Abstract:Cryptococcus neoformans
and
Cryptococcus gattii
can cause cryptococcosis, which has a high mortality rate. To treat the disease, amphotericin B and fluconazole are often used in clinic.
“…S4). Combining these observations of the cap59 Δ mutants and the fact that the dense network structure of polysaccharide capsule was severely damaged after treatment of SP1 ( 32 ), we postulated that SP1 destroyed the capsule to expose proteins or polysaccharide, and the interactions of these exposed substances might induce the flocculation of C. neoformans H99. When the flocs were treated with 3 mg/mL proteinase K, the cell aggregation caused by SP1 was dispersed ( Fig.…”
Section: Resultsmentioning
confidence: 83%
“…Previously, we reported that SP1 can specifically kill C. neoformans and Cryptococcus gatti ( 32 ). Scanning electronic microscopy showed that SP1 damaged the capsule of C. neoformans H99 ( 32 ).…”
Section: Resultsmentioning
confidence: 99%
“…Previously, we reported that SP1 can specifically kill C. neoformans and Cryptococcus gatti ( 32 ). Scanning electronic microscopy showed that SP1 damaged the capsule of C. neoformans H99 ( 32 ). When we treated C. neoformans strain H99 with 8 μM SP1, we noticed that the treatment caused a flocculation-like phenotype ( Fig.…”
Section: Resultsmentioning
confidence: 99%
“…SP1, an antifungal peptide derived from Saccharomyces cerevisiae GAPDH, has a specific antifungal effect against Cryptococcus ( 32 , 33 ). Interestingly, we observed that treatment with SP1 specifically damaged the capsule of C. neoformans ( 32 ).…”
Section: Introductionmentioning
confidence: 99%
“…SP1, an antifungal peptide derived from Saccharomyces cerevisiae GAPDH, has a specific antifungal effect against Cryptococcus ( 32 , 33 ). Interestingly, we observed that treatment with SP1 specifically damaged the capsule of C. neoformans ( 32 ). In this study, we investigated the possible mechanism for the capsule damage caused by SP1, providing a basis for a treatment strategy to control refractory fungal infections by inhibiting virulence factors.…”
C. neoformans
is an opportunistic pathogen that causes invasive infections with a high mortality rate. Currently, the clinical drugs available for the treatment of cryptococcosis are limited to amphotericin B, azoles, and flucytosine.
“…S4). Combining these observations of the cap59 Δ mutants and the fact that the dense network structure of polysaccharide capsule was severely damaged after treatment of SP1 ( 32 ), we postulated that SP1 destroyed the capsule to expose proteins or polysaccharide, and the interactions of these exposed substances might induce the flocculation of C. neoformans H99. When the flocs were treated with 3 mg/mL proteinase K, the cell aggregation caused by SP1 was dispersed ( Fig.…”
Section: Resultsmentioning
confidence: 83%
“…Previously, we reported that SP1 can specifically kill C. neoformans and Cryptococcus gatti ( 32 ). Scanning electronic microscopy showed that SP1 damaged the capsule of C. neoformans H99 ( 32 ).…”
Section: Resultsmentioning
confidence: 99%
“…Previously, we reported that SP1 can specifically kill C. neoformans and Cryptococcus gatti ( 32 ). Scanning electronic microscopy showed that SP1 damaged the capsule of C. neoformans H99 ( 32 ). When we treated C. neoformans strain H99 with 8 μM SP1, we noticed that the treatment caused a flocculation-like phenotype ( Fig.…”
Section: Resultsmentioning
confidence: 99%
“…SP1, an antifungal peptide derived from Saccharomyces cerevisiae GAPDH, has a specific antifungal effect against Cryptococcus ( 32 , 33 ). Interestingly, we observed that treatment with SP1 specifically damaged the capsule of C. neoformans ( 32 ).…”
Section: Introductionmentioning
confidence: 99%
“…SP1, an antifungal peptide derived from Saccharomyces cerevisiae GAPDH, has a specific antifungal effect against Cryptococcus ( 32 , 33 ). Interestingly, we observed that treatment with SP1 specifically damaged the capsule of C. neoformans ( 32 ). In this study, we investigated the possible mechanism for the capsule damage caused by SP1, providing a basis for a treatment strategy to control refractory fungal infections by inhibiting virulence factors.…”
C. neoformans
is an opportunistic pathogen that causes invasive infections with a high mortality rate. Currently, the clinical drugs available for the treatment of cryptococcosis are limited to amphotericin B, azoles, and flucytosine.
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