Affiliation:
1. School of Biological Sciences University of California San Diego La Jolla California
Abstract
AbstractOrsay virus infection in the nematode Caenorhabditis elegans presents an opportunity to study host‐virus interactions in an easily culturable, whole‐animal host. Previously, a major limitation of C. elegans as a model for studying antiviral immunity was the lack of viruses known to naturally infect the worm. With the 2011 discovery of the Orsay virus, a naturally occurring viral pathogen, C. elegans has emerged as a compelling model for research on antiviral defense. From the perspective of the host, the genetic tractability of C. elegans enables mechanistic studies of antiviral immunity while the transparency of this animal allows for the observation of subcellular processes in vivo. Preparing infective virus filtrate and performing infections can be achieved with relative ease in a laboratory setting. Moreover, several tools are available to measure the outcome of infection. Here, we describe workflows for generating infective virus filtrate, achieving reproducible infection of C. elegans, and assessing the outcome of viral infection using molecular biology approaches and immunofluorescence. © 2024 The Authors. Current Protocols published by Wiley Periodicals LLC.Basic Protocol 1: Preparation of Orsay virus filtrateSupport Protocol: Synchronize C. elegans development by bleachingBasic Protocol 2: Orsay virus infectionBasic Protocol 3: Quantification of Orsay virus RNA1/RNA2 transcript levels by qRT‐PCRBasic Protocol 4: Quantification of infection rate and fluorescence in situ hybridization (FISH) fluorescence intensityBasic Protocol 5: Immunofluorescent labeling of dsRNA in virus‐infected intestinal tissue
Funder
National Institutes of Health
National Science Foundation
Deutsche Forschungsgemeinschaft