Stage-specific expression and divergent functions of two insulinase-like proteases associated with host infectivity in Cryptosporidium

The determinants of differences in host infectivity among Cryptosporidium species and subtypes are poorly understood. Results from recent comparative genomic studies suggest that gains and losses of multicopy subtelomeric genes encoding insulinase-like proteases (INS-19 and INS-20 in Cryptosporidium...

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Veröffentlicht in:PLoS neglected tropical diseases 2025-01, Vol.19 (1), p.e0012777
Hauptverfasser: Huang, Yue, Pei, Shifeng, Lv, Xin, Yang, Fuxian, Gong, Xiaoqing, Li, Na, Guo, Yaqiong, Feng, Yaoyu, Xiao, Lihua
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container_title PLoS neglected tropical diseases
container_volume 19
creator Huang, Yue
Pei, Shifeng
Lv, Xin
Yang, Fuxian
Gong, Xiaoqing
Li, Na
Guo, Yaqiong
Feng, Yaoyu
Xiao, Lihua
description The determinants of differences in host infectivity among Cryptosporidium species and subtypes are poorly understood. Results from recent comparative genomic studies suggest that gains and losses of multicopy subtelomeric genes encoding insulinase-like proteases (INS-19 and INS-20 in Cryptosporidium parvum and their orthologs in closely related species) may potentially contribute to these differences. In this study, we investigated the expression and biological function of the INS-19 and INS-20 of C. parvum. CRISPR/Cas9 was used to endogenously tag both genes with the hemagglutinin epitope. Immunofluorescence analysis revealed that INS-19 and INS-20 are expressed at different developmental stages of the pathogen. Although knockout of either had no detectable effect on the in vitro growth of C. parvum, knockout of INS-20, deletion of its multiple domains, or mutation of the active motif in the functional domain reduced the intensity of C. parvum infection in IFN-γ knockout mice. Consistent with this, mice infected with the INS-20-deleted mutant had reduced intestinal damage and parasite burden. These results suggest that INS-19 and INS-20 have stage-specific expression with distinct biological functions, and that the presence of the INS-20 in zoonotic C. parvum contributes to its infectivity and fitness in mice.
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Results from recent comparative genomic studies suggest that gains and losses of multicopy subtelomeric genes encoding insulinase-like proteases (INS-19 and INS-20 in Cryptosporidium parvum and their orthologs in closely related species) may potentially contribute to these differences. In this study, we investigated the expression and biological function of the INS-19 and INS-20 of C. parvum. CRISPR/Cas9 was used to endogenously tag both genes with the hemagglutinin epitope. Immunofluorescence analysis revealed that INS-19 and INS-20 are expressed at different developmental stages of the pathogen. Although knockout of either had no detectable effect on the in vitro growth of C. parvum, knockout of INS-20, deletion of its multiple domains, or mutation of the active motif in the functional domain reduced the intensity of C. parvum infection in IFN-γ knockout mice. Consistent with this, mice infected with the INS-20-deleted mutant had reduced intestinal damage and parasite burden. 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subjects Animals
Biology and Life Sciences
CRISPR-Cas Systems
Cryptosporidiosis - parasitology
Cryptosporidium parvum - enzymology
Cryptosporidium parvum - genetics
Cryptosporidium parvum - pathogenicity
Engineering and Technology
Humans
Insulysin - genetics
Insulysin - metabolism
Medicine and Health Sciences
Mice
Mice, Inbred C57BL
Mice, Knockout
Protozoan Proteins - genetics
Protozoan Proteins - metabolism
Research and Analysis Methods
title Stage-specific expression and divergent functions of two insulinase-like proteases associated with host infectivity in Cryptosporidium
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