Structure B virus is approximately 200 nm in diameter and has a structure almost identical to that of
HSV1 and
HSV2. It has an
icosahedral capsid (T=16) consisting of 150
hexons and 12 pentons formed from 6 proteins. The envelope is loose around the viral capsid and contains at least 10 glycoproteins critical for
adsorption and
penetration into host cells. The
tegument, containing at least 14 proteins, lies between the capsid and the envelope. The tegument proteins are involved in
nucleic acid metabolism,
DNA synthesis, and
protein processing. The proteins in the tegument are
thymidine kinase,
thymidylate synthetase,
dUTPase,
ribonucleotide reductase,
DNA polymerase,
DNA helicase,
DNA primase, and
protein kinases.
Genome The B virus
genome was fully sequenced in 2003 from an isolate found in a
rhesus macaque. Like all herpes viruses, the B virus genome contains double-stranded
DNA and is approximately 157
kbp in length. Two unique regions (UL and US) are flanked by a pair of inverted repeats, two of which are found at the termini, with the other two internally located. This arrangement, which is identical in nature to HSV, results in four sequence-oriented isomers.
Cytosine and
guanine nucleotides represent 75% of the sequence. Sequence analyses suggest that B virus and HSV types 1 and 2 most likely diverged from a common ancestor during the evolution of these pathogens. Each gene-encoded
glycoprotein, including gB, gC, gD, gE and gG, has approximately 50% homology with HSV, with a slightly higher predilection towards HSV-2 over HSV-1. Additionally, glycoprotein sequences have demonstrated that all cysteine residues are conserved, as are most
glycosylation sites. One key difference between the B virus and the HSVs is that B virus does not have a homolog of the HSV γ134.5 gene, which codes for a neurovirulence factor. This indicates that B virus has different mechanisms from HSV for replicating inside
nerve cells, which could explain the drastically different effects of these viruses on humans. ==Infection==