{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"institution":[{"name":"bioRxiv"}],"indexed":{"date-parts":[[2026,6,24]],"date-time":"2026-06-24T05:51:23Z","timestamp":1782280283110,"version":"3.54.5"},"posted":{"date-parts":[[2025,8,19]]},"group-title":"Microbiology","reference-count":69,"publisher":"openRxiv","license":[{"start":{"date-parts":[[2025,8,19]],"date-time":"2025-08-19T00:00:00Z","timestamp":1755561600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.biorxiv.org\/about\/FAQ#license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"accepted":{"date-parts":[[2025,8,19]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                <jats:p>\n                  Upon exposure to echinocandins, growing yeast cells begin to accumulate cell wall damage and eventually die, resulting in therapeutic effects. While resistance to echinocandins is well studied, tolerance and persistence mechanisms that may also contribute to clinical failures and relapses remain understudied. In time-kill assays with micafungin\n                  <jats:italic>in vitro<\/jats:italic>\n                  , the opportunistic pathogen\n                  <jats:italic>Candida glabrata<\/jats:italic>\n                  exhibited biphasic kinetics of cell death. Modeling with exponential decay equations distinguished a fast-dying major population from a slow-dying minor population, indicative of persistence. A genome-wide forward-genetic screen revealed dozens of genes that appeared to regulate persistence and\/or tolerance, but not resistance. Several of those genes encoded calcineurin and its upstream regulators. Using individual gene knockout mutants and FK506, we show that calcineurin signaling increases the lifespans of most\n                  <jats:italic>C. glabrata<\/jats:italic>\n                  cells through a process that is largely independent of Crz1, one of its downstream effectors. The formation of long-lived persister-like cells (i.e. persistence) was strongly dependent on calcineurin signaling, independent of Crz1. Pre-activation of calcineurin using genetic or chemical stressors, such as manogepix, strongly increased tolerance and persistence in\n                  <jats:italic>C. glabrata<\/jats:italic>\n                  , suggesting antagonism of echinocandin efficacy by this new antifungal. Calcineurin signaling was also necessary for induction of tolerance and persistence in\n                  <jats:italic>Candida albicans<\/jats:italic>\n                  . The findings suggest that short-term administration of FK506 during the earliest stages of echinocandin treatment may improve clinical outcomes while possibly avoiding long-term immunosuppression.\n                <\/jats:p>\n                <jats:sec>\n                  <jats:title>IMPORTANCE<\/jats:title>\n                  <jats:p>\n                    Treatment of fungal infections is often unsuccessful. Potential causes of antifungal failure include tolerance and persistence, which are poorly understood processes used by fungal pathogens to survive our assaults. This study utilizes detailed experimental protocols and genome-wide screens to discover how\n                    <jats:italic>Candida glabrata<\/jats:italic>\n                    induces tolerance and persistence to a major class of antifungals. The findings suggest that a clinical immunosuppressant may be repurposed to combat tolerance and persistence in this pathogenic yeast as well as\n                    <jats:italic>Candida albicans<\/jats:italic>\n                    and perhaps others.\n                  <\/jats:p>\n                <\/jats:sec>","DOI":"10.1101\/2025.08.19.671059","type":"posted-content","created":{"date-parts":[[2025,8,20]],"date-time":"2025-08-20T05:35:28Z","timestamp":1755668128000},"source":"Crossref","is-referenced-by-count":0,"title":["Echinocandin tolerance and persistence\n                  <i>in vitro<\/i>\n                  are regulated by calcineurin signaling in\n                  <i>Candida glabrata<\/i>"],"prefix":"10.64898","author":[{"given":"Abigail A.","family":"Harrington","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Timothy J.","family":"Nickels","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6877-6321","authenticated-orcid":false,"given":"Kyle W.","family":"Cunningham","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"54368","reference":[{"key":"2025082204500748000_2025.08.19.671059v1.1","doi-asserted-by":"publisher","DOI":"10.3109\/10409238.2013.869543"},{"key":"2025082204500748000_2025.08.19.671059v1.2","doi-asserted-by":"publisher","DOI":"10.1038\/nrmicro.2016.34"},{"key":"2025082204500748000_2025.08.19.671059v1.3","doi-asserted-by":"publisher","DOI":"10.1016\/j.molcel.2019.09.028"},{"key":"2025082204500748000_2025.08.19.671059v1.4","doi-asserted-by":"publisher","DOI":"10.1038\/s41579-019-0322-2"},{"key":"2025082204500748000_2025.08.19.671059v1.5","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1038\/s44259-023-00007-2","article-title":"Molecular mechanisms governing antifungal drug resistance","volume":"1","year":"2023","journal-title":"NPJ Antimicrob Resist"},{"key":"2025082204500748000_2025.08.19.671059v1.6","doi-asserted-by":"publisher","DOI":"10.1016\/j.mib.2024.102439"},{"key":"2025082204500748000_2025.08.19.671059v1.7","doi-asserted-by":"crossref","unstructured":"Ben-Ami R , Zimmerman O , Finn T , Amit S , Novikov A , Wertheimer N , Lurie-Weinberger M , Berman J. 2016. 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