Hendra virus genotypes 1 and 2 differ in V protein-mediated immune evasion

Hendra virus (HeV) is a highly pathogenic virus endemic to Australia that causes lethal infections in horses and humans following spillover from bat reservoirs. There are two known genotypes: genotype 1 and 2 (HeV-g1 and HeV-g2). Both have caused lethal disease in horses, but HeV-g1 causes a more severe disease than HeV-g2 in non-human primates. The molecular mechanisms underlying these differences are poorly understood. The capacity of viruses to evade the interferon (IFN)-mediated antiviral innate immune response is important in infection and disease, and in HeV, the virulence factor V protein is a key mediator and one of the most divergent proteins between the genotypes. We compared the IFN antagonist functions of the V proteins of HeV-g1 and HeV-g2, finding that HeV-g1-V was more potent than HeV-g2-V in antagonizing the induction of type-I IFN; we further found that the proteins differ in nucleocytoplasmic localization. Consistent with these findings, HeV-g1 suppressed type-I IFN production more effectively than HeV-g2 during infection. These data reveal differences in the fundamental biology of HeV genotypes, which may be significant to pathogenesis.

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Publication Details

Journal
Journal of General Virology
Published
2026-04-21
DOI
https://doi.org/10.1099/jgv.0.002256
Primary Topic
Virology and Viral Diseases
Type
article
Field-Weighted Citation Impact
0.00

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article

Hendra virus genotypes 1 and 2 differ in V protein-mediated immune evasion

Stephen M. Rawlinson, Glenn A. Marsh, Kim Halpin, Gregory W. Moseley et al.
Journal of General Virology
Virology and Viral Diseases
article

Hendra virus genotypes 1 and 2 differ in V protein-mediated immune evasion

Stephen M. Rawlinson, Glenn A. Marsh, Kim Halpin, Gregory W. Moseley, Sarah J. Edwards, Melanie N. Tripp, Cassandra T. David
article en

Abstract

Hendra virus (HeV) is a highly pathogenic virus endemic to Australia that causes lethal infections in horses and humans following spillover from bat reservoirs. There are two known genotypes: genotype 1 and 2 (HeV-g1 and HeV-g2). Both have caused lethal disease in horses, but HeV-g1 causes a more severe disease than HeV-g2 in non-human primates. The molecular mechanisms underlying these differences are poorly understood. The capacity of viruses to evade the interferon (IFN)-mediated antiviral innate immune response is important in infection and disease, and in HeV, the virulence factor V protein is a key mediator and one of the most divergent proteins between the genotypes. We compared the IFN antagonist functions of the V proteins of HeV-g1 and HeV-g2, finding that HeV-g1-V was more potent than HeV-g2-V in antagonizing the induction of type-I IFN; we further found that the proteins differ in nucleocytoplasmic localization. Consistent with these findings, HeV-g1 suppressed type-I IFN production more effectively than HeV-g2 during infection. These data reveal differences in the fundamental biology of HeV genotypes, which may be significant to pathogenesis.

Journal of General VirologyVol. 107(4)
Commonwealth Scientific and Industrial Research Organisation (AU), Australian Centre for Disease Preparedness (AU), Australian Regenerative Medicine Institute (AU), Australian e-Health Research Centre (AU), Monash University (AU)
Australian Research Council, National Health and Medical Research Council
Openalex Percentile: Top 10%
Virology and Viral Diseases
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