Evidence map›Paper›PMID 25256667›Full record

ArticleJournal of biomolecular screening2015

Streptomyces: a screening tool for bacterial cell division inhibitors.

Charul Jani, Elitza I Tocheva, Scott McAuley, Arryn Craney, Grant J Jensen, Justin Nodwell

Open access · hybridAbstract read
In one paragraph

Article in Journal of biomolecular screening, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

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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 3 institutions in 2 countries.

Charul JaniDepartment of Biochemistry and Biomedical Sciences, Michael DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada.
Elitza I TochevaDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.
Scott McAuleyDepartment of Biochemistry, University of Toronto, Toronto, ON, Canada.
Arryn CraneyDepartment of Biochemistry and Biomedical Sciences, Michael DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada.
Grant J JensenDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA Howard Hughes Medical Institute, Chevy Chase, MD, USA.
Justin NodwellDepartment of Biochemistry and Biomedical Sciences, Michael DeGroote Institute for Infectious Diseases Research, McMaster University, Hamilton, ON, Canada Department of Biochemistry, University of Toronto, Toronto, ON, Canada justin.nodwell@utoronto.ca.
McMaster University · CACalifornia Institute of Technology · USUniversity of Toronto · CA

Funding

Structure and function of the prokaryotic cytoskeleton by electron cryotomographyR01GM094800 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI JENSEN, GRANT J · 2011 to 2015
$1.7M
CIHR MOP-133636Howard Hughes Medical InstituteNIGMS NIH HHS GM094800BNIGMS NIH HHS R01 GM094800
6 · The paper itself

Abstract

Cell division is essential for spore formation but not for viability in the filamentous streptomycetes bacteria. Failure to complete cell division instead blocks spore formation, a phenotype that can be visualized by the absence of gray (in Streptomyces coelicolor) and green (in Streptomyces venezuelae) spore-associated pigmentation. Despite the lack of essentiality, the streptomycetes divisome is similar to that of other prokaryotes. Therefore, the chemical inhibitors of sporulation in model streptomycetes may interfere with the cell division in rod-shaped bacteria as well. To test this, we investigated 196 compounds that inhibit sporulation in S. coelicolor. We show that 19 of these compounds cause filamentous growth in Bacillus subtilis, consistent with impaired cell division. One of the compounds is a DNA-damaging agent and inhibits cell division by activating the SOS response. The remaining 18 act independently of known stress responses and may therefore act on the divisome or on divisome positioning and stability. Three of the compounds (Fil-1, Fil-2, and Fil-3) confer distinct cell division defects on B. subtilis. They also block B. subtilis sporulation, which is mechanistically unrelated to the sporulation pathway of streptomycetes but is also dependent on the divisome. We discuss ways in which these differing phenotypes can be used in screens for cell division inhibitors.

Indexed as

Anti-Bacterial AgentsCell DivisionDrug Evaluation, PreclinicalMicrobial Sensitivity TestsSmall Molecule LibrariesSOS Response, GeneticsStreptomycesAnti-Bacterial AgentsSmall Molecule Librariesbacterial cell divisioncell-based assaysin vivo screeningsporulationStreptomyces

Identifiers

PMID25256667
PMCPMC4888893
OpenAlexW1968962968

What OpenQuestion holds

Textmetadata
LicenceTDM
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.