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Persons at greatest risk for B virus infection are veterinarians, laboratory workers, and others who have close contact with Old World macaques or monkey cell cultures.
Attachment of the viral glycoproteins to host receptors mediates endocytosis of the virus into the host cell.
Fusion with the plasma membrane to release the core and the tegument proteins into the host cytoplasm. The capsid is transported to the nuclear pore where the viral DNA is released into the nucleus. Transcription of immediate early genes which promote transcription of early genes and protect the virus against innate host immunity.
Transcription of early viral mRNA by host polymerase II, encoding proteins involved in replication of the viral DNA.

Assembly of the virus in nuclear viral factories and budding through the inner lamella of the nuclear membrane which has been modified by the insertion of herpes glycoproteins, throughout the Golgi and final release at the plasma membrane. Latent replication : replication of circular viral episome in tandem with the host cell DNA using the host cell replication machinery. Modulates the viral and host mRNA expression by exporting unspliced mRNA, thereby inducing alternative splicing. B virus is also commonly referred to as herpes B, monkey B virus, herpesvirus simiae, and herpesvirus B.The virus is found among macaque monkeys, including rhesus macaques, pig-tailed macaques, and cynomolgus monkeys (also called crab-eating or long-tailed macaques). Macaques housed in primate facilities usually become B virus positive by the time they reach adulthood.
However, infection in macaques can only be transmitted during active viral shedding through body fluids.Infection with B virus is extremely rare in humans.

When it does occur, the infection can result in severe brain damage or death if the patient is not treated soon after exposure (see Risks for Infection and Treatment sections). Infection in humans is typically caused by animal bites or scratches or by mucosal contact with body fluid or tissue.

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