Genome sequencing of Listeria monocytogenes "Quargel" listeriosis outbreak strains reveals two different strains with distinct in vitro virulence potential
Language English Country United States Media electronic-ecollection
Document type Historical Article, Journal Article, Research Support, Non-U.S. Gov't
Grant support
P 22703
Austrian Science Fund FWF - Austria
PubMed
24587155
PubMed Central
PMC3935953
DOI
10.1371/journal.pone.0089964
PII: PONE-D-13-45645
Knihovny.cz E-resources
- MeSH
- Cell Line MeSH
- History, 21st Century MeSH
- Species Specificity MeSH
- Disease Outbreaks history MeSH
- Phylogeny MeSH
- Genetic Variation * MeSH
- Genome, Bacterial genetics MeSH
- Humans MeSH
- Listeria monocytogenes classification genetics pathogenicity MeSH
- Listeriosis epidemiology MeSH
- Models, Genetic MeSH
- Molecular Sequence Data MeSH
- Likelihood Functions MeSH
- Base Sequence MeSH
- Sequence Analysis, DNA MeSH
- Virulence MeSH
- Check Tag
- History, 21st Century MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Historical Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Germany MeSH
- Austria MeSH
A large listeriosis outbreak occurred in Austria, Germany and the Czech Republic in 2009 and 2010. The outbreak was traced back to a traditional Austrian curd cheese called "Quargel" which was contaminated with two distinct serovar 1/2a Listeria monocytogenes strains (QOC1 and QOC2). In this study we sequenced and analysed the genomes of both outbreak strains in order to investigate the extent of genetic diversity between the two strains belonging to MLST sequence types 398 (QOC2) and 403 (QOC1). Both genomes are highly similar, but also display distinct properties: The QOC1 genome is approximately 74 kbp larger than the QOC2 genome. In addition, the strains harbour 93 (QOC1) and 45 (QOC2) genes encoding strain-specific proteins. A 21 kbp region showing highest similarity to plasmid pLMIV encoding three putative internalins is integrated in the QOC1 genome. In contrast to QOC1, strain QOC2 harbours a vip homologue, which encodes a LPXTG surface protein involved in cell invasion. In accordance, in vitro virulence assays revealed distinct differences in invasion efficiency and intracellular proliferation within different cell types. The higher virulence potential of QOC1 in non-phagocytic cells may be explained by the presence of additional internalins in the pLMIV-like region, whereas the higher invasion capability of QOC2 into phagocytic cells may be due to the presence of a vip homologue. In addition, both strains show differences in stress-related gene content. Strain QOC1 encodes a so-called stress survival islet 1, whereas strain QOC2 harbours a homologue of the uncharacterized LMOf2365_0481 gene. Consistently, QOC1 shows higher resistance to acidic, alkaline and gastric stress. In conclusion, our results show that strain QOC1 and QOC2 are distinct and did not recently evolve from a common ancestor.
Austrian Agency for Health and Food Safety Vienna Austria
Institute for Milk Hygiene University of Veterinary Medicine Vienna Vienna Austria
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