Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.

BACKGROUND: Human infections with highly pathogenic H5N1 avian influenza viruses have generally been confirmed by molecular amplification or culture-based methods. Serologic surveillance has potential advantages which have not been realized because rapid and specific serologic tests to detect H5N1 i...

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Main Authors: Mookkan Prabakaran, Hui-Ting Ho, Nayana Prabhu, Sumathy Velumani, Milene Szyporta, Fang He, Kwai-Peng Chan, Li-Mei Chen, Yumiko Matsuoka, Ruben O Donis, Jimmy Kwang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2642733?pdf=render
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spelling doaj-96659d21139b4e18bf7529de30e7a4d72020-11-25T02:22:01ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0142e456610.1371/journal.pone.0004566Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.Mookkan PrabakaranHui-Ting HoNayana PrabhuSumathy VelumaniMilene SzyportaFang HeKwai-Peng ChanLi-Mei ChenYumiko MatsuokaRuben O DonisJimmy KwangBACKGROUND: Human infections with highly pathogenic H5N1 avian influenza viruses have generally been confirmed by molecular amplification or culture-based methods. Serologic surveillance has potential advantages which have not been realized because rapid and specific serologic tests to detect H5N1 infection are not widely available. METHODOLOGY/PRINCIPAL FINDINGS: Here we describe an epitope-blocking ELISA to detect specific antibodies to H5N1 viruses in human or animal sera. The assay relies on a novel monoclonal antibody (5F8) that binds to an epitope comprising amino acid residues 274-281 (CNTKCQTP) in the HA1 region of H5 hemagglutinin. Database search analysis of publicly available sequences revealed that this epitope is conserved in 100% of the 163 H5N1 viruses isolated from humans. The sensitivity and specificity of the epitope-blocking ELISA for H5N1 were evaluated using chicken antisera to multiple virus clades and other influenza subtypes as well as serum samples from individuals naturally infected with H5N1 or seasonal influenza viruses. The epitope-blocking ELISA results were compared to those of hemagglutinin inhibition (HI) and microneutralization assays. Antibodies to H5N1 were readily detected in immunized animals or convalescent human sera by the epitope-blocking ELISA whereas specimens with antibodies to other influenza subtypes yielded negative results. The assay showed higher sensitivity and specificity as compared to HI and microneutralization. CONCLUSIONS/SIGNIFICANCE: The epitope-blocking ELISA based on a unique 5F8 mAb provided highly sensitive and 100% specific detection of antibodies to H5N1 influenza viruses in human sera.http://europepmc.org/articles/PMC2642733?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mookkan Prabakaran
Hui-Ting Ho
Nayana Prabhu
Sumathy Velumani
Milene Szyporta
Fang He
Kwai-Peng Chan
Li-Mei Chen
Yumiko Matsuoka
Ruben O Donis
Jimmy Kwang
spellingShingle Mookkan Prabakaran
Hui-Ting Ho
Nayana Prabhu
Sumathy Velumani
Milene Szyporta
Fang He
Kwai-Peng Chan
Li-Mei Chen
Yumiko Matsuoka
Ruben O Donis
Jimmy Kwang
Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.
PLoS ONE
author_facet Mookkan Prabakaran
Hui-Ting Ho
Nayana Prabhu
Sumathy Velumani
Milene Szyporta
Fang He
Kwai-Peng Chan
Li-Mei Chen
Yumiko Matsuoka
Ruben O Donis
Jimmy Kwang
author_sort Mookkan Prabakaran
title Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.
title_short Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.
title_full Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.
title_fullStr Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.
title_full_unstemmed Development of epitope-blocking ELISA for universal detection of antibodies to human H5N1 influenza viruses.
title_sort development of epitope-blocking elisa for universal detection of antibodies to human h5n1 influenza viruses.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-01-01
description BACKGROUND: Human infections with highly pathogenic H5N1 avian influenza viruses have generally been confirmed by molecular amplification or culture-based methods. Serologic surveillance has potential advantages which have not been realized because rapid and specific serologic tests to detect H5N1 infection are not widely available. METHODOLOGY/PRINCIPAL FINDINGS: Here we describe an epitope-blocking ELISA to detect specific antibodies to H5N1 viruses in human or animal sera. The assay relies on a novel monoclonal antibody (5F8) that binds to an epitope comprising amino acid residues 274-281 (CNTKCQTP) in the HA1 region of H5 hemagglutinin. Database search analysis of publicly available sequences revealed that this epitope is conserved in 100% of the 163 H5N1 viruses isolated from humans. The sensitivity and specificity of the epitope-blocking ELISA for H5N1 were evaluated using chicken antisera to multiple virus clades and other influenza subtypes as well as serum samples from individuals naturally infected with H5N1 or seasonal influenza viruses. The epitope-blocking ELISA results were compared to those of hemagglutinin inhibition (HI) and microneutralization assays. Antibodies to H5N1 were readily detected in immunized animals or convalescent human sera by the epitope-blocking ELISA whereas specimens with antibodies to other influenza subtypes yielded negative results. The assay showed higher sensitivity and specificity as compared to HI and microneutralization. CONCLUSIONS/SIGNIFICANCE: The epitope-blocking ELISA based on a unique 5F8 mAb provided highly sensitive and 100% specific detection of antibodies to H5N1 influenza viruses in human sera.
url http://europepmc.org/articles/PMC2642733?pdf=render
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