Abstract
Retroviruses are well known pathogens of mammals, birds and fish. Their potential to induce cancer in chickens was already described almost 100 years ago and murine retroviruses have been a subject of study for 50 years. The first human retroviruses, HTLV and HIV, were discovered more than 30 years ago, surprising researchers and physicians by the profound differences in the diseases they cause. HTLV-1 is able to induce, after decades of infection, lymphomas/leukemia or neuroimmune disorders whereas untreated HIV infection leads almost inevitably to AIDS. The recently described XMRV (xenotropic murine leukemia virus-related virus) appeared to possess many of the features known for HTLV and was regarded by some to be the third human retrovirus. However, recent publications by Knox et al. [1] and Paprotka et al. [2] have shed new light on this gammaretrovirus. Knox and colleagues clearly demonstrate that XMRV is absent in patients belonging to a chronic fatigue syndrome cohort who had previously been reported to be XMRV-positive [3]. This supports the growing suspicion that laboratory contamination was responsible for the postulated link between XMRV and the disease. Furthermore, Paprotka et al’s identification of XMRV’s origin and the phylogenetic analysis of known XMRV sequences are further nails in the coffin to the notion that XMRV is a clinically relevant infectious human retrovirus.
Highlights
Retroviruses are well known pathogens of mammals, birds and fish
XMRV was first reported as a potential new retrovirus of humans in 2006 [4] when a microarray approach revealed its presence predominantly in tissues from patients with familial prostate cancer who were homozygous for a mutation (R462Q)
Rhesus monkeys can be infected with very high amounts of XMRV [32], there is substantial evidence that the virus does not infect, replicate and circulate in humans
Summary
XMRV (xenotropic murine leukemia virus-related virus) was first reported as a potential new retrovirus of humans in 2006 [4] when a microarray approach revealed its presence predominantly in tissues from patients with familial prostate cancer who were homozygous for a mutation (R462Q). The presence of XMRV in prostate cancer patients was later confirmed by others [5,6,7], the virus was usually found in tumor cells and with no correlation to the RNASE L genotype. One critical result in 2009 seemed to support the link between XMRV and prostate cancer by discovering the virus in the primary prostate carcinoma-derived cell line 22Rv1 [15]
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