Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-021-22845-2
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dc.titleA peptidoglycan storm caused by β-lactam antibiotic’s action on host microbiota drives Candida albicans infection
dc.contributor.authorTan, Chew Teng
dc.contributor.authorXu, Xiaoli
dc.contributor.authorQiao, Yuan
dc.contributor.authorWang, Yue
dc.date.accessioned2022-10-11T07:48:31Z
dc.date.available2022-10-11T07:48:31Z
dc.date.issued2021-05-07
dc.identifier.citationTan, Chew Teng, Xu, Xiaoli, Qiao, Yuan, Wang, Yue (2021-05-07). A peptidoglycan storm caused by β-lactam antibiotic’s action on host microbiota drives Candida albicans infection. Nature Communications 12 (1) : 2560. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-021-22845-2
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/231948
dc.description.abstractThe commensal fungus Candida albicans often causes life-threatening infections in patients who are immunocompromised with high mortality. A prominent but poorly understood risk factor for the C. albicans commensal‒pathogen transition is the use of broad-spectrum antibiotics. Here, we report that β-lactam antibiotics cause bacteria to release significant quantities of peptidoglycan fragments that potently induce the invasive hyphal growth of C. albicans. We identify several active peptidoglycan subunits, including tracheal cytotoxin, a molecule produced by many Gram-negative bacteria, and fragments purified from the cell wall of Gram-positive Staphylococcus aureus. Feeding mice with β-lactam antibiotics causes a peptidoglycan storm that transforms the gut from a niche usually restraining C. albicans in the commensal state to promoting invasive growth, leading to systemic dissemination. Our findings reveal a mechanism underlying a significant risk factor for C. albicans infection, which could inform clinicians regarding future antibiotic selection to minimize this deadly disease incidence. © 2021, The Author(s).
dc.publisherNature Research
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.typeArticle
dc.contributor.departmentINSTITUTE OF MOLECULAR & CELL BIOLOGY
dc.description.doi10.1038/s41467-021-22845-2
dc.description.sourcetitleNature Communications
dc.description.volume12
dc.description.issue1
dc.description.page2560
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