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Genetic features of Mycobacterium tuberculosis modern Beijing sublineage

Mycobacterium tuberculosis (MTB) Beijing strains have caused a great concern because of their rapid emergence and increasing prevalence in worldwide regions. Great efforts have been made to investigate the pathogenic characteristics of Beijing strains such as hypervirulence, drug resistance and favo...

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Autores principales: Liu, Qingyun, Luo, Tao, Dong, Xinran, Sun, Gang, Liu, Zhu, Gan, Mingyun, Wu, Jie, Shen, Xin, Gao, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777927/
https://www.ncbi.nlm.nih.gov/pubmed/26905026
http://dx.doi.org/10.1038/emi.2016.14
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author Liu, Qingyun
Luo, Tao
Dong, Xinran
Sun, Gang
Liu, Zhu
Gan, Mingyun
Wu, Jie
Shen, Xin
Gao, Qian
author_facet Liu, Qingyun
Luo, Tao
Dong, Xinran
Sun, Gang
Liu, Zhu
Gan, Mingyun
Wu, Jie
Shen, Xin
Gao, Qian
author_sort Liu, Qingyun
collection PubMed
description Mycobacterium tuberculosis (MTB) Beijing strains have caused a great concern because of their rapid emergence and increasing prevalence in worldwide regions. Great efforts have been made to investigate the pathogenic characteristics of Beijing strains such as hypervirulence, drug resistance and favoring transmission. Phylogenetically, MTB Beijing family was divided into modern and ancient sublineages. Modern Beijing strains displayed enhanced virulence and higher prevalence when compared with ancient Beijing strains, but the genetic basis for this difference remains unclear. In this study, by analyzing previously published sequencing data of 1082 MTB Beijing isolates, we determined the genetic changes that were commonly present in modern Beijing strains but absent in ancient Beijing strains. These changes include 44 single-nucleotide polymorphisms (SNPs) and two short genomic deletions. Through bioinformatics analysis, we demonstrated that these genetic changes had high probability of functional effects. For example, 4 genes were frameshifted due to premature stop mutation or genomic deletions, 19 nonsynonymous SNPs located in conservative codons, and there is a significant enrichment in regulatory network for all nonsynonymous mutations. Besides, three SNPs located in promoter regions were verified to alter downstream gene expressions. Our study precisely defined the genetic features of modern Beijing strains and provided interesting clues for future researches to elucidate the mechanisms that underlie this sublineage's successful expansion. These findings from the analysis of the modern Beijing sublineage could provide us a model to understand the dynamics of pathogenicity of MTB.
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spelling pubmed-47779272016-03-10 Genetic features of Mycobacterium tuberculosis modern Beijing sublineage Liu, Qingyun Luo, Tao Dong, Xinran Sun, Gang Liu, Zhu Gan, Mingyun Wu, Jie Shen, Xin Gao, Qian Emerg Microbes Infect Original Article Mycobacterium tuberculosis (MTB) Beijing strains have caused a great concern because of their rapid emergence and increasing prevalence in worldwide regions. Great efforts have been made to investigate the pathogenic characteristics of Beijing strains such as hypervirulence, drug resistance and favoring transmission. Phylogenetically, MTB Beijing family was divided into modern and ancient sublineages. Modern Beijing strains displayed enhanced virulence and higher prevalence when compared with ancient Beijing strains, but the genetic basis for this difference remains unclear. In this study, by analyzing previously published sequencing data of 1082 MTB Beijing isolates, we determined the genetic changes that were commonly present in modern Beijing strains but absent in ancient Beijing strains. These changes include 44 single-nucleotide polymorphisms (SNPs) and two short genomic deletions. Through bioinformatics analysis, we demonstrated that these genetic changes had high probability of functional effects. For example, 4 genes were frameshifted due to premature stop mutation or genomic deletions, 19 nonsynonymous SNPs located in conservative codons, and there is a significant enrichment in regulatory network for all nonsynonymous mutations. Besides, three SNPs located in promoter regions were verified to alter downstream gene expressions. Our study precisely defined the genetic features of modern Beijing strains and provided interesting clues for future researches to elucidate the mechanisms that underlie this sublineage's successful expansion. These findings from the analysis of the modern Beijing sublineage could provide us a model to understand the dynamics of pathogenicity of MTB. Nature Publishing Group 2016-02 2016-02-24 /pmc/articles/PMC4777927/ /pubmed/26905026 http://dx.doi.org/10.1038/emi.2016.14 Text en Copyright © 2016 Shanghai Shangyixun Cultural Communication Co., Ltd http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Original Article
Liu, Qingyun
Luo, Tao
Dong, Xinran
Sun, Gang
Liu, Zhu
Gan, Mingyun
Wu, Jie
Shen, Xin
Gao, Qian
Genetic features of Mycobacterium tuberculosis modern Beijing sublineage
title Genetic features of Mycobacterium tuberculosis modern Beijing sublineage
title_full Genetic features of Mycobacterium tuberculosis modern Beijing sublineage
title_fullStr Genetic features of Mycobacterium tuberculosis modern Beijing sublineage
title_full_unstemmed Genetic features of Mycobacterium tuberculosis modern Beijing sublineage
title_short Genetic features of Mycobacterium tuberculosis modern Beijing sublineage
title_sort genetic features of mycobacterium tuberculosis modern beijing sublineage
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777927/
https://www.ncbi.nlm.nih.gov/pubmed/26905026
http://dx.doi.org/10.1038/emi.2016.14
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