A comprehensive update to the Mycobacterium tuberculosis H37Rv reference genome (vol 13, 7068, 2022)

被引:0
|
作者
Chitale, Poonam
Lemenze, Alexander D.
Fogarty, Emily C.
Shah, Avi
Grady, Courtney
Odom-Mabey, Aubrey R.
Johnson, W. Evan
Yang, Jason H.
Eren, A. Murat
Brosch, Roland
Kumar, Pradeep
Alland, David
机构
[1] Ray V. Lourenco Center for the Study of Emerging and Re-emerging Pathogens, Rutgers University – New Jersey Medical School, Newark, NJ
[2] Public Health Research Institute, Rutgers University – New Jersey Medical School, Newark, NJ
[3] Department of Pathology, Immunology and Laboratory Medicine, New Jersey Medical School, Rutgers—The State University of New Jersey, Newark, NJ
[4] Department of Medicine, University of Chicago, Chicago, IL
[5] Committee on Microbiology, University of Chicago, Chicago, IL
[6] Department of Microbiology, Biochemistry and Molecular Genetics, Rutgers University- New Jersey Medical School, Newark, NJ
[7] Division of Computational Biomedicine, Boston University School of Medicine and Bioinformatics Program, Boston University, Boston, MA
[8] Bioinformatics Program, Boston University, Boston, MA
[9] Center for Data Science, Rutgers University – New Jersey Medical School, Newark, NJ
[10] Helmholtz Institute for Functional Marine Biodiversity (HIFMB), Oldenburg
[11] Bay Paul Center, Marine Biological Laboratory, Woods Hole, MA
[12] Institut Pasteur, Université Paris Cité, Unit for Integrated Mycobacterial Pathogenomics, CNRS UMR 6047, Paris
基金
美国国家卫生研究院;
关键词
D O I
10.1038/s41467-022-35402-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
H37Rv is the most widely used Mycobacterium tuberculosis strain, and its genome is globally used as the M. tuberculosis reference sequence. Here, we present Bact-Builder, a pipeline that uses consensus building to generate complete and accurate bacterial genome sequences and apply it to three independently cultured and sequenced H37Rv aliquots of a single laboratory stock. Two of the 4,417,942 base-pair long H37Rv assemblies are 100% identical, with the third differing by a single nucleotide. Compared to the existing H37Rv reference, the new sequence contains ~6.4 kb additional base pairs, encoding ten new regions that include insertions in PE/PPE genes and new paralogs of esxN and esxJ, which are differentially expressed compared to the reference genes. New sequencing and de novo assemblies with Bact-Builder confirm that all 10 regions, plus small additional polymorphisms, are also present in the commonly used H37Rv strains NR123, TMC102, and H37Rv1998. Thus, Bact-Builder shows promise as an improved method to perform accurate and reproducible de novo assemblies of bacterial genomes, and our work provides important updates to the primary M. tuberculosis reference genome. © 2022, The Author(s).
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