Functional divergence of the Bhanja virus NSs protein modulates interferon antagonism and viral fitness across divergent lineages

@article{clarke2026functional,
  title = {{Functional divergence of the Bhanja virus NSs protein modulates interferon antagonism and viral fitness across divergent lineages}},
  author = {Andrew T. Clarke and Kelsey Davies and Mazigh Fares and Agnieszka M. Szemiel and Diogo Correa Mendonca and Karen Kerr and Vanessa Herder and Lesley Bell-Sakyi and Brian J. Willett and Arvind H. Patel and Alain Kohl and Benjamin Brennan},
  journal = {PLOS Pathogens},
  year = {2026},
  month = sep,
  doi = {10.1371/journal.ppat.1014645},
  url = {https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1014645},
  note = {CC BY 4.0},
}

TY  - JOUR
TI  - Functional divergence of the Bhanja virus NSs protein modulates interferon antagonism and viral fitness across divergent lineages
AU  - Andrew T. Clarke
AU  - Kelsey Davies
AU  - Mazigh Fares
AU  - Agnieszka M. Szemiel
AU  - Diogo Correa Mendonca
AU  - Karen Kerr
AU  - Vanessa Herder
AU  - Lesley Bell-Sakyi
AU  - Brian J. Willett
AU  - Arvind H. Patel
AU  - Alain Kohl
AU  - Benjamin Brennan
PY  - 2026
DA  - 2026/09/24
JO  - PLOS Pathogens
DO  - 10.1371/journal.ppat.1014645
UR  - https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1014645
AB  - Bhanja virus (BHAV) is a tick-borne bandavirus (Family Phenuiviridae) with a broad geographic distribution and documented neuroinvasive capacity, yet its molecular biology remains poorly understood. Within the genus Bandavirus, the non-structural protein NSs functions as the primary antagonist of innate immune responses, although mechanistic details for BHAV remain unknown. We established a reverse genetics platform for BHAV by combining virion RNA sequencing with terminal untranslated region mapping, enabling generation of recombinant viruses and systematic investigation of viral determinants. Using this system, we characterized recombinant BHAV replication in mammalian and arthropod cell lines and demonstrated that interferon competence is a critical determinant of viral replication in mammalian cells. Notably, we observed substantial amino acid divergence within the NSs protein across geographically distinct BHAV isolates, despite higher conservation of other viral proteins. To investigate the functional significance of this variation, we generated recombinant viruses expressing heterologous NSs proteins from African and European isolates. Viruses expressing NSs from ibAr2709 or R1819 isolates exhibited enhanced capacity to suppress interferon-beta induction compared to the prototype IG690 strain, correlating with increased viral protein accumulation in interferon-competent cells. Mechanistic studies revealed that BHAV NSs proteins inhibit interferon induction upstream of IRF3, with ibAr2709 and R1819 NSs showing selective inhibition of TBK1 phosphorylation. However, unlike highly pathogenic bandaviruses such as severe fever with thrombocytopenia syndrome virus (SFTSV), BHAV NSs proteins exhibit comparatively weak antagonism of downstream interferon signalling. In vivo studies using interferon alpha/beta receptor-deficient mice demonstrated that NSs sequence variation influences viral replication in splenic tissue without substantially altering disease phenotype. Together, these findings establish BHAV reverse genetics tools for future investigation and reveal how naturally-occurring NSs divergence modulates innate immune antagonism and viral fitness while maintaining an overall attenuated disease phenotype. Author summary: Bhanja virus is a tick-borne virus distributed across Asia, Africa, and Europe that causes neurological disease, yet little is known about how it replicates or evades immunity. We developed the laboratory tools to create recombinant Bhanja viruses and investigate viral functions. We discovered that the virus replicates efficiently in cells lacking interferon responses but is severely restricted in normal immune-competent cells, revealing interferon as a major barrier to viral growth. We observed that Bhanja virus isolates from distinct geographic regions have different versions of a viral protein called NSs that suppresses interferon responses. Isolates from Africa and Europe were better at blocking interferon production than the original Asian strain, correlating with increased viral growth in immune-competent cells. However, unlike related viruses that cause more serious disease such as SFTSV, BHAV NSs proteins only partially antagonise interferon. While this weak antagonism likely contributes to the attenuated phenotype observed in our experimental systems, the natural pathogenesis of Bhanja virus in human hosts and tick vectors remains to be determined. This study provides tools for examining Bhanja virus biology and demonstrates that small viral differences in viral sequence can meaningfully influence evasion of innate immunity and viral fitness without triggering severe disease.
SN  - 1553-7374
ER  -