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Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association

Trypanosomatid parasites are significant causes of human disease and are ubiquitous in insects. Despite the importance of Drosophila melanogaster as a model of infection and immunity and a long awareness that trypanosomatid infection is common in the genus, no trypanosomatid parasites naturally infe...

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Autores principales: Hamilton, Phineas T., Votýpka, Jan, Dostálová, Anna, Yurchenko, Vyacheslav, Bird, Nathan H., Lukeš, Julius, Lemaitre, Bruno, Perlman, Steve J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600116/
https://www.ncbi.nlm.nih.gov/pubmed/26374124
http://dx.doi.org/10.1128/mBio.01356-15
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author Hamilton, Phineas T.
Votýpka, Jan
Dostálová, Anna
Yurchenko, Vyacheslav
Bird, Nathan H.
Lukeš, Julius
Lemaitre, Bruno
Perlman, Steve J.
author_facet Hamilton, Phineas T.
Votýpka, Jan
Dostálová, Anna
Yurchenko, Vyacheslav
Bird, Nathan H.
Lukeš, Julius
Lemaitre, Bruno
Perlman, Steve J.
author_sort Hamilton, Phineas T.
collection PubMed
description Trypanosomatid parasites are significant causes of human disease and are ubiquitous in insects. Despite the importance of Drosophila melanogaster as a model of infection and immunity and a long awareness that trypanosomatid infection is common in the genus, no trypanosomatid parasites naturally infecting Drosophila have been characterized. Here, we establish a new model of trypanosomatid infection in Drosophila—Jaenimonas drosophilae, gen. et sp. nov. As far as we are aware, this is the first Drosophila-parasitic trypanosomatid to be cultured and characterized. Through experimental infections, we find that Drosophila falleni, the natural host, is highly susceptible to infection, leading to a substantial decrease in host fecundity. J. drosophilae has a broad host range, readily infecting a number of Drosophila species, including D. melanogaster, with oral infection of D. melanogaster larvae resulting in the induction of numerous immune genes. When injected into adult hemolymph, J. drosophilae kills D. melanogaster, although interestingly, neither the Imd nor the Toll pathway is induced and Imd mutants do not show increased susceptibility to infection. In contrast, mutants deficient in drosocrystallin, a major component of the peritrophic matrix, are more severely infected during oral infection, suggesting that the peritrophic matrix plays an important role in mediating trypanosomatid infection in Drosophila. This work demonstrates that the J. drosophilae-Drosophila system can be a powerful model to uncover the effects of trypanosomatids in their insect hosts.
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spelling pubmed-46001162015-10-12 Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association Hamilton, Phineas T. Votýpka, Jan Dostálová, Anna Yurchenko, Vyacheslav Bird, Nathan H. Lukeš, Julius Lemaitre, Bruno Perlman, Steve J. mBio Research Article Trypanosomatid parasites are significant causes of human disease and are ubiquitous in insects. Despite the importance of Drosophila melanogaster as a model of infection and immunity and a long awareness that trypanosomatid infection is common in the genus, no trypanosomatid parasites naturally infecting Drosophila have been characterized. Here, we establish a new model of trypanosomatid infection in Drosophila—Jaenimonas drosophilae, gen. et sp. nov. As far as we are aware, this is the first Drosophila-parasitic trypanosomatid to be cultured and characterized. Through experimental infections, we find that Drosophila falleni, the natural host, is highly susceptible to infection, leading to a substantial decrease in host fecundity. J. drosophilae has a broad host range, readily infecting a number of Drosophila species, including D. melanogaster, with oral infection of D. melanogaster larvae resulting in the induction of numerous immune genes. When injected into adult hemolymph, J. drosophilae kills D. melanogaster, although interestingly, neither the Imd nor the Toll pathway is induced and Imd mutants do not show increased susceptibility to infection. In contrast, mutants deficient in drosocrystallin, a major component of the peritrophic matrix, are more severely infected during oral infection, suggesting that the peritrophic matrix plays an important role in mediating trypanosomatid infection in Drosophila. This work demonstrates that the J. drosophilae-Drosophila system can be a powerful model to uncover the effects of trypanosomatids in their insect hosts. American Society of Microbiology 2015-09-15 /pmc/articles/PMC4600116/ /pubmed/26374124 http://dx.doi.org/10.1128/mBio.01356-15 Text en Copyright © 2015 Hamilton et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hamilton, Phineas T.
Votýpka, Jan
Dostálová, Anna
Yurchenko, Vyacheslav
Bird, Nathan H.
Lukeš, Julius
Lemaitre, Bruno
Perlman, Steve J.
Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association
title Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association
title_full Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association
title_fullStr Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association
title_full_unstemmed Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association
title_short Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association
title_sort infection dynamics and immune response in a newly described drosophila-trypanosomatid association
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4600116/
https://www.ncbi.nlm.nih.gov/pubmed/26374124
http://dx.doi.org/10.1128/mBio.01356-15
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