2015
DOI: 10.1016/j.meegid.2015.01.007
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Unexpected spatiotemporal abundance of infected Culex restuans suggest a greater role as a West Nile virus vector for this native species

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Cited by 38 publications
(44 citation statements)
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“…Culex mosquitoes, disease ecology, pathogen transmission, urban ecology, vector control, vectorial capacity, West Nile virus transmission season presents the opportunity to investigate the likelihood that Cx. restuans contributes to enzootic WNv transmission by extending the transmission season and/or by being involved in WNv overwintering (Johnson, Robson, & Fonseca, 2015;Reiter, 1988).…”
Section: Introductionmentioning
confidence: 99%
“…Culex mosquitoes, disease ecology, pathogen transmission, urban ecology, vector control, vectorial capacity, West Nile virus transmission season presents the opportunity to investigate the likelihood that Cx. restuans contributes to enzootic WNv transmission by extending the transmission season and/or by being involved in WNv overwintering (Johnson, Robson, & Fonseca, 2015;Reiter, 1988).…”
Section: Introductionmentioning
confidence: 99%
“…The lack of statistical significance could be due to the small sample sizes, as Cx. pipiens is primarily an urban mosquito that occurs with low frequency in natural sites . Additionally, lower frequency and diversity of resistant alleles in the large and medium wetland sites may be due to the poor penetration of ground‐applied adulticides in these areas.…”
Section: Discussionmentioning
confidence: 99%
“…Once DNA collection was completed, we handled filter membranes with flame‐sterilized tweezers, cut pieces approximately 14 mm 2 from the center of the filter with flame‐sterilized scissors, and extracted DNA using an affordable and readily available HotSHOT extraction (Johnson et al . ) (Panel 1). To assess the presence of BMSB DNA in these samples, we used a TaqMan quantitative polymerase chain reaction (qPCR) assay designed specifically for BMSB (for details regarding assessments of specificity and sensitivity, see Valentin et al .…”
Section: Methodsmentioning
confidence: 99%
“…Following one methodology in the eDNA literature (eg Rees et al 2014;Turner et al 2014), we used a peristaltic pump (Pegasus Alexis, Pegasus Pump Company, Bradenton, FL) and a 10μm polycarbonate track-etched (PCTE) filter membrane (GVS North America, Sanford, ME) combination to remove the DNA from the water. Once DNA collection was completed, we handled filter membranes with flame-sterilized tweezers, cut pieces approximately 14 mm 2 from the center of the filter with flame-sterilized scissors, and extracted DNA using an affordable and readily available HotSHOT extraction (Johnson et al 2015) (Panel 1). To assess the presence of BMSB DNA in these samples, we used a TaqMan quantitative polymerase chain reaction (qPCR) assay designed specifically for BMSB (for details regarding assessments of specificity and sensitivity, see Valentin et al 2016).…”
Section: Target Edna Collectionmentioning
confidence: 99%