» Articles » PMID: 28734764

Comparative Genomic Analysis of Mycobacterium Tuberculosis Beijing-like Strains Revealed Specific Genetic Variations Associated with Virulence and Drug Resistance

Overview
Date 2017 Jul 24
PMID 28734764
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Isolates of the Mycobacterium tuberculosis lineage 2/East-Asian are considered one of the most successful strains due to their increased pathogenicity, hyper-virulence associated with drug resistance, and high transmission. Recent studies in Colombia have shown that the Beijing-like genotype is associated with multidrug-resistance and high prevalence in the southwest of the country, but the genetic basis of its success in dissemination is unknown. In contribution to this matter, we obtained the whole sequences of six genomes of clinical isolates assigned to the Beijing-like genotype. The genomes were compared with the reference genome of M. tuberculosis H37Rv and 53 previously published M. tuberculosis genomes. We found that the six Beijing-like isolates belong to a modern Beijing sub-lineage and share specific genomic variants: i.e. deletion in the PPE8 gene, in Rv3806c (ubiA) responsible of high ethambutol resistance and in Rv3862c (whiB6) which is involved in granuloma formation and virulence, are some of them. Moreover, each isolated has exclusively single nucleotide polymorphisms (SNPs) in genes related with cell wall processes and cell metabolism. We identified polymorphisms in genes related to drug resistance that could explain the drug-resistant phenotypes found in the six isolates from Colombia. We hypothesize that changes due to these genetic variations contribute to the success of these strains. Finally, we analyzed the IS6110 insertion sequences finding very low variance between them, suggesting that SNPs is the major cause of variability found in Beijing-like strains circulating in Colombia.

Citing Articles

Diversification of gene content in the complex is determined by phylogenetic and ecological signatures.

Silva-Pereira T, Soler-Camargo N, Guimaraes A Microbiol Spectr. 2024; 12(2):e0228923.

PMID: 38230932 PMC: 10871547. DOI: 10.1128/spectrum.02289-23.


Close Related Drug-Resistance Beijing Isolates of Reveal a Different Transcriptomic Signature in a Murine Disease Progression Model.

Cerezo-Cortes M, Rodriguez-Castillo J, Mata-Espinosa D, Bini E, Barrios-Payan J, Zatarain-Barron Z Int J Mol Sci. 2022; 23(9).

PMID: 35563545 PMC: 9100210. DOI: 10.3390/ijms23095157.


Whole-genome comparative analysis at the lineage/sublineage level discloses relationships between genotype and clinical phenotype.

Negrete-Paz A, Vazquez-Marrufo G, Vazquez-Garciduenas M PeerJ. 2021; 9:e12128.

PMID: 34589306 PMC: 8434806. DOI: 10.7717/peerj.12128.


Profiling the immune response to Beijing family infection: a perspective from the transcriptome.

Maria Irene C, Juan German R, Gamaliel L, Dulce Adriana M, Estela Isabel B, Brenda Nohemi M Virulence. 2021; 12(1):1689-1704.

PMID: 34228582 PMC: 8265813. DOI: 10.1080/21505594.2021.1936432.


Genome analyses of 174 strains of provide insight into the evolution of drug resistance and reveal potential drug targets.

Verma H, Nagar S, Vohra S, Pandey S, Lal D, Negi R Microb Genom. 2021; 7(3).

PMID: 33750515 PMC: 8190606. DOI: 10.1099/mgen.0.000542.