular identification of blood meals and species composition in Culicoides biting midges. Med Vet Entomol. 2013;27:104–12.

    CAS  Article  Google Scholar 

  78. 78.

    Malmqvist B, Strasevicius D, Hellgren O, Adler PH, Bensch S. Vertebrate host specificity of wild-caught blackflies revealed by mitochondrial DNA in blood. Proc R Soc Lond B Biol Sci. 2004;271:152–5.

    Article  Google Scholar 

  79. 79.

    Santiago-Alarcon D, Havelka P, Schaefer HM, Segelbacher G. Bloodmeal analysis reveals avian Plasmodium infections and broad host preferences of Culicoides (Diptera: Ceratopogonidae) vectors. PLoS One. 2012;7:e31098.

    CAS  Article  Google Scholar 

  80. 80.

    Santiago-Alarcon D, Havelka P, Pineda E, Segelbacher G, Schaefer H. Urban forests as hubs for novel zoonosis: Blood meal analysis, seasonal variation in Culicoides (Diptera: Ceratopogonidae) vectors, and avian haemosporidians. Parasitology. 2013;140:1799–810.

    Article  Google Scholar 

  81. 81.

    Lassen SB, Nielsen SA, Kristensen M. Identity and diversity of blood meal hosts of biting midges (Diptera: Ceratopogonidae: Culicoides Latreille) in Denmark. Parasit Vectors. 2012;5:143.

    CAS  Article  Google Scholar 

  82. 82.

    Bobeva A, Zehtindjiev P, Ilieva M, Dimitrov D, Mathis A, Bensch S. Host preferences of ornithophilic biting midges of the genus Culicoides in the eastern Balkans. Med Vet Entomol. 2015;29:290–6.

  83. 83.

    Valkiūnas G. Haemosporidian vector research: marriage of molecular and microscopical approaches is essential. Mol Ecol. 2011;20:3084–6.

    Article  Google Scholar 

  84. 84.

    Valkiūnas G, Kazlauskienė R, Bernotienė R, Palinauskas V, Iezhova TA. Abortive long-lasting sporogony of two Haemoproteus species (Haemosporida, Haemoproteidae) in the mosquito Ochlerotatus cantans with perspectives on haemosporidian vector research. Parasitol Res. 2013;112:2159–69.

    Article  Google Scholar 

  85. 85.

    Drovetski SV, Aghayan SA, Mata VA, Lopes RJ, Mode NA, Harvey JA, et al. Does the niche breadth or trade-off hypothesis explain the abundance-occupancy relationship in avian haemosporidia? Mol Ecol. 2014;23:3322–9.

    Article  Google Scholar 

  86. 86.

    Dimitrov D, Zehtindjiev P, Bensch S. Genetic diversity of avian blood parasites in SE Europe: cytochrome b lineages of the genera Plasmodium and Haemoproteus (Haemosporida) from Bulgaria. Acta Parasitol. 2010;55:201–9.

    CAS  Article  Google Scholar 

  87. 87.

    Synek P, Popelková A, Koubínová D, Šťastný K, Langrová I, Votýpka J, et al. Haemosporidian infections in the Tengmalm’s Owl (Aegolius funereus) and potential insect vectors of their transmission. Parasitol Res. 2016;115:291–8.

    Article  Google Scholar 

  88. 88.

    Shurulinkov P, Golemansky V. Haemoproteids (Haemosporida: Haemoproteidae) of wild birds in Bulgaria. Acta Protozool. 2002;41:359–74.

    Google Scholar 

  89. 89.

    Valkiūnas G, Iezhova T. Parasitic Protozoa of the blood of birds in the USSR. 6. Haemoproteidae of columbiformes and coraciiformes. Ekologija. 1990;2:86–103 (In Russian).

    Google Scholar 

  90. 90.

    Cleaveland S, Laurenson MK, Taylor LH. Diseases of humans and their domestic mammals: pathogen characteristics, host range and the risk of emergence. Philos Trans R Soc Lond B Biol Sci. 2001;356:991–9.

  91. 91.

    Atkinson CT, Thomas NJ, Hunter DB. Parasitic Diseases of Wild Birds. Ames: Wiley-Blackwell; 2008.

    Book  Google Scholar 

Download references

Acknowledgements

Francisco Collantes provided helpful advice concerning trapping methods. Domingo Álvarez, Isabel Martín and Laura Gómez helped in the laboratory analyses.

Funding

JV was funded by the Spanish Ministry of Economy, Industry and Competitiveness by means of a predoctoral grant (grant no. BES-2015-075951). FV and JF received financial support from the Spanish Ministry of Economy and Competitiveness, and the European Regional Development Fund (CGL2014-55969-P; CGL2015-65055-P). JMP was partially supported by a 2017 Leonardo Grant for Researchers and Cultural Creators, BBVA Foundation. The Foundation accepts no responsibility for the opinions, statements and contents included in the project and/or the results thereof, which are entirely the responsibility of the authors. We acknowledge support of the publication fees by the CSIC Open Access Publication Support Initiative through its Unit of Information Resources for Research (URICI).

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author upon reasonable request. The new lineage sequence of H. coraciae was submitted to the GenBank database under the accession number MH237967.

Author information

Affiliations

  1. Departamento de Ecología Funcional y Evolutiva, Estación Experimental de Zonas Áridas (EEZA-CSIC), Ctra. de Sacramento s/n, La Cañada de San Urbano, E-04120, Almería, Spain

    Jesús Veiga & Francisco Valera

  2. Departamento de Ecología de Humedales, Estación Biológica de Doñana (EBD-CSIC), Seville, Spain

    Josué Martínez-de la Puente & Jordi Figuerola

  3. Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain

    Josué Martínez-de la Puente & Jordi Figuerola

  4. Institute of Zoology, Slovak Academy of Sciences, Dúbravská cesta 9, SK-84506, Bratislava, Slovakia

    Radovan Václav

Authors
  1. Jesús Veiga
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Josué Martínez-de la Puente
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Radovan Václav
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Jordi Figuerola
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Francisco Valera
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Conceived and designed the experiments: JV, RV and FV. Fieldwork: JV and FV. Contributed reagents/materials/analysis tools: JV, JMP, JF and FV. All authors contributed toward writing the manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Jesús Veiga.

Ethics declarations

Ethics approval

Bird trapping was carried out with all the necessary permits issued by the Junta de Andalucía.

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

Verify currency and authenticity via CrossMark

Cite this article

Veiga, J., Martínez-de la Puente, J., Václav, R. et al. Culicoides paolae and C. circumscriptus as potential vectors of avian haemosporidians in an arid ecosystem. Parasites Vectors 11, 524 (2018). https://doi.org/10.1186/s13071-018-3098-8

Download citation

Keywords

  • Biting midges
  • Haemoproteus
  • Vector-borne
  • Arid area
  • Endophagy
  • Blood meal
  • Coracias garrulus

Parasites & Vectors

ISSN: 1756-3305

Contact us