Pythium insidiosum-antigen enhances neutrophil-mediated killing of zoospores

Pythium insidiosum-antigen (PIA) immunotherapy has been used to treat human pythiosis. This study compared PIA-stimulated and unstimulated neutrophils on zoospore viability of P. insidiosum strains. We cultured and collected zoospores of 6 P. insidiosum strains, CBS 777.84, ATCC 58643, ATCC 90586, PEC1, PC10, and CBS 101039. PIA concentrations of 0.01, 0.1, 1, and 10 µg/ml were prepared and were used to stimulate neutrophils isolated from healthy volunteers. The MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide) assay was used to calculate the zoospore viability of P. insidiosum strains. Neutrophils stimulated with 0.01 or 0.1 µg/ml PIA, or both, showed a significant reduction in the viability of zoospores of CBS 777.84, ATCC 58643, CBS 101039, PC10, and PEC1 strains. Furthermore, 1 µg/ml PIA-induced neutrophils elicited a significant decrease in the viability of zoospores of ATCC 58643, CBS 101039, and PC10 strains. However, a higher dose of PIA (10 µg/ml) did not demonstrate superiority in reducing the zoospore viability of all six strains. Our findings suggest that PIA immunotherapy improves the zoospore-killing activity of neutrophils, and neutrophils might be involved in the forefront mechanism responsible for the beneficial effects of PIA immunotherapy.

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Publication Details

Journal
Scientific Reports
Published
2025-02-12
DOI
https://doi.org/10.1038/s41598-025-88962-w
Citations
1
Primary Topic
Infectious Diseases and Mycology
Type
article
Field-Weighted Citation Impact
2.35

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Pythium insidiosum-antigen enhances neutrophil-mediated killing of zoospores

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Pythium insidiosum-antigen enhances neutrophil-mediated killing of zoospores

Sadeep Medhasi, Navaporn Worasilchai, Ariya Chindamporn, Apichaya Sriwarom, Nitipong Permpalung, Rongpong Plongla, Pattama Torvorapanit
article en
1 citations

Abstract

Pythium insidiosum-antigen (PIA) immunotherapy has been used to treat human pythiosis. This study compared PIA-stimulated and unstimulated neutrophils on zoospore viability of P. insidiosum strains. We cultured and collected zoospores of 6 P. insidiosum strains, CBS 777.84, ATCC 58643, ATCC 90586, PEC1, PC10, and CBS 101039. PIA concentrations of 0.01, 0.1, 1, and 10 µg/ml were prepared and were used to stimulate neutrophils isolated from healthy volunteers. The MTT (3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide) assay was used to calculate the zoospore viability of P. insidiosum strains. Neutrophils stimulated with 0.01 or 0.1 µg/ml PIA, or both, showed a significant reduction in the viability of zoospores of CBS 777.84, ATCC 58643, CBS 101039, PC10, and PEC1 strains. Furthermore, 1 µg/ml PIA-induced neutrophils elicited a significant decrease in the viability of zoospores of ATCC 58643, CBS 101039, and PC10 strains. However, a higher dose of PIA (10 µg/ml) did not demonstrate superiority in reducing the zoospore viability of all six strains. Our findings suggest that PIA immunotherapy improves the zoospore-killing activity of neutrophils, and neutrophils might be involved in the forefront mechanism responsible for the beneficial effects of PIA immunotherapy.

Scientific ReportsVol. 15(1)
Thai Red Cross Society (TH), Johns Hopkins University (US), Chulalongkorn University (TH), Johns Hopkins Medicine (US), King Chulalongkorn Memorial Hospital (TH)
Chulalongkorn University, Thailand Science Research and Innovation, Faculty of Allied Health Sciences, Chulalongkorn University
Zero hunger
Openalex Percentile: Top 17%
Infectious Diseases and Mycology
2.35
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