Host JAK-STAT activity is a target of parasitoid wasp virulence strategies.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
01 Jul 2024
Historique:
received: 22 12 2023
accepted: 17 06 2024
medline: 1 7 2024
pubmed: 1 7 2024
entrez: 1 7 2024
Statut: aheadofprint

Résumé

Innate immune responses that allow hosts to survive infection depend on the action of multiple conserved signaling pathways. Pathogens and parasites in turn have evolved virulence factors to target these immune signaling pathways in an attempt to overcome host immunity. Consequently, the interactions between host immune molecules and pathogen virulence factors play an important role in determining the outcome of an infection. The immune responses of Drosophila melanogaster provide a valuable model to understand immune signaling and host-pathogen interactions. Flies are commonly infected by parasitoid wasps and mount a coordinated cellular immune response following infection. This response is characterized by the production of specialized blood cells called lamellocytes that form a tight capsule around wasp eggs in the host hemocoel. The conserved JAK-STAT signaling pathway has been implicated in lamellocyte proliferation and is required for successful encapsulation of wasp eggs. Here we show that activity of Stat92E, the D. melanogaster STAT ortholog, is induced in immune tissues following parasitoid infection. Virulent wasp species are able to suppress Stat92E activity during infection, suggesting they target JAK-STAT pathway activation as a virulence strategy. Furthermore, two wasp species (Leptopilina guineaensis and Ganaspis xanthopoda) suppress phenotypes associated with a gain-of-function mutation in hopscotch, the D. melanogaster JAK ortholog, indicating that they inhibit the activity of the core signaling components of the JAK-STAT pathway. Our data suggest that parasitoid wasp virulence factors block JAK-STAT signaling to overcome fly immune defenses.

Identifiants

pubmed: 38950076
doi: 10.1371/journal.ppat.1012349
pii: PPATHOGENS-D-23-02268
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1012349

Informations de copyright

Copyright: © 2024 Brantley et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Susanna E Brantley (SE)

Department of Cell Biology, Duke University Medical Center, Durham, North Carolina, United States of America.

Corinne M Stouthamer (CM)

Department of Entomology, University of Arizona, Tucson, Arizona, United States of America.

Pooja Kr (P)

School of Biological Sciences, Illinois State University, Normal, Illinois, United States of America.

Mary L Fischer (ML)

School of Biological Sciences, Illinois State University, Normal, Illinois, United States of America.

Joshua Hill (J)

School of Biological Sciences, Illinois State University, Normal, Illinois, United States of America.

Todd A Schlenke (TA)

Department of Entomology, University of Arizona, Tucson, Arizona, United States of America.

Nathan T Mortimer (NT)

School of Biological Sciences, Illinois State University, Normal, Illinois, United States of America.
Department of Biochemistry & Biophysics, Oregon State University, Corvallis, Oregon, United States of America.

Classifications MeSH