A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity

Background: In order to promote infection, the blood-borne parasite Trypanosoma brucei releases factors that upregulate arginase expression and activity in myeloid cells. Methodology/Principal findings: By screening a cDNA library of T. brucei with an antibody neutralizing the arginaseinducing activity of parasite released factors, we identified a Kinesin Heavy Chain isoform, termed TbKHC1, as responsible for this effect. Following interaction with mouse myeloid cells, natural or recombinant TbKHC1 triggered SIGN-R1 receptordependent induction of IL-10 production, resulting in arginase-1 activation concomitant with reduction of nitric oxide (NO) synthase activity. This TbKHC1 activity was IL-4Ra-independent and did not mirror M2 activation of myeloid cells. As compared to wild-type T. brucei, infection by TbKHC1 KO parasites was characterized by strongly reduced parasitaemia and prolonged host survival time. By treating infected mice with ornithine or with NO synthase inhibitor, we observed that during the first wave of parasitaemia the parasite growth-promoting effect of TbKHC1-mediated arginase activation resulted more from increased polyamine production than from reduction of NO synthesis. In late stage infection, TbKHC1- mediated reduction of NO synthesis appeared to contribute to liver damage linked to shortening of host survival time. Conclusion: A kinesin heavy chain released by T. brucei induces IL-10 and arginase-1 through SIGN-R1 signaling in myeloid cells, which promotes early trypanosome growth and favors parasite settlement in the host. Moreover, in the late stage of infection, the inhibition of NO synthesis by TbKHC1 contributes to liver pathogenicity.

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Main Authors: De Muylder, Géraldine, Daulouède, Sylvie, Lecordier, Laurence, Uzureau, Pierrick, Morias, Yannick, Van Den Abbeele, Jan, Caljon, Guy, Hérin, Michel, Holzmuller, Philippe, Semballa, Silla, Courtois, Pierrette, Vanhamme, Luc, Stijlemans, Benoît, De Baetselier, Patrick, Barrett, Michael P., Barlow, Jilian L., McKenzie, Andrew N.J., Barron, Luke, Wynn, Thomas A., Beschin, Alain, Vincendeau, Philippe, Pays, Etienne
Format: article biblioteca
Language:eng
Published: PLOS
Subjects:L73 - Maladies des animaux, L72 - Organismes nuisibles des animaux,
Online Access:http://agritrop.cirad.fr/571659/
http://agritrop.cirad.fr/571659/1/document_571659.pdf
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spelling dig-cirad-fr-5716592024-12-19T12:33:34Z http://agritrop.cirad.fr/571659/ http://agritrop.cirad.fr/571659/ A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity. De Muylder Géraldine, Daulouède Sylvie, Lecordier Laurence, Uzureau Pierrick, Morias Yannick, Van Den Abbeele Jan, Caljon Guy, Hérin Michel, Holzmuller Philippe, Semballa Silla, Courtois Pierrette, Vanhamme Luc, Stijlemans Benoît, De Baetselier Patrick, Barrett Michael P., Barlow Jilian L., McKenzie Andrew N.J., Barron Luke, Wynn Thomas A., Beschin Alain, Vincendeau Philippe, Pays Etienne. 2013. PLoS Pathogens, 9 (10):e1003731, 14 p.https://doi.org/10.1371/journal.ppat.1003731 <https://doi.org/10.1371/journal.ppat.1003731> A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity De Muylder, Géraldine Daulouède, Sylvie Lecordier, Laurence Uzureau, Pierrick Morias, Yannick Van Den Abbeele, Jan Caljon, Guy Hérin, Michel Holzmuller, Philippe Semballa, Silla Courtois, Pierrette Vanhamme, Luc Stijlemans, Benoît De Baetselier, Patrick Barrett, Michael P. Barlow, Jilian L. McKenzie, Andrew N.J. Barron, Luke Wynn, Thomas A. Beschin, Alain Vincendeau, Philippe Pays, Etienne eng 2013 PLOS PLoS Pathogens L73 - Maladies des animaux L72 - Organismes nuisibles des animaux Background: In order to promote infection, the blood-borne parasite Trypanosoma brucei releases factors that upregulate arginase expression and activity in myeloid cells. Methodology/Principal findings: By screening a cDNA library of T. brucei with an antibody neutralizing the arginaseinducing activity of parasite released factors, we identified a Kinesin Heavy Chain isoform, termed TbKHC1, as responsible for this effect. Following interaction with mouse myeloid cells, natural or recombinant TbKHC1 triggered SIGN-R1 receptordependent induction of IL-10 production, resulting in arginase-1 activation concomitant with reduction of nitric oxide (NO) synthase activity. This TbKHC1 activity was IL-4Ra-independent and did not mirror M2 activation of myeloid cells. As compared to wild-type T. brucei, infection by TbKHC1 KO parasites was characterized by strongly reduced parasitaemia and prolonged host survival time. By treating infected mice with ornithine or with NO synthase inhibitor, we observed that during the first wave of parasitaemia the parasite growth-promoting effect of TbKHC1-mediated arginase activation resulted more from increased polyamine production than from reduction of NO synthesis. In late stage infection, TbKHC1- mediated reduction of NO synthesis appeared to contribute to liver damage linked to shortening of host survival time. Conclusion: A kinesin heavy chain released by T. brucei induces IL-10 and arginase-1 through SIGN-R1 signaling in myeloid cells, which promotes early trypanosome growth and favors parasite settlement in the host. Moreover, in the late stage of infection, the inhibition of NO synthesis by TbKHC1 contributes to liver pathogenicity. article info:eu-repo/semantics/article Journal Article info:eu-repo/semantics/publishedVersion http://agritrop.cirad.fr/571659/1/document_571659.pdf application/pdf Cirad license info:eu-repo/semantics/openAccess https://agritrop.cirad.fr/mention_legale.html https://doi.org/10.1371/journal.ppat.1003731 10.1371/journal.ppat.1003731 info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.ppat.1003731 info:eu-repo/semantics/altIdentifier/purl/https://doi.org/10.1371/journal.ppat.1003731
institution CIRAD FR
collection DSpace
country Francia
countrycode FR
component Bibliográfico
access En linea
databasecode dig-cirad-fr
tag biblioteca
region Europa del Oeste
libraryname Biblioteca del CIRAD Francia
language eng
topic L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
spellingShingle L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
De Muylder, Géraldine
Daulouède, Sylvie
Lecordier, Laurence
Uzureau, Pierrick
Morias, Yannick
Van Den Abbeele, Jan
Caljon, Guy
Hérin, Michel
Holzmuller, Philippe
Semballa, Silla
Courtois, Pierrette
Vanhamme, Luc
Stijlemans, Benoît
De Baetselier, Patrick
Barrett, Michael P.
Barlow, Jilian L.
McKenzie, Andrew N.J.
Barron, Luke
Wynn, Thomas A.
Beschin, Alain
Vincendeau, Philippe
Pays, Etienne
A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity
description Background: In order to promote infection, the blood-borne parasite Trypanosoma brucei releases factors that upregulate arginase expression and activity in myeloid cells. Methodology/Principal findings: By screening a cDNA library of T. brucei with an antibody neutralizing the arginaseinducing activity of parasite released factors, we identified a Kinesin Heavy Chain isoform, termed TbKHC1, as responsible for this effect. Following interaction with mouse myeloid cells, natural or recombinant TbKHC1 triggered SIGN-R1 receptordependent induction of IL-10 production, resulting in arginase-1 activation concomitant with reduction of nitric oxide (NO) synthase activity. This TbKHC1 activity was IL-4Ra-independent and did not mirror M2 activation of myeloid cells. As compared to wild-type T. brucei, infection by TbKHC1 KO parasites was characterized by strongly reduced parasitaemia and prolonged host survival time. By treating infected mice with ornithine or with NO synthase inhibitor, we observed that during the first wave of parasitaemia the parasite growth-promoting effect of TbKHC1-mediated arginase activation resulted more from increased polyamine production than from reduction of NO synthesis. In late stage infection, TbKHC1- mediated reduction of NO synthesis appeared to contribute to liver damage linked to shortening of host survival time. Conclusion: A kinesin heavy chain released by T. brucei induces IL-10 and arginase-1 through SIGN-R1 signaling in myeloid cells, which promotes early trypanosome growth and favors parasite settlement in the host. Moreover, in the late stage of infection, the inhibition of NO synthesis by TbKHC1 contributes to liver pathogenicity.
format article
topic_facet L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
author De Muylder, Géraldine
Daulouède, Sylvie
Lecordier, Laurence
Uzureau, Pierrick
Morias, Yannick
Van Den Abbeele, Jan
Caljon, Guy
Hérin, Michel
Holzmuller, Philippe
Semballa, Silla
Courtois, Pierrette
Vanhamme, Luc
Stijlemans, Benoît
De Baetselier, Patrick
Barrett, Michael P.
Barlow, Jilian L.
McKenzie, Andrew N.J.
Barron, Luke
Wynn, Thomas A.
Beschin, Alain
Vincendeau, Philippe
Pays, Etienne
author_facet De Muylder, Géraldine
Daulouède, Sylvie
Lecordier, Laurence
Uzureau, Pierrick
Morias, Yannick
Van Den Abbeele, Jan
Caljon, Guy
Hérin, Michel
Holzmuller, Philippe
Semballa, Silla
Courtois, Pierrette
Vanhamme, Luc
Stijlemans, Benoît
De Baetselier, Patrick
Barrett, Michael P.
Barlow, Jilian L.
McKenzie, Andrew N.J.
Barron, Luke
Wynn, Thomas A.
Beschin, Alain
Vincendeau, Philippe
Pays, Etienne
author_sort De Muylder, Géraldine
title A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity
title_short A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity
title_full A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity
title_fullStr A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity
title_full_unstemmed A Trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity
title_sort trypanosoma brucei kinesin heavy chain promotes parasite growth by triggering host arginase activity
publisher PLOS
url http://agritrop.cirad.fr/571659/
http://agritrop.cirad.fr/571659/1/document_571659.pdf
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