Evidence map›Paper›PMID 29884996›Full record

ArticleMolecular microbiology2018

The lytic transglycosylase MltB connects membrane homeostasis and in vivo fitness of Acinetobacter baumannii.

Sébastien Crépin, Elizabeth N Ottosen, Katharina Peters, Sara N Smith, Stephanie D Himpsl, Waldemar Vollmer, Harry L T Mobley

Open access · hybridAbstract read
In one paragraph

Article in Molecular microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

35 citing papers in PubMed, 46 citations in OpenAlex.

  1. Adaptive Response ofAntibiotics (Basel, Switzerland) · 2026
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  8. The interplay betweenInfection and immunity · 2025
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  9. Multidrug resistantCurrent research in microbial sciences · 2025
    Review
  10. Pathogenomic Insights intoLife (Basel, Switzerland) · 2024
    Article
  11. Article
  12. Virulence Factors and Pathogenicity Mechanisms ofAntibiotics (Basel, Switzerland) · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Deciphering the virulence factors, regulation, and immune response toFrontiers in cellular and infection microbiology · 2023
    Review
  19. Article
  20. Strain Specific Variations inFrontiers in immunology · 2022
    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

7 authors at 2 institutions in 2 countries.

Sébastien CrépinDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
Elizabeth N OttosenDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
Katharina PetersCentre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne, UK.
Sara N SmithDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
Stephanie D HimpslDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
Waldemar VollmerCentre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Newcastle University, Newcastle upon Tyne, UK.
Harry L T MobleyDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USNewcastle University · GB

Funding

Genome-wide identification of virulence genes in Acinetobacter baumannii in vivoR21AI107184 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOBLEY, HARRY L. · 2014 to 2015
$428k
NIAID NIH HHS R21 AI107184Wellcome TrustWellcome Trust 101824/Z/13/Z
6 · The paper itself

Abstract

Acinetobacter baumannii has emerged as a leading nosocomial pathogen, infecting a wide range of anatomic sites including the respiratory tract and the bloodstream. In addition to being multi-drug resistant, little is known about the molecular basis of A. baumannii pathogenesis. To better understand A. baumannii virulence, a combination of a transposon-sequencing (TraDIS) screen and the neutropenic mouse model of bacteremia was used to identify the full set of fitness genes required during bloodstream infection. The lytic transglycosylase MltB was identified as a critical fitness factor. MltB cleaves the MurNAc-GlcNAc bond of peptidoglycan, which leads to cell wall remodeling. Here we show that MltB is part of a complex network connecting resistance to stresses, membrane homeostasis, biogenesis of pili and in vivo fitness. Indeed, inactivation of mltB not only impaired resistance to serum complement, cationic antimicrobial peptides and oxygen species, but also altered the cell envelope integrity, activated the envelope stress response, drastically reduced the number of pili at the cell surface and finally, significantly decreased colonization of both the bloodstream and the respiratory tract.

Indexed as

Acinetobacter baumanniiAcinetobacter InfectionsAnimalsAntimicrobial Cationic PeptidesCell MembraneComplement System ProteinsFemaleGlycosyltransferasesHigh-Throughput Nucleotide SequencingMiceMice, Inbred CBAMuramic AcidsPeptidoglycanStress, PhysiologicalAntimicrobial Cationic PeptidesComplement System ProteinsGlycosyltransferasesMuramic Acidsmurein transglycosylaseN-acetylmuramic acidPeptidoglycan

Identifiers

PMID29884996
PMCPMC6185781
OpenAlexW2805091853

What OpenQuestion holds

Textmetadata
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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.