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Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism

BACKGROUND: The trematode Fasciola hepatica is the most widespread causative agent of fasciolosis, a parasitic disease that mainly affects humans and ruminants worldwide. During F. hepatica infection, newly excysted juveniles (FhNEJ) emerge in the duodenum of the mammalian host and migrate towards t...

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Autores principales: Serrat, Judit, Becerro-Recio, David, Torres-Valle, María, Simón, Fernando, Valero, María Adela, Bargues, María Dolores, Mas-Coma, Santiago, Siles-Lucas, Mar, González-Miguel, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155961/
https://www.ncbi.nlm.nih.gov/pubmed/37083884
http://dx.doi.org/10.1371/journal.pntd.0010936
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author Serrat, Judit
Becerro-Recio, David
Torres-Valle, María
Simón, Fernando
Valero, María Adela
Bargues, María Dolores
Mas-Coma, Santiago
Siles-Lucas, Mar
González-Miguel, Javier
author_facet Serrat, Judit
Becerro-Recio, David
Torres-Valle, María
Simón, Fernando
Valero, María Adela
Bargues, María Dolores
Mas-Coma, Santiago
Siles-Lucas, Mar
González-Miguel, Javier
author_sort Serrat, Judit
collection PubMed
description BACKGROUND: The trematode Fasciola hepatica is the most widespread causative agent of fasciolosis, a parasitic disease that mainly affects humans and ruminants worldwide. During F. hepatica infection, newly excysted juveniles (FhNEJ) emerge in the duodenum of the mammalian host and migrate towards their definitive location, the intra-hepatic biliary ducts. Understanding how F. hepatica traverses the intestinal wall and migrates towards the liver is pivotal for the development of more successful strategies against fasciolosis. The central enzyme of the mammalian fibrinolytic system is plasmin, a serine protease whose functions are exploited by a number of parasite species owing to its broad spectrum of substrates, including components of tissue extracellular matrices. The aim of the present work is to understand whether FhNEJ co-opt the functions of their host fibrinolytic system as a mechanism to facilitate trans-intestinal migration. METHODOLOGY/PRINCIPAL FINDINGS: A tegument-enriched antigenic extract of FhNEJ (FhNEJ-Teg) was obtained in vitro, and its capability to bind the zymogen plasminogen (PLG) and enhance its conversion to the active protease, plasmin, were analyzed by a combination of enzyme-linked immunosorbent, chromogenic and immunofluorescence assays. Additionally, PLG-binding proteins in FhNEJ-Teg were identified by bidimensional electrophoresis coupled to mass spectrometry analysis, and the interactions were validated using FhNEJ recombinant proteins. CONCLUSIONS/SIGNIFICANCE: Our results show that FhNEJ-Teg contains proteins that bind PLG and stimulate its activation to plasmin, which could facilitate the traversal of the intestinal wall by FhNEJ and contribute to the successful establishment of the parasite within its mammalian host. Altogether, our findings contribute to a better understanding of host-parasite relationships during early fasciolosis and may be exploited from a pharmacological and/or immunological perspective for the development of treatment and control strategies against this global disease.
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spelling pubmed-101559612023-05-04 Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism Serrat, Judit Becerro-Recio, David Torres-Valle, María Simón, Fernando Valero, María Adela Bargues, María Dolores Mas-Coma, Santiago Siles-Lucas, Mar González-Miguel, Javier PLoS Negl Trop Dis Research Article BACKGROUND: The trematode Fasciola hepatica is the most widespread causative agent of fasciolosis, a parasitic disease that mainly affects humans and ruminants worldwide. During F. hepatica infection, newly excysted juveniles (FhNEJ) emerge in the duodenum of the mammalian host and migrate towards their definitive location, the intra-hepatic biliary ducts. Understanding how F. hepatica traverses the intestinal wall and migrates towards the liver is pivotal for the development of more successful strategies against fasciolosis. The central enzyme of the mammalian fibrinolytic system is plasmin, a serine protease whose functions are exploited by a number of parasite species owing to its broad spectrum of substrates, including components of tissue extracellular matrices. The aim of the present work is to understand whether FhNEJ co-opt the functions of their host fibrinolytic system as a mechanism to facilitate trans-intestinal migration. METHODOLOGY/PRINCIPAL FINDINGS: A tegument-enriched antigenic extract of FhNEJ (FhNEJ-Teg) was obtained in vitro, and its capability to bind the zymogen plasminogen (PLG) and enhance its conversion to the active protease, plasmin, were analyzed by a combination of enzyme-linked immunosorbent, chromogenic and immunofluorescence assays. Additionally, PLG-binding proteins in FhNEJ-Teg were identified by bidimensional electrophoresis coupled to mass spectrometry analysis, and the interactions were validated using FhNEJ recombinant proteins. CONCLUSIONS/SIGNIFICANCE: Our results show that FhNEJ-Teg contains proteins that bind PLG and stimulate its activation to plasmin, which could facilitate the traversal of the intestinal wall by FhNEJ and contribute to the successful establishment of the parasite within its mammalian host. Altogether, our findings contribute to a better understanding of host-parasite relationships during early fasciolosis and may be exploited from a pharmacological and/or immunological perspective for the development of treatment and control strategies against this global disease. Public Library of Science 2023-04-21 /pmc/articles/PMC10155961/ /pubmed/37083884 http://dx.doi.org/10.1371/journal.pntd.0010936 Text en © 2023 Serrat et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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
Serrat, Judit
Becerro-Recio, David
Torres-Valle, María
Simón, Fernando
Valero, María Adela
Bargues, María Dolores
Mas-Coma, Santiago
Siles-Lucas, Mar
González-Miguel, Javier
Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism
title Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism
title_full Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism
title_fullStr Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism
title_full_unstemmed Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism
title_short Fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism
title_sort fasciola hepatica juveniles interact with the host fibrinolytic system as a potential early-stage invasion mechanism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155961/
https://www.ncbi.nlm.nih.gov/pubmed/37083884
http://dx.doi.org/10.1371/journal.pntd.0010936
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