Evidence map›Paper›PMID 40243034›Full record

ArticleMolecular microbiology2025

Protein Homeostasis Impairment Alters Phenotypic Heterogeneity of Biofilm Communities.

Judith Matavacas, Claes von Wachenfeldt

Abstract read
In one paragraph

Article in Molecular microbiology, 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

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

1 citing paper in PubMed.

  1. Recent insights into HSP70: proteostasis and beyond.Frontiers in molecular biosciences · 2026
    Review
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

2 authors.

Judith MatavacasThe Microbiology Group, Department of Biology, Lund University, Lund, Sweden.
Claes von WachenfeldtThe Microbiology Group, Department of Biology, Lund University, Lund, Sweden.ORCID 0000-0001-8950-3218

Funding

Jörgen Lindström's FoundationKungliga Fysiografiska Sällskapet i LundVetenskapsrådet 2023-05271
6 · The paper itself

Abstract

Biofilms are highly organized, cooperating communities of microorganisms encased in a self-produced extracellular matrix, providing resilience against external stress such as antimicrobial agents and host defenses. A hallmark of biofilms is their phenotypic heterogeneity, which enhances the overall growth and survival of the community. In this study, we demonstrate that removing the dnaK and tig genes encoding the core molecular chaperones DnaK (Hsp70 homolog) and Trigger factor disrupted protein homeostasis in Bacillus subtilis and resulted in the formation of an extremely mucoid biofilm with aberrant architecture, compromised structural integrity, and altered phenotypic heterogeneity. These changes include a large reduction in the motile subpopulation and an overrepresentation of matrix producers and endospores. Overproduction of poly-γ-glutamic acid contributed crucially to the mucoid phenotype and aberrant biofilm architecture. Homeostasis impairment, triggered by elevated temperatures, in wild-type cells led to mucoid and aberrant biofilm phenotypes similar to those observed in strains lacking both dnaK and tig. Our findings show that disruption of protein homeostasis, whether due to the absence of molecular chaperones or because of environmental factors, severely changes biofilm features.

Indexed as

Bacillus subtilisBacterial ProteinsBiofilmsProteostasisGene Expression Regulation, BacterialHomeostasisHSP70 Heat-Shock ProteinsMolecular ChaperonesPhenotypePolyglutamic AcidBacterial ProteinsHSP70 Heat-Shock ProteinsMolecular ChaperonesPolyglutamic AcidBacillus subtilisDnaKmolecular chaperonephenotypic heterogeneityproteostasistrigger factor

Identifiers

PMID40243034
PMCPMC12242103

What OpenQuestion holds

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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.