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Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats

BACKGROUND: Presently, few data exist on the level and duration of anti-protective antigen (PA) IgG in vaccinated livestock. Various adaptation of enzyme-linked immunosorbent assays (ELISAs) have been developed in studies to assess immune response following vaccination, albeit mostly in laboratory r...

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Autores principales: Ndumnego, Okechukwu C, Crafford, Jannie, Beyer, Wolfgang, van Heerden, Henriette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892015/
https://www.ncbi.nlm.nih.gov/pubmed/24373579
http://dx.doi.org/10.1186/1746-6148-9-265
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author Ndumnego, Okechukwu C
Crafford, Jannie
Beyer, Wolfgang
van Heerden, Henriette
author_facet Ndumnego, Okechukwu C
Crafford, Jannie
Beyer, Wolfgang
van Heerden, Henriette
author_sort Ndumnego, Okechukwu C
collection PubMed
description BACKGROUND: Presently, few data exist on the level and duration of anti-protective antigen (PA) IgG in vaccinated livestock. Various adaptation of enzyme-linked immunosorbent assays (ELISAs) have been developed in studies to assess immune response following vaccination, albeit mostly in laboratory rodent models. The quantitative anti-anthrax IgG ELISA in this study describes a method of enumerating the concentration of anti-PA specific IgG present in sera of immunized goats, with the aid of an affinity-purified caprine polyclonal anti-anthrax PA-83 IgG standard. This was compared with the anthrax toxin neutralization assay (TNA) which measures a functional subset of toxin neutralizing anti-PA IgG. RESULTS: The measured concentrations obtained in the standard curve correlated with the known concentration at each dilution. Percentage recovery of the standard concentrations ranged from 89 to 98% (lower and upper asymptote respectively). Mean correlation coefficient (r(2)) of the standard curve was 0.998. Evaluation of the intra-assay coefficient of variation showed ranges of 0.23-16.90% and 0.40-12.46% for days 28 and 140 sera samples respectively, following vaccination. The mean inter-assay coefficient of variation for triplicate samples repeated on 5 different days was 18.53 and 12.17% for days 28 and 140 sera samples respectively. Spearman’s rank correlation of log-transformed IgG concentrations and TNA titres showed strong positive correlation (r(s) = 0.942; p = 0.01). CONCLUSION: This study provides evidence that an indirect ELISA can be used for the quantification of anti-anthrax PA IgG in goats with the added advantage of using single dilutions to save time and resources. The use of such related immunoassays can serve as potential adjuncts to potency tests for Sterne and other vaccine types under development in ruminant species. This is the first report on the correlation of polyclonal anti-anthrax PA83 antibody with the TNA in goats.
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spelling pubmed-38920152014-01-15 Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats Ndumnego, Okechukwu C Crafford, Jannie Beyer, Wolfgang van Heerden, Henriette BMC Vet Res Methodology Article BACKGROUND: Presently, few data exist on the level and duration of anti-protective antigen (PA) IgG in vaccinated livestock. Various adaptation of enzyme-linked immunosorbent assays (ELISAs) have been developed in studies to assess immune response following vaccination, albeit mostly in laboratory rodent models. The quantitative anti-anthrax IgG ELISA in this study describes a method of enumerating the concentration of anti-PA specific IgG present in sera of immunized goats, with the aid of an affinity-purified caprine polyclonal anti-anthrax PA-83 IgG standard. This was compared with the anthrax toxin neutralization assay (TNA) which measures a functional subset of toxin neutralizing anti-PA IgG. RESULTS: The measured concentrations obtained in the standard curve correlated with the known concentration at each dilution. Percentage recovery of the standard concentrations ranged from 89 to 98% (lower and upper asymptote respectively). Mean correlation coefficient (r(2)) of the standard curve was 0.998. Evaluation of the intra-assay coefficient of variation showed ranges of 0.23-16.90% and 0.40-12.46% for days 28 and 140 sera samples respectively, following vaccination. The mean inter-assay coefficient of variation for triplicate samples repeated on 5 different days was 18.53 and 12.17% for days 28 and 140 sera samples respectively. Spearman’s rank correlation of log-transformed IgG concentrations and TNA titres showed strong positive correlation (r(s) = 0.942; p = 0.01). CONCLUSION: This study provides evidence that an indirect ELISA can be used for the quantification of anti-anthrax PA IgG in goats with the added advantage of using single dilutions to save time and resources. The use of such related immunoassays can serve as potential adjuncts to potency tests for Sterne and other vaccine types under development in ruminant species. This is the first report on the correlation of polyclonal anti-anthrax PA83 antibody with the TNA in goats. BioMed Central 2013-12-27 /pmc/articles/PMC3892015/ /pubmed/24373579 http://dx.doi.org/10.1186/1746-6148-9-265 Text en Copyright © 2013 Ndumnego et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Ndumnego, Okechukwu C
Crafford, Jannie
Beyer, Wolfgang
van Heerden, Henriette
Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats
title Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats
title_full Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats
title_fullStr Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats
title_full_unstemmed Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats
title_short Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats
title_sort quantitative anti-pa igg elisa; assessment and comparability with the anthrax toxin neutralization assay in goats
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892015/
https://www.ncbi.nlm.nih.gov/pubmed/24373579
http://dx.doi.org/10.1186/1746-6148-9-265
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