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

Show simple item record

dc.contributor.author Ndumnego, Okechukwu Chinazo
dc.contributor.author Crafford, Jan Ernst
dc.contributor.author Beyer, Wolfgang
dc.contributor.author Van Heerden, Henriette
dc.date.accessioned 2014-04-17T08:41:38Z
dc.date.available 2014-04-17T08:41:38Z
dc.date.issued 2013-12-27
dc.description.abstract 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 (r2) 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 (rs = 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. en
dc.description.librarian am2014 en
dc.description.librarian ab2014
dc.description.sponsorship The Deutsche Forschungsgemeinschaft (German Research Foundation) en
dc.description.uri http://www.biomedcentral.com/1746-6148/9/265 en
dc.identifier.citation Ndumnego et al.: Quantitative anti-PA IgG ELISA; assessment and comparability with the anthrax toxin neutralization assay in goats. BMC Veterinary Research 2013 9:265. en
dc.identifier.issn 1746-6148
dc.identifier.other 10.1186/1746-6148-9-265
dc.identifier.uri http://hdl.handle.net/2263/39669
dc.language.iso en en
dc.publisher BioMed Central en
dc.relation.requires Adobe Acrobat Reader en
dc.rights © 2013 Ndumnego et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License en
dc.subject Protective antigen en
dc.subject Indirect ELISA en
dc.subject Toxin neutralization assay en
dc.subject Immunoglobulin en
dc.subject Sterne vaccine en
dc.subject.lcsh Goats en
dc.subject.lcsh Anthrax en
dc.subject.lcsh Enzyme-linked immunosorbent assay en
dc.title Quantitative anti-PA IgG ELISA : assessment and comparability with the anthrax toxin neutralization assay in goats en
dc.type Article en


Files in this item

This item appears in the following Collection(s)

Show simple item record