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Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[2026,4,28]]},"abstract":"<jats:p>\n                    Microbial interactions, particularly bacteria\u2013fungus interactions, are research hotspots within microbial ecology and pathogenic biology. However, their underlying molecular mechanisms remain poorly understood, especially how bacterial pathogens recognize and exploit fungal signaling molecules for fungal predation. Here, we demonstrate that\n                    <jats:italic toggle=\"yes\">Pseudomonas aeruginosa<\/jats:italic>\n                    employs an integrated tripartite farnesol-sensing system to detect and eliminate\n                    <jats:italic toggle=\"yes\">Candida albicans<\/jats:italic>\n                    hyphae: The chemoreceptor PctA mediates directional migration toward hyphae; the type IV pilus sensor PilJ activates antifungal type III secretion system (T3SS) expression; and the quorum regulator PqsR monitors farnesol levels to coordinate virulence-metabolic switching. This mechanism enables bacteria to convert farnesol into their own signaling language (\n                    <jats:italic toggle=\"yes\">Pseudomonas<\/jats:italic>\n                    quinolone signal) according to fungi status, thereby adaptively modulating their virulence expression and metabolism to cope with complex competitive microbial environments. Furthermore, bioinformatics analysis and functional validation confirm that the PctA\u2013PilJ\u2013PqsR triad is conserved across\n                    <jats:italic toggle=\"yes\">P<\/jats:italic>\n                    .\n                    <jats:italic toggle=\"yes\">aeruginosa<\/jats:italic>\n                    , suggesting that this interkingdom communication is widespread. In conclusion, this study reveals that\n                    <jats:italic toggle=\"yes\">P<\/jats:italic>\n                    .\n                    <jats:italic toggle=\"yes\">aeruginosa<\/jats:italic>\n                    orchestrates a targeted predation strategy against filamentous fungi by coordinating three interkingdom receptors, providing a theoretical foundation and potential molecular targets for understanding of interkingdom communication strategies among microorganisms and the development of signal molecule\u2013based microbial prevention and control technologies.\n                  <\/jats:p>","DOI":"10.1073\/pnas.2529531123","type":"journal-article","created":{"date-parts":[[2026,4,20]],"date-time":"2026-04-20T19:01:46Z","timestamp":1776711706000},"update-policy":"https:\/\/doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":2,"title":["A farnesol-sensing triad in\n                    <i>Pseudomonas aeruginosa<\/i>\n                    drives interkingdom predation on\n                    <i>Candida albicans<\/i>\n                    via signal transduction"],"prefix":"10.1073","volume":"123","author":[{"given":"Zhiyan","family":"Wei","sequence":"first","affiliation":[{"name":"State Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of Agricultural and Environmental Microbiology, College of Life Sciences, Northwest Agriculture and Forestry University","place":["Yangling, Shaanxi, People\u2019s Republic of China"]},{"name":"College of Plant Protection, Northwest Agriculture and Forestry University","place":["Yangling, Shaanxi, People\u2019s Republic of China"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7791-6111","authenticated-orcid":false,"given":"Changfu","family":"Li","sequence":"additional","affiliation":[{"name":"State Key Laboratory for Crop Stress Resistance and High-Efficiency Production, Shaanxi Key Laboratory of 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