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Involvement of apoptosis in syncytial cell death induced by canine distemper virus
T Nishi1, K Tsukiyama-Kohara, K Togashi
1Laboratory of Animal Research Center, Institution of Medical Science, The University of Tokyo, 4-6-1 Shirokanedai Minato-ku, Tokyo 108-8639, Japan.
Abstract:
The Yanaka strain, a field isolate of Canine distemper virus (CDV), caused extensive syncytial cytopathic effects (CPEs) followed by cell death in vitro. Syncytium formation is an important aspect of CDV pathogenicity, but the mechanism of the fusion-induced cell death is still not understood. In this study, the involvement of apoptosis in the CDV-induced CPE was investigated. We also examined apoptosis in cells infected with a persistent strain of CDV, the Yanaka-BP strain derived from the Yanaka strain, because this strain does not cause obvious CPE. DNA laddering together with Terminal transferase dUTP nick endlabeling (TUNEL) assay indicated that the Yanaka strain infection, but not the Yanaka-BP infection induced apoptosis. In addition, flow cytometric analysis similarly indicated that the Yanaka-BP strain induced apoptosis significantly less frequently than the Yanaka strain did. Thus, absence of apoptosis may be implicated in the CPE and establishment of persistent CDV infection.
Insights
Canine distemper virus (CDV) causes cell death through apoptosis. A persistent CDV strain, Yanaka-BP, induced less apoptosis, suggesting its absence may lead to persistent infection.
Area of Science:
- Virology
- Cell Biology
- Immunology
Background:
- Canine distemper virus (CDV) causes syncytium formation and cell death.
- The mechanism of CDV-induced cell death, particularly apoptosis, remains unclear.
- Persistent CDV strains may evade apoptosis, contributing to chronic infection.
Purpose of the Study:
- To investigate the role of apoptosis in CDV-induced cytopathic effects (CPE).
- To compare apoptosis induction between a virulent CDV strain (Yanaka) and a persistent strain (Yanaka-BP).
Main Methods:
- In vitro infection of cells with Yanaka and Yanaka-BP CDV strains.
- DNA laddering assay to detect apoptosis.
- Terminal transferase dUTP nick endlabeling (TUNEL) assay for apoptosis.
- Flow cytometry to quantify apoptosis.
Main Results:
- The Yanaka strain induced significant apoptosis, evidenced by DNA laddering and TUNEL assay.
- The Yanaka-BP strain induced significantly less apoptosis compared to the Yanaka strain.
- Flow cytometry confirmed lower apoptosis rates in cells infected with Yanaka-BP.
Conclusions:
- Apoptosis plays a crucial role in CDV-induced CPE.
- The reduced induction of apoptosis by the Yanaka-BP strain may contribute to persistent CDV infections.
- Understanding apoptosis evasion is key to developing strategies against persistent CDV.
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