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A novel Ancestral Beijing sublineage of Mycobacterium tuberculosis suggests the transition site to Modern Beijing sublineages.

Pravech Ajawatanawong | Hideki Yanai | Nat Smittipat | Areeya Disratthakit | Norio Yamada | Reiko Miyahara | Supalert Nedsuwan | Worarat Imasanguan | Pacharee Kantipong | Boonchai Chaiyasirinroje | Jiraporn Wongyai | Supada Plitphonganphim | Pornpen Tantivitayakul | Jody Phelan | Julian Parkhill | Taane G Clark | Martin L Hibberd | Wuthiwat Ruangchai | Panawun Palittapongarnpim | Tada Juthayothin | Yuttapong Thawornwattana | Wasna Viratyosin | Sissades Tongsima | Surakameth Mahasirimongkol | Katsushi Tokunaga | Prasit Palittapongarnpim
Scientific reports | 2019

Global Mycobacterium tuberculosis population comprises 7 major lineages. The Beijing strains, particularly the ones classified as Modern groups, have been found worldwide, frequently associated with drug resistance, younger ages, outbreaks and appear to be expanding. Here, we report analysis of whole genome sequences of 1170 M. tuberculosis isolates together with their patient profiles. Our samples belonged to Lineage 1-4 (L1-L4) with those of L1 and L2 being equally dominant. Phylogenetic analysis revealed several new or rare sublineages. Differential associations between sublineages of M. tuberculosis and patient profiles, including ages, ethnicity, HIV (human immunodeficiency virus) infection and drug resistance were demonstrated. The Ancestral Beijing strains and some sublineages of L4 were associated with ethnic minorities while L1 was more common in Thais. L2.2.1.Ancestral 4 surprisingly had a mutation that is typical of the Modern Beijing sublineages and was common in Akha and Lahu tribes who have migrated from Southern China in the last century. This may indicate that the evolutionary transition from the Ancestral to Modern Beijing sublineages might be gradual and occur in Southern China, where the presence of multiple ethnic groups might have allowed for the circulations of various co-evolving sublineages which ultimately lead to the emergence of the Modern Beijing strains.

Pubmed ID: 31548561

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Associated grants

  • Agency: FIC NIH HHS, United States
    Id: D43 TW009522
  • Agency: Medical Research Council, United Kingdom
    Id: MR/M01360X/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/N010469/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/R025576/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/R020973/1
  • Agency: Biotechnology and Biological Sciences Research Council, United Kingdom
    Id: BB/R013063/1
  • Agency: Wellcome Trust, United Kingdom
    Id: WT096249/Z/11/B
  • Agency: Wellcome Trust, United Kingdom
    Id: WT088559MA
  • Agency: Wellcome Trust, United Kingdom
    Id: WT081814/Z/06/Z
  • Agency: Wellcome Trust, United Kingdom
    Id: WT098051

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Jalview (tool)

RRID:SCR_006459

A free program for multiple sequence alignment editing, visualisation and analysis that is available in two forms: a lightweight Java applet for use in web applications, and a powerful desktop application that employs web services for sequence alignment, secondary structure prediction and the retrieval of alignments, sequences, annotation and structures from public databases and any DAS 1.53 compliant sequence or annotation server. Use it to view and edit sequence alignments, analyse them with phylogenetic trees and principal components analysis (PCA) plots and explore molecular structures and annotation. Jalview has built in DNA, RNA and protein sequence and structure visualisation and analysis capabilities. It uses Jmol to view 3D structures, and VARNA to display RNA secondary structure.

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RRID:SCR_008515

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RRID:SCR_012813

Data analysis service to predict whether an amino acid substitution affects protein function based on sequence homology and the physical properties of amino acids. SIFT can be applied to naturally occurring nonsynonymous polymorphisms and laboratory-induced missense mutations. (entry from Genetic Analysis Software) Web service is also available.

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