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J Gen Virol 75 (1994), 513-527; DOI 10.1099/0022-1317-75-3-513
© 1994 Society for General Microbiology

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Quantitative analysis of genomic polymorphism of herpes simplex virus type 1 strains from six countries: studies of molecular evolution and molecular epidemiology of the virus

Hiroshi Sakaoka1, Keiko Kurita1, Yoichi Iida2, Shigeyuki Takada2, Kenichi Umene3, Young Tae Kim4, Chang Shang Ren5 and Andre J. Nahmias6

1 Department of Oral Bacteriology
and2 Department of Chemistry, Hokkaido University, Sapporo
3 Department of Virology, Kyushu University, Fukuoka, Japan
4 Department of Dermatology, Hanyang University, Seoul, Korea
5 Department of Immunology, China Medical College, Shenyang, China
and6 Department of Pediatrics, Emory University, Atlanta, Georgia, U.S.A.

Using the presence or absence of 63 variable restriction endonuclease (RE) sites selected from 225 sites with six REs, genomic polymorphism of 242 herpes simplex virus type 1 (HSV-1) strains from six countries (Japan, Korea, China, Sweden, U.S.A. and Kenya) was quantitatively analysed. Twenty-five of the 63 sites were found to differ between Korean and Kenyan strains. In contrast, only three and six sites were found to differ between isolates from Sweden and the U.S.A. and between those from Korea and China, respectively, suggesting that they are closely related to each other. In this way, characterization of 63 sites enabled us to categorize 186 distinct HSV-1 genotypes from 242 individuals. Some strains from Japan, Korea and China shared the same genotypes, indicating that they are phylogenetically closely related. Many significant correlation coefficients (|r | > 0.42; P < 0.01) between pairs of sites were found in isolates from the three Asian countries (Japan, Korea and China) as well as in those from Sweden and the U.S.A., suggesting that HSV-1 strains from within the same ethnic groups are evolutionarily closer. The average number of nucleotide substitutions per nucleotide, as defined by nucleotide diversity ({pi}), was estimated for HSV-1 genomes within ({pi}X or {pi}Y) and between ({pi}XY) countries. On the basis of 225 sites, nucleotide diversity for Kenyan isolates was 0.0056, almost three times higher than that for Korean isolates, implying that Kenyan HSV-1 genomes are much more diverse than those from Korea. In addition, the diversity between HSV-1 isolates from different countries ({pi}XY) was highest between isolates from the three Asian countries and Kenya (0.0075 to 0.0081) and lowest among those from the three Asian countries (0.0032 to 0.0040). The mutation rate ({lambda}) for HSV-1 was estimated to be 3.5 x 10-8/site/year. All these findings show that the evolution of HSV-1 may be host-dependent and very slow.

Received 30 April 1993; accepted 18 October 1993.


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