Literature DB >> 20019077

Pan-genome analysis provides much higher strain typing resolution than multi-locus sequence typing.

Barry G Hall1,2, Garth D Ehrlich3,1, Fen Z Hu3,1.   

Abstract

The most widely used DNA-based method for bacterial strain typing, multi-locus sequence typing (MLST), lacks sufficient resolution to distinguish among many bacterial strains within a species. Here, we show that strain typing based on the presence or absence of distributed genes is able to resolve all completely sequenced genomes of six bacterial species. This was accomplished by the development of a clustering method, neighbour grouping, which is completely consistent with the lower-resolution MLST method, but provides far greater resolving power. Because the presence/absence of distributed genes can be determined by low-cost microarray analyses, it offers a practical, high-resolution alternative to MLST that could provide valuable diagnostic and prognostic information for pathogenic bacterial species.

Mesh:

Year:  2009        PMID: 20019077      PMCID: PMC2889442          DOI: 10.1099/mic.0.035188-0

Source DB:  PubMed          Journal:  Microbiology (Reading)        ISSN: 1350-0872            Impact factor:   2.777


  28 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-19       Impact factor: 11.205

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Authors:  Tristan Lefébure; Michael J Stanhope
Journal:  Genome Biol       Date:  2007       Impact factor: 13.583

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  23 in total

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2.  Comparison of Whole-Genome Sequencing Methods for Analysis of Three Methicillin-Resistant Staphylococcus aureus Outbreaks.

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Review 3.  Microbial sequence typing in the genomic era.

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Review 6.  Diversity and Evolution in the Genome of Clostridium difficile.

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8.  Comparative genome-scale modelling of Staphylococcus aureus strains identifies strain-specific metabolic capabilities linked to pathogenicity.

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10.  Rapid bacterial whole-genome sequencing to enhance diagnostic and public health microbiology.

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Journal:  JAMA Intern Med       Date:  2013-08-12       Impact factor: 21.873

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