Weast Nile Virus Serosurveillance in Iowa White-Tailed Deer (1999-2003)

Authors

Julian Santatella, USDA/APHIS/WS National Wildlife Research Center, University of Caldas, Manizales. Columbia; University Hygienic Laboratory. University of lowa, Colorado State University, Coe College
Robert McLean, USDA/APHIS/WS National Wildlife Research Center, University of Caldas, Manizales, Columbia, University Hygienic Laboratory, University of Iowa, Department of Biomedical Sciences, Colorado State University, Coe College
Jeffrey S. Hall, USDA/APHIS/WS National Wildlife Research Center, University of Caldas, Manizales. Columbia; University Hygienic Laboratory. University of lowa, Colorado State University, Coe College
James S. Gill, USDA/APHIS/WS National Wildlife Research Center, University of Caldas, Manizales. Columbia; University Hygienic Laboratory. University of lowa, Colorado State University, Coe College
Richard A. Bowen, USDA/APHIS/WS National Wildlife Research Center, University of Caldas, Manizales. Columbia; University Hygienic Laboratory. University of lowa, Colorado Stare University, Coe College
Harlo H. Hadow, USDA/APHIS/WS National Wildlife Research Center, University of Caldas, Manizales. Columbia; University Hygienic Laboratory. University of lowa, Colorado State University, Coe College
Larry Clark, USDA/APHIS/WS National Wildlife Research CenterFollow

Date of this Version

6-1-2005

Abstract

Sera from white-tailed deer (Odocoileus virginianus) were collected in Iowa during the winter months (1999-2003), 2 years before and after West Nile virus (WNV) was first reported in Iowa (2001), and were analyzed for antibodies to WNV. Samples from 1999 to 2001 were antibody negalive by blocking enzyme-linikedI immunosorbent assay (bELISA) and plaque reduction neutralization test (PRNT₉₀). Prevalence derived from bELISA (2002, 12.7%; 2003. 11.2%) and WNV PRNT₉₀ (2002,7.9%; 2003, 8.5%) assays were similar. All sanlples were negative for antibodies against St. Louis encephalitis virus as determined by PRNT₉₀. Antibodies to flaviviruses were detected by indirect enzyme-linked immunosorbent assay (iELISA) prior to the first WNV cases reported in Iowa (1999-2001) with prevalence ranging from 2.2% to 3.2%, suggesting the circulation of an additional undescribed flavivirus prior to the introduction of WNV into the area. Flavivirus prevalence as determined by iELISA increased in 2002 and 2003 (23.3% and 31.9%, respectively). The increase in prevalence exceeded estimates of WNV prevalence. suggesting that conditions favored general flavivirus transmission (including WNV) during the 2002-2003 epizootic. These data indicate that serologic analysis of deer sera collected from hunter harvests may prove useful for surveillance and evidence of local transmission of WNV and other pathogens and identify white-tailed deer as a species for further studies for host competency.