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Published on: November 2, 2013
Hypothesis on the molecular basis of nononcogenic retroviral diseases
Abstract:
Oncogenic and nononcogenic retroviruses have similar structures and replicate by reverse transcription of their viral RNAs. The nononcogenic retroviruses are distinguished from the oncogenic retroviruses by virtue of the chronic inflammatory or degenerative disease they cause. These diseases include visna-maedi of sheep, caprine arthritis and encephalitis, equine infectious anemia, and chronic spongiform polioencephalomyelopathy of mice. The basis for the particular disease caused by the nononcogenic retroviruses seems to be the selective infection of specific end-stage cells. A common factor in these slowly progressing diseases is lifelong persistence of virus with viral spread either in the face of host immunity-antigenic drift or by modulation of the host immune response. The molecular basis for antigenic drift in visna virus and its biologic significance are discussed.
Insights
Nononcogenic retroviruses cause chronic diseases like visna-maedi by infecting specific cells and persisting lifelong. Viral spread occurs despite host immunity through antigenic drift or immune modulation.
Area of Science:
- Virology
- Immunology
- Pathology
Background:
- Retroviruses, both oncogenic and nononcogenic, share similar structures and replicate via reverse transcription.
- Nononcogenic retroviruses are characterized by the chronic inflammatory or degenerative diseases they induce.
- Examples of diseases caused by nononcogenic retroviruses include visna-maedi in sheep, caprine arthritis and encephalitis, equine infectious anemia, and chronic spongiform polioencephalomyelopathy in mice.
Purpose of the Study:
- To differentiate nononcogenic retroviruses from oncogenic ones based on disease outcomes.
- To explore the mechanisms underlying chronic disease development caused by nononcogenic retroviruses.
- To discuss the molecular basis and biological significance of antigenic drift in visna virus.
Main Methods:
- Comparative analysis of retroviral structures and replication.
- Identification of specific end-stage cells targeted by nononcogenic retroviruses.
- Investigation of viral persistence and spread mechanisms in the face of host immunity.
- Molecular analysis of antigenic drift in visna virus.
Main Results:
- Nononcogenic retroviruses selectively infect specific end-stage cells, leading to chronic diseases.
- Lifelong viral persistence is a common feature, with viral spread occurring despite host immunity.
- Mechanisms of viral spread include antigenic drift and modulation of the host immune response.
- The molecular basis and biological significance of antigenic drift in visna virus were examined.
Conclusions:
- Nononcogenic retroviruses cause specific chronic inflammatory or degenerative diseases through selective cell tropism.
- Viral persistence and evasion of host immunity, via antigenic drift or immune modulation, are key to disease progression.
- Understanding these mechanisms is crucial for managing retroviral infections and associated diseases.
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