The fragments of simian retrovirus genome STLV-1Ph detected in lymphomatous specimens from baboons dead from malignant lymphoma in different periods of a many-year (22 years) outbreak are studied. African and Asian subtypes of STLV-1Ph retrovirus circulate in the animals: the African type predominates during the first and Asian during the second half of the outbreak.Key Words: baboons; outbreak of malignant lymphoma; STL V-1Ph retrovirus; African and Asian subtypes Many-year (1967Many-year ( -1991 outbreak of malignant lymphoma among baboons (primarily Papio hamadryas) in the Sukhumi Breeding Center began with inoculation of human leukemic material to several animals and led to death of almost 400 adult baboons [ 1 ]. A group of baboons at a high risk of lymphoma was formed including a total of 4158 animals over the entire period of experiment. Control group consisted of 800 baboons brought to the center and living at an isolated territory, which had no contacts with lymphomatous animals. No cases of lymphoma were detected in the control group during at least 15 years. Immunophenotypically, malignant lymphomas of baboons were identified as non-Hodgkin's lymphomas (NHL) of T or B cell similar to human tumors. Testing for STLV-1 in 68 cases of T-cell NHL by PCR showed that retrovirus can be present in all cytological variants of identified T-cell baboon lymphomas [3,11].Horizontal dissemination of lymphoma and the presence of type C retrovirus particles in lymphoid Department of Immunology and Oncovirology, Institute of Medical Primatolocjy, Russian Academy of Medical Sciences, Adler--Sochi cells, lungs, kidneys, and salivary glands of sick animals confirmed viral origin of lymphoma. In further studies the virus was identified as simian T-lymphotropic retrovirus (STLV-IPh or PTLV-1) [4,7] belonging to human HTLV-1 subfamily. Serum antibodies to STLV-1 were detected in 40-45% adult animals in the high-risk group and in almost 100% of baboons with T-cell malignant lymphomas [3]. Moreover, antibodies to STLV-1 were detected in the blood of 7% healthy adult animals in the control group. For detecting the possible biomolecular differences between the viruses isolated in the control and lymphomatous groups, we compared sequenced fragments of STLV-1 from lymphomatous baboons (STLV-1PhL) and healthy carriers (STLV-1PhN) in the control group. Different degree of homology with HTLV-1 and between STLV-1PhL and STLV-1PhN was detected in the sequenced env and tax sites [7,10]. The forest variant of STLV-1PhN had 96% homology with HTLV-1 and only 83% with STLV-1PhL. The data on the molecular structure of sequenced fragments of STLV-1/HTLV-1 were sufficient for phylogenetic analysis and grouping of viruses of this family into two 0007-4888/99/0007-0733522.00 9KluwerAcademic/PlenumPublishers