Tick-transmitted thogotovirus gains high virulence by a single MxA escape mutation in the viral nucleoprotein

• Published in: PLoS pathogens 2020-11, Vol.16 (11), p.e1009038
• Main Authors: Fuchs, Jonas, Oschwald, Alexander, Graf, Laura, Kochs, Georg
• Format: Article
• Language: English
• Subjects: Amino Acid Substitution; Analysis; Animals; Antiviral Agents; Arachnids; Biology and life sciences; Chlorocebus aethiops; Control; Diagnosis; Humans; Impact analysis; In vivo methods and tests; Infections; Influenza; Loci; Measurement; Medicine and Health Sciences; Mice; Mice, Transgenic; Microbial mutation; Mutation; Myxovirus resistance proteins; Myxovirus Resistance Proteins - genetics; Myxovirus Resistance Proteins - metabolism; Nucleoproteins; Nucleoproteins - genetics; Nucleoproteins - metabolism; Orthomyxoviridae Infections - transmission; Orthomyxoviridae Infections - virology; Research and analysis methods; RNA viruses; Statistical analysis; Thogotovirus - genetics; Thogotovirus - pathogenicity; Thogotovirus - physiology; Tick-borne diseases; Ticks - virology; Transgenic animals; Transgenic mice; Variance analysis; Vero Cells; Viral Proteins - genetics; Viral Proteins - metabolism; Virulence; Virulence (Microbiology); Viruses; Zoonoses
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1009038

Infections with emerging and re-emerging arboviruses are of increasing concern for global health. Tick-transmitted RNA viruses of the genus Thogotovirus in the Orthomyxoviridae family have considerable zoonotic potential, as indicated by the recent emergence of Bourbon virus in the USA. To successfully infect humans, arboviruses have to escape the restrictive power of the interferon defense system. This is exemplified by the high sensitivity of thogotoviruses to the antiviral action of the interferon-induced myxovirus resistance protein A (MxA) that inhibits the polymerase activity of incoming viral ribonucleoprotein complexes. Acquiring resistance to human MxA would be expected to enhance the zoonotic potential of these pathogens. Therefore, we screened a panel of 10 different thogotovirus isolates obtained from various parts of the world for their sensitivity to MxA. A single isolate from Nigeria, Jos virus, showed resistance to the antiviral action of MxA in cell culture and in MxA-transgenic mice, whereas the prototypic Sicilian isolate SiAr126 was fully MxA-sensitive. Further analysis identified two amino acid substitutions (G327R and R328V) in the viral nucleoprotein as determinants for MxA resistance. Importantly, when introduced into SiAr126, the R328V mutation resulted in complete MxA escape of the recombinant virus, without causing any viral fitness loss. The escape mutation abolished viral nucleoprotein recognition by MxA and allowed unhindered viral growth in MxA-expressing cells and in MxA-transgenic mice. These findings demonstrate that thogotoviruses can overcome the species barrier by escaping MxA restriction and reveal that these tick-transmitted viruses may have a greater zoonotic potential than previously suspected.