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MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates
BACKGROUND: Since 1950, Brucella melitensis has been the predominant strain associated with human brucellosis in China. In this study we investigated the genotypic characteristics of B. melitensis isolates from China using a multiple-locus variable-number tandem-repeat analysis (MLVA) and evaluated...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3233519/ https://www.ncbi.nlm.nih.gov/pubmed/22108057 http://dx.doi.org/10.1186/1471-2180-11-256 |
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author | Jiang, Hai Fan, Mengguang Chen, Jingdiao Mi, Jingchuan Yu, Ruiping Zhao, Hongyan Piao, Dongri Ke, Changwen Deng, Xiaoling Tian, Guozhong Cui, Buyun |
author_facet | Jiang, Hai Fan, Mengguang Chen, Jingdiao Mi, Jingchuan Yu, Ruiping Zhao, Hongyan Piao, Dongri Ke, Changwen Deng, Xiaoling Tian, Guozhong Cui, Buyun |
author_sort | Jiang, Hai |
collection | PubMed |
description | BACKGROUND: Since 1950, Brucella melitensis has been the predominant strain associated with human brucellosis in China. In this study we investigated the genotypic characteristics of B. melitensis isolates from China using a multiple-locus variable-number tandem-repeat analysis (MLVA) and evaluated the utility of MLVA with regards to epidemiological trace-back investigation. RESULTS: A total of 105 B. melitensis strains isolated from throughout China were divided into 69 MLVA types using MLVA-16. Nei's genetic diversity indices for the various loci ranged between 0.00 - 0.84. 12 out 16 loci were the low diversity with values < 0.2 and the most discriminatory markers were bruce16 and bruce30 with a diversity index of > 0.75 and containing 8 and 7 alleles, respectively. Many isolates were single-locus or double-locus variants of closely related B. melitensis isolates from different regions, including the north and south of China. Using panel 1, the majority of strains (84/105) were genotype 42 clustering to the 'East Mediterranean' B. melitensis group. Chinese B. melitensis are classified in limited number of closely related genotypes showing variation mainly at the panel 2B loci. CONCLUSION: The MLVA-16 assay can be useful to reveal the predominant genotypes and strain relatedness in endemic or non-endemic regions of brucellosis. However it is not suitable for biovar differentiation of B. melitensis. Genotype 42 is widely distributed throughout China during a long time. Bruce 16 and bruce 30 in panel 2B markers are most useful for typing Chinese isolates. |
format | Online Article Text |
id | pubmed-3233519 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32335192011-12-08 MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates Jiang, Hai Fan, Mengguang Chen, Jingdiao Mi, Jingchuan Yu, Ruiping Zhao, Hongyan Piao, Dongri Ke, Changwen Deng, Xiaoling Tian, Guozhong Cui, Buyun BMC Microbiol Research Article BACKGROUND: Since 1950, Brucella melitensis has been the predominant strain associated with human brucellosis in China. In this study we investigated the genotypic characteristics of B. melitensis isolates from China using a multiple-locus variable-number tandem-repeat analysis (MLVA) and evaluated the utility of MLVA with regards to epidemiological trace-back investigation. RESULTS: A total of 105 B. melitensis strains isolated from throughout China were divided into 69 MLVA types using MLVA-16. Nei's genetic diversity indices for the various loci ranged between 0.00 - 0.84. 12 out 16 loci were the low diversity with values < 0.2 and the most discriminatory markers were bruce16 and bruce30 with a diversity index of > 0.75 and containing 8 and 7 alleles, respectively. Many isolates were single-locus or double-locus variants of closely related B. melitensis isolates from different regions, including the north and south of China. Using panel 1, the majority of strains (84/105) were genotype 42 clustering to the 'East Mediterranean' B. melitensis group. Chinese B. melitensis are classified in limited number of closely related genotypes showing variation mainly at the panel 2B loci. CONCLUSION: The MLVA-16 assay can be useful to reveal the predominant genotypes and strain relatedness in endemic or non-endemic regions of brucellosis. However it is not suitable for biovar differentiation of B. melitensis. Genotype 42 is widely distributed throughout China during a long time. Bruce 16 and bruce 30 in panel 2B markers are most useful for typing Chinese isolates. BioMed Central 2011-11-22 /pmc/articles/PMC3233519/ /pubmed/22108057 http://dx.doi.org/10.1186/1471-2180-11-256 Text en Copyright ©2011 Jiang 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 Jiang, Hai Fan, Mengguang Chen, Jingdiao Mi, Jingchuan Yu, Ruiping Zhao, Hongyan Piao, Dongri Ke, Changwen Deng, Xiaoling Tian, Guozhong Cui, Buyun MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates |
title | MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates |
title_full | MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates |
title_fullStr | MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates |
title_full_unstemmed | MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates |
title_short | MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates |
title_sort | mlva genotyping of chinese human brucella melitensis biovar 1, 2 and 3 isolates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3233519/ https://www.ncbi.nlm.nih.gov/pubmed/22108057 http://dx.doi.org/10.1186/1471-2180-11-256 |
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