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. 2018 Aug 2;9(8):396.
doi: 10.3390/genes9080396.

Genomic Diversity of Listeria monocytogenes Isolated from Clinical and Non-Clinical Samples in Chile

Affiliations

Genomic Diversity of Listeria monocytogenes Isolated from Clinical and Non-Clinical Samples in Chile

Viviana Toledo et al. Genes (Basel). .

Abstract

Listeria monocytogenes is the causative agent of listeriosis, which is an uncommon but severe infection associated with high mortality rates in humans especially in high-risk groups. This bacterium survives a variety of stress conditions (e.g., high osmolality, low pH), which allows it to colonize different niches especially niches found in food processing environments. Additionally, a considerable heterogeneity in pathogenic potential has been observed in different strains. In this study, 38 isolates of L. monocytogenes collected in Chile from clinical samples (n = 22) and non-clinical samples (n = 16) were analyzed using whole genome sequencing (WGS) to determine their genomic diversity. A core genome Single Nucleotide Polymorphism (SNP) tree using 55 additional L. monocytogenes accessions classified the Chilean isolates in lineages I (n = 25) and II (n = 13). In silico, Multi-locus sequence typing (MLST) differentiated the isolates into 13 sequence types (ST) in which the most common were ST1 (15 isolates) and ST9 (6 isolates) and represented 55% of the isolates. Genomic elements associated with virulence (i.e., LIPI-1, LIPI-3, inlA, inlB, inlC, inlG, inlH, inlD, inlE, inlK, inlF, and inlJ) and stress survival (i.e., stress survival islet 1 and stress survival islet 2) were unevenly distributed among clinical and non-clinical isolates. In addition, one novel inlA premature stop codon (PMSC) was detected. Comparative analysis of L. monocytogenes circulating in Chile revealed the presence of globally distributed sequence types along with differences among the isolates analyzed at a genomic level specifically associated with virulence and stress survival.

Keywords: Chile; Listeria monocytogenes; genomic diversity; single nucleotide polymorphism; whole genome sequencing.

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Conflict of interest statement

The authors declared no conflict of interest.

Figures

Figure 1
Figure 1
Phylogenetic tree of 38 L. monocytogenes isolates from Chile inferred from single nucleotide polymorphisms (SNPs) of whole genome sequencing data and the distribution of their genetic elements associated with virulence and stress survival. Isolates from clinical samples are colored in blue and isolates from non-clinical samples are colored in green. Columns on the right of the tree indicate the presence (purple) or absence (white) of genetic elements. Isolates with premature stop codon mutations (PMSCs) in inlA are in pink and isolates with 3 aa deletions are yellow. The number of intact prophages predicted with PHAST is added.

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