Comparative Pathobiology of Macaque Lymphocryptoviruses

Lymphocryptoviruses (LCVs) have been identified as naturally occurring infections of both Old and New World nonhuman primates. These viruses are closely related to Epstein–Barr virus (EBV, Human herpesvirus 4) and share similar genomic organization and biological properties. Nonhuman primate LCVs have the ability to immortalize host cells and express a similar complement of viral lytic and latent genes as those found in EBV. Recent evidence indicates that nonhuman primate LCVs can immortalize B cells from genetically related species, suggesting a close evolutionary relationship between these viruses and their respective hosts. Early work with EBV in tamarins and owl monkeys revealed that cross species transmission of lymphocryptoviruses from the natural to inadvertent host may be associated with oncogenesis and the development of malignant lymphoma. Moreover, simian LCVs have the ability to induce malignant lymphomas in immunodeficient hosts and have been associated with posttransplantation lymphoproliferative disease in cynomolgus macaques undergoing solid organ transplantation. This review will focus on the comparative pathobiology of lymphocryptoviral infection and discuss the derivation of specific pathogen-free animals.Abbreviations: EBER, EBV-encoded small RNA; EBNA, Epstein–Barr nuclear antigen; EBV, Epstein–Barr virus; LCV, lymphocryptovirus; LMP, latent membrane protein; NHL, non-Hodgkin lymphoma; PTLD, posttransplantation lymphoproliferative disease; RhLCV, rhesus LCV; SHIV, simian–human immunodeficiency virus; sVCA, small viral capsid antigenThe herpesviridae family shares a number of genetic and biologic properties and is composed of 3 subfamilies: the alphaherpesvirinae, betaherpesvirinae and gammaherpesvirinae. Regardless of subfamily, herpes virions have similar ultrastructural morphology, which comprises an envelope, a capsid with icosahedral symmetry, and a centrally located core containing a linear genome of double-stranded DNA 100 to 200 kb in length. Productive replication of herpesviruses occurs within the host cell nucleus, resulting in cell lysis, and histopathologic diagnosis of these infections often is aided by the presence of intranuclear inclusion bodies, which consist of viral protein complexes. As a group, herpesviruses have large, complex genomes and often include acquired cellular homolog genes that manipulate host immunologic and cellular responses, allowing these viruses to persist for the life of the host. Pathogen–host adaptation and coevolution has resulted in, for the most part, infections of low virulence. However, these viruses often do not have strict host specificity, and there are numerous examples of severe disease resulting from cross-species transmission. An early example of this phenomenon was the experimental transmission of 2 gammaherpesvirinae, Epstein–Barr virus (EBV, Human herpesvirus 4) and herpesvirus saimiri (Saimiriine herpesvirus 2), to tamarins and owl monkeys, resulting in malignant lymphoma within several weeks of inoculation.^1,6,39,48,53The gammaherpesvirinae subfamily contains a number of important human and animal pathogens and is subdivided into the lymphocryptovirus (γ1 herpesvirus) and rhadinovirus (γ2 herpesvirus) genera.⁷⁵ The rhadinovirus genus contains Kaposi sarcoma-associated herpesvirus (Human herpesvirus 8), rhesus rhadinovirus (Cercopithecine herpesvirus 17), and retroperitoneal fibromatosis-associated herpes virus and is discussed separately in this issue.⁹³ The γ1 herpesvirus genus contains EBV and the nonhuman primate lymphocryptoviruses.²⁸ Viruses from this genus have been isolated from many species of both Old and New World nonhuman primates, and although the isolates show considerable genomic and biologic similarity, they tend to have restricted ability for immortalizing B cells from all but closely related species.^{21,37,56,70,73} This review will examine the comparative pathobiology of primate lymphocryptoviruses and explore the derivation of macaque colonies that are specific pathogen-free of these agents.