Murine Norovirus: Additional Protocols for Basic and Antiviral Studies

Author:

Wobus Christiane E.1,Peiper Amy M.2,McSweeney Alice M.3,Young Vivienne L.3,Chaika Maryna4,Lane Miranda Sophie4,Lingemann Marit4,Deerain Joshua M.5,Strine Madison S.6,Alfajaro Mia Madel6,Helm Emily W.2,Karst Stephanie M.2,Mackenzie Jason M.5,Taube Stefan4,Ward Vernon K.3,Wilen Craig B.6

Affiliation:

1. Department of Microbiology and Immunology University of Michigan Ann Arbor Michigan

2. Department of Molecular Genetics & Microbiology University of Florida Gainesville Florida

3. Department of Microbiology & Immunology University of Otago Dunedin New Zealand

4. Institute of Virology and Cell Biology University of Lübeck Lübeck Germany

5. Department of Microbiology and Immunology University of Melbourne Melbourne Australia

6. Departments of Immunobiology and Laboratory Medicine Yale University School of Medicine New Haven Connecticut

Abstract

AbstractMurine norovirus (MNV) is a positive‐sense, plus‐stranded RNA virus in the Caliciviridae family. Viruses in this family replicate in the intestine and are transmitted by the fecal‐oral route. MNV is related to the human noroviruses, which cause the majority of nonbacterial gastroenteritis worldwide. Given the technical challenges in studying human norovirus, MNV is often used to study mechanisms in norovirus biology since it combines the availability of a cell culture and reverse genetics system with the ability to study infection in the native host. Adding to our previous protocol collection, here we describe additional techniques that have since been developed to study MNV biology. © 2023 The Authors. Current Protocols published by Wiley Periodicals LLC.Basic Protocol 1: Indirect method for measuring cell cytotoxicity and antiviral activityBasic Protocol 2: Measuring murine norovirus genome titers by RT‐qPCRSupport Protocol 1: Preparation of standardBasic Protocol 3: Generation of recombinant murine norovirus with minimal passagingBasic Protocol 4: Generation of recombinant murine norovirus via circular polymerase extension reaction (CPER)Basic Protocol 5: Expression of norovirus NS1‐2 in insect cell suspension cultures using a recombinant baculovirusSupport Protocol 2: Isotope labelling of norovirus NS1‐2 in insect cellsSupport Protocol 3: Purification of the norovirus NS1‐2 proteinSupport Protocol 4: Expression of norovirus NS1‐2 in mammalian cells by transduction with a recombinant baculovirusBasic Protocol 6: Infection of enteroids in transwell inserts with murine norovirusSupport Protocol 5: Preparation of conditioned medium for enteroids cultureSupport Protocol 6: Isolation of crypts for enteroids generationSupport Protocol 7: Enteroid culture passaging and maintenanceBasic Protocol 7: Quantification of murine norovirus‐induced diarrhea using neonatal mouse infectionsAlternate Protocol 1: Intragastric inoculation of neonatal miceAlternate Protocol 2: Scoring colon contents

Publisher

Wiley

Subject

Medical Laboratory Technology,Health Informatics,General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Neuroscience

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