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Genetic variability of the envelope gene of Type D simian retrovirus-2 (SRV-2) subtypes associated with SAIDS-related retroperitoneal fibromatosis in different macaque species.

TitleGenetic variability of the envelope gene of Type D simian retrovirus-2 (SRV-2) subtypes associated with SAIDS-related retroperitoneal fibromatosis in different macaque species.
Publication TypeJournal Article
Year of Publication2006
AuthorsPhilipp-Staheli, J, Marquardt, T, Thouless, ME, A Bruce, G, Grant, RF, Tsai, C-C, Rose, TM
JournalVirol J
Volume3
Pagination11
Date Published2006
ISSN1743-422X
KeywordsAmino Acid Sequence, Animals, Gene Expression Regulation, Viral, Genetic Variation, Macaca, Mason-Pfizer monkey virus, Molecular Sequence Data, Phylogeny, Retroperitoneal Fibrosis, Simian Acquired Immunodeficiency Syndrome, Species Specificity, Viral Envelope Proteins
Abstract

BACKGROUND: D-type simian retrovirus-2 (SRV-2) causes an AIDS-like immune deficiency syndrome (SAIDS) in various macaque species. SAIDS is often accompanied by retroperitoneal fibromatosis (RF), an aggressive fibroproliferative disorder reminiscent of Kaposi's sarcoma in patients with HIV-induced AIDS. In order to determine the association of SRV-2 subtypes with SAIDS-RF, and study the evolution and transmission of SRV-2 in captive macaque populations, we have molecularly characterized the env gene of a number of SRV-2 isolates from different macaque species with and without RF.

RESULTS: We sequenced the env gene from eighteen SRV-2 isolates and performed sequence comparisons and phylogenetic analyses. Our studies revealed the presence of six distinct subtypes of SRV-2, three of which were associated with SAIDS-RF cases. We found no association between SRV-2 subtypes and a particular macaque species. Little sequence variation was detected in SRV-2 isolates from the same individual, even after many years of infection, or from macaques housed together or related by descent from a common infected parent. Seventy-two amino acid changes were identified, most occurring in the larger gp70 surface protein subunit. In contrast to the lentiviruses, none of the amino acid variations involved potential N-linked glycosylation sites. Structural analysis of a domain within the gp22/gp20 transmembrane subunit that was 100% conserved between SRV-2 subtypes, revealed strong similarities to a disulfide-bonded loop that is crucial for virus-cell fusion and is found in retroviruses and filoviruses.

CONCLUSION: Our study suggests that separate introductions of at least six parental SRV-2 subtypes into the captive macaque populations in the U.S. have occurred with subsequent horizontal transfer between macaque species and primate centers. No specific association of a single SRV-2 subtype with SAIDS-RF was seen. The minimal genetic variability of the env gene within a subtype over time suggests that a strong degree of adaptation to its primate host has occurred during evolution of the virus.

DOI10.1186/1743-422X-3-11
Alternate JournalVirol. J.
PubMed ID16515713
PubMed Central IDPMC1450265
Grant ListK02 AI49275 / AI / NIAID NIH HHS / United States
RR00166 / RR / NCRR NIH HHS / United States
RR13154 / RR / NCRR NIH HHS / United States