Volume 13, Number 12—December 2007
Dispatch
Host-Feeding Patterns of Culex Mosquitoes in Relation to Trap Habitat
Abstract
Mosquito feeding patterns identify vertebrate species potentially involved in the amplification of West Nile virus. In New York, northern cardinals (Cardinalis cardinalis) were the predominant hosts in most habitats. Crow (Corvus sp.) blood meals were most frequently identified from sewage treatment plant and storm water catch basin habitats.
In the northeastern United States, Culex pipiens and Cx. restuans are the most important vectors of West Nile virus (WNV), according to the frequency of viral detection, vector competence, and their largely ornithophilic feeding habits (1–4). Mosquito feeding studies suggest that American robins (Turdus migratorius) are the preferred avian hosts that support enzootic transmission in the Northeast (4,5). A shift in hosts from birds to mammals, including humans, as robins begin fall migratory movements is hypothesized to be responsible for the seasonal rise in human WNV cases (5). We identified blood meals of Culex mosquitoes collected in New York and found feeding patterns unlike those previously reported (4,5). We suggest caution in applying findings for epidemiologic purposes across different habitats and large geographic areas.
We determined host species of Cx. pipiens and Cx. restuans mosquitoes collected by mosquito surveillance programs in 2001 and 2002 in Nassau (89 identified/100 tested), Orange (66/87), Rockland (83/96), and Westchester (20/20) counties and in 2005 and 2006 in Tompkins County (46/52) (1). Dry ice–baited CDC light traps and gravid traps were used to capture host-seeking and ovipositing females, respectively. Seventy percent of mosquitoes were collected from traps located in public places such as parks, preserves, woodlots, cemeteries, and golf courses (hereafter, parks and preserves). The remaining 30% were collected on residential properties, near storm water basins and sewage treatment plants, and at a university composting facility and dairy barn. Culex species were identified molecularly with taxon-specific primers (6).
Genomic DNA was extracted from each mosquito by using DNAzol-BD (Molecular Research Center, Cincinnati, OH, USA) or DNeasy Blood & Tissue Kits (QIAGEN, Germantown, MD, USA). Blood meals were initially identified by PCR-heteroduplex assays (7). We subsequently used DNA sequencing with cytochrome b primers as follows: Cyt F 5′-GCHGAYACHWVHHYHGCHTTYTCHTC-3′ and Cyt H 5′-CCCCTCAGAATGATATTTGTCCTCA-3′, in which W = A or T, H = A, C, or T, Y = C or T, and V = A, C, or G. Cycling conditions were 94°C for 2 min, followed by 55 cycles at 94°C for 45 s, 50°C for 50 s, and 72°C for 1 min with a final extension at 72°C for 7 min. PCR amplifications were conducted by using Taq PCR Core Kits (QIAGEN). Expected 300-bp PCR products were purified with an exonuclease-alkaline phosphate kit (Exo SAP-IT, USB Corporation, Cleveland, OH, USA). Samples were sequenced at the Biotechnology Resource Center (Cornell University, Ithaca, NY, USA) with a 3730 DNA Analyzer (Applied Biosystems, Foster City, CA, USA). Sequences were identified by using BLASTn searches in the GenBank database to compare fragments (8).
We identified host species in 183 Cx. pipiens and 119 Cx. restuans (Appendix Table). Cx. pipiens fed on birds (n = 171, 92.9% of Cx. pipiens blood meals), mammals (n = 12, 6.5%), and a northern brown snake (Storeria d. dekayi) (n = 1, 0.5%). Cx. restuans fed exclusively on birds. Avian host species were similar to those previously reported (3,4), except that northern cardinals (Cardinalis cardinalis), not American robins, were the principal hosts throughout the season, and feeding patterns differed somewhat, depending on the habitat of the trap site. Mosquitoes trapped in parks and preserves fed on 32 species of birds. Northern cardinal, gray catbird (Dumetella carolinensis), American robin, and blue jay (Cyanocitta cristata) accounted for 64% of the identifications. On residential properties, 52% of the blood meals were from cardinals. American robin blood meals accounted for only 12% of the blood meals and were found only in parks, preserves, and residential and storm water catch basins habitats. Crows (Corvus spp.) accounted for 26% of the blood meals from storm water catch basins and sewage treatment plant sites but only 2% of the collections from parks and preserves. No crow blood meals were identified from other habitats. American crows (C. brachyrhynchos) and fish crows (C. ossifragus) are found where crow-fed mosquitoes were collected. Mammalian blood meals were identified in June (human, white-tailed deer, and raccoon), July (deer and Virginia opossum), and August (human, 3 white-tailed deer, and 2 eastern gray squirrels). The percentage of northern cardinal and American robin blood meals was relatively constant throughout the summer (p = 0.261, Fisher exact test) (Table). The proportion of gray catbird–derived blood meals increased somewhat late in the summer (p = 0.668, Fisher exact test).
The avifauna was not censused in Nassau, Orange, Rockland and Westchester Counties. However, data on breeding bird communities were available for mosquito trap locations, and all species detected in blood meals were known to be present there (9,10). In Tompkins County, 10-min point-count censuses within a 50-m radius of mosquito traps were conducted 2–3 times each month from June through September 2006, totaling 140 counts. Sites included 8 residential properties, a university composting facility, and a wooded area. Of the 84 avian species recorded, the most frequent were northern cardinal (n = 110), black-capped chickadee (Poecile atricapillus) (n = 109), American robin (n = 103), blue jay (n = 102), and American crow (n = 100). Although the relative frequency of northern cardinals and American robins was approximately the same at Tompkins County sites, northern cardinals were 7.7 times more likely than American robins to be selected at those sites.
We found northern cardinals, rather than American robins, to be the predominant hosts of Cx. pipiens and Cx. restuans in all habitat types except storm water catch basins, where crows were identified most frequently. Robin-derived blood meals were less common than reported elsewhere (4,5). No seasonal decline in robin-fed Cx. pipiens or shift to other birds or mammals was found. We found that 7% of Cx. pipiens fed on mammals, similar to findings of a study in Connecticut (4).
The infrequent identification of crow-derived blood meals relative to their local abundance is an enigma (3,4). However, the spatial and temporal distribution and social behavior of crows have never been considered. Unless mosquito traps are located where crows are present at dusk or sleeping, the probability of collecting a crow-fed mosquito in the area sampled is low. This caveat is particularly relevant for mosquitoes with relatively short flight ranges such as Cx. pipiens and Cx. restuans, which presumably would not travel far to find suitable hosts.
Why American robins were the predominant hosts found in host-feeding studies in Connecticut, Maryland, and Washington, DC (4,5) and why northern cardinals were the preferred hosts in our study are not clear. At the Tompkins County, New York, sites, the relative abundance of cardinals and robins was comparable throughout the season. Thus, host abundance does not explain the frequency of cardinal-derived blood meals, at least at those sites. Cardinals and robins are common, share similar habitats, and are capable of amplifying WNV (11,12). WNV seroprevalence rates in northern cardinals, American robins, and other birds differ across geographic areas from year to year (13). Whether host-feeding patterns parallel those findings is not known.
Cx. pipiens fed on humans in June and August and on deer throughout the summer. In areas experiencing recurrent human WNV infection, future blood meal analyses should focus on peridomestic populations of Culex spp. to better understand their predilection for avian and/or mammalian feeding and the spatial and temporal dynamics of their host-feeding activities.
Dr Patrican is a medical entomologist and visiting scientist in the Department of Population Medicine and Diagnostic Sciences, Cornell University, Ithaca, New York. Her professional interests include the transmission dynamics of arboviruses and ecology of vectorborne diseases.
Acknowledgments
We thank New York State Department of Health county surveillance programs for collecting and contributing mosquitoes and Elliot Swarthout, Linda Chapman, JoAnne Oliver, John Howard, Amy Glaser, Laura Kramer, Glen Howser, Anne Clark, and Phil Kaufman for contributing blood and tissue samples. We thank Kevin McGowan and Anne Clark for critical review of the manuscript.
This work was funded in part by the National Institutes of Health.
References
- Lukacik G, Anand M, Shusas EJ, Howard JH, Oliver J, Chen H, West Nile surveillance in mosquitoes in New York State. J Am Mosq Control Assoc. 2006;22:254–71. DOIPubMedGoogle Scholar
- Turell MJ, Dohm DJ, Sardelis MR, O’Guinn ML, Andreadis TG, Blow JA. An update on the potential of North American mosquitoes (Diptera: Culicidae) to transmit West Nile virus. J Med Entomol. 2005;42:57–62. DOIPubMedGoogle Scholar
- Apperson CS, Hassan HK, Harrison BA, Savage HM, Aspen SE, Farajollahi A, Host feeding patterns of established and potential mosquito vectors of West Nile virus in the eastern United States. Vector Borne Zoonotic Dis. 2004;4:71–82. DOIPubMedGoogle Scholar
- Molaei G, Andreadis TG, Armstrong PM, Anderson JF, Vossbrinck CR. Host feeding patterns of Culex mosquitoes and West Nile virus transmission, northeastern United States. Emerg Infect Dis. 2006;12:468–74.PubMedGoogle Scholar
- Kilpatrick AM, Kramer LD, Jones MJ, Marra PP, Daszak P. West Nile virus epidemics in North America are driven by shifts in mosquito feeding behavior. PLoS Biol. 2006;4:e82. DOIPubMedGoogle Scholar
- Crabtree MB, Savage HM, Miller BR. Development of a species-diagnostic polymerase chain reaction assay for the identification of Culex vectors of St. Louis encephalitis virus based on interspecies sequence variation in ribosomal DNA spacers. Am J Trop Med Hyg. 1995;53:105–9.PubMedGoogle Scholar
- Lee JH, Hassan H, Hill G, Cupp EW, Higazi TB, Mitchell CJ, Identification of mosquito avian-derived blood meals by polymerase chain reaction heteroduplex analysis. Am J Trop Med Hyg. 2002;66:599–604.PubMedGoogle Scholar
- National Center for Biotechnology Information. GenBank [cited 2006 Nov 20]. Available from http://www.ncbi.nlm.nih.gov/blast
- Levine E. Bull’s birds of New York State. Ithaca (NY): Cornell University Press; 1998.
- New York State Department of Environmental Conservation. New York State Breeding Bird Atlas Interim Database. Albany (NY): The Department; 2005 [cited 2006 Nov 10]. Available from http://www.dec.state.ny.us/cfmx/extapps/bba
- Komar N, Langevin S, Hinten S, Nemeth N, Edwards E, Hettler D, Experimental infection of North American birds with the New York 1999 strain of West Nile virus. Emerg Infect Dis. 2003;9:311–22.PubMedGoogle Scholar
- Komar N, Panella NA, Langevin SA, Brault AC, Amador M, Edwards E, Avian hosts for West Nile virus in St. Tammany Parish, Louisiana, 2002. Am J Trop Med Hyg. 2005;73:1031–7.PubMedGoogle Scholar
- Beveroth TA, Ward MP, Lampman RL, Ringia AM, Novak RJ. Changes in seroprevalence of West Nile virus across Illinois in free-ranging birds from 2001 through 2004. Am J Trop Med Hyg. 2006;74:174–9.PubMedGoogle Scholar
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Cite This Article1Current affiliation: Cornell University, Ithaca, New York, USA
2Current affiliation: State of New York Department of Health, Syracuse, New York, USA
3Current affiliation: University of North Texas–Health Science Center, Fort Worth, Texas, USA
Table of Contents – Volume 13, Number 12—December 2007
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Lisa A. Patrican, Diagnostic Laboratory, Cornell University, Ithaca, NY 14853, USA;
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