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.

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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