Evidence map›Paper›PMID 37140436›Full record

ArticlemBio2023

Hypermucoviscosity Regulator RmpD Interacts with Wzc and Controls Capsular Polysaccharide Chain Length.

Olga G Ovchinnikova, Logan P Treat, Tanisha Teelucksingh, Bradley R Clarke, Taryn A Miner, Chris Whitfield, Kimberly A Walker, Virginia L Miller

Open access · goldAbstract read
In one paragraph

Article in mBio, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 64 citations in OpenAlex.

  1. Review
  2. Article
  3. Hypermucoviscosity inJournal of bacteriology · 2026
    Review
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  5. Article
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  8. Infection and immunity · 2026
    Article
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  13. Connections betweenInfection and immunity · 2026
    Article
  14. Article
  15. The acquisition ofmBio · 2026
    Article
  16. Review
  17. Antibiotics accumulate inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  18. Article
  19. Sugar Import SuppressesbioRxiv : the preprint server for biology · 2025
    Article
  20. 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

8 authors at 2 institutions in 2 countries.

Olga G Ovchinnikova *Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.
Logan P Treat *Department of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.ORCID 0009-0008-2877-7432
Tanisha TeelucksinghDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.
Bradley R ClarkeDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.ORCID 0000-0003-2233-1268
Taryn A MinerDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
Chris WhitfieldDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.ORCID 0000-0002-5267-7027
Kimberly A WalkerDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
Virginia L MillerDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.ORCID 0000-0002-9522-1767
University of Guelph · CAUniversity of North Carolina at Chapel Hill · US

Funding

Understanding hypermucoviscosity in KlebsiellaR01AI148197 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MILLER, VIRGINIA L, WHITFIELD, CHRIS · 2020 to 2023
$1.8M
NIAID NIH HHS R01 AI148197
6 · The paper itself

Abstract

Klebsiella pneumoniae is a leading cause of nosocomial infections, including pneumonia, bacteremia, and urinary tract infections. Treatment options are increasingly restricted by the high prevalence of resistance to frontline antibiotics, including carbapenems, and the recently identified plasmid-conferred colistin resistance. The classical pathotype (cKp) is responsible for most of the nosocomial infections observed globally, and these isolates are often multidrug resistant. The hypervirulent pathotype (hvKp) is a primary pathogen capable of causing community-acquired infections in immunocompetent hosts. The hypermucoviscosity (HMV) phenotype is strongly associated with the increased virulence of hvKp isolates. Recent studies demonstrated that HMV requires capsule (CPS) synthesis and the small protein RmpD but is not dependent on the increased amount of capsule associated with hvKp. Here, we identified the structure of the capsular and extracellular polysaccharide isolated from hvKp strain KPPR1S (serotype K2) with and without RmpD. We found that the polymer repeat unit structure is the same in both strains and that it is identical to the K2 capsule. However, the chain length of CPS produced by strains expressing

Indexed as

Cross InfectionKlebsiella InfectionsAnti-Bacterial AgentsEscherichia coliHumansKlebsiella pneumoniaePolysaccharidesVirulenceVirulence FactorsAnti-Bacterial AgentsPolysaccharidesVirulence Factorscapsulecapsule chain lengthhypermucoviscosityhypervirulentKlebsiellaRmpDWzc

Identifiers

PMID37140436
PMCPMC10294653
OpenAlexW4368357025

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.