The unique Efg1 fungal virulence regulon in the catheterized bladder environment

A Alyssa Ann La Bella (Department of Biological Sciences, University of Notre Dame) N Nicholas C. Gervais (Department of Molecular and Cellular Biology, University of Guelph) K Kurt N. Kohler (Department of Biological Sciences, University of Notre Dame) H Hope Akegbe (Department of Biological Sciences, University of Notre Dame) C Chloe L. P. Obernuefemann (Department of Molecular Microbiology, Washington University School of Medicine) C Christopher Gager (Department of Biological Sciences, University of Notre Dame) C Catherine May May Hubbard (Department of Biological Sciences, University of Notre Dame) A Armando M. Marrufo (Department of Biological Sciences, University of Notre Dame) I Ilse D. Jacobsen (Research Group Microbial Immunology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute) R Rebecca S. Shapiro M Michael G. Caparon (Department of Molecular Microbiology, Washington University School of Medicine) S Scott J. Hultgren (Department of Molecular Microbiology, Washington University School of Medicine) A Ana Lidia Flores-Mireles (Department of Biological Sciences, University of Notre Dame) F Felipe Hiram Santiago-Tirado (Department of Biological Sciences, University of Notre Dame)

Abstract

Urinary catheterization, a frequent procedure in hospitals, nursing homes, and other healthcare facilities, is a primary driver of nosocomial infections. The most common of these are catheter-associated urinary tract infections (CAUTIs), which often progress to severe complication, sepsis, and ultimately death. The fungus Candida albicans is a primary causative agent of CAUTIs; yet, its tissue-specific pathogenesis remains poorly understood, which complicates development of efficient treatments. While Efg1 is a known virulence driver in CAUTI, its specific downstream targets within the unique bladder environment have not been defined. Here, we identify and validate the EFG1 regulon that is active during conditions that mimic the human catheterized bladder and, additionally, confirm the regulon by transcriptional profiling of catheters retrieved from patients with C. albicans infection. We found that this urine-specific signature is highly conserved in clinical samples, with Efg1-dependent genes being among the most robustly induced transcripts during active human infection. Furthermore, we characterized two of these key factors, ECE1 and EED1 , validating their roles in infection both in vitro in human urine and in vivo using a CAUTI mouse model. Elucidating this tissue-specific regulon offers a strategic roadmap for the development of targeted therapies to mitigate these ever-increasing life-threatening fungal infections.

Article Details

Volume / Issue Vol. 123, Issue 30
Published July 28, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (14)

A

Alyssa Ann La Bella

Department of Biological Sciences, University of Notre Dame

N

Nicholas C. Gervais

Department of Molecular and Cellular Biology, University of Guelph

K

Kurt N. Kohler

Department of Biological Sciences, University of Notre Dame

H

Hope Akegbe

Department of Biological Sciences, University of Notre Dame

C

Chloe L. P. Obernuefemann

Department of Molecular Microbiology, Washington University School of Medicine

C

Christopher Gager

Department of Biological Sciences, University of Notre Dame

C

Catherine May May Hubbard

Department of Biological Sciences, University of Notre Dame

A

Armando M. Marrufo

Department of Biological Sciences, University of Notre Dame

I

Ilse D. Jacobsen

Research Group Microbial Immunology, Leibniz Institute for Natural Product Research and Infection Biology-Hans Knöll Institute

R

Rebecca S. Shapiro

M

Michael G. Caparon

Department of Molecular Microbiology, Washington University School of Medicine

S

Scott J. Hultgren

Department of Molecular Microbiology, Washington University School of Medicine

A

Ana Lidia Flores-Mireles

Department of Biological Sciences, University of Notre Dame

F

Felipe Hiram Santiago-Tirado

Department of Biological Sciences, University of Notre Dame