Infection Dynamics and Immune Response in a Newly Described Drosophila-Trypanosomatid Association
Date
2015-09
Authors
Hamilton, Phineas
Votýpka, Jan
Dostálová, Anna
Yurchenko, Vyacheslav
Bird, Nathan
Lukeš, Julius
Lemaitre, Bruno
Perlman, Steve
Journal Title
Journal ISSN
Volume Title
Publisher
mBio
Abstract
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.
Description
Keywords
Citation
Hamilton, P.T. et al. (2015). Infection dynamics and immune response in a newly described Drosophila-trypanosomatid association. mBio, 6(5):e01356-15, 1-11. doi:10.1128/mBio.01356-15