Evidence map›Paper›PMID 39843522›Full record

ArticleNature communications2025

Klebsiella pneumoniae employs a type VI secretion system to overcome microbiota-mediated colonization resistance.

Andrew S Bray, Christopher A Broberg, Andrew W Hudson, Weisheng Wu, Ravinder K Nagpal, Maidul Islam, Juan D Valencia-Bacca, Fawaz Shahid, Giovanna E Hernandez, Noah A Nutter and 7 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

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  14. Connections betweenInfection and immunity · 2026
    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

17 authors.

Andrew S BrayDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
Christopher A BrobergDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Andrew W HudsonDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
Weisheng WuBRCF Bioinformatics Core, University of Michigan, Ann Arbor, MI, USA.
Ravinder K NagpalDepartment of Nutrition & Integrative Physiology, Florida State University College of Health and Human Sciences, Tallahassee, FL, USA.ORCID http://orcid.org/0000-0002-4250-1749
Maidul IslamDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
Juan D Valencia-BaccaDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.ORCID http://orcid.org/0009-0005-7368-4719
Fawaz ShahidWake Forest University, Winston Salem, Winston Salem, NC, USA.
Giovanna E HernandezDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.ORCID http://orcid.org/0000-0001-5498-3469
Noah A NutterDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
Kimberly A WalkerDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Emma F BennettDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
Taylor M YoungDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
Andrew J BarnesDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
David A OrnellesDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA.
Virginia L MillerDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
M Ammar ZafarDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston Salem, NC, USA. mzafar@wakehealth.edu.ORCID http://orcid.org/0000-0002-3737-0422

Funding

INFECTIOUS DISEASE PATHOGENESIS TRAININGT32AI007151 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JULIANO, JONATHAN J · 1985 to 2024
$5.5M
TRAINING PROGRAM IN IMMUNOLOGY AND PATHOGENESIST32AI007401 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Martha Ann Alexander-Miller · 1991 to 2026
$4.4M
Mechanisms of Klebsiella pneumoniae gastrointestinal colonizationR01AI173244 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ZAFAR, MUHAMMAD AMMAR · 2023 to 2025
$1.8M
Redox Biology and Medicine Training ProgramT32GM127261 · NIGMS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI FURDUI, CRISTINA MARIA, POOLE, LESLIE B · 2018 to 2022
$975k
Regulators of Klebsiella VirulenceR21AI132925 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MILLER, VIRGINIA L · 2018 to 2019
$428k
Role of B cells in controlling Klebsiella pneumoniae associated disease statesR21AI178595 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HAAS, KAREN M, ZAFAR, MUHAMMAD AMMAR · 2023 to 2024
$426k
Biology of hypervirulent Klebsiella pneumoniae translocation from the gastrointestinal tractR21AI166642 · NIAID · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ZAFAR, MUHAMMAD AMMAR · 2022 to 2023
$426k
NIAID NIH HHS R01 AI173244NIAID NIH HHS R21 AI132925NIAID NIH HHS R21 AI166642NIAID NIH HHS R21 AI178595NIAID NIH HHS T32 AI007151NIAID NIH HHS T32 AI007401NIGMS NIH HHS T32 GM127261U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI166642U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI173244U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI178595
6 · The paper itself

Abstract

Microbial species must compete for space and nutrients to persist in the gastrointestinal (GI) tract, and our understanding of the complex pathobiont-microbiota interactions is far from complete. Klebsiella pneumoniae, a problematic, often drug-resistant nosocomial pathogen, can colonize the GI tract asymptomatically, serving as an infection reservoir. To provide insight on how K. pneumoniae interacts with the resident gut microbiome, we conduct a transposon mutagenesis screen using a murine model of GI colonization with an intact microbiota. Among the genes identified were those encoding a type VI secretion system (T6SS), which mediates contact-dependent killing of gram-negative bacteria. From several approaches, we demonstrate that the T6SS is critical for K. pneumoniae gut colonization. Metagenomics and in vitro killing assays reveal that K. pneumoniae reduces Betaproteobacteria species in a T6SS-dependent manner, thus identifying specific species targeted by K. pneumoniae. We further show that T6SS gene expression is controlled by several transcriptional regulators and that expression only occurs in vitro under conditions that mimic the gut environment. By enabling K. pneumoniae to thrive in the gut, the T6SS indirectly contributes to the pathogenic potential of this organism. These observations advance our molecular understanding of how K. pneumoniae successfully colonizes the GI tract.

Indexed as

Gastrointestinal MicrobiomeKlebsiella InfectionsKlebsiella pneumoniaeType VI Secretion SystemsAnimalsBacterial ProteinsDNA Transposable ElementsFemaleGastrointestinal TractGene Expression Regulation, BacterialMiceBacterial ProteinsDNA Transposable ElementsType VI Secretion Systems

Identifiers

PMID39843522
PMCPMC11754592

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.