Development of reverse genetics system for Guanarito virus: substitution of E1497K in the L protein of Guanarito virus S-26764 strain changes plaque phenotype and growth kinetics

Author:

Taniguchi Satoshi12ORCID,Maruyama Junki1ORCID,Saito Takeshi1,Littlefield Kirsten3,Reyna Rachel A.1ORCID,Manning John T.1,Huang Cheng1ORCID,Saijo Masayuki2ORCID,Paessler Slobodan1ORCID

Affiliation:

1. Department of Pathology, University of Texas Medical Branch, Galveston, Texas, USA

2. Department of Virology I, National Institute of Infectious Diseases, Shinjuku-ku, Tokyo, Japan

3. Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, Texas, USA

Abstract

Guanarito virus (GTOV) is a rodent-borne virus. GTOV causes fever, prostration, headache, arthralgia, cough, sore throat, nausea, vomiting, diarrhea, epistaxis, bleeding gums, menorrhagia, and melena in humans. The lethality rate is 23.1% or higher. Vero cell-adapted GTOV S-26764 shows a clear cytopathic effect (CPE), whereas the parental virus shows unclear CPE in Vero cells. We generated a reverse genetics system to rescue recombinant GTOVs and found that E1497K in the L protein was responsible for the formation of clear plaques as well as enhanced viral RNA replication and transcription efficiency. This reverse genetic system will accelerate vaccine and antiviral drug developments, and the findings of this study contribute to the understanding of the function of GTOV L as an RNA polymerase.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

John S. Dunn Foundation

HHS | U.S. Public Health Service

Publisher

American Society for Microbiology

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