We have isolated and characterised two divergent simian T-lymphotropic viruses (STLV), not belonging to the established human and simian T-lymphotropic virus lineages HTLV-1/STLV-1 and HTLV-2. STLV-L, from an Eritrean sacred baboon (Papio hamadryas), has been typed as a third type of simian T-lymphotropic virus, distinct from HTLV-1/STLV-1 and HTLV-2. The other virus, isolated from Congolese bonobos (Pan paniscus), is a distinct member of the HTLV-2 clade and has been designated STLV-2. The isolation of these two simian viruses shows that the spectrum of HTLVs/STLVs is larger than previously expected. Our data indicate that the two lineages STLV-L and HTLV-2/STLV-2 are of African origin, while the HTLV-1/STLV-1 lineage has been shown to be of Asian origin. These data, together with our phylogenetic analyses, suggest an African origin of the HTLV/STLV ancestor, which provides new clues about virus dissemination. Furthermore, the atypical serological profiles exhibited by STLV-L or STLV-2 infected animals in western blot, raise questions about the efficiency of current screening methods to type highly divergent HTLVs/STLVs. Considering the growing interest in xenotransplantations, more epidemiological and biological knowledge of simian and human T-lymphotropic viruses is necessary to estimate the risk of interspecies transmissions.

Download full-text PDF

Source
http://dx.doi.org/10.1002/(sici)1099-1654(199907/09)9:3<155::aid-rmv242>3.0.co;2-3DOI Listing

Publication Analysis

Top Keywords

simian t-lymphotropic
12
t-lymphotropic viruses
8
t-lymphotropic virus
8
htlv-1/stlv-1 htlv-2
8
african origin
8
simian
5
discovery divergent
4
divergent stlvs
4
stlvs implications
4
implications evolution
4

Similar Publications

Lymphoproliferative disorders of natural killer (NK)-cell lineage are well documented in humans but have yet to be documented in non-human primates (NHPs). Here we describe a case of NK-cell lymphoproliferative disorder/leukemia in a 20-y-old captive female rhesus macaque (). The animal clinically had mild splenomegaly and marked lymphocytosis with small-to-medium lymphocytes in blood smears.

View Article and Find Full Text PDF

Simian immunodeficiency viruses (SIV) infecting chimpanzees (SIVcpz) and sooty mangabeys (SIVsm) are, respectively, the biological precursors of human immunodeficiency viruses (HIV) Types 1 and 2. Former French colonies in West Africa are the regions where retroviruses first jumped from primates to humans. Ivory Coast is nowadays a country of over 29 million people, being 2% (580,000) persons living with HIV (PLWH).

View Article and Find Full Text PDF
Article Synopsis
  • STLV-1 is a retrovirus similar to HTLV-1 that causes adult T-cell leukemia and is highly prevalent in Japanese macaques, yet its molecular epidemiology hasn't been fully studied.
  • A study analyzed the complete genome sequences of STLV-1 from 68 JMs across 5 different troops, revealing high genome similarity within troops and low nucleotide diversity overall.
  • The findings suggest that the high homogeneity of STLV-1 genomes in JMs is partly due to the absence of G-to-A hypermutation, which is often seen in HTLV-1 in humans and African primates.
View Article and Find Full Text PDF

Vulnerability to APOBEC3G linked to the pathogenicity of deltaretroviruses.

Proc Natl Acad Sci U S A

March 2024

Department of Hematology, Rheumatology and Infectious Diseases, Faculty of Life Sciences, Kumamoto University, Kumamoto 860-8556, Japan.

Article Synopsis
  • Human retroviruses like HIV and HTLV-1 originate from simian viruses and can lead to serious diseases in humans, despite being less harmful to their natural hosts.
  • Research revealed that the human protein APOBEC3G (A3G) causes G-to-A mutations primarily in HTLV-1, while HTLV-2 and STLV-1 have mechanisms to resist these mutations.
  • The study found that the antisense proteins from these retroviruses interact differently with A3G, with HTLV-1 exploiting A3G to promote cell growth in a way tied to cancer development, while HTLV-2 and STLV-1 do not have this effect.
View Article and Find Full Text PDF

Background: BK polyomavirus-associated nephropathy (BKPyVAN) has become a major cause of kidney dysfunction and graft loss in kidney transplant recipients. On rare occasion, polyomavirus has also been known to affect native kidneys of immunocompromised individuals. Only a small number of opportunistic infections have been reported in the carrier phase of human T-lymphotropic virus type 1 (HTLV-1).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!