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A comprehensive update to the Mycobacterium tuberculosis H37Rv reference genome. | LitMetric

AI Article Synopsis

  • H37Rv is the primary strain of Mycobacterium tuberculosis used as a reference genome, and researchers have developed a new pipeline called Bact-Builder for accurate bacterial genome sequencing.
  • Two out of three H37Rv samples sequenced were identical, while one differed by just one nucleotide, and the new analysis revealed about 6.4 kb of extra DNA sequence with ten new regions compared to the existing reference.
  • Bact-Builder has validated that these new genomic regions are also present in other common H37Rv strains, indicating its effectiveness for de novo genome assemblies and enhancing the M. tuberculosis reference genome.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673877PMC
http://dx.doi.org/10.1038/s41467-022-34853-xDOI Listing

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