Evidence map›Paper›PMID 40705813›Full record

ArticlePloS one2025

Human whole blood influences the expression of Acinetobacter baumannii genes related to translation and siderophore production.

Hannaneh Ghavanloughajar, Moamen M Elmassry, Amanda M V Brown, Abdul N Hamood

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

1 citing paper in PubMed.

  1. microPublication biology · 2025
    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

4 authors.

Hannaneh GhavanloughajarDepartment of Biological Sciences, Texas Tech University, Lubbock, Texas, United States of America.ORCID https://orcid.org/0009-0003-9376-1107
Moamen M ElmassryDepartment of Molecular Biology, Princeton University, Princeton, New Jersey, United States of America.
Amanda M V BrownDepartment of Biological Sciences, Texas Tech University, Lubbock, Texas, United States of America.
Abdul N HamoodDepartment of Immunology & Molecular Microbiology, Texas Tech University Health Sciences Center, Lubbock, Texas, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acinetobacter baumannii is a major cause of bloodstream infections, yet its adaptation and survival mechanisms in human blood remain poorly understood. While previous studies focused on individual blood components, the impact of human whole blood on A. baumannii gene expression has not been explored. To address this, we used an ex vivo model where A. baumannii was grown in human whole blood from healthy volunteers (WBHV) and compared its gene expression to that in Luria-Bertani (LB) broth using RNA-seq. Our lab has previously employed a similar WBHV vs. LB comparison in Pseudomonas aeruginosa, validating this approach. Our results showed that ribosome biogenesis was the most upregulated pathway in WBHV, with 51 out of 55 ribosomal protein genes exhibiting increased expression. We then examined virulence related genes and found upregulation in iron and zinc acquisition systems (acinetobactin, znuABC) and biofilm/quorum sensing regulators, including the csu operon. Given these findings, we hypothesized that WBHV exposure enhances virulence. Using the Galleria mellonella infection model, we confirmed that A. baumannii caused higher larval mortality when grown in WBHV than when grown in LB. Upregulation of the csu operon, involved in pili assembly, led us to investigate twitching motility, where we observed a significant increase in WBHV. Additionally, since A. baumannii exhibits high drug resistance through the regulation of various outer membrane proteins (OMPs), we analyzed OMP expression in response to WBHV. SDS-PAGE and LC-MS/MS analysis identified three OMPs-Omp33-36, CarO, and OmpA-that were downregulated in WBHV. As these proteins mediate carbapenem uptake, we tested imipenem resistance using a minimum bactericidal concentration (MBC) assay and found that WBHV exposure increased A. baumannii's MBC to imipenem, suggesting reduced susceptibility. Our findings provide valuable insights into the adaptive mechanisms of A. baumannii in human whole blood, highlighting potential targets for combating its persistence and antibiotic resistance in bloodstream infections.

Indexed as

Acinetobacter baumanniiGene Expression Regulation, BacterialProtein BiosynthesisSiderophoresAcinetobacter InfectionsAnimalsBacterial ProteinsBiofilmsHumansRibosomal ProteinsVirulenceBacterial ProteinsRibosomal ProteinsSiderophores

Identifiers

PMID40705813
PMCPMC12289009

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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.