F. Mcomish et al., GEOGRAPHICAL-DISTRIBUTION OF HEPATITIS-C VIRUS GENOTYPES IN BLOOD-DONORS - AN INTERNATIONAL COLLABORATIVE SURVEY, Journal of clinical microbiology, 32(4), 1994, pp. 884-892
The frequency of infection with the six classified major genotypes of
hepatitis C virus (HCV) was investigated in 447 infected volunteer blo
od donors from the following nine countries: Scotland, Finland, The Ne
therlands, Hungary, Australia, Egypt, Japan, Hong Kong, and Taiwan. Vi
ral sequences in plasma from blood donors infected with HCV were ampli
fied in the 5'-noncoding region and were typed by restriction fragment
length polymorphism analysis. Electrophoresis of DNA fragments produc
ed by cleavage with HaeIII-RsaI and ScrFI-HinfI allowed HCV types 1 (o
r 5), 2, 3, 4, and 6 to be identified. Further analysis with Mval-Hinf
I allowed sequences of the type 5 genotype to be distinguished from se
quences of the type I genotype. Types 1, 2, and 3 accounted for almost
all infections in donors from Scotland, Finland, The Netherlands, and
Australia. Types 2 and 3 were not found in the eastern European count
ry (Hungary), where all but one of the donors were infected with type
1. Donors from Japan and Taiwan were infected only with type 1 or 2, w
hile types 1, 2, and 6 were found in those from Hong Kong. HCV infecti
on among Egyptians was almost always by type 4. Donors infected with H
CV type 1 showed broad serological reactivity with all four antigens o
f the second generation Chiron RIBA-2 assay (Chiron Corporation, Emery
ville, Calif.), while infection with divergent HCV genotypes elicited
antibodies mainly reactive to c22-3 and c33c. Reactivities with antibo
dies 5-1-1 and c100-3 were infrequent and were generally weak, irrespe
ctive of the geographical origin of the donor. Because the envelope re
gion of HCV is even more variable than the NS-4 region, it is likely t
hat vaccines based on these proteins need to be multivalent and perhap
s specifically adapted for different geographical regions.