Evidence map›Paper›PMID 23267677›Full record

ArticleBMC microbiology2012

Polyphasic characterization and genetic relatedness of low-virulence and virulent Listeria monocytogenes isolates.

Sylvie M Roche, Olivier Grépinet, Annaëlle Kerouanton, Marie Ragon, Alexandre Leclercq, Stéphanie Témoin, Brigitte Schaeffer, Gilbert Skorski, Laurent Mereghetti, Alban Le Monnier and 1 more

Abstract read
In one paragraph

Article in BMC microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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  6. Predominance of DistinctMicroorganisms · 2020
    Article
  7. First Detection ofFrontiers in veterinary science · 2020
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Sylvie M RocheINRA, UR 1282 Infectiologie Animale et Santé Publique, Agents transmissibles et Infectiologie, F-37380, Nouzilly and IFR, 136, France. sylvie.roche@tours.inra.fr
Olivier Grépinet
Annaëlle Kerouanton
Marie Ragon
Alexandre Leclercq
Stéphanie Témoin
Brigitte Schaeffer
Gilbert Skorski
Laurent Mereghetti
Alban Le Monnier
Philippe Velge

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrently, food regulatory authorities consider all Listeria monocytogenes isolates as equally virulent. However, an increasing number of studies demonstrate extensive variations in virulence and pathogenicity of L. monocytogenes strains. Up to now, there is no comprehensive overview of the population genetic structure of L. monocytogenes taking into account virulence level. We have previously demonstrated that different low-virulence strains exhibit the same mutations in virulence genes suggesting that they could have common evolutionary pathways. New low-virulence strains were identified and assigned to phenotypic and genotypic Groups using cluster analysis. Pulsed-field gel electrophoresis, virulence gene sequencing and multi-locus sequence typing analyses were performed to study the genetic relatedness and the population structure between the studied low-virulence isolates and virulent strains.

resultsThese methods showed that low-virulence strains are widely distributed in the two major lineages, but some are also clustered according to their genetic mutations. These analyses showed that low-virulence strains initially grouped according to their lineage, then to their serotypes and after which, they lost their virulence suggesting a relatively recent emergence.

conclusionsLoss of virulence in lineage II strains was related to point mutation in a few virulence genes (prfA, inlA, inlB, plcA). These strains thus form a tightly clustered, monophyletic group with limited diversity. In contrast, low-virulence strains of lineage I were more dispersed among the virulence strains and the origin of their loss of virulence has not been identified yet, even if some strains exhibited different mutations in prfA or inlA.

Indexed as

Genetic VariationAnimalsCluster AnalysisDisease Models, AnimalElectrophoresis, Gel, Pulsed-FieldGenotypeHumansListeria monocytogenesMiceMolecular Sequence DataMultilocus Sequence TypingSequence Analysis, DNAVirulenceVirulence FactorsVirulence Factors

Identifiers

PMID23267677
PMCPMC3558321

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.