A major capsid protein (MCP) gene homologue of porcine cytomegalovirus (PCM
V) was identified. Sequence analysis indicated that the PCMV MCP gene is 4,
026 nucleotides in length encoding a protein of 1,341 amino acid residues.
The predicted molecular weight of the PCMV MCP is 151,456 Da, equivalent to
those of other herpesvirus MCP counterparts. Phylogenetic analysis using h
erpesviral MCP gene sequences confirmed that PCMV is a betaherpesvirus with
higher homology with human herpesvirus-6 and -7 than human and mouse cytom
egaloviruses. The serum of pig experimentally infected with PCMV did not re
act with bacterially expressed MCP, suggesting that the PCMV MCP may not be
related to the humoral immune response in the course of PCMV infection. Al
so, we established polymerase chain reaction (PCR) protocols using primers
corresponding to MCP gene sequences fur detection of PCMV infection. The PC
R protocol would be effective for the diagnosis of slow-growing PCMV infect
ion, for which traditional methods involving virus-isolation are not useful
.