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Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays

BACKGROUND: Our previous studies revealed that a new disease form of streptococcal toxic shock syndrome (STSS) is associated with specific Streptococcus suis serotype 2 (SS2) strains. To achieve a better understanding of the pathogenicity and evolution of SS2 at the whole-genome level, comparative g...

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Autores principales: Wu, Zuowei, Li, Ming, Wang, Changjun, Li, Jing, Lu, Na, Zhang, Ruifen, Jiang, Yongqiang, Yang, Ruifu, Liu, Cuihua, Liao, Hui, Gao, George F, Tang, Jiaqi, Zhu, Baoli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118785/
https://www.ncbi.nlm.nih.gov/pubmed/21554741
http://dx.doi.org/10.1186/1471-2164-12-219
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author Wu, Zuowei
Li, Ming
Wang, Changjun
Li, Jing
Lu, Na
Zhang, Ruifen
Jiang, Yongqiang
Yang, Ruifu
Liu, Cuihua
Liao, Hui
Gao, George F
Tang, Jiaqi
Zhu, Baoli
author_facet Wu, Zuowei
Li, Ming
Wang, Changjun
Li, Jing
Lu, Na
Zhang, Ruifen
Jiang, Yongqiang
Yang, Ruifu
Liu, Cuihua
Liao, Hui
Gao, George F
Tang, Jiaqi
Zhu, Baoli
author_sort Wu, Zuowei
collection PubMed
description BACKGROUND: Our previous studies revealed that a new disease form of streptococcal toxic shock syndrome (STSS) is associated with specific Streptococcus suis serotype 2 (SS2) strains. To achieve a better understanding of the pathogenicity and evolution of SS2 at the whole-genome level, comparative genomic analysis of 18 SS2 strains, selected on the basis of virulence and geographic origin, was performed using NimbleGen tiling arrays. RESULTS: Our results demonstrate that SS2 isolates have highly divergent genomes. The 89K pathogenicity island (PAI), which has been previously recognized as unique to the Chinese epidemic strains causing STSS, was partially included in some other virulent and avirulent strains. The ABC-type transport systems, encoded by 89K, were hypothesized to greatly contribute to the catastrophic features of STSS. Moreover, we identified many polymorphisms in genes encoding candidate or known virulence factors, such as PlcR, lipase, sortases, the pilus-associated proteins, and the response regulator RevS and CtsR. On the basis of analysis of regions of differences (RDs) across the entire genome for the 18 selected SS2 strains, a model of microevolution for these strains is proposed, which provides clues into Streptococcus pathogenicity and evolution. CONCLUSIONS: Our deep comparative genomic analysis of the 89K PAI present in the genome of SS2 strains revealed details into how some virulent strains acquired genes that may contribute to STSS, which may lead to better environmental monitoring of epidemic SS2 strains.
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spelling pubmed-31187852011-06-21 Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays Wu, Zuowei Li, Ming Wang, Changjun Li, Jing Lu, Na Zhang, Ruifen Jiang, Yongqiang Yang, Ruifu Liu, Cuihua Liao, Hui Gao, George F Tang, Jiaqi Zhu, Baoli BMC Genomics Research Article BACKGROUND: Our previous studies revealed that a new disease form of streptococcal toxic shock syndrome (STSS) is associated with specific Streptococcus suis serotype 2 (SS2) strains. To achieve a better understanding of the pathogenicity and evolution of SS2 at the whole-genome level, comparative genomic analysis of 18 SS2 strains, selected on the basis of virulence and geographic origin, was performed using NimbleGen tiling arrays. RESULTS: Our results demonstrate that SS2 isolates have highly divergent genomes. The 89K pathogenicity island (PAI), which has been previously recognized as unique to the Chinese epidemic strains causing STSS, was partially included in some other virulent and avirulent strains. The ABC-type transport systems, encoded by 89K, were hypothesized to greatly contribute to the catastrophic features of STSS. Moreover, we identified many polymorphisms in genes encoding candidate or known virulence factors, such as PlcR, lipase, sortases, the pilus-associated proteins, and the response regulator RevS and CtsR. On the basis of analysis of regions of differences (RDs) across the entire genome for the 18 selected SS2 strains, a model of microevolution for these strains is proposed, which provides clues into Streptococcus pathogenicity and evolution. CONCLUSIONS: Our deep comparative genomic analysis of the 89K PAI present in the genome of SS2 strains revealed details into how some virulent strains acquired genes that may contribute to STSS, which may lead to better environmental monitoring of epidemic SS2 strains. BioMed Central 2011-05-10 /pmc/articles/PMC3118785/ /pubmed/21554741 http://dx.doi.org/10.1186/1471-2164-12-219 Text en Copyright ©2011 Wu 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
Wu, Zuowei
Li, Ming
Wang, Changjun
Li, Jing
Lu, Na
Zhang, Ruifen
Jiang, Yongqiang
Yang, Ruifu
Liu, Cuihua
Liao, Hui
Gao, George F
Tang, Jiaqi
Zhu, Baoli
Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays
title Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays
title_full Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays
title_fullStr Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays
title_full_unstemmed Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays
title_short Probing genomic diversity and evolution of Streptococcus suis serotype 2 by NimbleGen tiling arrays
title_sort probing genomic diversity and evolution of streptococcus suis serotype 2 by nimblegen tiling arrays
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3118785/
https://www.ncbi.nlm.nih.gov/pubmed/21554741
http://dx.doi.org/10.1186/1471-2164-12-219
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