Evidence map›Paper›PMID 24748614›Full record

ArticleJournal of bacteriology2014

Hypermotility in Clostridium perfringens strain SM101 is due to spontaneous mutations in genes linked to cell division.

Hualan Liu, Kristin D McCord, Jonathon Howarth, David L Popham, Roderick V Jensen, Stephen B Melville

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Effects of Bile Acids and Nisin on the Production of Enterotoxin byInternational journal of microbiology · 2018
    Article
  3. 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

6 authors at 1 institution in 1 country.

Hualan LiuDepartment of Biological Sciences, Virginia Tech, Blacksburg, Virginia, USA.
Kristin D McCordDepartment of Biological Sciences, Virginia Tech, Blacksburg, Virginia, USA.
Jonathon HowarthDepartment of Biological Sciences, Virginia Tech, Blacksburg, Virginia, USA.
David L PophamDepartment of Biological Sciences, Virginia Tech, Blacksburg, Virginia, USA.
Roderick V JensenDepartment of Biological Sciences, Virginia Tech, Blacksburg, Virginia, USA.
Stephen B MelvilleDepartment of Biological Sciences, Virginia Tech, Blacksburg, Virginia, USA melville@vt.edu.
Virginia Tech · US

Funding

Characterization of a Type II secretion system in a Gram-positive pathogenR21AI109391 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI MELVILLE, STEPHEN · 2014 to 2015
$413k
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 R21 AI088298NIAID NIH HHS R21 AI109391
6 · The paper itself

Abstract

Clostridium perfringens is a Gram-positive anaerobic pathogen of humans and animals. Although they lack flagella, C. perfringens bacteria can still migrate across surfaces using a type of gliding motility that involves the formation of filaments of bacteria lined up in an end-to-end conformation. In strain SM101, hypermotile variants are often found arising from the edges of colonies on agar plates. Hypermotile cells are longer than wild-type cells, and video microscopy of their gliding motility suggests that they form long, thin filaments that move rapidly away from a colony, analogously to swarmer cells in bacteria with flagella. To identify the cause(s) of the hypermotility phenotype, the genome sequences of normal strains and their direct hypermotile derivatives were determined and compared. Strains SM124 and SM127, hypermotile derivatives of strains SM101 and SM102, respectively, contained 10 and 6 single nucleotide polymorphisms (SNPs) relative to their parent strains. While SNPs were located in different genes in the two sets of strains, one feature in common was mutations in cell division genes, an ftsI homolog in strain SM124 (CPR_1831) and a minE homolog in strain SM127 (CPR_2104). Complementation of these mutations with wild-type copies of each gene restored the normal motility phenotype. A model explaining the principles underlying the hypermotility phenotype is presented.

Indexed as

Anti-Bacterial AgentsBacterial ProteinsCell DivisionCephalexinClostridium perfringensGene Expression Regulation, BacterialGenetic Complementation TestMovementMutationAnti-Bacterial AgentsBacterial ProteinsCephalexin

Identifiers

PMID24748614
PMCPMC4054169
OpenAlexW2135585649

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.