Sequence and Phylogenetic Analysis of Respiratory Syncytial Virus Isolated from Korea

국내에서 유행한 Respiratory Syncytial 바이러스의 염기서열 및 계통분석

  • Kwon, Soon-Young (Department of Microbiology, College of Medicine, Institute for Viral Diseases, Korea University) ;
  • Choi, Young-Ju (Department of Microbiology, College of Medicine, Institute for Viral Diseases, Korea University) ;
  • Kim, So-Youn (Department of Microbiology, College of Medicine, Institute for Viral Diseases, Korea University) ;
  • Song, Ki-Joon (Department of Microbiology, College of Medicine, Institute for Viral Diseases, Korea University) ;
  • Lee, Yong-Ju (Department of Microbiology, College of Medicine, Institute for Viral Diseases, Korea University) ;
  • Choi, Jong-Ouck (Department of Otolaryngology, College of Medicine, Korea University) ;
  • Seong, In-Wha (Department of Microbiology, College of Medicine, Institute for Viral Diseases, Korea University)
  • 권순영 (고려대학교 의과대학 미생물학교실, 고려대학교 바이러스병연구소) ;
  • 최영주 (고려대학교 의과대학 미생물학교실, 고려대학교 바이러스병연구소) ;
  • 김소연 (고려대학교 의과대학 미생물학교실, 고려대학교 바이러스병연구소) ;
  • 송기준 (고려대학교 의과대학 미생물학교실, 고려대학교 바이러스병연구소) ;
  • 이용주 (고려대학교 의과대학 미생물학교실, 고려대학교 바이러스병연구소) ;
  • 최종욱 (고려대학교 의과대학 이비인후과학교실) ;
  • 성인화 (고려대학교 의과대학 미생물학교실, 고려대학교 바이러스병연구소)
  • Published : 1996.06.30

Abstract

Respiratory Syncytial virus (RSV) is an important cause of acute lower respiratory tract infections in human, with infants and young children being particularly susceptible. In the temperate zones, sharp annual outbreaks of RSV occur during the colder months, in both the northern and the southern hemisphere. RSV is unusual in that it can repeatedly reinfect individuals throughout life and infect babies in the presence of maternal antibody. RSV isolates can be divided into two subgroups, A and B, on the basis of their reactions with monoclonal antibodies, and the two subgroups are also distinct at the nucleotide sequence level. The specific diagnosis of RSV infection was best made by isolation of virus in tissue culture, identification of viral antigen, or by specific serologic procedures. Recently, rapid detection of RSV and analysis of RSV strain variation became possible by development of methods of reverse transcription and polymerase chain reaction amplification. In this study, to determine the genetic diversity of RSV found in Korea, 173 bp and 164 bp spanning selected regions of the RSV F and SH genes were enzymatically amplified and sequenced, respectively. Eight for F gene and three for SH gene were detected in 66 nasopharyngeal swap samples tested. Two major antigenic subgroups, A and B were confirmed from Korean samples (seven for subgroup A and one for subgroup B). At the nucleotide level of the F gene region, Korean subgroup A strains showed 95-99% homologies compared to the prototype A2 strain of subgroup A and 93-100% homologies among Korean subgroup A themselves. For the SH gene region, Korean subgroup A strain showed 97.5% homology compared to the prototype A2 strain of subgroup A, and Korean subgroup B strain showed 97% homology compared to the prototype 18537 strain of subgroup B. Most of base changes were transition and occured in codon position 3, which resulted in amino acid conservation. Using the maximum parsimony method, phylogenetic analysis indicated that Korean RSV strains formed a group with other RSV strains isolated from the United States, Canada, the Great Britain and Australia.

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