| Literature DB >> 26245135 |
Swapnil Doijad1, Markus Weigel1, Sukhadeo Barbuddhe2, Jochen Blom3, Alexander Goesmann3, Torsten Hain1, Trinad Chakraborty1.
Abstract
The precise delineation of lineages and clonal groups are a prerequisite to examine within-species genetic variations, particularly with respect to pathogenic potential. A whole-genome-based approach was used to subtype and subgroup isolates of Listeria monocytogenes. Core-genome typing was performed, employing 3 different approaches: total core genes (CG), high-scoring segment pairs (HSPs), and average nucleotide identity (ANI). Examination of 113 L. monocytogenes genomes available in-house and in public domains revealed 33 phylogenomic groups (PGs). Each PG could be differentiated into a number of genomic types (GTs), depending on the approach used: HSPs (n = 57 GTs), CG (n = 71 GTs), and ANI (n = 83 GTs). Demarcation of the PGs was concordant with the 4 known lineages and led to the identification of sublineages in the lineage groups I, II, and III. In addition, PG assignments had discriminatory power similar to multi-virulence-locus sequence typing types and clonal complexes of multilocus sequence typing. Clustering of genomically highly similar isolates from different countries, sources, and isolation dates using whole-genome-based PG suggested that dispersion of phylogenomic clones of L. monocytogenes preceded their subsequent evolution. Classification according to PG may act as a guideline for future epidemiological studies.Entities:
Keywords: L. monocytogenes; SGE; WGS; core-genome typing; typage du génome central
Mesh:
Year: 2015 PMID: 26245135 DOI: 10.1139/cjm-2015-0281
Source DB: PubMed Journal: Can J Microbiol ISSN: 0008-4166 Impact factor: 2.419