The Role of Henosepilachna vigintioctopunctata in Facilitating the Spread of Tomato Brown Rugose Fruit Virus (ToBRFV) Among Hosts.
- 2025-12-03
- Insects 16(12)
- PubMed: 41465664
- DOI: 10.3390/insects16121225
Study Design
- Population
- Hadda beetle (Henosepilachna vigintioctopunctata) and solanaceous hosts (tomato, black nightshade, pepper, eggplant)
- Methods
- Beetle-mediated transmission efficiency, persistence of virus-carrying capacity, and ability to vector to various hosts evaluated using reverse transcription quantitative PCR (RT-qPCR)
- Duration
- up to 48 hours
- Funding
- Unclear
Tomato brown rugose fruit virus (ToBRFV), a highly stable and mechanically transmissible tobamovirus, poses a significant threat to solanaceous crops worldwide, particularly tomato (Solanum lycopersicum). While its transmission via human activities and contaminated materials is well-documented, the role of common phytophagous insects in its epidemiology remains less understood. Henosepilachna vigintioctopunctata, the Hadda beetle, is a common pest of Solanaceae with a host range that overlaps extensively with that of ToBRFV. This study aimed to quantify the beetle's capacity to act as a mechanical vector and to assess its potential epidemiological impact. Using reverse transcription quantitative PCR (RT-qPCR), we evaluated beetle-mediated transmission efficiency, the persistence of its virus-carrying capacity, and its ability to vector the virus to various solanaceous hosts. Our results demonstrate that H. vigintioctopunctata efficiently acquires and transmits ToBRFV to tomato and other key hosts, including black nightshade (S. nigrum), pepper (Capsicum annuum), and eggplant (Solanum melongena). The virus was retained and remained transmissible by beetles for up to 48 h post-acquisition, providing a significant window for dispersal. Viral particles were most abundant in the digestive tract, consistent with ingestion of infected tissue, and declined rapidly on external body parts, confirming a non-circulative, mechanical transmission mechanism. Furthermore, feeding wounds created by non-viruliferous beetles increased plant susceptibility to subsequent infection from environmental contamination. We conclude that H. vigintioctopunctata acts as a potential mechanical vector that might amplify ToBRFV spread at local and landscape levels. This highlights a synergistic interaction between a native pest and an invasive pathogen, underscoring the necessity of incorporating beetle management into integrated strategies for controlling ToBRFV.
Research Insights
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