期刊论文详细信息
PLoS Pathogens
Macaque Homologs of EBV and KSHV Show Uniquely Different Associations with Simian AIDS-related Lymphomas
Patrick Lewis1  Che-Chung Tsai2  A. Gregory Bruce2  Serge Barcy2  Helle Bielefeldt-Ohmann3  Angela M. Bakke4  Robert D. Murnane4  Timothy M. Rose5 
[1] Northwestern University, Evanston, Illinois, United States of America;Seattle Children's Research Institute, Seattle, Washington, United States of America;University of Queensland, Gatton, Queensland, Australia;University of Washington, Seattle, Washington, United States of America;Washington National Primate Research Center, Seattle, Washington, United States of America
关键词: Macaque;    Lymphomas;    Cell staining;    Cytoplasmic staining;    Viral load;    Nuclear staining;    B cells;    Kaposi's sarcoma-associated herpesvirus;   
DOI  :  10.1371/journal.ppat.1002962
学科分类:生物科学(综合)
来源: Public Library of Science
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【 摘 要 】

Two gammaherpesviruses, Epstein-Barr virus (EBV) (Lymphocryptovirus genus) and Kaposi's sarcoma-associated herpesvirus (KSHV) (Rhadinovirus genus) have been implicated in the etiology of AIDS-associated lymphomas. Homologs of these viruses have been identified in macaques and other non-human primates. In order to assess the association of these viruses with non-human primate disease, archived lymphoma samples were screened for the presence of macaque lymphocryptovirus (LCV) homologs of EBV, and macaque rhadinoviruses belonging to the RV1 lineage of KSHV homologs or the more distant RV2 lineage of Old World primate rhadinoviruses. Viral loads were determined by QPCR and infected cells were identified by immunolabeling for different viral proteins. The lymphomas segregated into three groups. The first group (n = 6) was associated with SIV/SHIV infections, contained high levels of LCV (1–25 genomes/cell) and expressed the B-cell antigens CD20 or BLA.36. A strong EBNA-2 signal was detected in the nuclei of the neoplastic cells in one of the LCV-high lymphomas, indicative of a type III latency stage. None of the lymphomas in this group stained for the LCV viral capsid antigen (VCA) lytic marker. The second group (n = 5) was associated with D-type simian retrovirus-2 (SRV-2) infections, contained high levels of RV2 rhadinovirus (9–790 genomes/cell) and expressed the CD3 T-cell marker. The third group (n = 3) was associated with SIV/SHIV infections, contained high levels of RV2 rhadinovirus (2–260 genomes/cell) and was negative for both CD20 and CD3. In both the CD3-positive and CD3/CD20-negative lymphomas, the neoplastic cells stained strongly for markers of RV2 lytic replication. None of the lymphomas had detectable levels of retroperitoneal fibromatosis herpesvirus (RFHV), the macaque RV1 homolog of KSHV. Our data suggest etiological roles for both lymphocryptoviruses and RV2 rhadinoviruses in the development of simian AIDS-associated lymphomas and indicate that the virus-infected neoplastic lymphoid cells are derived from different lymphocyte lineages and differentiation stages.

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