ArticleBMC microbiology2025
Xanthomonas citri subsp. citri requires a polyketide cyclase to activate the type III secretion system for virulence.
Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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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.
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Who cites it
3 citing papers in PubMed.
- Shikimic acid pathway drives the phase-dependent antibacterial activity of Bacillus amyloliquefaciens against Xanthomonas citri subsp. citri.BMC microbiology · 2026Article
- Review
- Getting a grip on StAR-related lipid-transfer (START) domain proteins in bacteria.FEMS microbiology reviews · 2026Review
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
backgroundXanthomonas citri subsp. citri is the causal agent of citrus canker, which causes substantial losses in citrus production. Here, we report the role of a polyketide cyclase (PKC) on the virulence in X. citri subsp. citri.
methodsThe structure of PKC was precisely predicted using Alphafold3. Promoter GUS fusion constructs and real-time quantitative reverse transcription (qRT-PCR) were employed to study the pattern of expression of the polyketide gene. A deletion mutation was created to explore the role of PKC in virulence and metabolic change.
resultsThe PKC was determined to have a signal peptide, a START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC (SRPBCC) domain, and a GyrI-like small molecule binding domain. The expression of the PKC gene was induced in planta, as well as under stress by CuSO
conclusionsThe overall data indicate that the PKC affects bacterial virulence by modulating the type III secretion system, possibly through the biosynthesis of particular metabolites.
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Registered trials
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