M. N. Mangada, Halimah Mohamed, Leticia del Carmen Castillo, F. Hasebe, A. Igarashi
{"title":"EFFECT OF INCUBATION TEMPERATURE ON DENGUE-2 VIRAL ANTIGEN PRODUCTION AND VIRAL RNA SYNTHESIS IN INFECTED Aedes albopictus CLONE C6/36 CELL LINE","authors":"M. N. Mangada, Halimah Mohamed, Leticia del Carmen Castillo, F. Hasebe, A. Igarashi","doi":"10.11418/JTCA1981.14.4_213","DOIUrl":null,"url":null,"abstract":"Increase in the incubation temperature of infected Aedes albopictus clone C6/36 cells from its optimal growth temperature of 28°C to 32 and 37°C showed a concomitant rise in the production of dengue virus type 2 antigen and genomic RNA. The quantitative reverse transcription-polymerase chain reaction using an internal standard as a measuring tool for the viral genomic RNA showed that RNA production was higher in the cells and in the extracellular fluid from the cultures incubated at 32 and 37°C than at 28°C. The presence of viral antigen and viral genomic RNA was also detected 1-2 days earlier in the cultures incubated at elevated temperatures.","PeriodicalId":308966,"journal":{"name":"Tissue culture research communications : the journal of experimental & applied cell culture research","volume":"58 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1995-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tissue culture research communications : the journal of experimental & applied cell culture research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11418/JTCA1981.14.4_213","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3
Abstract
Increase in the incubation temperature of infected Aedes albopictus clone C6/36 cells from its optimal growth temperature of 28°C to 32 and 37°C showed a concomitant rise in the production of dengue virus type 2 antigen and genomic RNA. The quantitative reverse transcription-polymerase chain reaction using an internal standard as a measuring tool for the viral genomic RNA showed that RNA production was higher in the cells and in the extracellular fluid from the cultures incubated at 32 and 37°C than at 28°C. The presence of viral antigen and viral genomic RNA was also detected 1-2 days earlier in the cultures incubated at elevated temperatures.