Evidence map›Paper›PMID 20123713›Full record

ArticleInfection and immunity2010

Critical role of dispensable genes in Mycoplasma agalactiae interaction with mammalian cells.

Eric Baranowski, Sébastien Guiral, Eveline Sagné, Agnès Skapski, Christine Citti

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

31 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Regulation of potassium homeostasis inFrontiers in microbiology · 2026
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  4. Bacterial conjugation in the ruminant pathogenApplied and environmental microbiology · 2025
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  5. Article
  6. Article
  7. Genes required for survival and proliferation ofApplied and environmental microbiology · 2024
    Article
  8. Article
  9. Review
  10. Impacts ofMicrobial genomics · 2022
    Article
  11. Article
  12. Metal utilization in genome-reduced bacteria: Do human mycoplasmas rely on iron?Computational and structural biotechnology journal · 2021
    Review
  13. Novel Secreted Protein ofFrontiers in immunology · 2021
    Article
  14. Article
  15. Article
  16. Extracellular DNA: A Nutritional Trigger ofFrontiers in microbiology · 2019
    Article
  17. Large-Scale Analysis of theFrontiers in microbiology · 2019
    Article
  18. Article
  19. Article
  20. Article
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

5 authors at 1 institution in 1 country.

Eric BaranowskiINRA, UMR 1225, F-31076 Toulouse, France.
Sébastien Guiral
Eveline Sagné
Agnès Skapski
Christine Citti
Université de Toulouse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycoplasmas are minimal bacteria whose genomes barely exceed the smallest amount of information required to sustain autonomous life. Despite this apparent simplicity, several mycoplasmas are successful pathogens of humans and animals, in which they establish intimate interactions with epithelial cells at mucosal surfaces. To identify biological functions mediating mycoplasma interactions with mammalian cells, we produced a library of transposon knockout mutants in the ruminant pathogen Mycoplasma agalactiae and used this library to identify mutants displaying a growth-deficient pheonotype in cell culture. M. agalactiae mutants displaying a 3-fold reduction in CFU titers to nearly complete extinction in coculture with HeLa cells were identified. Mapping of transposon insertion sites revealed 18 genomic regions putatively involved in the interaction of M. agalactiae with HeLa cells. Several of these regions encode proteins with features of membrane lipoproteins and/or were involved in horizontal gene transfer with phylogenetically distant pathogenic mycoplasmas of ruminants. Two mutants with the most extreme phenotype carry a transposon in a genomic region designated the NIF locus which encodes homologues of SufS and SufU, two proteins presumably involved in [Fe-S] cluster biosynthesis in Gram-positive bacteria. Complementation studies confirmed the conditional essentiality of the NIF locus, which was found to be critical for proliferation in the presence of HeLa cells and several other mammalian cell lines but dispensable for axenic growth. While our results raised questions regarding essential functions in mycoplasmas, they also provide a means for studying the role of mycoplasmas as minimal pathogens.

Indexed as

Bacterial AdhesionBacterial ProteinsCoculture TechniquesColony Count, MicrobialDNA Transposable ElementsEpithelial CellsGene Knockout TechniquesGenes, EssentialGenetic Complementation TestHeLa CellsHumansMutagenesis, InsertionalMycoplasma agalactiaeVirulence FactorsBacterial ProteinsDNA Transposable ElementsVirulence Factors

Identifiers

PMID20123713
PMCPMC2849427
OpenAlexW2168687274

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.