Evidence map›Paper›PMID 31760080›Full record

ArticleAnaerobe2020

The early stage peptidoglycan biosynthesis Mur enzymes are antibacterial and antisporulation drug targets for recurrent Clostridioides difficile infection.

Madhab Sapkota, Ravi K R Marreddy, Xiaoqian Wu, Manish Kumar, Julian G Hurdle

Open access · greenAbstract read
In one paragraph

Article in Anaerobe, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 10 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

5 authors at 2 institutions in 1 country.

Madhab SapkotaUniversity of Texas at Arlington, Department of Biology, Arlington, TX, 76019, United States.
Ravi K R MarreddyTexas A & M University Health Science Center, Biosciences and Technology, Houston, TX, 77030, United States.
Xiaoqian WuTexas A & M University Health Science Center, Biosciences and Technology, Houston, TX, 77030, United States.
Manish KumarUniversity of Texas at Arlington, Department of Biology, Arlington, TX, 76019, United States.
Julian G HurdleTexas A & M University Health Science Center, Biosciences and Technology, Houston, TX, 77030, United States. Electronic address: jhurdle@tamu.edu.
Texas A&M Health Science Center · USThe University of Texas at Arlington · US

Funding

Investigation of the FAS-II enzyme, FabK, as a druggable target for C. difficileR21AI126755 · NIAID · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI HEVENER, KIRK EDWARD, HURDLE, JULIAN G · 2016 to 2017
$424k
NIAID NIH HHS R21 AI126755
6 · The paper itself

Abstract

Sporulation during Clostridioides difficile infection (CDI) contributes to recurrent disease. Cell division and sporulation both require peptidoglycan biosynthesis. We show C. difficile growth and sporulation is attenuated by antisenses to murA and murC or the MurA inhibitor fosfomycin. Thus, targeting the early steps of peptidoglycan biosynthesis might reduce the onset of recurrent CDI.

Indexed as

Alkyl and Aryl TransferasesAnti-Bacterial AgentsClostridioides difficileClostridium InfectionsEnzyme ActivationEnzyme InhibitorsGene Expression Regulation, BacterialHumansPeptidoglycanSpores, BacterialAlkyl and Aryl TransferasesAnti-Bacterial AgentsEnzyme InhibitorsPeptidoglycanUDP-N-acetylglucosamine 1-carboxyvinyltransferaseAntibiotic drug-targetsHeat-resistant spore cortexMur ligasesPeptidoglycan

Identifiers

PMID31760080
PMCPMC8811877
OpenAlexW2989705908

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.