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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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. |
doi_str_mv | 10.1371/journal.pntd.0012777 |
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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.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0012777</identifier><identifier>PMID: 39804945</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>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</subject><ispartof>PLoS neglected tropical diseases, 2025-01, Vol.19 (1), p.e0012777</ispartof><rights>Copyright: © 2025 Huang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>2025 Huang et al 2025 Huang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1570-703c41a0ce67b423defefc9f4da3a0712d5e850c9dbdad40cc019e55b6f77f983</cites><orcidid>0000-0001-8532-2727</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11760560/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11760560/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2915,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39804945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Yue</creatorcontrib><creatorcontrib>Pei, Shifeng</creatorcontrib><creatorcontrib>Lv, Xin</creatorcontrib><creatorcontrib>Yang, Fuxian</creatorcontrib><creatorcontrib>Gong, Xiaoqing</creatorcontrib><creatorcontrib>Li, Na</creatorcontrib><creatorcontrib>Guo, Yaqiong</creatorcontrib><creatorcontrib>Feng, Yaoyu</creatorcontrib><creatorcontrib>Xiao, Lihua</creatorcontrib><title>Stage-specific expression and divergent functions of two insulinase-like proteases associated with host infectivity in Cryptosporidium</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><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.</description><subject>Animals</subject><subject>Biology and Life Sciences</subject><subject>CRISPR-Cas Systems</subject><subject>Cryptosporidiosis - parasitology</subject><subject>Cryptosporidium parvum - enzymology</subject><subject>Cryptosporidium parvum - genetics</subject><subject>Cryptosporidium parvum - pathogenicity</subject><subject>Engineering and Technology</subject><subject>Humans</subject><subject>Insulysin - genetics</subject><subject>Insulysin - metabolism</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Protozoan Proteins - genetics</subject><subject>Protozoan Proteins - metabolism</subject><subject>Research and Analysis Methods</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc9uGyEQxlHVqvnTvkEUcexlXTCL2T1FkZW0kSL10PaMMAw2yRo2DOvEL9DnLlHcKD3xwXzzDaMfIWeczbhQ_OtdmnI0w2yMxc0Y43Ol1DtyzHshm7kS8v0bfUROEO8Yk73s-EdyJPqOtX0rj8mfn8WsocERbPDBUngaMyCGFKmJjrqwg7yGWKifoi31GWnytDwmGiJOQ4gGoRnCPdAxpwL1htQgJhtMAUcfQ9nQTcJS7R5qwC6UfdV0mfdjSTimHFyYtp_IB28GhM-H85T8vr76tfze3P74drO8vG0sl4o1ignbcsMsLNSqnQsHHrztfeuMMEzxuZPQSWZ7t3LGtcxaxnuQcrXwSvm-E6fk4iV3nFZbcLZuls2gxxy2Ju91MkH_X4lho9dppzlXCyYXrCZ8OSTk9DABFr0NaGEYTIQ0oRZcSiE7IXi1ti9WmxNiBv86hzP9zFAfGOpnhvrAsLadv_3ja9M_aOIvlRCiIA</recordid><startdate>20250113</startdate><enddate>20250113</enddate><creator>Huang, Yue</creator><creator>Pei, Shifeng</creator><creator>Lv, Xin</creator><creator>Yang, Fuxian</creator><creator>Gong, Xiaoqing</creator><creator>Li, Na</creator><creator>Guo, Yaqiong</creator><creator>Feng, Yaoyu</creator><creator>Xiao, Lihua</creator><general>Public Library of Science</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8532-2727</orcidid></search><sort><creationdate>20250113</creationdate><title>Stage-specific expression and divergent functions of two insulinase-like proteases associated with host infectivity in Cryptosporidium</title><author>Huang, Yue ; Pei, Shifeng ; Lv, Xin ; Yang, Fuxian ; Gong, Xiaoqing ; Li, Na ; Guo, Yaqiong ; Feng, Yaoyu ; Xiao, Lihua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1570-703c41a0ce67b423defefc9f4da3a0712d5e850c9dbdad40cc019e55b6f77f983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Animals</topic><topic>Biology and Life Sciences</topic><topic>CRISPR-Cas Systems</topic><topic>Cryptosporidiosis - parasitology</topic><topic>Cryptosporidium parvum - enzymology</topic><topic>Cryptosporidium parvum - genetics</topic><topic>Cryptosporidium parvum - pathogenicity</topic><topic>Engineering and Technology</topic><topic>Humans</topic><topic>Insulysin - genetics</topic><topic>Insulysin - metabolism</topic><topic>Medicine and Health Sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Protozoan Proteins - genetics</topic><topic>Protozoan Proteins - metabolism</topic><topic>Research and Analysis Methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Yue</creatorcontrib><creatorcontrib>Pei, Shifeng</creatorcontrib><creatorcontrib>Lv, Xin</creatorcontrib><creatorcontrib>Yang, Fuxian</creatorcontrib><creatorcontrib>Gong, Xiaoqing</creatorcontrib><creatorcontrib>Li, Na</creatorcontrib><creatorcontrib>Guo, Yaqiong</creatorcontrib><creatorcontrib>Feng, Yaoyu</creatorcontrib><creatorcontrib>Xiao, Lihua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>PLoS neglected tropical diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Yue</au><au>Pei, Shifeng</au><au>Lv, Xin</au><au>Yang, Fuxian</au><au>Gong, Xiaoqing</au><au>Li, Na</au><au>Guo, Yaqiong</au><au>Feng, Yaoyu</au><au>Xiao, Lihua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stage-specific expression and divergent functions of two insulinase-like proteases associated with host infectivity in Cryptosporidium</atitle><jtitle>PLoS neglected tropical diseases</jtitle><addtitle>PLoS Negl Trop Dis</addtitle><date>2025-01-13</date><risdate>2025</risdate><volume>19</volume><issue>1</issue><spage>e0012777</spage><pages>e0012777-</pages><issn>1935-2735</issn><issn>1935-2727</issn><eissn>1935-2735</eissn><abstract>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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>39804945</pmid><doi>10.1371/journal.pntd.0012777</doi><orcidid>https://orcid.org/0000-0001-8532-2727</orcidid><oa>free_for_read</oa></addata></record> |
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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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