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E/NS1 modifications of dengue 2 virus after serial passages in mammalian and/or mosquito cells

  • Wei June Chen*
  • , Hsin Rong Wu
  • , Shyang Song Chiou
  • *此作品的通信作者
  • National Taiwan University
  • Chang Gung University

研究成果: 期刊稿件文章同行評審

51 引文 斯高帕斯(Scopus)

摘要

Objective: Dengue viruses are routinely maintained in nature by transmission cycles involving the passage of virus between humans and Aedes mosquitoes. The number of dengue virus lineages has been increasing over time. The aim of this study was to identify the genetic diversity of dengue 2 virus serially transferred in mammalian and/or mosquito cells. Methods: The E/NS1 gene of dengue 2 virus variants derived from serial passages in Vero or C6/36 cells, or alternately in both cell systems, was amplified and sequenced in order to observe gene modification after serial passages. Results: Three nucleotides (two in E and one in NS1) or two amino acids (one each in E and NS1) changed in the virus that was continuously cultured in Vero cells for 20 passages, whereas four nucleotides (two each in E and NS1) or three amino acids (one in E and two in NS1) changed in the virus cultured for 30 passages. The genome of dengue 2 virus remained stable even when the virus was serially transferred in C6/36 cells for 30 generations. However, there was one amino acid substitution (E)46 I→V) resulting from a single nucleotide change in the E region of dengue 2 virus alternately transferred in C6/36 and Vero cells for either 20 or 30 passages. In addition, dengue 2 virus obtained from serially cultured Vero cells usually replicated better when it reinfected Vero cells, reflecting its high adaptation fitness to the host cell. Con-clusions: It is concluded that genetic changes of dengue 2 virus are constrained in Vero (mammalian) cells, resulting in a variety of genome-related quasispecies populations. Some populations of the virus are subsequently selected by and genetically (at least in the E/NS1 portion of the viral genome) maintained in C6/36 (mosquito) cells during replicative competition.

原文英語
頁(從 - 到)289-295
頁數7
期刊Intervirology
46
發行號5
DOIs
出版狀態已出版 - 2003

UN SDG

此研究成果有助於以下永續發展目標

  1. SDG3 健康與福祉
    SDG3 健康與福祉

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