H. Hebart et al., INTERSTRAIN VARIATION OF IMMEDIATE-EARLY DNA-SEQUENCES AND GLYCOPROTEIN-B GENOTYPES IN CYTOMEGALOVIRUS CLINICAL ISOLATES, Medical microbiology and immunology, 186(2-3), 1997, pp. 135-138
Cytomegalovirus (CMV) disease is associated with a high mortality in r
ecipients of an allogeneic stem cell transplant. Apparent differences
in biological behaviour have been noted among clinical CMV isolates. B
y amplifying specific functionally relevant regions of the CMV genome
[immediate early (IE) exon 3, glycoprotein B (gB)], a possible associa
tion of strain variation and clinical symptoms of infection was analys
ed in 24 patients. A high number of genome mutations of the IE exon 3
region could be documented translating into amino acid changes of vira
l isolated of 8 out of 15 patients with symptomatic and 2 out of 9 pat
ients with asymptomatic CMV infection. Identical IE mutations and gB t
ypes were observed in isolates from two different sites in 6 patients.
gB strain 2 was found to be associated with symptomatic CMV infection
(P=0.03). Thus, apart from host factors viral factors might influence
the virus-host interaction in severely immunosuppressed patients.