Evaluation of the Function of ASFV Gene E66L in the Process of Virus Replication and Virulence in Swine

Author:

Ramirez-Medina Elizabeth1,Vuono Elizabeth A.1,Rai Ayushi12,Espinoza Nallely1,Valladares Alyssa12,Spinard Edward1,Velazquez-Salinas Lauro1,Gladue Douglas P.1ORCID,Borca Manuel V.1

Affiliation:

1. Plum Island Animal Disease Center, Agricultural Research Service, United States Department of Agriculture, Greenport, NY 11944, USA

2. Oak Ridge Institute for Science and Education (ORISE), Oak Ridge, TN 37830, USA

Abstract

African swine fever virus (ASFV) is the etiological agent of an economically important disease of swine currently affecting large areas of Africa, Eurasia and the Caribbean. ASFV has a complex structure harboring a large dsDNA genome which encodes for more than 160 proteins. One of the proteins, E66L, has recently been involved in arresting gene transcription in the infected host cell. Here, we investigate the role of E66L in the processes of virus replication in swine macrophages and disease production in domestic swine. A recombinant ASFV was developed (ASFV-G-∆E66L), from the virulent parental Georgia 2010 isolate (ASFV-G), harboring the deletion of the E66L gene as a tool to assess the role of the gene. ASFV-G-∆E66L showed that the E66L gene is non-essential for ASFV replication in primary swine macrophages when compared with the parental highly virulent field isolate ASFV-G. Additionally, domestic pigs infected with ASFV-G-∆E66L developed a clinical disease undistinguishable from that produced by ASFV-G. Therefore, E66L is not involved in virus replication or virulence in domestic pigs.

Funder

National Pork Board

Agriculture Research (ROAR) grant

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference42 articles.

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