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Caenorhabditis elegans immune responses to microsporidia and viruses.
González, Rubén; Félix, Marie-Anne.
Afiliación
  • González R; Institut de Biologie de l'École Normale Supérieure, CNRS, INSERM, 75005, Paris, France. Electronic address: ruben.gonzalez@bio.ens.psl.eu.
  • Félix MA; Institut de Biologie de l'École Normale Supérieure, CNRS, INSERM, 75005, Paris, France.
Dev Comp Immunol ; 154: 105148, 2024 May.
Article en En | MEDLINE | ID: mdl-38325500
ABSTRACT
The model organism Caenorhabditis elegans is susceptible to infection by obligate intracellular pathogens, specifically microsporidia and viruses. These intracellular pathogens infect intestinal cells, or, for some microsporidia, epidermal cells. Strikingly, intestinal cell infections by viruses or microsporidia trigger a common transcriptional response, activated in part by the ZIP-1 transcription factor. Among the strongest activated genes in this response are ubiquitin-pathway members and members of the pals family, an intriguing gene family with cross-regulations of different members of genomic clusters. Some of the induced genes participate in host defense against the pathogens, for example through ubiquitin-mediated inhibition. Other mechanisms defend the host specifically against viral infections, including antiviral RNA interference and uridylation. These various immune responses are altered by environmental factors and by intraspecific genetic variation of the host. These pathogens were first isolated 15 years ago and much remains to be discovered using C. elegans genetics; also, other intracellular pathogens of C. elegans may yet to be discovered.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus / Microsporidios / Proteínas de Caenorhabditis elegans Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Dev Comp Immunol Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus / Microsporidios / Proteínas de Caenorhabditis elegans Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Dev Comp Immunol Año: 2024 Tipo del documento: Article
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