Evidence map›Paper›PMID 22530965›Full record

ArticleBMC genomics2012

Comparative genomics and transcriptomics of lineages I, II, and III strains of Listeria monocytogenes.

Torsten Hain, Rohit Ghai, André Billion, Carsten Tobias Kuenne, Christiane Steinweg, Benjamin Izar, Walid Mohamed, Mobarak Abu Mraheil, Eugen Domann, Silke Schaffrath and 12 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
9.8field-weighted citation impact, top 1% of its field
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

53 citing papers in PubMed, 91 citations in OpenAlex.

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  18. An Immunomodulatory Transcriptional Signature Associated With PersistentFrontiers in cellular and infection microbiology · 2021
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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

22 authors at 8 institutions in 2 countries.

Torsten HainInstitute of Medical Microbiology, Justus-Liebig-University, Schubertstrasse 81, Giessen, D-35392, Germany.
Rohit Ghai
André Billion
Carsten Tobias Kuenne
Christiane Steinweg
Benjamin Izar
Walid Mohamed
Mobarak Abu Mraheil
Eugen Domann
Silke Schaffrath
Uwe Kärst
Alexander Goesmann
Sebastian Oehm
Alfred Pühler
Rainer Merkl
Sonja Vorwerk
Philippe Glaser
Patricia Garrido
Christophe Rusniok
Carmen Buchrieser
Werner Goebel
Trinad Chakraborty
University of Giessen · DEBielefeld University · DECentre National de la Recherche Scientifique · FRBioMed X Institute · DEHelmholtz Centre for Infection Research · DEInstitute of Medical Microbiology and Hygiene · DEInstitut Pasteur · FRUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundListeria monocytogenes is a food-borne pathogen that causes infections with a high-mortality rate and has served as an invaluable model for intracellular parasitism. Here, we report complete genome sequences for two L. monocytogenes strains belonging to serotype 4a (L99) and 4b (CLIP80459), and transcriptomes of representative strains from lineages I, II, and III, thereby permitting in-depth comparison of genome- and transcriptome -based data from three lineages of L. monocytogenes. Lineage III, represented by the 4a L99 genome is known to contain strains less virulent for humans.

resultsThe genome analysis of the weakly pathogenic L99 serotype 4a provides extensive evidence of virulence gene decay, including loss of several important surface proteins. The 4b CLIP80459 genome, unlike the previously sequenced 4b F2365 genome harbours an intact inlB invasion gene. These lineage I strains are characterized by the lack of prophage genes, as they share only a single prophage locus with other L. monocytogenes genomes 1/2a EGD-e and 4a L99. Comparative transcriptome analysis during intracellular growth uncovered adaptive expression level differences in lineages I, II and III of Listeria, notable amongst which was a strong intracellular induction of flagellar genes in strain 4a L99 compared to the other lineages. Furthermore, extensive differences between strains are manifest at levels of metabolic flux control and phosphorylated sugar uptake. Intriguingly, prophage gene expression was found to be a hallmark of intracellular gene expression. Deletion mutants in the single shared prophage locus of lineage II strain EGD-e 1/2a, the lma operon, revealed severe attenuation of virulence in a murine infection model.

conclusionComparative genomics and transcriptome analysis of L. monocytogenes strains from three lineages implicate prophage genes in intracellular adaptation and indicate that gene loss and decay may have led to the emergence of attenuated lineages.

Indexed as

PhylogenyAnimalsBacteriophagesDisease Models, AnimalFlagellinGene DuplicationGene Expression ProfilingGene Expression Regulation, BacterialGenes, ViralGenetic LociGene Transfer, HorizontalGenome, BacterialGenomicsHumansListeria monocytogenesListeriosisFlagellinMembrane ProteinsNucleotides

Identifiers

PMID22530965
PMCPMC3464598
OpenAlexW2127411591

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LicenceCC BY
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Registered trials

None linked

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.