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Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction
OBJECTIVE: Dichelobacter nodosus is the causative agent of footrot in sheep. Ovine footrot is a major problem in Australia that results in large economic losses and a represents a very significant animal welfare issue. D. nodosus is divided into 10 serogroups (A–I, M), based on sequence variation in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804069/ https://www.ncbi.nlm.nih.gov/pubmed/29415761 http://dx.doi.org/10.1186/s13104-018-3229-5 |
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author | Best, Nickala Gwozdz, Jacek Suter, Robert Rawlin, Grant Beddoe, Travis |
author_facet | Best, Nickala Gwozdz, Jacek Suter, Robert Rawlin, Grant Beddoe, Travis |
author_sort | Best, Nickala |
collection | PubMed |
description | OBJECTIVE: Dichelobacter nodosus is the causative agent of footrot in sheep. Ovine footrot is a major problem in Australia that results in large economic losses and a represents a very significant animal welfare issue. D. nodosus is divided into 10 serogroups (A–I, M), based on sequence variation in the type IV fimbriae gene, fimA. Control of the bacteria is possible through use of serogroup-specific vaccination, however traditional identification of the serogroups of D. nodosus on infected sheep is time-consuming and costly. With the aim of reducing time and cost, a PCR assay was used to identify serogroups of D. nodosus directly from foot swabs of infected sheep in Victoria. RESULTS: It was shown that serogroup B was most common (10 locations), followed by A, G and H (4 locations), I and C (2 locations), D, E and F (1 location). Infections with multiple serotypes were observed in 50% of farms, with the remaining 50% having only a single serogroup detected. The ability to identify serogroups quickly and cheaply direct from foot swabs will aid the understanding of the epidemiology of D. nodosus and support control programs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3229-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5804069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58040692018-02-14 Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction Best, Nickala Gwozdz, Jacek Suter, Robert Rawlin, Grant Beddoe, Travis BMC Res Notes Research Note OBJECTIVE: Dichelobacter nodosus is the causative agent of footrot in sheep. Ovine footrot is a major problem in Australia that results in large economic losses and a represents a very significant animal welfare issue. D. nodosus is divided into 10 serogroups (A–I, M), based on sequence variation in the type IV fimbriae gene, fimA. Control of the bacteria is possible through use of serogroup-specific vaccination, however traditional identification of the serogroups of D. nodosus on infected sheep is time-consuming and costly. With the aim of reducing time and cost, a PCR assay was used to identify serogroups of D. nodosus directly from foot swabs of infected sheep in Victoria. RESULTS: It was shown that serogroup B was most common (10 locations), followed by A, G and H (4 locations), I and C (2 locations), D, E and F (1 location). Infections with multiple serotypes were observed in 50% of farms, with the remaining 50% having only a single serogroup detected. The ability to identify serogroups quickly and cheaply direct from foot swabs will aid the understanding of the epidemiology of D. nodosus and support control programs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13104-018-3229-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-07 /pmc/articles/PMC5804069/ /pubmed/29415761 http://dx.doi.org/10.1186/s13104-018-3229-5 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 | Research Note Best, Nickala Gwozdz, Jacek Suter, Robert Rawlin, Grant Beddoe, Travis Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction |
title | Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction |
title_full | Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction |
title_fullStr | Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction |
title_full_unstemmed | Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction |
title_short | Direct serogrouping of Dichelobacter nodosus from Victorian farms using conventional multiplex polymerase chain reaction |
title_sort | direct serogrouping of dichelobacter nodosus from victorian farms using conventional multiplex polymerase chain reaction |
topic | Research Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5804069/ https://www.ncbi.nlm.nih.gov/pubmed/29415761 http://dx.doi.org/10.1186/s13104-018-3229-5 |
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