Evidence map›Paper›PMID 24699671›Full record

ArticlePloS one2014

Experimental infections with Mycoplasma agalactiae identify key factors involved in host-colonization.

Eric Baranowski, Dominique Bergonier, Eveline Sagné, Marie-Claude Hygonenq, Patricia Ronsin, Xavier Berthelot, Christine Citti

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Genomic Characterization of aVeterinary sciences · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Metal utilization in genome-reduced bacteria: Do human mycoplasmas rely on iron?Computational and structural biotechnology journal · 2021
    Review
  8. Contagious Agalactia In Sheep And Goats: Current Perspectives.Veterinary medicine (Auckland, N.Z.) · 2019
    Review
  9. Extracellular DNA: A Nutritional Trigger ofFrontiers in microbiology · 2019
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Eric BaranowskiINRA, UMR 1225, IHAP, Toulouse, France; Université de Toulouse, INP-ENVT, UMR 1225, IHAP, Toulouse, France.
Dominique BergonierUniversité de Toulouse, INP-ENVT, UMR 1225, IHAP, Toulouse, France; INRA, UMR 1225, IHAP, Toulouse, France.
Eveline SagnéUniversité de Toulouse, INP-ENVT, UMR 1225, IHAP, Toulouse, France; INRA, UMR 1225, IHAP, Toulouse, France.
Marie-Claude HygonenqINRA, UMR 1225, IHAP, Toulouse, France; Université de Toulouse, INP-ENVT, UMR 1225, IHAP, Toulouse, France.
Patricia RonsinUniversité de Toulouse, INP-ENVT, UMR 1225, IHAP, Toulouse, France.
Xavier BerthelotUniversité de Toulouse, INP-ENVT, UMR 1225, IHAP, Toulouse, France; INRA, UMR 1225, IHAP, Toulouse, France.
Christine CittiINRA, UMR 1225, IHAP, Toulouse, France; Université de Toulouse, INP-ENVT, UMR 1225, IHAP, Toulouse, France.
École Nationale Vétérinaire de Toulouse · FRInteraction Hôtes Agents Pathogènes · FRUniversité de Toulouse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanisms underlying pathogenic processes in mycoplasma infections are poorly understood, mainly because of limited sequence similarities with classical, bacterial virulence factors. Recently, large-scale transposon mutagenesis in the ruminant pathogen Mycoplasma agalactiae identified the NIF locus, including nifS and nifU, as essential for mycoplasma growth in cell culture, while dispensable in axenic media. To evaluate the importance of this locus in vivo, the infectivity of two knock-out mutants was tested upon experimental infection in the natural host. In this model, the parental PG2 strain was able to establish a systemic infection in lactating ewes, colonizing various body sites such as lymph nodes and the mammary gland, even when inoculated at low doses. In these PG2-infected ewes, we observed over the course of infection (i) the development of a specific antibody response and (ii) dynamic changes in expression of M. agalactiae surface variable proteins (Vpma), with multiple Vpma profiles co-existing in the same animal. In contrast and despite a sensitive model, none of the knock-out mutants were able to survive and colonize the host. The extreme avirulent phenotype of the two mutants was further supported by the absence of an IgG response in inoculated animals. The exact role of the NIF locus remains to be elucidated but these data demonstrate that it plays a key role in the infectious process of M. agalactiae and most likely of other pathogenic mycoplasma species as many carry closely related homologs.

Indexed as

AnimalsBacterial ProteinsFemaleGenetic LociHost-Pathogen InteractionsMutationMycoplasma agalactiaeMycoplasma InfectionsSheepSheep DiseasesBacterial Proteins

Identifiers

PMID24699671
PMCPMC3974822
OpenAlexW1995184475

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.