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ECHOウイルス11型の性状に関する研究 : II. Large plaque(Lp)及びSmall plaque(Sp)変異ウイルスとHeLa細胞の系における持続感染について(ECHOウイルス11型の性状に関する研究)


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タイトル: ECHOウイルス11型の性状に関する研究 : II. Large plaque(Lp)及びSmall plaque(Sp)変異ウイルスとHeLa細胞の系における持続感染について(ECHOウイルス11型の性状に関する研究)
その他のタイトル: Studies on Mutants of ECHO Virus Type 11 : II. Properties of Carrier Culture of HeLa Cells Infected with Large (Lp) and Small (Sp) Plaque Variants of ECHO Virus Type 11
著者: 陳, 境津
著者(別表記) : Chen, Jeng Jieng
発行日: 1971年 6月30日
出版者: 長崎大学熱帯医学研究所 / Institute of Tropical Medicine, Nagasaki University
引用: 熱帯医学 Tropical medicine 13(2). p53-60, 1971
抄録: Carrier culture of HeLa cells persistently infected with ECHO virus type 11, Gregory strain, produced large plaque (Lp) and small plaque (Sp) variant viruses at the initial period of carrier state. After several passages of subculture, however, Lp virus was eliminated from carrier state and only Sp virus was released in the culture fluid. Such phenomenon was also investigated in case of Sp virus carrier culture challenged with Lp virus. On the other hand, Lp virus carrier culture challenged with Sp virus produced only Sp virus. In order to maintain an equilibrium of such carrier culture, antibody need not be supplied in culture medium. Generation time of Sp virus carrier HeLa cells was given 38.6 hours as same as that of normal HeLa cells. The proportion of infected cells in Sp virus carrier culture was 88.8% at the 11th passage and it reduced to 51.9% at the 25th passage. The subcultures of HeLa cells persistently infected with Sp virus became not produced the virus after the 102nd passage (HeLa sp 102). The adsorption of Lp or Sp virus onto that cells was allowed at the rate of 35% or 85% respectively, and the cells escaped from cytopathic effect caused by virus infection. Culture fluid of HeLa sp 102 cells was adjusted pH to 2.0 by adding N-HCl solution, then, kept at 4℃ for 4 days. After readjusting pH to 7.4, the fluid was centrifuged at 100,000g for 2 hours and the supernatant was used for the test of interferon-like activity. The yield of Sp virus particularly Lp virus in normal HeLa cells treated with the supernatant was markedly reduced. On the other hand, these events were not investigated by heating the supernatant at 60℃ for 1 hour. No effect of the supernatant prepared from normal HeLa cells on the yield of Lp or Sp viruses was observed. Consequently, it would be said that the substance prepared from culture fluid of HeLa sp 102 cells indicated the interferon-like activity and Lp virus was more sensitive to it than Sp virus.
URI: http://hdl.handle.net/10069/4090
ISSN: 03855643
資料タイプ: Departmental Bulletin Paper
出現コレクション:第13巻 第2号

引用URI : http://hdl.handle.net/10069/4090

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