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Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera

BACKGROUND: Lawsonia intracellularis is a common cause of chronic diarrhoea and poor performance in young growing pigs. Diagnosis of this obligate intracellular bacterium is based on the demonstration of the microbe or microbial DNA in tissue specimens or faecal samples, or the demonstration of L. i...

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Autores principales: Jacobson, Magdalena, Wallgren, Per, Nordengrahn, Ann, Merza, Malik, Emanuelson, Ulf
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080824/
https://www.ncbi.nlm.nih.gov/pubmed/21453555
http://dx.doi.org/10.1186/1751-0147-53-23
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author Jacobson, Magdalena
Wallgren, Per
Nordengrahn, Ann
Merza, Malik
Emanuelson, Ulf
author_facet Jacobson, Magdalena
Wallgren, Per
Nordengrahn, Ann
Merza, Malik
Emanuelson, Ulf
author_sort Jacobson, Magdalena
collection PubMed
description BACKGROUND: Lawsonia intracellularis is a common cause of chronic diarrhoea and poor performance in young growing pigs. Diagnosis of this obligate intracellular bacterium is based on the demonstration of the microbe or microbial DNA in tissue specimens or faecal samples, or the demonstration of L. intracellularis-specific antibodies in sera. The aim of the present study was to evaluate a blocking ELISA in the detection of serum antibodies to L. intracellularis, by comparison to the previously widely used immunofluorescent antibody test (IFAT). METHODS: Sera were collected from 176 pigs aged 8-12 weeks originating from 24 herds with or without problems with diarrhoea and poor performance in young growing pigs. Sera were analyzed by the blocking ELISA and by IFAT. Bayesian modelling techniques were used to account for the absence of a gold standard test and the results of the blocking ELISA was modelled against the IFAT test with a "2 dependent tests, 2 populations, no gold standard" model. RESULTS: At the finally selected cut-off value of percent inhibition (PI) 35, the diagnostic sensitivity of the blocking ELISA was 72% and the diagnostic specificity was 93%. The positive predictive value was 0.82 and the negative predictive value was 0.89, at the observed prevalence of 33.5%. CONCLUSION: The sensitivity and specificity as evaluated by Bayesian statistic techniques differed from that previously reported. Properties of diagnostic tests may well vary between countries, laboratories and among populations of animals. In the absence of a true gold standard, the importance of validating new methods by appropriate statistical methods and with respect to the target population must be emphasized.
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spelling pubmed-30808242011-04-22 Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera Jacobson, Magdalena Wallgren, Per Nordengrahn, Ann Merza, Malik Emanuelson, Ulf Acta Vet Scand Research BACKGROUND: Lawsonia intracellularis is a common cause of chronic diarrhoea and poor performance in young growing pigs. Diagnosis of this obligate intracellular bacterium is based on the demonstration of the microbe or microbial DNA in tissue specimens or faecal samples, or the demonstration of L. intracellularis-specific antibodies in sera. The aim of the present study was to evaluate a blocking ELISA in the detection of serum antibodies to L. intracellularis, by comparison to the previously widely used immunofluorescent antibody test (IFAT). METHODS: Sera were collected from 176 pigs aged 8-12 weeks originating from 24 herds with or without problems with diarrhoea and poor performance in young growing pigs. Sera were analyzed by the blocking ELISA and by IFAT. Bayesian modelling techniques were used to account for the absence of a gold standard test and the results of the blocking ELISA was modelled against the IFAT test with a "2 dependent tests, 2 populations, no gold standard" model. RESULTS: At the finally selected cut-off value of percent inhibition (PI) 35, the diagnostic sensitivity of the blocking ELISA was 72% and the diagnostic specificity was 93%. The positive predictive value was 0.82 and the negative predictive value was 0.89, at the observed prevalence of 33.5%. CONCLUSION: The sensitivity and specificity as evaluated by Bayesian statistic techniques differed from that previously reported. Properties of diagnostic tests may well vary between countries, laboratories and among populations of animals. In the absence of a true gold standard, the importance of validating new methods by appropriate statistical methods and with respect to the target population must be emphasized. BioMed Central 2011-04-01 /pmc/articles/PMC3080824/ /pubmed/21453555 http://dx.doi.org/10.1186/1751-0147-53-23 Text en Copyright ©2011 Jacobson 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.
spellingShingle Research
Jacobson, Magdalena
Wallgren, Per
Nordengrahn, Ann
Merza, Malik
Emanuelson, Ulf
Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera
title Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera
title_full Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera
title_fullStr Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera
title_full_unstemmed Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera
title_short Evaluation of a blocking ELISA for the detection of antibodies against Lawsonia intracellularis in pig sera
title_sort evaluation of a blocking elisa for the detection of antibodies against lawsonia intracellularis in pig sera
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080824/
https://www.ncbi.nlm.nih.gov/pubmed/21453555
http://dx.doi.org/10.1186/1751-0147-53-23
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