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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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 |
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L73 - Maladies des animaux L72 - Organismes nuisibles des animaux L73 - Maladies des animaux L72 - Organismes nuisibles des animaux |
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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 |
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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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