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Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases
Serine protease inhibitors (serpins) regulate proteolytic events within diverse biological processes, including digestion, coagulation, inflammation and immune responses. The presence of serpins in Fasciola hepatica excretory-secretory products indicates that the parasite exploits these to regulate...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437470/ https://www.ncbi.nlm.nih.gov/pubmed/32760059 http://dx.doi.org/10.1371/journal.pntd.0008510 |
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author | De Marco Verissimo, Carolina Jewhurst, Heather L. Tikhonova, Irina G. Urbanus, Rolf T. Maule, Aaron G. Dalton, John P. Cwiklinski, Krystyna |
author_facet | De Marco Verissimo, Carolina Jewhurst, Heather L. Tikhonova, Irina G. Urbanus, Rolf T. Maule, Aaron G. Dalton, John P. Cwiklinski, Krystyna |
author_sort | De Marco Verissimo, Carolina |
collection | PubMed |
description | Serine protease inhibitors (serpins) regulate proteolytic events within diverse biological processes, including digestion, coagulation, inflammation and immune responses. The presence of serpins in Fasciola hepatica excretory-secretory products indicates that the parasite exploits these to regulate proteases encountered during its development within vertebrate hosts. Interrogation of the F. hepatica genome identified a multi-gene serpin family of seven members that has expanded by gene duplication and divergence to create an array of inhibitors with distinct specificities. We investigated the molecular properties and functions of two representatives, FhSrp1 and FhSrp2, highly expressed in the invasive newly excysted juvenile (NEJ). Consistent with marked differences in the reactive centre loop (RCL) that executes inhibitor-protease complexing, the two recombinant F. hepatica serpins displayed distinct inhibitory profiles against an array of mammalian serine proteases. In particular, rFhSrp1 efficiently inhibited kallikrein (K(i) = 40 nM) whilst rFhSrp2 was a highly potent inhibitor of chymotrypsin (K(i) = 0.07 nM). FhSrp1 and FhSrp2 are both expressed on the NEJ surface, predominantly around the oral and ventral suckers, suggesting that these inhibitors protect the parasites from the harmful proteolytic effects of host proteases, such as chymotrypsin, during invasion. Furthermore, the unusual inhibition of kallikrein suggests that rFhSrp1 modulates host responses such as inflammation and vascular permeability by interfering with the kallikrein-kinin system. A vaccine combination of rFhSrp1 and rFhSrp2 formulated in the adjuvant Montanide ISA 206VG elicited modest but non-significant protection against a challenge infection in a rat model, but did induce some protection against liver pathogenesis when compared to a control group and a group vaccinated with two well-studied vaccine candidates, F. hepatica cathepsin L2 and L3. This work highlights the importance of F. hepatica serpins to regulate host responses that enables parasite survival during infection and, coupled with the vaccine data, encourages future vaccine trials in ruminants. |
format | Online Article Text |
id | pubmed-7437470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74374702020-08-25 Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases De Marco Verissimo, Carolina Jewhurst, Heather L. Tikhonova, Irina G. Urbanus, Rolf T. Maule, Aaron G. Dalton, John P. Cwiklinski, Krystyna PLoS Negl Trop Dis Research Article Serine protease inhibitors (serpins) regulate proteolytic events within diverse biological processes, including digestion, coagulation, inflammation and immune responses. The presence of serpins in Fasciola hepatica excretory-secretory products indicates that the parasite exploits these to regulate proteases encountered during its development within vertebrate hosts. Interrogation of the F. hepatica genome identified a multi-gene serpin family of seven members that has expanded by gene duplication and divergence to create an array of inhibitors with distinct specificities. We investigated the molecular properties and functions of two representatives, FhSrp1 and FhSrp2, highly expressed in the invasive newly excysted juvenile (NEJ). Consistent with marked differences in the reactive centre loop (RCL) that executes inhibitor-protease complexing, the two recombinant F. hepatica serpins displayed distinct inhibitory profiles against an array of mammalian serine proteases. In particular, rFhSrp1 efficiently inhibited kallikrein (K(i) = 40 nM) whilst rFhSrp2 was a highly potent inhibitor of chymotrypsin (K(i) = 0.07 nM). FhSrp1 and FhSrp2 are both expressed on the NEJ surface, predominantly around the oral and ventral suckers, suggesting that these inhibitors protect the parasites from the harmful proteolytic effects of host proteases, such as chymotrypsin, during invasion. Furthermore, the unusual inhibition of kallikrein suggests that rFhSrp1 modulates host responses such as inflammation and vascular permeability by interfering with the kallikrein-kinin system. A vaccine combination of rFhSrp1 and rFhSrp2 formulated in the adjuvant Montanide ISA 206VG elicited modest but non-significant protection against a challenge infection in a rat model, but did induce some protection against liver pathogenesis when compared to a control group and a group vaccinated with two well-studied vaccine candidates, F. hepatica cathepsin L2 and L3. This work highlights the importance of F. hepatica serpins to regulate host responses that enables parasite survival during infection and, coupled with the vaccine data, encourages future vaccine trials in ruminants. Public Library of Science 2020-08-06 /pmc/articles/PMC7437470/ /pubmed/32760059 http://dx.doi.org/10.1371/journal.pntd.0008510 Text en © 2020 De Marco Verissimo et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article De Marco Verissimo, Carolina Jewhurst, Heather L. Tikhonova, Irina G. Urbanus, Rolf T. Maule, Aaron G. Dalton, John P. Cwiklinski, Krystyna Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases |
title | Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases |
title_full | Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases |
title_fullStr | Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases |
title_full_unstemmed | Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases |
title_short | Fasciola hepatica serine protease inhibitor family (serpins): Purposely crafted for regulating host proteases |
title_sort | fasciola hepatica serine protease inhibitor family (serpins): purposely crafted for regulating host proteases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7437470/ https://www.ncbi.nlm.nih.gov/pubmed/32760059 http://dx.doi.org/10.1371/journal.pntd.0008510 |
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