ABSTRACr Integrated viral DNA sequences were detected in tissues from two gibbon apes, a leukemic gibbon (60-1) from whose leukocytes a distinct strain of gibbon ape leukemia virus (GaLVH) was isolated, and gibbon 604, a contact of 6G-1 from the same colony that had uremia and cachexia of unknown origin. Although 6G4 had no detectable neoplasia or viral proteins, its serum contained persistent antibody against GaLV antigens. Whereas DNA from most of the tissues of 60-1 contained GaLV provirus, DNA from only three tissues (kidney, spleen, and liver) from 604 showed detectable viral sequences, and the extent of hybridization in each case was lower than with 6G-1. After cleavage with BamHI, two virus-specific DNA fragments were detected in tissues of 60-1. Only one of these fragments was detected in the positive tissues of 6G4. The results indicate that: (i) 6G4 was exposed to and infected by GaLV; (ii) early target sites for infection of gibbon by GaLV may be limited to a few tissues; and (iii) infection can be contained by integration of only partial provirus in a few tissues.We recently reported the isolation of a type C virus from a gibbon with spontaneous malignant lymphoma and leukemia (1). This virus, designated GaLVH, is in the same family that contains other gibbon ape leukemia virus isolates (2-5) and the simian sarcoma virus (SSV) and simian sarcoma-associated virus (SSAV) isolated from a fibrosarcoma of a pet woolly monkey (6, 7). Although closely related, the members of this group including GaLVH may be distinguished from each other by analysis of their RNA (8) or of the gp70 envelope protein (9). Proviral DNA and viral RNA and proteins were detected in most tissues of the leukemic gibbon (6G-1), and virus was recovered from all tissues, including tissues of the oral cavity (1). In addition to leukemic gibbon 6G-1, at least four of the eight animals of this colony were also exposed to GaLVH as indicated by the detection of serum antibodies (9, 10) even though none was viremic. For unknown reasons, one of the antibody-positive, nonleukemic, nonviremic animals, designated 6G-4, developed renal failure, became emaciated, and died. This provided an opportunity for search for proviral sequences in DNA from various tissues of this gibbon and to compare these sequences to those of 6G-1, the leukemic, viremic animal.Here we report results of molecular hybridization experiments showing that proviral sequences were present in 6G-4 but only in DNA extracted from liver, kidney, and spleen, and the plateau hybridization values were much lower than those obtained with DNA from 6G-1. Using restriction enzyme cleavage of cellular DNA followed by hybridization of the fragments to 125I-labeled viral RNA, we confirmed and extended our previous finding of proviral DNA in tissues from 6G-1. Two viral fragments were detected after cleavage with BamHI. More interestingly, DNA from the positive tissues of 6G-4 was shown to contain only one of these viral fragments, indicating that only part of the GaLV provirus is integrated ...