Evidence map›Paper›PMID 39146259›Full record

ReviewPLoS pathogens2024

Biomolecular condensates as stress sensors and modulators of bacterial signaling.

Moeka Sasazawa, Dylan T Tomares, W Seth Childers, Saumya Saurabh

Abstract readReview
In one paragraph

Review in PLoS pathogens, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Divergent condensates tune transcriptional responses during stress.bioRxiv : the preprint server for biology · 2026
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Mechanisms and Pathological Significance of Liquid-Liquid Phase Separation in Bacteria.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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.

Moeka SasazawaDepartment of Chemistry, New York University, New York, New York, United States of America.
Dylan T TomaresDepartment of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
W Seth ChildersDepartment of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Saumya SaurabhDepartment of Chemistry, New York University, New York, New York, United States of America.ORCID 0000-0002-7524-7548

Funding

Biomolecular condensates as organizers of mRNA decay in bacteriaR01GM136863 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI William Seth Childers · 2020 to 2026
$1.9M
Exploring the function of bacterial condensates in adaptation and evolutionR35GM157103 · NIGMS · NEW YORK UNIVERSITY · PI Saumya Saurabh · 2024 to 2026
$1.2M
NIGMS NIH HHS R01 GM136863NIGMS NIH HHS R35 GM157103
6 · The paper itself

Abstract

Microbes exhibit remarkable adaptability to environmental fluctuations. Signaling mechanisms, such as two-component systems and secondary messengers, have long been recognized as critical for sensing and responding to environmental cues. However, recent research has illuminated the potential of a physical adaptation mechanism in signaling-phase separation, which may represent a ubiquitous mechanism for compartmentalizing biochemistry within the cytoplasm in the context of bacteria that frequently lack membrane-bound organelles. This review considers the broader prospect that phase separation may play critical roles as rapid stress sensing and response mechanisms within pathogens. It is well established that weak multivalent interactions between disordered regions, coiled-coils, and other structured domains can form condensates via phase separation and be regulated by specific environmental parameters in some cases. The process of phase separation itself acts as a responsive sensor, influenced by changes in protein concentration, posttranslational modifications, temperature, salts, pH, and oxidative stresses. This environmentally triggered phase separation can, in turn, regulate the functions of recruited biomolecules, providing a rapid response to stressful conditions. As examples, we describe biochemical pathways organized by condensates that are essential for cell physiology and exhibit signaling features. These include proteins that organize and modify the chromosome (Dps, Hu, SSB), regulate the decay, and modification of RNA (RNase E, Hfq, Rho, RNA polymerase), those involved in signal transduction (PopZ, PodJ, and SpmX) and stress response (aggresomes and polyphosphate granules). We also summarize the potential of proteins within pathogens to function as condensates and the potential and challenges in targeting biomolecular condensates for next-generation antimicrobial therapeutics. Together, this review illuminates the emerging significance of biomolecular condensates in microbial signaling, stress responses, and regulation of cell physiology and provides a framework for microbiologists to consider the function of biomolecular condensates in microbial adaptation and response to diverse environmental conditions.

Indexed as

BacteriaBiomolecular CondensatesSignal TransductionStress, PhysiologicalBacterial Physiological PhenomenaBacterial ProteinsBacterial Proteins

Identifiers

PMID39146259
PMCPMC11326607

What OpenQuestion holds

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Registered trials

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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.