2015
DOI: 10.7589/2014-07-175
|View full text |Cite
|
Sign up to set email alerts
|

West Nile Virus Antibody Decay Rate in Free-Ranging Birds

Abstract: ABSTRACT:Antibody duration, following a humoral immune response to West Nile virus (WNV) infection, is poorly understood in free-ranging avian hosts. Quantifying antibody decay rate is important for interpreting serologic results and for understanding the potential for birds to serorevert and become susceptible again. We sampled free-ranging birds in Chicago, Illinois, US, from 2005 to 2011 and Atlanta, Georgia, US, from 2010 to 2012 to examine the dynamics of antibody decay following natural WNV infection. Us… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
8
0

Year Published

2016
2016
2020
2020

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 15 publications
(8 citation statements)
references
References 41 publications
0
8
0
Order By: Relevance
“…36,43,44 We used avian serum from blood samples to test for the presence of WNV antibodies using an inhibition enzyme-linked immunosorbent assay (ELISA). 17,45 For Culex mosquitoes, DNA was extracted from pools of whole-bodied host-seeking female individuals that were collected from the same sites and at the same time. Extractions were carried out with Qiagen (Hilden, Germany) blood and tissue kits following the manufacturer's protocol.…”
Section: Methodsmentioning
confidence: 99%
“…36,43,44 We used avian serum from blood samples to test for the presence of WNV antibodies using an inhibition enzyme-linked immunosorbent assay (ELISA). 17,45 For Culex mosquitoes, DNA was extracted from pools of whole-bodied host-seeking female individuals that were collected from the same sites and at the same time. Extractions were carried out with Qiagen (Hilden, Germany) blood and tissue kits following the manufacturer's protocol.…”
Section: Methodsmentioning
confidence: 99%
“…Our method can be applied to understand the patterns and mechanisms of seasonal infection risk in pathogens of concern for wildlife and humans including plague, avian influenza, West Nile virus, and myxomatosis in rabbits (Kerr 1997; McKee et al 2015; Pepin et al 2017), where longitudinal antibody and serosurveillance data already exist. However, high-resolution longitudinal antibody data is not a necessary prerequisite to use the survival analysis framework we present here, as our method is a generalization of serology methods that only use seroprevalence data to estimate infection risk, with no information on TOI (Heisey et al 2006; Hens et al 2012).…”
Section: Discussionmentioning
confidence: 99%
“…Possibly, the rather high prevalence of WNV in the simulations, as well as the high values of 0 , are an artifact arising from this simplified situation. Another questionable assumption is that birds are not allowed to recover, though antibody-positive birds are not difficult to find in endemic areas (Jozan et al, 2003;Mckee et al, 2015). Including a compartment of recovered birds would not change the values of 0 but would certainly decrease infection prevalence.…”
Section: Discussionmentioning
confidence: 99%