Evidence map›Paper›PMID 37294840›Full record

ArticlePLoS pathogens2023

Replicative Acinetobacter baumannii strains interfere with phagosomal maturation by modulating the vacuolar pH.

Jesus S Distel, Gisela Di Venanzio, Joseph J Mackel, David A Rosen, Mario F Feldman

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. IntracellularProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. InvasiveMicrobiology (Reading, England) · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. An interstrand DNA crosslink glycosylase aidsProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Antibiotics (Basel, Switzerland) · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jesus S DistelDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri, United States of America.
Gisela Di VenanzioDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri, United States of America.
Joseph J MackelDepartment of Pediatrics, Division of Infectious Diseases, Washington University School of Medicine, Saint Louis, Missouri, United States of America.
David A RosenDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri, United States of America.
Mario F FeldmanDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri, United States of America.ORCID 0000-0003-4497-0976
Washington University in St. Louis · US

Funding

Molecular Insights into the Uropathogenesis of MDR Acinetobacter baumanniiR01AI144120 · NIAID · WASHINGTON UNIVERSITY · PI Mario Feldman · 2019 to 2026
$4.1M
NIAID NIH HHS R01 AI144120
6 · The paper itself

Abstract

Bacterial pneumonia is a common infection of the lower respiratory tract that can afflict patients of all ages. Multidrug-resistant strains of Acinetobacter baumannii are increasingly responsible for causing nosocomial pneumonias, thus posing an urgent threat. Alveolar macrophages play a critical role in overcoming respiratory infections caused by this pathogen. Recently, we and others have shown that new clinical isolates of A. baumannii, but not the common lab strain ATCC 19606 (19606), can persist and replicate in macrophages within spacious vacuoles that we called Acinetobacter Containing Vacuoles (ACV). In this work, we demonstrate that the modern A. baumannii clinical isolate 398, but not the lab strain 19606, can infect alveolar macrophages and produce ACVs in vivo in a murine pneumonia model. Both strains initially interact with the macrophage endocytic pathway, as indicated by EEA1 and LAMP1 markers; however, the fate of these strains diverges at a later stage. While 19606 is eliminated in an autophagy pathway, 398 replicates in ACVs and are not degraded. We show that 398 reverts the natural acidification of the phagosome by secreting large amounts of ammonia, a by-product of amino acid catabolism. We propose that this ability to survive within macrophages may be critical for the persistence of clinical A. baumannii isolates in the lung during a respiratory infection.

Indexed as

Acinetobacter baumanniiPneumonia, BacterialRespiratory Tract InfectionsAnimalsAnti-Bacterial AgentsDrug Resistance, Multiple, BacterialHumansHydrogen-Ion ConcentrationLungMiceMicrobial Sensitivity TestsVacuolesAnti-Bacterial Agents

Identifiers

PMID37294840
PMCPMC10286980
OpenAlexW4380085076

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.