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A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep

The accurate diagnosis of parasitic nematode infections in livestock (including sheep and goats) is central to their effective control and the detection of the anthelmintic resistance. Traditionally, the faecal egg count reduction test (FECRT), combined with the technique of larval culture (LC), has...

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Autores principales: Roeber, Florian, Larsen, John W. A., Anderson, Norman, Campbell, Angus J. D., Anderson, Garry A., Gasser, Robin B., Jex, Aaron R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358350/
https://www.ncbi.nlm.nih.gov/pubmed/22629381
http://dx.doi.org/10.1371/journal.pone.0037327
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author Roeber, Florian
Larsen, John W. A.
Anderson, Norman
Campbell, Angus J. D.
Anderson, Garry A.
Gasser, Robin B.
Jex, Aaron R.
author_facet Roeber, Florian
Larsen, John W. A.
Anderson, Norman
Campbell, Angus J. D.
Anderson, Garry A.
Gasser, Robin B.
Jex, Aaron R.
author_sort Roeber, Florian
collection PubMed
description The accurate diagnosis of parasitic nematode infections in livestock (including sheep and goats) is central to their effective control and the detection of the anthelmintic resistance. Traditionally, the faecal egg count reduction test (FECRT), combined with the technique of larval culture (LC), has been used widely to assess drug-susceptibility/resistance in strongylid nematodes. However, this approach suffers from a lack of specificity, sensitivity and reliability, and is time-consuming and costly to conduct. Here, we critically assessed a specific PCR assay to support FECRT, in a well-controlled experiment on sheep with naturally acquired strongylid infections known to be resistant to benzimidazoles. We showed that the PCR results were in close agreement with those of total worm count (TWC), but not of LC. Importantly, albendazole resistance detected by PCR-coupled FECRT was unequivocally linked to Teladorsagia circumcincta and, to lesser extent, Trichostrongylus colubriformis, a result that was not achievable by LC. The key findings from this study demonstrate that our PCR-coupled FECRT approach has major merit for supporting anthelmintic resistance in nematode populations. The findings also show clearly that our PCR assay can be used as an alternative to LC, and is more time-efficient and less laborious, which has important practical implications for the effective management and control strongylid nematodes of sheep.
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spelling pubmed-33583502012-05-24 A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep Roeber, Florian Larsen, John W. A. Anderson, Norman Campbell, Angus J. D. Anderson, Garry A. Gasser, Robin B. Jex, Aaron R. PLoS One Research Article The accurate diagnosis of parasitic nematode infections in livestock (including sheep and goats) is central to their effective control and the detection of the anthelmintic resistance. Traditionally, the faecal egg count reduction test (FECRT), combined with the technique of larval culture (LC), has been used widely to assess drug-susceptibility/resistance in strongylid nematodes. However, this approach suffers from a lack of specificity, sensitivity and reliability, and is time-consuming and costly to conduct. Here, we critically assessed a specific PCR assay to support FECRT, in a well-controlled experiment on sheep with naturally acquired strongylid infections known to be resistant to benzimidazoles. We showed that the PCR results were in close agreement with those of total worm count (TWC), but not of LC. Importantly, albendazole resistance detected by PCR-coupled FECRT was unequivocally linked to Teladorsagia circumcincta and, to lesser extent, Trichostrongylus colubriformis, a result that was not achievable by LC. The key findings from this study demonstrate that our PCR-coupled FECRT approach has major merit for supporting anthelmintic resistance in nematode populations. The findings also show clearly that our PCR assay can be used as an alternative to LC, and is more time-efficient and less laborious, which has important practical implications for the effective management and control strongylid nematodes of sheep. Public Library of Science 2012-05-22 /pmc/articles/PMC3358350/ /pubmed/22629381 http://dx.doi.org/10.1371/journal.pone.0037327 Text en Roeber et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Roeber, Florian
Larsen, John W. A.
Anderson, Norman
Campbell, Angus J. D.
Anderson, Garry A.
Gasser, Robin B.
Jex, Aaron R.
A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep
title A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep
title_full A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep
title_fullStr A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep
title_full_unstemmed A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep
title_short A Molecular Diagnostic Tool to Replace Larval Culture in Conventional Faecal Egg Count Reduction Testing in Sheep
title_sort molecular diagnostic tool to replace larval culture in conventional faecal egg count reduction testing in sheep
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3358350/
https://www.ncbi.nlm.nih.gov/pubmed/22629381
http://dx.doi.org/10.1371/journal.pone.0037327
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