Programmed −2/−1 Ribosomal Frameshifting in Simarteriviruses: an Evolutionarily Conserved Mechanism

Author:

Li Yanhua12,Firth Andrew E.2ORCID,Brierley Ian2,Cai Yingyun3,Napthine Sawsan2,Wang Tao14,Yan Xingyu1,Kuhn Jens H.3,Fang Ying1

Affiliation:

1. Department of Diagnostic Medicine and Pathobiology, Kansas State University, Manhattan, Kansas, USA

2. Division of Virology, Department of Pathology, University of Cambridge, Cambridge, United Kingdom

3. Integrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Frederick, Maryland, USA

4. Yangzhou University, Yangzhou, People’s Republic of China

Abstract

Simarteriviruses are a group of arteriviruses infecting nonhuman primates, and a number of new species have been established in recent years. Although these arteriviruses are widely distributed among African nonhuman primates of different species, and some of them cause lethal hemorrhagic fever disease, this group of viruses has been undercharacterized. Since wild nonhuman primates are historically important sources or reservoirs of human pathogens, there is concern that simarteriviruses may be preemergent zoonotic pathogens. Thus, molecular characterization of simarteriviruses is becoming a priority in arterivirology. In this study, we demonstrated that an evolutionarily conserved ribosomal frameshifting mechanism is used by simarteriviruses and other distantly related arteriviruses for the expression of additional viral proteins. This mechanism is unprecedented in eukaryotic systems. Given the crucial role of ribosome function in all living systems, the potential impact of the in-depth characterization of this novel mechanism reaches beyond the field of virology.

Funder

Wellcome Trust

European Research Council

HHS | NIH | National Institute of Allergy and Infectious Diseases

U.S. Department of Agriculture

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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