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qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture
Although a number of genetically diverse Yersinia ruckeri strains are present in Norwegian aquaculture environments, most if not all outbreaks of yersiniosis in Atlantic salmon in Norway are associated with a single specific genetic lineage of serotype O1, termed clonal complex 1. To investigate the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545435/ https://www.ncbi.nlm.nih.gov/pubmed/35648597 http://dx.doi.org/10.1111/jfd.13656 |
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author | Riborg, Andreas Gulla, Snorre Strand, David Wiik‐Nielsen, Jannicke Rønneseth, Anita Welch, Timothy J. Spilsberg, Bjørn Colquhoun, Duncan J. |
author_facet | Riborg, Andreas Gulla, Snorre Strand, David Wiik‐Nielsen, Jannicke Rønneseth, Anita Welch, Timothy J. Spilsberg, Bjørn Colquhoun, Duncan J. |
author_sort | Riborg, Andreas |
collection | PubMed |
description | Although a number of genetically diverse Yersinia ruckeri strains are present in Norwegian aquaculture environments, most if not all outbreaks of yersiniosis in Atlantic salmon in Norway are associated with a single specific genetic lineage of serotype O1, termed clonal complex 1. To investigate the presence and spread of virulent and putatively avirulent strains in Norwegian salmon farms, PCR assays specific for Y. ruckeri (species level) and Y. ruckeri clonal complex 1 were developed. Following extensive screening of water and biofilm, the widespread prevalence of putatively avirulent Y. ruckeri strains was confirmed in freshwater salmon hatcheries, while Y. ruckeri clonal complex 1 was found in fewer farms. The formalin‐killed bacterin yersiniosis vaccine was detected in environmental samples by both PCR assays for several weeks post‐vaccination. It is thus important to interpret results from recently vaccinated fish with great care. Moreover, field studies and laboratory trials confirmed that stressful management procedures may result in increased shedding of Y. ruckeri by sub‐clinically infected fish. Analysis of sea water sampled throughout thermal delousing procedures proved effective for detection of Y. ruckeri in sub‐clinically infected populations. |
format | Online Article Text |
id | pubmed-9545435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95454352022-10-14 qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture Riborg, Andreas Gulla, Snorre Strand, David Wiik‐Nielsen, Jannicke Rønneseth, Anita Welch, Timothy J. Spilsberg, Bjørn Colquhoun, Duncan J. J Fish Dis Research Articles Although a number of genetically diverse Yersinia ruckeri strains are present in Norwegian aquaculture environments, most if not all outbreaks of yersiniosis in Atlantic salmon in Norway are associated with a single specific genetic lineage of serotype O1, termed clonal complex 1. To investigate the presence and spread of virulent and putatively avirulent strains in Norwegian salmon farms, PCR assays specific for Y. ruckeri (species level) and Y. ruckeri clonal complex 1 were developed. Following extensive screening of water and biofilm, the widespread prevalence of putatively avirulent Y. ruckeri strains was confirmed in freshwater salmon hatcheries, while Y. ruckeri clonal complex 1 was found in fewer farms. The formalin‐killed bacterin yersiniosis vaccine was detected in environmental samples by both PCR assays for several weeks post‐vaccination. It is thus important to interpret results from recently vaccinated fish with great care. Moreover, field studies and laboratory trials confirmed that stressful management procedures may result in increased shedding of Y. ruckeri by sub‐clinically infected fish. Analysis of sea water sampled throughout thermal delousing procedures proved effective for detection of Y. ruckeri in sub‐clinically infected populations. John Wiley and Sons Inc. 2022-06-01 2022-08 /pmc/articles/PMC9545435/ /pubmed/35648597 http://dx.doi.org/10.1111/jfd.13656 Text en © 2022 The Authors. Journal of Fish Diseases published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Riborg, Andreas Gulla, Snorre Strand, David Wiik‐Nielsen, Jannicke Rønneseth, Anita Welch, Timothy J. Spilsberg, Bjørn Colquhoun, Duncan J. qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture |
title |
qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture |
title_full |
qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture |
title_fullStr |
qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture |
title_full_unstemmed |
qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture |
title_short |
qPCR screening for Yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in Norwegian aquaculture |
title_sort | qpcr screening for yersinia ruckeri clonal complex 1 against a background of putatively avirulent strains in norwegian aquaculture |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545435/ https://www.ncbi.nlm.nih.gov/pubmed/35648597 http://dx.doi.org/10.1111/jfd.13656 |
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