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Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea

BACKGROUND: A Brucella eradication program has been executed in Korea. To effectively prevent and control brucellosis, a molecular method for genetic identification and epidemiological trace-back must be established. As part of that, the MLVA typing assay was evaluated and applied to B. abortus isol...

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Autores principales: Her, Moon, Kang, Sung-Il, Cho, Dong-Hee, Cho, Yun-Sang, Hwang, In-Yeong, Heo, Young-Ran, Jung, Suk-Chan, Yoo, Han-Sang
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774859/
https://www.ncbi.nlm.nih.gov/pubmed/19863821
http://dx.doi.org/10.1186/1471-2180-9-230
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author Her, Moon
Kang, Sung-Il
Cho, Dong-Hee
Cho, Yun-Sang
Hwang, In-Yeong
Heo, Young-Ran
Jung, Suk-Chan
Yoo, Han-Sang
author_facet Her, Moon
Kang, Sung-Il
Cho, Dong-Hee
Cho, Yun-Sang
Hwang, In-Yeong
Heo, Young-Ran
Jung, Suk-Chan
Yoo, Han-Sang
author_sort Her, Moon
collection PubMed
description BACKGROUND: A Brucella eradication program has been executed in Korea. To effectively prevent and control brucellosis, a molecular method for genetic identification and epidemiological trace-back must be established. As part of that, the MLVA typing assay was evaluated and applied to B. abortus isolates for analyzing the characteristics of the regional distribution and relationships of foreign isolates. RESULTS: A total of 177 isolates originating from 105 cattle farms for the period 1996 to 2008 were selected as representatives for the nine provinces of South Korea. A dendrogram of strain relatedness was constructed in accordance with the number of tandem repeat units for 17 loci so that it was possible to trace back in the restricted areas. Even in a farm contaminated by one source, however, the Brucella isolates showed an increase or decrease in one TRs copy number at some loci with high DI values. Moreover, those 17 loci was confirmed in stability via in-vitro and in-vivo passage, and found to be sufficiently stable markers that can readily identify the inoculated strain even if minor changes were detected. In the parsimony analysis with foreign Brucella isolates, domestic isolates were clustered distinctively, and located near the Central and Southern American isolates. CONCLUSION: The MLVA assay has enough discrimination power in the Brucella species level and can be utilized as a tool for the epidemiological trace-back of the B. abortus isolates. But it is important to consider that Brucella isolates may be capable of undergoing minor changes at some loci in the course of infection or in accordance with the changes of the host.
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spelling pubmed-27748592009-11-10 Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea Her, Moon Kang, Sung-Il Cho, Dong-Hee Cho, Yun-Sang Hwang, In-Yeong Heo, Young-Ran Jung, Suk-Chan Yoo, Han-Sang BMC Microbiol Research article BACKGROUND: A Brucella eradication program has been executed in Korea. To effectively prevent and control brucellosis, a molecular method for genetic identification and epidemiological trace-back must be established. As part of that, the MLVA typing assay was evaluated and applied to B. abortus isolates for analyzing the characteristics of the regional distribution and relationships of foreign isolates. RESULTS: A total of 177 isolates originating from 105 cattle farms for the period 1996 to 2008 were selected as representatives for the nine provinces of South Korea. A dendrogram of strain relatedness was constructed in accordance with the number of tandem repeat units for 17 loci so that it was possible to trace back in the restricted areas. Even in a farm contaminated by one source, however, the Brucella isolates showed an increase or decrease in one TRs copy number at some loci with high DI values. Moreover, those 17 loci was confirmed in stability via in-vitro and in-vivo passage, and found to be sufficiently stable markers that can readily identify the inoculated strain even if minor changes were detected. In the parsimony analysis with foreign Brucella isolates, domestic isolates were clustered distinctively, and located near the Central and Southern American isolates. CONCLUSION: The MLVA assay has enough discrimination power in the Brucella species level and can be utilized as a tool for the epidemiological trace-back of the B. abortus isolates. But it is important to consider that Brucella isolates may be capable of undergoing minor changes at some loci in the course of infection or in accordance with the changes of the host. BioMed Central 2009-10-29 /pmc/articles/PMC2774859/ /pubmed/19863821 http://dx.doi.org/10.1186/1471-2180-9-230 Text en Copyright ©2009 Her 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 article
Her, Moon
Kang, Sung-Il
Cho, Dong-Hee
Cho, Yun-Sang
Hwang, In-Yeong
Heo, Young-Ran
Jung, Suk-Chan
Yoo, Han-Sang
Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea
title Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea
title_full Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea
title_fullStr Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea
title_full_unstemmed Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea
title_short Application and evaluation of the MLVA typing assay for the Brucella abortus strains isolated in Korea
title_sort application and evaluation of the mlva typing assay for the brucella abortus strains isolated in korea
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774859/
https://www.ncbi.nlm.nih.gov/pubmed/19863821
http://dx.doi.org/10.1186/1471-2180-9-230
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