Evidence map›Paper›PMID 24664503›Full record

ArticleInfection and immunity2014

Clostridium difficile extracytoplasmic function σ factor σV regulates lysozyme resistance and is necessary for pathogenesis in the hamster model of infection.

Theresa D Ho, Kyle B Williams, Yan Chen, Richard F Helm, David L Popham, Craig D Ellermeier

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Identification of a family of peptidoglycan transpeptidases reveals thatProceedings of the National Academy of Sciences of the United States of America · 2024
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  3. Identification ofJournal of bacteriology · 2024
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  4. Review
  5. Identification of DraRS inJournal of bacteriology · 2023
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  6. Review
  7. Article
  8. Article
  9. Activation of the extracytoplasmic function σ factor σCurrent opinion in microbiology · 2022
    Review
  10. Article
  11. Article
  12. 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

6 authors at 2 institutions in 1 country.

Theresa D HoDepartment of Microbiology, University of Iowa, Iowa City, Iowa, USA.
Kyle B Williams
Yan Chen
Richard F Helm
David L Popham
Craig D Ellermeier
University of Iowa · USVirginia Tech · US

Funding

TRAINING IN MECHANISMS OF PARASITISMT32AI007511 · NIAID · UNIVERSITY OF IOWA · PI BUTLER, NOAH SULLIVAN, WEBER, MARY · 1996 to 2025
$8.1M
Identification of daptomycin resistance mechanisms in Clostridioides difficileR01AI087834 · NIAID · UNIVERSITY OF IOWA · PI ELLERMEIER, CRAIG D · 2011 to 2025
$5.6M
Proteomic Analyses of Clostridium difficile Spore Germination ApparatusR21AI088298 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI HELM, RICHARD, JENSEN, RODERICK V · 2010 to 2011
$410k
NIAID NIH HHS R01 AI087834NIAID NIH HHS R01AI087834NIAID NIH HHS R21 AI088298NIAID NIH HHS R21AI088298NIAID NIH HHS T32 AI007511NIAID NIH HHS T32AI007511
6 · The paper itself

Abstract

Clostridium difficile is a clinically important pathogen and the most common cause of hospital-acquired infectious diarrhea. Expression of the C. difficile gene csfV, which encodes σ(V), an extracytoplasmic function σ factor, is induced by lysozyme, which damages the peptidoglycan of bacteria. Here we show that σ(V) is required for lysozyme resistance in C. difficile. Using microarray analysis, we identified the C. difficile genes whose expression is dependent upon σ(V) and is induced by lysozyme. Although the peptidoglycan of wild-type C. difficile is intrinsically highly deacetylated, we have found that exposure to lysozyme leads to additional peptidoglycan deacetylation. This lysozyme-induced deacetylation is dependent upon σ(V). Expression of pdaV, which encodes a putative peptidoglycan deacetylase, was able to increase lysozyme resistance of a csfV mutant. The csfV mutant strain is severely attenuated compared to wild-type C. difficile in a hamster model of C. difficile-associated disease. We conclude that the σ(V) signal transduction system, which senses the host innate immune defense enzyme lysozyme, is required for lysozyme resistance and is necessary during C. difficile infection.

Indexed as

AnimalsAnti-Bacterial AgentsClostridioides difficileCricetinaeDisease Models, AnimalDNA, BacterialEnterocolitis, PseudomembranousMicroarray AnalysisMicrobial Sensitivity TestsMuramidaseSigma FactorVirulenceAnti-Bacterial AgentsDNA, BacterialMuramidaseSigma Factor

Identifiers

PMID24664503
PMCPMC4019185
OpenAlexW2164424979

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.