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Mitochondrial protein CHCHD10 inhibits NDV replication and reduces pathological changes.
Xibing Yu1, Hexiang Jiang2, Jindou Li1
1State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, Institute of Zoonosis, and College of Veterinary Medicine, Jilin University, Changchun 130062, China.
Newcastle disease virus (NDV) infection significantly reduces coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10) protein levels. Lower CHCHD10 expression in mice correlates with higher viral loads and severe disease.
Area of Science:
- Veterinary Virology
- Molecular Biology
- Immunology
Background:
- Newcastle disease (ND) poses a significant threat to the global poultry industry.
- The pathogenic mechanisms of virulent Newcastle disease virus (NDV) are not fully understood.
- Proteomic analysis of NDV-infected cells is crucial for understanding host-pathogen interactions.
Purpose of the Study:
- To investigate the role of coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10) protein during NDV infection.
- To determine the expression patterns of CHCHD10 in response to NDV.
- To assess the impact of CHCHD10 expression levels on viral load and disease severity.
Main Methods:
- Proteomic analysis of NDV-infected cells.
- In vivo and in vitro detection of CHCHD10 expression after NDV infection.
- Assessment of viral loads and pathological damage in C57BL/6 mice with altered CHCHD10 expression.
Main Results:
- CHCHD10 protein levels significantly decreased at the late stage of NDV infection.
- CHCHD10 expression was notably reduced both in vivo and in vitro following NDV infection.
- Silencing CHCHD10 in mice led to increased viral loads and exacerbated pathological damage, while overexpression had the opposite effect.
Conclusions:
- CHCHD10 plays a protective role against Newcastle disease virus infection.
- Reduced CHCHD10 expression is associated with increased NDV pathogenicity.
- CHCHD10 may represent a potential therapeutic target for managing Newcastle disease.
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