A replication-defective Chikungunya Virus platform for high-throughput drug screening and diagnostics

Chikungunya virus (CHIKV) is a mosquito-borne alphavirus that poses a significant global health threat. Although vaccines have recently been approved, the requirement for Biosafety Level 3 (BSL-3) containment substantially impedes therapeutic and diagnostic development for CHIKV. Here, we engineered an RNA replication-defective CHIKV (CHIKV-ΔnsP4) via trans-complementation, wherein the deleted nsP4 gene product is supplied in trans. CHIKV-ΔnsP4 replicates exclusively in nsP4-expressing cells, completing a full infectious cycle, while exhibiting no detectable replication in naïve cells. Consistent with this, CHIKV-ΔnsP4 demonstrated high attenuation in animal models. Building upon this platform, we generated an mCherry-expressing RNA replication-defective reporter virus, which enabled high-content antiviral screening and serological diagnostics. Collectively, this study establishes the RNA replication-defective strategy as a safe and effective platform for CHIKV research.

Authors

Publication Details

Journal
Figshare
Published
2026-11-10
DOI
https://doi.org/10.6084/m9.figshare.34969987
Primary Topic
Mosquito-borne diseases and control
Type
article
Field-Weighted Citation Impact
0.00
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article

A replication-defective Chikungunya Virus platform for high-throughput drug screening and diagnostics

Zherui Zhang, Qiuyan Zhang, Yue Li, Jing Wang et al.
Figshare
Mosquito-borne diseases and control
article

A replication-defective Chikungunya Virus platform for high-throughput drug screening and diagnostics

Zherui Zhang, Qiuyan Zhang, Yue Li, Jing Wang, Chenglin Deng, Bo Zhang, Jiaqi Li, Yanan Zhang, Jie Huang
article en

Abstract

Chikungunya virus (CHIKV) is a mosquito-borne alphavirus that poses a significant global health threat. Although vaccines have recently been approved, the requirement for Biosafety Level 3 (BSL-3) containment substantially impedes therapeutic and diagnostic development for CHIKV. Here, we engineered an RNA replication-defective CHIKV (CHIKV-ΔnsP4) via trans-complementation, wherein the deleted nsP4 gene product is supplied in trans. CHIKV-ΔnsP4 replicates exclusively in nsP4-expressing cells, completing a full infectious cycle, while exhibiting no detectable replication in naïve cells. Consistent with this, CHIKV-ΔnsP4 demonstrated high attenuation in animal models. Building upon this platform, we generated an mCherry-expressing RNA replication-defective reporter virus, which enabled high-content antiviral screening and serological diagnostics. Collectively, this study establishes the RNA replication-defective strategy as a safe and effective platform for CHIKV research.

Figshare
Mosquito-borne diseases and control
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