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Cryptococcus neoformans trehalose-6-phosphate synthase (tps1) promotes organ-specific virulence and fungal protection against multiple lines of host defenses.

Publication ,  Journal Article
Goughenour, K; Creech, A; Xu, J; He, X; Hissong, R; Giamberardino, C; Tenor, J; Toffaletti, D; Perfect, J; Olszewski, M
Published in: Front Cell Infect Microbiol
2024

Trehalose-6-phosphate synthase (TPS1) was identified as a virulence factor for Cryptococcus neoformans and a promising therapeutic target. This study reveals previously unknown roles of TPS1 in evasion of host defenses during pulmonary and disseminated phases of infection. In the pulmonary infection model, TPS1-deleted (tps1Δ) Cryptococci are rapidly cleared by mouse lungs whereas TPS1-sufficent WT (H99) and revertant (tps1Δ:TPS1) strains expand in the lungs and disseminate, causing 100% mortality. Rapid pulmonary clearance of tps1Δ mutant is T-cell independent and relies on its susceptibility to lung resident factors and innate immune factors, exemplified by tps1Δ but not H99 inhibition in a coculture with dispersed lung cells and its rapid clearance coinciding with innate leukocyte infiltration. In the disseminated model of infection, which bypasses initial lung-fungus interactions, tps1Δ strain remains highly attenuated. Specifically, tps1Δ mutant is unable to colonize the lungs from the bloodstream or expand in spleens but is capable of crossing into the brain, where it remains controlled even in the absence of T cells. In contrast, strains H99 and tps1Δ:TPS1 rapidly expand in all studied organs, leading to rapid death of the infected mice. Since the rapid pulmonary clearance of tps1Δ mutant resembles a response to acapsular strains, the effect of tps1 deletion on capsule formation in vitro and in vivo was examined. Tps1Δ cryptococci form capsules but with a substantially reduced size. In conclusion, TPS1 is an important virulence factor, allowing C. neoformans evasion of resident pulmonary and innate defense mechanisms, most likely via its role in cryptococcal capsule formation.

Duke Scholars

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Published In

Front Cell Infect Microbiol

DOI

EISSN

2235-2988

Publication Date

2024

Volume

14

Start / End Page

1392015

Location

Switzerland

Related Subject Headings

  • Virulence Factors
  • Virulence
  • Spleen
  • Mice, Inbred C57BL
  • Mice
  • Lung
  • Immunity, Innate
  • Immune Evasion
  • Host-Pathogen Interactions
  • Glucosyltransferases
 

Citation

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Chicago
ICMJE
MLA
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Goughenour, K., Creech, A., Xu, J., He, X., Hissong, R., Giamberardino, C., … Olszewski, M. (2024). Cryptococcus neoformans trehalose-6-phosphate synthase (tps1) promotes organ-specific virulence and fungal protection against multiple lines of host defenses. Front Cell Infect Microbiol, 14, 1392015. https://doi.org/10.3389/fcimb.2024.1392015
Goughenour, Kristie, Arianna Creech, Jintao Xu, Xiumiao He, Rylan Hissong, Charles Giamberardino, Jennifer Tenor, Dena Toffaletti, John Perfect, and Michal Olszewski. “Cryptococcus neoformans trehalose-6-phosphate synthase (tps1) promotes organ-specific virulence and fungal protection against multiple lines of host defenses.Front Cell Infect Microbiol 14 (2024): 1392015. https://doi.org/10.3389/fcimb.2024.1392015.
Goughenour K, Creech A, Xu J, He X, Hissong R, Giamberardino C, et al. Cryptococcus neoformans trehalose-6-phosphate synthase (tps1) promotes organ-specific virulence and fungal protection against multiple lines of host defenses. Front Cell Infect Microbiol. 2024;14:1392015.
Goughenour, Kristie, et al. “Cryptococcus neoformans trehalose-6-phosphate synthase (tps1) promotes organ-specific virulence and fungal protection against multiple lines of host defenses.Front Cell Infect Microbiol, vol. 14, 2024, p. 1392015. Pubmed, doi:10.3389/fcimb.2024.1392015.
Goughenour K, Creech A, Xu J, He X, Hissong R, Giamberardino C, Tenor J, Toffaletti D, Perfect J, Olszewski M. Cryptococcus neoformans trehalose-6-phosphate synthase (tps1) promotes organ-specific virulence and fungal protection against multiple lines of host defenses. Front Cell Infect Microbiol. 2024;14:1392015.

Published In

Front Cell Infect Microbiol

DOI

EISSN

2235-2988

Publication Date

2024

Volume

14

Start / End Page

1392015

Location

Switzerland

Related Subject Headings

  • Virulence Factors
  • Virulence
  • Spleen
  • Mice, Inbred C57BL
  • Mice
  • Lung
  • Immunity, Innate
  • Immune Evasion
  • Host-Pathogen Interactions
  • Glucosyltransferases