Molecular species identification, host preference and detection of myxoma virus in the Anopheles maculipennis complex (Diptera: Culicidae) in southern England, UK
© Brugman et al. 2015
Received: 8 June 2015
Accepted: 5 August 2015
Published: 15 August 2015
Determining the host feeding patterns of mosquitoes by identifying the origin of their blood-meals is an important part of understanding the role of vector species in current and future disease transmission cycles. Collecting large numbers of blood-fed mosquitoes from the field is difficult, therefore it is important to maximise the information obtained from each specimen. This study aimed to use mosquito genome sequence to identify the species within Anopheles maculipennis sensu lato (An. maculipennis s.l.), identify the vertebrate hosts of field-caught blood-fed An. maculipennis s.l. , and to test for the presence of myxoma virus (Poxviridae, genus Leporipoxvirus) in specimens found to have fed on the European rabbit (Oryctolagus cuniculus).
Blood-fed An. maculipennis s.l. were collected from resting sites at Elmley Nature Reserve, Kent, between June and September 2013. Hosts that An. maculipennis s.l. had fed on were determined by a PCR-sequencing approach based on the partial amplification of the mitochondrial cytochrome C oxidase subunit I gene. Mosquitoes were then identified to species by sequencing a region of the internal transcribed spacer-2. DNA extracts from all mosquitoes identified as having fed on rabbits were subsequently screened using PCR for the presence of myxoma virus.
A total of 94 blood-fed Anopheles maculipennis s.l. were collected, of which 43 (46 %) provided positive blood-meal identification results. Thirty-six of these specimens were identified as Anopheles atroparvus, which had fed on rabbit (n = 33, 92 %) and cattle (n = 3, 8 %). Seven mosquitoes were identified as Anopheles messeae, which had fed on cattle (n = 6, 86 %) and dog (n = 1, 14 %). Of the 33 An. atroparvus that contained rabbit blood, nine (27 %) were positive for myxoma virus.
Results demonstrate that a single DNA extract from a blood-fed mosquito can be successfully used for molecular identification of members of the An. maculipennis complex, blood-meal identification, and for the targeted detection of a myxoma virus. This study shows that An. atroparvus has a strong feeding preference for both healthy and myxoma-infected rabbits, providing evidence that this species may play a significant role in the transmission of myxomatosis among wild rabbit populations in the United Kingdom (UK).
The identification of blood-meal origin in haematophagous arthropods such as mosquitoes provides important information concerning vector-host interactions and associated disease transmission dynamics . Molecular techniques for blood-meal identification and the increasing volume of openly accessible databases of host species identification data such as GenBank  and The Barcode of Life Database  have facilitated this area of research. Systematic characterisation of bird and mammalian host genetics in particular has increased the specificity of studies carried out driven by the use of polymerase chain reaction techniques. These techniques have largely replaced serological methods for blood meal identification such as the precipitin test and enzyme-linked immunosorbent assays (ELISA) . The high copy number and conserved nature of mitochondrial genes such as cytochrome b and cytochrome c oxidase I (COI) have made them popular targets for identification applied to host-feeding preference studies . Ribosomal genes such as the internal transcribed spacer-2 (ITS-2) are also commonly used in species identification . For example, both COI and ITS-2 markers helped to identify a third member of the An. maculipennis complex, An. daciae, Linton, Nicolescu & Harbach 2004, from the previously recognised species An. atroparvus van Thiel 1927 and An. messeae Falleroni 1926 . Identifying mosquitoes to species level is important in blood-feeding studies as sibling species may exhibit marked differences in feeding preferences which are likely to influence their role in patterns of disease transmission (reviewed in ).
Reported rabbit-feeding behaviour of British mosquitoes and their association with the myxoma virus prior to this study
Evidence of natural rabbit feeding
Identification of rabbit feeding through analysis of blood-meals
Wild-caught mosquitoes positive for Myxoma virus
Anopheles atroparvus a
Yes DC, BC
Culex pipiens s.l.
Yes; DC, BC
A major limitation to mosquito blood-feeding studies lies with the difficulty in collecting large numbers of blood-fed individuals with blood-meals that are sufficiently undigested to allow successful DNA amplification . This study aimed to maximise the data obtained from each blood-fed specimen by assessing whether a single DNA extract could be used for multiple purposes: firstly to identify the blood-meal origin in members of the An. maculipennis s.l using a cocktail of ‘universal’ barcoding primers and secondly to identify individual species of the An. maculipennis s.l. present in the study area to assess whether different species exhibited different feeding preferences. An. maculipennis s.l. was abundant at the site during the collecting visits and the dominant anopheline species captured. During a visit to Elmley, Kent, in the summer of 2013, it was also observed that rabbits were frequently present within 25 metres of areas where human biting activity of mosquitoes had been reported by farm workers. On a subsequent visit, wild rabbits with obvious facial lesions indicative of myxomatosis were observed. Therefore, a further aim of the study was to test whether blood-meal samples that originated specifically from rabbits also contained evidence of myxoma virus infection.
Collection of blood-fed mosquitoes
DNA extraction from mosquito abdomens
Mosquitoes were identified based on morphological features as An. maculipennis s.l. following the key of Snow . Abdomens of engorged mosquitoes were separated from the rest of the body on a chilled plate using forceps, and placed into individual 1.5 mL eppendorf tubes containing 200 μl phosphate buffered saline (PBS). The abdomens were pressed against the wall of the tube using the forceps to release the blood-meal. The remaining head and thorax of each mosquito was stored at −20 °C for morphological reference. Forceps were cleaned between specimens using a three stage wash to avoid cross-contamination. The first wash consisted of 5 % decon, the second of 100 % ethanol and the third of sterile water, at which point all excess liquid was removed with task wipes (Kimtech Science, Roswell, Georgia, USA). Each sample was incubated with 20 μl proteinase K and 200 μl buffer AL for 30 min at 56 °C in a water bath. DNA extraction was carried out using the DNeasy Blood and Tissue Kit (QIAgen, Manchester, UK), following the manufacturer’s spin column-protocol. All DNA extractions were stored at 4 °C until processing.
Identification of blood-meal host
Vertebrate host species in the blood-meal were identified using a vertebrate specific, M13-tailed, triple-primer cocktail (VF1_t1 + VF1d_t1 + VF1i_t1/VR1_t1 + VR1d_t1 + VD1i_t1) targeting a 685 base pair (bp) sequence of the COI gene [26, 27]. This primer combination was expected to amplify all vertebrate species. Reaction contents were obtained from Sigma-Aldrich (Sigma-Aldrich, Dorset, UK) unless otherwise stated. The final PCR reaction mix of 50 μl consisted of: 31.075 μl H2O, 5 μl GeneAmp 10X PCR buffer I (Applied Biosystems, Life Technologies Ltd, Paisley, UK), 1 μl dNTPs (at 0.2 mM/μl), 1 μl of each primer (at 10pmol/μl), 0.25 μl AmpliTaq Gold DNA Polymerase (10 units/μl) (Applied Biosystems, Life Technologies Ltd, Paisley, UK), 0.675 μl dimethyl sulfoxide (DMSO), 1 μl tetramethylammonium chloride (TMAC) and 5 μl extracted DNA. The thermal profile consisted of an initial denaturation step at 94 °C for 10 minutes followed by 40 cycles of: 94 °C for 30 seconds, 53 °C for 30 seconds, 72 °C for one minute, followed by a final elongation step of 72 °C for 10 minutes. PCR products were separated on a 1.5 % agarose gel and samples producing a positive result were sequenced. Sequencing was performed using M13 primers  at 1pmol/μl. Amplification products were sequenced in both directions using the ABI PRISM® BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Life Technologies Ltd, Paisley, UK). All sequences were edited using Lasergene version 12.1 (DNASTAR, Inc, Madison, Wisconsin, USA) and assigned to a particular vertebrate species when agreement was ≥98 % to sequences of known species in GenBank .
Species identification within Anopheles maculipennis s.l.
Species level identification was obtained by amplification of a 435 bp region of ITS-2 using the primers 5.8SF and 28SR of Collins & Paskewitz . PCR products were obtained using an optimised real-time PCR assay in a Mx3000P real-time PCR system (Stratagene, Agilent Technologies, Cheshire, UK) in the following reaction mix, final volume 40 μl: 2 μl of DNA template, 14 μl H2O, 20 μl SYBRGreen JumpStart Taq ReadyMix (Sigma-Aldrich, Dorset, UK) and 2 μl of each primer (each at 10 pmol/μl). The thermal profile consisted of an initial denaturation step at 94 °C for 10 minutes followed by 35 cycles of: 94 °C for 30 seconds, 53 °C for 30 seconds, 72 °C for one minute, followed by a final elongation step of 72 °C for 10 minutes. PCR products were visualized on a 1.5 % agarose gel, and samples showing bands of the correct size were sequenced in both directions using the ABI PRISM® BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems). All sequences were edited in Lasergene version 12.1 (DNASTAR) and assigned to a particular mosquito species when agreement was ≥98 % to sequences of known species in GenBank. ITS-2 sequences for each of the species within An. maculipennis s.l. found in the UK are available.
Detection of myxoma virus
Myxoma virus genome was detected using two previously published methods. Samples were initially screened using Low-GC PCR primers that amplified a 220 bp sequence of the myxoma virus genome . Samples giving a positive result were also amplified using a primer pair (M135Rfor/M135Rrev)  that produced a 650 bp amplicon. Amplified products were excised from a 2 % agarose gel and purified using a gel extraction kit (QIAgen, Manchester, UK). The resulting amplicon was then sequenced using flanking primers and ABI PRISM® BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Life Technologies Ltd, Paisley, UK) following the manufacturer’s instructions. The presence of myxoma virus was confirmed by BLAST (NCBI) search of the sequence.
Hosts selected by mosquito species at Elmley, Kent, between June and September 2013
Total of blood-fed
The molecular identification of the species from the same DNA samples using the ITS-2 region revealed that 36 specimens were An. atroparvus (98–100 % identity following BLAST search) and seven specimens were An. messeae (99–100 % identity following BLAST search). For the latter sequences, all shared greater than 99 % identity with published An. messeae ITS-2 sequences (GenBank accession number AY238412) and we are confident that no blood-fed samples of An. daciae were detected at the site. When the blood-feeding hosts were analyzed by species, An. atroparvus fed mainly on rabbits (n = 33, 92 %) and cattle (n = 3, 8 %). In contrast, An. messeae was found to have fed on cattle (n = 6, 86 %) and dog (n = 1, 14 %) (Table 2).
This study demonstrates that a single DNA extract from the abdomen of a blood-fed mosquito can be successfully used for three purposes in a sequential workflow: (1) for the identification of the vertebrate origin of a blood-meal by sequencing of a 685 bp region of the COI gene, followed by (2) the molecular identification of members of An. maculipennis s.l. by sequencing of a 435 bp region of ITS-2, then (3) the detection of a pathogen, in this case the myxoma virus. This approach provided definitive evidence that An. atroparvus feeds extensively on both healthy and myxoma-infected rabbits, thus indicating that this mosquito could play a more significant role in the transmission of myxomatosis in wild rabbit populations in the UK than was previously suspected.
Early studies on the feeding behaviour of An. atroparvus [18, 22] were limited to morphological identification of specimens. Despite suggestions as far back as the 1930s of a third member of the An. maculipennis s.l. in the UK , it was not until recent sequencing of ITS-2 was performed that a third member, An. daciae, was discovered . Applying current molecular techniques to delineate mosquito species complexes is important as morphologically indistinguishable sibling species may exhibit different feeding behaviours that will affect their capacity to act as disease vectors. Owing to its recent discovery in the UK the feeding preferences of An. daciae have not been extensively studied, however one study indicated it may differ from An. atroparvus and An. messeae by feeding on birds as well mammals . In the present study no An. daciae were found but An. atroparvus and An. messeae were successfully identified by amplification of ITS-2 . The presence of both species in the same collection site is to be expected as Elmley sits at the interface between the saline coastal habitats generally favoured by An. atroparvus and freshwater breeding habitats in the grazing marshes more suited to An. messeae (see  for a review). Both these species were found to feed only on mammals, corresponding with previous studies . However, 92 % of An. atroparvus blood-meals were taken from rabbits, whereas An. messeae was found to have fed only on cattle (86 %) and dog (14 %). It is worthy of note that although the 14 % of An. messeae comprises only a single mosquito, only one dog is present on site (this belongs to the site owners; other dogs are not permitted) and thus the host abundance of this species is considerably lower than that of rabbits around the collection site. Nonetheless it is evident that further blood-fed collections from the site are required to draw conclusions on whether these results reflect a true difference in feeding preferences between the two mosquito species. Prior to this study, there have been no published reports of rabbit blood being detected in field-caught specimens of An. atroparvus in the UK (Table 1). The molecular approach used in this study facilitated the finding of this result as sequencing of the ‘universal’ barcoding region of the COI gene precludes the need to pre-select hosts on which mosquito feeding is considered most likely, a necessary step in the preparation of species-specific sera for serological assays such as the precipitin test or when designing primers for a multiplex assay. The previous study collecting An. maculipennis s.l. from a similar area of Kent utilised a multiplex assay design that did not include rabbit and therefore was not able to inform on rabbit-feeding behaviour .
The apparent strong feeding preference of An. atroparvus for rabbits is somewhat surprising considering the low numbers captured previously in a study employing direct capture of mosquitoes, rabbit-baited traps and precipitin testing in the UK . There, only two individuals of the An. maculipennis s.l. were collected, both of which were negative for rabbit blood by precipitin testing and neither mosquito were identified to species. A recent host preference study in Spain provided evidence that An. atroparvus populations did feed on rabbits in the wild, albeit at a frequency of less than 2 % (2/115 blood-meals) . This contrasts with observations of strong feeding preferences for rabbits by An. atroparvus elsewhere in Europe , raising the question of whether different populations of the same species may exhibit different feeding preferences driven mainly by the local availability of hosts rather than an intrinsic preference . Collecting larger numbers of blood-fed An. maculipennis s.l. from several sites across the UK taking into account local rabbit abundance may provide evidence to this effect. Elmley Nature Reserve is a grazing marsh with cattle present close to the area of collection and throughout the collection period. It would appear that rabbits are being preferentially selected for feeding by An. atroparvus despite the presence of larger mammalian hosts, although host-baited choice experiments in the field or laboratory would provide stronger evidence for this behaviour (reviewed in ).
It is important to maximise the data that can be obtained from a single blood-fed specimen as collecting large numbers of blood-fed mosquitoes in the UK by currently available methods is challenging . Furthermore, the likelihood of successfully identifying blood-meal host decreases rapidly with time as digestion within the insect takes place (reviewed in ). The primer cocktail used in this study  successfully identified the blood-meal host in 46 % of the captured blood-fed mosquitoes. The time between feeding and collection was not known for mosquitoes in this study but assessing mosquitoes in future studies using the Sella score to rate level of digestion would be beneficial to assess the efficacy of this approach according to the degree of digestion .
The concomitant identification of both the mosquito and its blood-meal host allowed for the targeted selection of specimens of epidemiological relevance for subsequent pathogen screening, saving both time and resources. In this instance we have screened samples for a mechanically transmitted pathogen. Prior to this study, there was little evidence from fieldwork studies that mosquitoes played an important role in the transmission of myxomatosis among wild rabbit populations in the UK. Evidence for occasional involvement in transmission to and within domestic rabbit populations has been reported  supported by laboratory transmission data . This study found that 27 % of blood-meals derived from rabbit were positive for myxoma virus. According to evidence that arthropod transmission is mechanical and therefore requires the presence of a lesion through which mouthpart contamination will occur , this finding demonstrates that wild, myxomatosis-infected rabbits are being fed upon by An. atroparvus at Elmley. However, it is the observation that over two-thirds of rabbit-derived blood-meals were negative for myxoma virus that is most important and differs from previous studies in the UK as this suggests that An. atroparvus is not simply opportunistically feeding on diseased rabbits, but also readily feeds on healthy rabbits in wild populations. We therefore conclude that mosquitoes could contribute to the transmission of the virus. Mosquito collections in this study were conducted between June and September, the period broadly considered to be the peak vector season in the UK [21, 40], however, the number of mosquitoes collected make interpreting seasonal influences uncertain. If the peak incidence of myxomatosis in the rabbit population were to be closely associated with the peak period of An. atroparvus activity, then this would provide evidence of seasonal shifts in the relative importance of different vector groups in the area.
The myxoma virus possesses a DNA genome and was therefore present following the extraction procedure. However, using a DNA- or RNA-specific extraction protocol provides an additional limitation to the data that can be obtained from each specimen. Therefore, we advocate the use of a co-extraction procedure such as that of Griffiths  that would preserve both DNA and RNA, greatly widening the information that could be obtained from a single mosquito specimen. Further applications of such an approach could include screening for human viral pathogens present in mosquitoes that had fed on humans for the purposes of xenosurveillance .
This study shows that a single DNA extraction can be successfully used to identify blood-meal host, delineate to species level members of the An. maculipennis s.l. and to subsequently detect the presence of an animal pathogen, myxoma virus. This tripartite approach revealed that healthy and myxomatosis-infected rabbits are a major blood-feeding host at Elmley, Kent, and therefore provides further evidence that An. atroparvus may play an important role in the transmission of this disease in wild rabbit populations.
The authors would like to acknowledge the help of the farm owners and workers at Elmley Nature Reserve, especially the contribution of Steve Gordon, warden of Elmley, who sadly passed away during the preparation of this paper. Funding was provided by the Department for Environment and Rural Affairs (DEFRA) through grants SV3045, SE4215 and SE4112. The authors thank Simon Carpenter and Jolyon Medlock for critical reading of this manuscript, and three anonymous reviewers for their constructive comments.
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