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Spectrum of Trained Innate Immunity Induced by Low-Virulence Candida Species against Lethal Polymicrobial
Elizabeth A Lilly1, Junko Yano1, Shannon K Esher1
1Center of Excellence in Oral and Craniofacial Biology, Louisiana State University Health Sciences Center School of Dentistry, New Orleans, Louisiana, USA.
Abstract:
Polymicrobial intra-abdominal infections (IAI) are clinically prevalent and cause significant morbidity and mortality, especially those involving fungi. Our laboratory developed a mouse model of polymicrobial IAI and demonstrated that coinfection with Candida albicans and Staphylococcus aureus (C. albicans/S. aureus) results in 80 to 90% mortality in 48 to 72 h due to robust local and systemic inflammation. Surprisingly, inoculation with Candida dubliniensis and S. aureus resulted in minimal mortality, and rechallenge of mice with lethal C. albicans/S. aureus conferred >90% protection up to 60 days postinoculation. Protection was mediated by Gr-1+ polymorphonuclear leukocytes, indicating a novel form of trained innate immunity (TII). The purpose of this study was to determine the microbial requirements and spectrum of innate-mediated protection. In addition to Candida dubliniensis, several other low-virulence Candida species (C. glabrata, C. auris, and C. albicansefg1Δ/Δ cph1Δ/Δ) and Saccharomyces cerevisiae conferred significant protection with or without S. aureus For C. dubliniensis-mediated protection, hyphal formation was not required, with protection conferred as early as 7 days after primary challenge but not at 120 days, and also following multiple lethal C. albicans/S. aureus rechallenges. This protection also extended to a lethal intravenous (i.v.) C. albicans challenge but had no effect in the C. albicans vaginitis model. Finally, studies revealed the ability of the low-virulence Candida species that conferred protection to invade the bone marrow by 24 h post-primary challenge, with a positive correlation between femoral bone marrow fungal infiltration at 48 h and protection upon rechallenge. These results support and further extend the characterization of this novel TII in protection against lethal fungal-bacterial IAI and sepsis.
Insights
Low-virulence fungi, like Candida dubliniensis, induce trained innate immunity (TII) offering protection against lethal polymicrobial intra-abdominal infections. This TII, mediated by specific immune cells, provides a novel defense mechanism against severe fungal-bacterial sepsis.
Area of Science:
- Immunology
- Microbiology
- Infectious Diseases
Background:
- Polymicrobial intra-abdominal infections (IAI) involving fungi cause high mortality.
- A mouse model showed coinfection with *Candida albicans* and *Staphylococcus aureus* leads to high mortality.
- Coinfection with *Candida dubliniensis* and *S. aureus* resulted in minimal mortality, surprisingly.
Purpose of the Study:
- To determine the microbial requirements for innate-mediated protection against IAI.
- To characterize the spectrum of this novel trained innate immunity (TII).
Main Methods:
- Developed a mouse model of polymicrobial IAI.
- Used various *Candida* species and *Saccharomyces cerevisiae* for primary challenge.
- Assessed protection via rechallenge with lethal *C. albicans*/*S. aureus* and *C. albicans* i.v. challenge.
- Investigated fungal infiltration in bone marrow post-challenge.
Main Results:
- *Candida dubliniensis*, *C. glabrata*, *C. auris*, *S. cerevisiae*, and *C. albicans* efg1Δ/Δ cph1Δ/Δ conferred significant protection.
- Protection was mediated by Gr-1+ polymorphonuclear leukocytes, indicating TII.
- Hyphal formation was not required for *C. dubliniensis*-mediated protection.
- Protection was observed up to 60 days and effective against i.v. *C. albicans* challenge, but not in a vaginitis model.
- Fungal infiltration into bone marrow correlated positively with protection.
Conclusions:
- Low-virulence *Candida* species can induce a protective TII against lethal fungal-bacterial IAI and sepsis.
- This TII is mediated by polymorphonuclear leukocytes and involves fungal invasion of bone marrow.
- Findings extend the characterization of TII as a potential therapeutic strategy.
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