Specific T-cell subsets have a role in anti-viral immunity and pathogenesis but not viral dynamics or onwards vector transmission of an important livestock arbovirus.

INTRODUCTION

Bluetongue virus (BTV) is an arthropod-borne that is almost solely transmitted by biting midges and causes a globally important haemorrhagic disease, bluetongue (BT), in susceptible ruminants. Infection with BTV is characterised by immunosuppression and substantial lymphopenia at peak viraemia in the host.

METHODS

In this study, the role of cell-mediated immunity and specific T-cell subsets in BTV pathogenesis, clinical outcome, viral dynamics, immune protection, and onwards transmission to a susceptible vector is defined in unprecedented detail for the first time, using an arboviral infection model system that closely mirrors natural infection and transmission of BTV. Individual circulating CD4, CD8, or WC1 γδ T-cell subsets in sheep were depleted through the administration of specific monoclonal antibodies.

RESULTS

The absence of cytotoxic CD8 T cells was consistently associated with less severe clinical signs of BT, whilst the absence of CD4 and WC1 γδ T cells both resulted in an increased clinical severity. The absence of CD4 T cells also impaired both a timely protective neutralising antibody response and the production of IgG antibodies targeting BTV non-structural protein, NS2, highlighting that the CD4 T-cell subset is important for a timely protective immune response. T cells did not influence viral replication characteristics, including onset/dynamics of viraemia, shedding, or onwards transmission of BTV to . We also highlight differences in T-cell dependency for the generation of immunoglobulin subclasses targeting BTV NS2 and the structural protein, VP7.

DISCUSSION

This study identifies a diverse repertoire of T-cell functions during BTV infection in sheep, particularly in inducing specific anti-viral immune responses and disease manifestation, and will support more effective vaccination strategies.