Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 1 de 1
Filtrer
Plus de filtres










Base de données
Gamme d'année
1.
Nat Commun ; 14(1): 1456, 2023 03 16.
Article de Anglais | MEDLINE | ID: mdl-36928642

RÉSUMÉ

Cryptosporidium infects gastrointestinal epithelium and is a leading cause of infectious diarrhea and diarrheal-related death in children worldwide. There are no vaccines and no fully effective therapy available for the infection. Type II and III interferon (IFN) responses are important determinants of susceptibility to infection but the role for type I IFN response remains obscure. Cryptosporidium parvum virus 1 (CSpV1) is a double-stranded RNA (dsRNA) virus harbored by Cryptosporidium spp. Here we show that intestinal epithelial conditional Ifnar1-/- mice (deficient in type I IFN receptor) are resistant to C. parvum infection. CSpV1-dsRNAs are delivered into host cells and trigger type I IFN response in infected cells. Whereas C. parvum infection attenuates epithelial response to IFN-γ, loss of type I IFN signaling or inhibition of CSpV1-dsRNA delivery can restore IFN-γ-mediated protective response. Our findings demonstrate that type I IFN signaling in intestinal epithelial cells is detrimental to intestinal anti-C. parvum defense and Cryptosporidium uses CSpV1 to activate type I IFN signaling to evade epithelial antiparasitic response.


Sujet(s)
Cryptosporidiose , Cryptosporidium parvum , Interactions hôte-parasite , Interféron de type I , Animaux , Souris , Antiparasitaires/métabolisme , Antiparasitaires/pharmacologie , Cryptosporidiose/étiologie , Cryptosporidiose/parasitologie , Cryptosporidiose/virologie , Cryptosporidium/pathogénicité , Cryptosporidium/virologie , Cryptosporidium parvum/pathogénicité , Cryptosporidium parvum/virologie , Interactions hôte-parasite/génétique , Interféron de type I/métabolisme , Interféron de type I/pharmacologie , Virus à ARN double brin/métabolisme
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE