Abstract

BackgroundBased on results of earlier studies, brain, heart and kidney are most commonly used for West Nile virus (WNV) detection in avian species. Both monoclonal and polyclonal antibodies have been used for the immunohistochemical diagnosis of WNV in these species. Thus far, no studies have been performed to compare the sensitivity and specificity of monoclonal and polyclonal antibodies in detecting WNV in American crows (Corvus brachyrhynchos). Our objectives were to determine 1) the comparative sensitivities of monoclonal and polyclonal antibodies for immunohistochemical (IHC) diagnosis of WNV infection in free-ranging American crows, 2) which organ(s) is/are most suitable for IHC-based diagnosis of WNV, and 3) how real-time RT-PCR on RNA extracted from formalin-fixed paraffin-embedded tissues compared to IHC for the diagnosis of WNV infection.MethodsVarious combinations, depending on tissue availability, of sections of heart, kidney, brain, liver, lung, spleen, and small intestine from 85 free-ranging American crows were stained using a rabbit-polyclonal anti-WNV antibody as well as a monoclonal antibody directed against an epitope on Domain III of the E protein of WNV. The staining intensity and the extent of staining were determined for each organ using both antibodies. Real-time RT-PCR on formalin-fixed paraffin-embedded tissues from all 85 crows was performed.ResultsForty-three crows were IHC-positive in at least one of the examined organs with the polyclonal antibody, and of these, only 31 were positive when IHC was performed with the monoclonal antibody. Real-time RT-PCR amplified WNV-specific sequences from tissue extracts of the same 43 crows that were IHC-positive using the polyclonal antibody. All other 42 crows tested negative for WNV with real-time PCR and IHC staining. Both antibodies had a test specificity of 100% when compared to PCR results. The test sensitivity of monoclonal antibody-based IHC staining was only 72%, compared to 100% when using the polyclonal antibody.ConclusionThe most sensitive, readily identified, positively staining organs for IHC are the kidney, liver, lung, spleen, and small intestine. Real-time RT-PCR and IHC staining using a polyclonal antibody on sections of these tissues are highly sensitive diagnostic tests for the detection of WNV in formalin-fixed tissues of American crows.

Highlights

  • Based on results of earlier studies, brain, heart and kidney are most commonly used for West Nile virus (WNV) detection in avian species

  • The objectives of this study were to determine: 1) if there is a significant difference in IHC staining for WNV using monoclonal versus polyclonal antibodies in naturally WNV-infected, free-ranging American crows (AMCRs), 2) which organ(s) is/ are the most appropriate for the detection of WNV infection by these IHC techniques, based upon sensitivity and staining intensity, and 3) how real-time RT-PCR performed on RNA extracted from formalin-fixed paraffinembedded tissues compared to IHC for the diagnosis of WNV infection

  • The test sensitivity of IHC staining for the detection of WNV infection in AMCRs using a polyclonal antibody with the Benchmark IHC System is superior to that of the 7H2 monoclonal antibody

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Summary

Introduction

Based on results of earlier studies, brain, heart and kidney are most commonly used for West Nile virus (WNV) detection in avian species. Both monoclonal and polyclonal antibodies have been used for the immunohistochemical diagnosis of WNV in these species. West Nile virus (WNV) first emerged in the Western hemisphere during the 1999 New York City outbreak and has since spread across the United States, into Canada, and to the Caribbean Islands and Central America [1,2,3,4,5,6]. These unusually high mortality rates may be due to the introduction of WNV in naïve avian populations, or due to the emergence of a new virulent strain [1,2,3,4]

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