# Establishment of a Cell-Fusing Agent Virus Infection Model in Aedes albopictus and Its Impact on Vector Competence for Zika Virus

**Authors:** Dongqin Li, Ningxin Zhou, Li Xiong, Xi Pu, Mingqiang Li, Qing Liu, Lu Liu, Rui Xiao, Yuanhang Wang, Hengduan Zhang, Xiaoxia Guo, Dan Xing, Tongyan Zhao, Jiahong Wu, Yuting Jiang

PMC · DOI: 10.3390/v18030384 · Viruses · 2026-03-19

## TL;DR

Researchers tested a virus that could potentially block Zika virus transmission in a different mosquito species but found limited effectiveness and challenges in using this approach.

## Contribution

Established a CFAV infection model in Aedes albopictus and evaluated its impact on Zika virus transmission.

## Key findings

- CFAV can infect Aedes albopictus with high viral loads but does not block Zika virus replication.
- CFAV does not vertically transmit in Aedes albopictus.
- CFAV pre-infection in Aedes aegypti reduces Zika virus infection in ovaries and salivary glands.

## Abstract

The overuse of chemical insecticides highlights the urgent need for novel vector control strategies. Insect-specific viruses (ISVs), such as the cell-fusing agent virus (CFAV), have shown potential to block arbovirus transmission by inhibiting viral replication in mosquitoes. However, the effects of CFAV beyond its natural host, Aedes aegypti, remain largely unexplored. In this study, we established a CFAV infection model in Aedes albopictus, a major vector for Zika virus (ZIKV), via intrathoracic injection. Stable infection was achieved, with viral loads reaching up to 107 copies per mosquito by day 10 post-injection. Nevertheless, high post-injection mortality (median survival: 3 days) was observed, which we attribute primarily to mechanical injury. No evidence of vertical transmission of CFAV was detected in Ae. albopictus. Co-injection of CFAV and ZIKV did not significantly affect ZIKV replication in this species. In contrast, in Ae. aegypti pre-infected with CFAV followed by oral ZIKV challenge, CFAV significantly reduced ZIKV infection rates in the ovaries at day 4 and viral loads in salivary glands at day 10. These findings demonstrate that while CFAV can productively infect Ae. albopictus, it does not undergo vertical transmission in this species, and has no inhibitory effect on ZIKV under the co-infection conditions tested. This study underscores challenges associated with using single ISVs such as CFAV for arbovirus control and highlights the complex, bidirectional role of multiple ISV co-infections. While exploring multi-ISV combinations may offer a potential strategy to enhance antiviral efficacy, their net effect—whether suppression or enhancement of arboviruses—warrants careful investigation.

## Linked entities

- **Species:** Aedes albopictus (taxon 7160), Aedes aegypti (taxon 7159)

## Full-text entities

- **Diseases:** Infection (MESH:D007239), mechanical injury (MESH:D041781)
- **Species:** Aedes albopictus (Asian tiger mosquito, species) [taxon 7160], Cell fusing agent virus (no rank) [taxon 31658], Zika virus (no rank) [taxon 64320], Aedes aegypti (yellow fever mosquito, species) [taxon 7159]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030859/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030859/full.md

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Source: https://tomesphere.com/paper/PMC13030859