Genotypic Variations among Human Calciviruses in Korea: 1987-1994.
- Author:
Ki Bum NAM
;
Ji Aee KIM
;
Kyung Hee KIM
;
Jai Myung YANG
- Publication Type:Original Article
- MeSH:
Amino Acid Motifs;
Amino Acid Sequence;
Animals;
Child;
Clone Cells;
DNA, Complementary;
Epidemiology;
Gastroenteritis;
Genetic Variation;
Genome;
Genotype;
Humans*;
Korea*;
Norwalk virus;
Polymerase Chain Reaction;
RNA Replicase;
Snow
- From:Journal of the Korean Society of Virology
1997;27(2):185-196
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Sequence comparison of the RNA-dependent RNA polymerase of human caliciviruses (HuCVs) from Korean children with gastroenteritis revealed significant genetic variation among them. cDNA clones were produced from the HuCVs collected from pediatric population during a period of 1987-1994. The application of reverse transcription-polymerase chain reaction (RT-PCR) using primers directed to the RNA-dependent RNA polymerase region within ORF1 of Norwalk virus (NV) showed that 13.7% of HuCVs yielded PCR products of similar size to the NV prototype, NV8Flla/68/US, with exceptions of HuCV185/87/Korea and HuCV1115/90/Korea. Computer analyses showed that the PCR products had a continuous protein encoding frame on the positive strand, and contained GLPSG and YGDD amino acid motifs at the predicted distance from primers. Alignment of the amino acid sequences of HuCVs with previously published sequences for Snow Mountain agent (SMA), NV, and Sapporo/82/Japan indicated that these strains can be divided into four major genogroups. There were 10 (45%) SMA-like CVs, one (4.5%) NV-like HuCVs, two (9%) Sapporo-like HuCVs, and nine (41%) unidentified HuCVs. This fourth genogroup should be investigated further. HuCV185/87/Korea and HuCV1115/90/Korea, Sapporo-like CVs, were genetically distinct from previously characterized HuCVs and more closely related to known animal CVs. One of the animal CV-like strain, HuCV185/87/Korea, showed nucleotide and amino acid homology of only 67% and 73% with the prototype Sapporo/82/Japan. Further characterization of animal and human CV genomes and studies of possible cross-transmission of CVs from animals to humans are likely to be beneficial in understanding the epidemiology of HuCVs.
