Role of Trim5α in the Suppression of Cross-Species Transmission and its Defence Against Human Immunodeficiency Virus
Madhuri P. Puvvada and Snehal S. Patel
Pages 601-609 (9)
Acquired Immunodeficiency Syndrome (AIDS) was discovered 30 years ago and was followed by the
identification and characterization of its causative agent, Human Immunodeficiency Virus (HIV). Increasing spread of
retroviral infections has impelled science to understand the evolution of retroviruses from primates to humans. In the
course of evolution, host cells have developed intracellular proteins to counteract the transforming viral defence system.
Such inhibitory endogenous intracellular proteins are known as restriction factors. Tripartite motif protein isoform 5 alpha
(TRIM5α), Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like (APOBEC), and Tetherin proteins are few
important restriction factors that have been extensively studied. Several evidences have conveyed information regarding
specific adaptations occurring in HIV-1 and its relatives to inhibit these host defenses; making the study more interesting.
The characteristic potential of restriction factors to restrict the replication of retroviruses was enticing when studies were
found that HIV-1 virus cannot infect nonhuman primate species. This review emphasizes on TRIM5α as a restriction
factor and its significance in the evolution of retroviruses. It also accentuates the role of polymorphism within the regions
of TRIM5α in both human and primate species that eventually affect the cross-species transmission of immunodeficiency
Acquired immunodeficiency syndrome, human immunodeficiency virus, restriction factor, transmission, TRIM5α.
Department of Pharmacology, Institute of Pharmacy, Nirma University, Ahmedabad, Gujarat, India.