Evidence map›Paper›PMID 41709304›Full record

ArticleMicrobiome2026

Microbiota-derived propionate suppresses Salmonella virulence gene expression via LuxS quorum sensing.

Qianyun Zhang, Qidong Zhu, Yunqi Xiao, Shiyong Liao, Shangzhou Liu, Shourong Shi

Abstract read
In one paragraph

Article in Microbiome, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

6 authors.

Qianyun ZhangJiangsu lnstitute of Poultry Science, Yangzhou, 225125, China.
Qidong ZhuJiangsu lnstitute of Poultry Science, Yangzhou, 225125, China.
Yunqi XiaoJiangsu lnstitute of Poultry Science, Yangzhou, 225125, China.
Shiyong LiaoJiangsu lnstitute of Poultry Science, Yangzhou, 225125, China.
Shangzhou LiuJiangsu lnstitute of Poultry Science, Yangzhou, 225125, China.
Shourong ShiJiangsu lnstitute of Poultry Science, Yangzhou, 225125, China. ssr236@163.com.

Funding

Agriculture Research System of China CARS-41-G01National Natural Science Foundation of China 32573258Yangzhou Science and Technology Program YZ2024242
6 · The paper itself

Abstract

backgroundDespite mounting evidence that commensal microbes enhance host defenses, whether and how they directly suppress pathogen virulence remains elusive. Here, we investigate metabolites from the gut microbiota of infection‑resistant Tibetan chickens for their ability to reduce Salmonella virulence gene expression and elucidate the molecular mechanism by which these compounds inhibit the LuxS/AI‑2 quorum‑sensing system.

resultsInitially, we compared the expression of the quorum‑sensing gene luxS and biofilm-associated virulence genes in Tibetan chickens and broiler chickens post-Salmonella infection. Notably, Tibetan chickens exhibited significantly lower virulence gene expression than broiler chickens. Subsequently, fecal microbiota transplantation (FMT) from Tibetan chickens to broiler chickens reduced virulence gene expression in infected recipients. Further, 16S rRNA gene sequencing of cecal contents revealed that FMT enhanced microbial diversity and altered composition in infected broiler chickens, specifically enriching short-chain fatty acids (SCFA)-producing beneficial bacteria (e.g., Bacteroides, Rikenellaceae_RC9_gut_group, Phascolarctobacterium, Desulfovibrio). Critically, using Transwell chambers to separate microbes and metabolites, we identified metabolites as mediators of this effect. Subsequent liquid chromatography-mass spectrometry (LC-MS) quantification demonstrated significantly elevated propionate concentrations in both uninfected and infected Tibetan chickens, and FMT-recipient broiler chickens. Propionate levels correlated negatively with key virulence factor expression. Moreover, in vitro experiments showed that propionate inhibited Salmonella biofilm formation, reduced autoinducer-2 (AI-2) activity, and downregulated the expression of virulence genes. In vivo, we further confirmed that propionate decreased the expression of Salmonella virulence genes. Taken together, these results support that propionate suppresses Salmonella virulence gene expression by targeting the LuxS/AI-2 quorum-sensing pathway. To validate this mechanism, we generated a luxS knockout strain by homologous recombination; strikingly, propionate failed to attenuate virulence gene expression in this mutant, thereby establishing the essential role of LuxS/AI-2. Finally, molecular docking identified propionate-LuxS binding sites (Ile53), and site-directed mutagenesis validated critical functional residues, highlighting structural determinants for virulence gene expression regulation.

conclusionThese findings underscore the role of the gut-derived metabolite propionate in directly modulating pathogen virulence gene expression by targeting the LuxS/AI-2 quorum‑sensing system, offering novel insights into microbiota-based strategies for infectious disease management.

Indexed as

Bacterial ProteinsCarbon-Sulfur LyasesGastrointestinal MicrobiomePropionatesQuorum SensingSalmonellaSalmonella Infections, AnimalAnimalsBiofilmsCecumChickensFatty Acids, VolatileFecesGene Expression Regulation, BacterialHomoserineLactonesBacterial ProteinsCarbon-Sulfur LyasesFatty Acids, VolatileHomoserineLactonesLuxS protein, BacteriaN-octanoylhomoserine lactonePropionatesRNA, Ribosomal, 16SVirulence FactorsLuxSPropionateQuorum sensingSalmonellaVirulence gene expression

Identifiers

PMID41709304
PMCPMC12918161

What Socratic 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 Socratic graph.