Deletion of MGF505-2R Gene Activates the cGAS-STING Pathway Leading to Attenuation and Protection against Virulent African Swine Fever Virus

Author:

Sunwoo Sun-Young1ORCID,García-Belmonte Raquel2,Walczak Marek3ORCID,Vigara-Astillero Gonzalo2ORCID,Kim Dae-Min4ORCID,Szymankiewicz Krzesimir3ORCID,Kochanowski Maciej3ORCID,Liu Lihong5,Tark Dongseob4ORCID,Podgórska Katarzyna3ORCID,Revilla Yolanda2,Pérez-Núñez Daniel2ORCID

Affiliation:

1. Careside Co., Ltd., Sagimakgol-ro 45 Beongil 14, Seongnam-si 13209, Gyeonggi-do, Republic of Korea

2. Microbes in Health and Welfare Department, Centro de Biologia Molecular Severo Ochoa (CBM), CSIC-UAM, c/Nicolás Cabrera 1, 28049 Madrid, Spain

3. Department of Swine Diseases, National Veterinary Research Institute, 57 Partyzantów Avenue, 24-100 Pulawy, Poland

4. Laboratory for Infectious Disease Prevention, Korea Zoonosis Research Institute, Jeonbuk National University, 79 Gobong-ro, Ma-dong, Iksan 54531, Jeollabuk-do, Republic of Korea

5. Department of Microbiology, Swedish Veterinary Agency, 751 89 Uppsala, Sweden

Abstract

African swine fever virus (ASFV) is the etiological agent causing African swine fever (ASF), affecting domestic pigs and wild boar, which is currently the biggest animal epidemic in the world and a major threat to the swine sector. At present, some safety concerns about using LAVs against ASFV still exist despite a commercial vaccine licensed in Vietnam. Therefore, the efforts to identify virulence factors and their mechanisms, as well as to generate new vaccine prototypes, are of major interest. In this work, we have identified the MGF505-2R gene product as an inhibitor of the cGAS/STING pathway, specifically through its interaction with STING protein, controlling IFN-β production. In addition, immunization of a recombinant virus lacking this gene, Arm/07-ΔMGF505-2R, resulted in complete attenuation, demonstrating its involvement in ASFV virulence. Finally, immunization with Arm/07-ΔMGF505-2R induced the generation of antibodies and proved to be partially protective against virulent ASFV strains. These results identify MGF505-2R, as well as its mechanism of action, as a gene contributing to understanding the molecular mechanisms of ASFV virulence, which will be of great value in the design of future vaccine prototypes.

Funder

Agencia Estatal Investigación”

National Centre for Research and Development

Careside Co., Ltd.

Publisher

MDPI AG

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