Sand fly saliva reprograms skin fibroblasts to enhance arbovirus infection

Arbovirus transmission by sand flies is a growing public health concern, yet the early skin events shaping infection outcomes remain undefined. We establish a mouse model of Toscana virus (TOSV) infection that incorporates sand fly salivary factors to mimic natural transmission. Saliva from two distinct sand fly genera significantly enhanced infection and promoted neurological signs and joint inflammation, recapitulating key features of human TOSV disease. In the skin, dermal macrophages and fibroblasts were the main infected cell types, but only fibroblasts generated infectious virus. Saliva reprogrammed fibroblasts into a wound-healing state permissive to viral replication, driving local viral amplification, systemic spread, and thereby clinical disease. These findings identify skin fibroblasts as central determinants of host susceptibility and reveal that sand fly saliva actively remodels the skin to exacerbate viral pathogenesis. This work redefines the skin’s role in sand fly-transmitted infection and highlights new targets for therapeutic and vaccine development.

Publication Details

Journal
White Rose Research Online (University of Leeds, The University of Sheffield, University of York)
Published
2025-11-21
Primary Topic
Viral Infections and Vectors
Type
article
Field-Weighted Citation Impact
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article

Sand fly saliva reprograms skin fibroblasts to enhance arbovirus infection

White Rose Research Online (University of Leeds, The University of Sheffield, University of York)
Viral Infections and Vectors
article

Sand fly saliva reprograms skin fibroblasts to enhance arbovirus infection

article en

Abstract

Arbovirus transmission by sand flies is a growing public health concern, yet the early skin events shaping infection outcomes remain undefined. We establish a mouse model of Toscana virus (TOSV) infection that incorporates sand fly salivary factors to mimic natural transmission. Saliva from two distinct sand fly genera significantly enhanced infection and promoted neurological signs and joint inflammation, recapitulating key features of human TOSV disease. In the skin, dermal macrophages and fibroblasts were the main infected cell types, but only fibroblasts generated infectious virus. Saliva reprogrammed fibroblasts into a wound-healing state permissive to viral replication, driving local viral amplification, systemic spread, and thereby clinical disease. These findings identify skin fibroblasts as central determinants of host susceptibility and reveal that sand fly saliva actively remodels the skin to exacerbate viral pathogenesis. This work redefines the skin’s role in sand fly-transmitted infection and highlights new targets for therapeutic and vaccine development.

White Rose Research Online (University of Leeds, The University of Sheffield, University of York)
Good health and well-being
Openalex Percentile: Top 33%
Viral Infections and Vectors
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