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Restriction of host range of xenotropic pseudotype murine sarcoma virus by helper leukemia virus
Abstract:
We investigated the restriction of the host range to infectivity of MSV by helper leukemia virus in vivo. When newborn SD-rats were inoculated intracerebrally, subcutaneously, intraperitoneally or intramuscularly with xenotropic pseudotype Kirsten MSV, Ki-MSV(BV2), either brain tumors or myogenic sarcomas were induced, depending upon the route of inoculation. However, no tumors developed in SW-Icr mice inoculated with Ki-MSV(BV2) either intracerebrally or intramuscularly at birth. Ecotropic Ki-MSV(Ki-MuLV) induced myogenic sarcomas in mice when inoculated intramuscularly and also induced brain tumors and myogenic sarcomas in rats when inoculated intracerebrally and intramuscularly, respectively. Thus, the host range of pseudotype MSV appeared to depend on a helper leukemia virus.
Insights
The host range of Moloney Sarcoma Virus (MSV) depends on the helper leukemia virus. Different virus types induced tumors in rats and mice, varying by inoculation site and route.
Area of Science:
- Virology
- Oncology
- Molecular Biology
Background:
- Murine sarcoma virus (MSV) is an oncogenic retrovirus.
- The host range of MSV infection is influenced by helper viruses.
- Understanding these interactions is crucial for cancer research.
Purpose of the Study:
- To investigate how helper leukemia viruses restrict the host range of MSV infectivity in vivo.
- To determine the role of different pseudotype MSV and helper virus combinations in tumor induction in rats and mice.
Main Methods:
- Inoculation of newborn SD-rats and SW-Icr mice with xenotropic pseudotype Kirsten MSV (Ki-MSV(BV2)) and ecotropic Ki-MSV (Ki-MSV(Ki-MuLV)).
- Various routes of inoculation were used: intracerebral, subcutaneous, intraperitoneal, and intramuscular.
- Tumor development (brain tumors, myogenic sarcomas) was monitored in inoculated animals.
Main Results:
- Xenotropic Ki-MSV(BV2) induced brain tumors or myogenic sarcomas in rats depending on inoculation route, but no tumors in mice.
- Ecotropic Ki-MSV(Ki-MuLV) induced myogenic sarcomas in mice and both brain tumors and myogenic sarcomas in rats.
- Tumorigenesis varied significantly between rat and mouse models and was dependent on the specific MSV pseudotype and helper virus.
Conclusions:
- The host range of pseudotype MSV is significantly restricted by the helper leukemia virus.
- The tropism of MSV infection and subsequent tumor formation is determined by the specific helper virus and host species.
- These findings highlight the critical role of helper viruses in MSV-mediated oncogenesis.