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[Cellular tropism and adaptation of the measles virus]
1Department of Virology, Faculty of Medicine, Kyushu University, Japan. soono@virology.med.kyushu-u.ac.jp
Abstract:
Measles virus (MV) is a member of the genus Morbillivirus in the family Paramyxoviridae. Clinical isolates of MV use signaling lymphocyte activating molecule (SLAM) as a cellular receptor. SLAM is mainly expressed on immune cells such as immature thymocytes, activated lymphocytes and mature dendritic cells. This distribution of SLAM can account for the lymphotropism of MV. On the other hand, laboratory strains of MV use CD46 as an alternative receptor, through amino acid change(s) in the receptor binding hemagglutinin protein. Recently, several reports imply the existence of the cellular receptor(s) other than SLAM and CD46. In this review, we discuss the receptor usage of MV and its adaptation to cultured cells.
Insights
Measles virus (MV) uses signaling lymphocyte activating molecule (SLAM) or CD46 as cellular receptors. Research suggests other receptors may also exist, influencing MV adaptation to cell cultures.
Area of Science:
- Virology
- Immunology
- Cell Biology
Background:
- Measles virus (MV), a Morbillivirus, primarily infects immune cells.
- Clinical MV strains utilize signaling lymphocyte activating molecule (SLAM) as a receptor, explaining their lymphotropism.
- Laboratory strains of MV can adapt to use CD46 as an alternative receptor.
Purpose of the Study:
- To review the known cellular receptors used by Measles virus.
- To discuss the implications of receptor usage on MV tropism and cell culture adaptation.
- To explore emerging evidence for novel MV cellular receptors.
Main Methods:
- Literature review of studies on Measles virus receptor usage.
- Analysis of viral adaptation mechanisms in cell culture.
- Synthesis of data on SLAM and CD46 interactions with MV.
Main Results:
- SLAM is the primary receptor for wild-type MV, found on immune cells.
- CD46 serves as an alternative receptor for adapted MV strains, often due to hemagglutinin mutations.
- Recent findings indicate potential additional cellular receptors for MV beyond SLAM and CD46.
Conclusions:
- MV receptor usage is multifaceted, involving SLAM, CD46, and possibly other cellular factors.
- Understanding MV receptor tropism is crucial for studying viral pathogenesis and developing cell culture models.
- Further research is needed to fully elucidate the spectrum of MV cellular receptors and their roles.
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