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Updated: May 5, 2026

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High-Throughput Transcriptome Analysis for Investigating Host-Pathogen Interactions
Published on: March 5, 2022
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Time-Resolved Transcriptomic Profiling of Chandipura Virus Infection Reveals Dynamic Host Responses and Host-Directed
Dhwani Jhala1, Prachi Shah1, Dhruvi Shah1
1Gujarat Biotechnology Research Centre, Gandhinagar 382011, India.
International Journal of Molecular Sciences
|May 4, 2026
Summary
Chandipura virus (CHPV) infection triggers dynamic host responses, including immune activation and metabolic shifts. This study reveals host targets for developing new antiviral therapies against this neurotropic virus.
Area of Science:
- Virology
- Molecular Biology
- Immunology
Background:
- Chandipura virus (CHPV) causes acute encephalitis with high mortality, particularly in India.
- The host molecular mechanisms underlying CHPV infection are not well understood.
- There is a need to identify host-directed therapeutic targets for CHPV.
Purpose of the Study:
- To characterize the temporal host response to CHPV infection using transcriptomics.
- To identify host pathways that can be pharmacologically targeted for antiviral development.
Main Methods:
- Human HEK293T cells were infected with CHPV.
- Time-resolved RNA sequencing (RNA-seq) was performed at 6, 12, 18, and 24 hours post-infection.
- Host-directed compounds were evaluated for antiviral activity in vitro.
Main Results:
- CHPV infection induced a temporal cascade of host responses, starting with innate immunity and inflammation.
- Metabolic reprogramming, particularly lipid metabolism, was observed by 18 hours post-infection.
- Global transcriptional shutdown occurred by 24 hours post-infection, associated with cytopathic effects.
- Host-directed compounds demonstrated antiviral activity against CHPV in neuronal cells.
Conclusions:
- This study provides the first time-resolved transcriptomic landscape of CHPV infection in human cells.
- Identified host pathways and compounds offer potential strategies for CHPV antiviral development.
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