{"title":"荧光、dna结合染料快速检测沙眼衣原体。","authors":"K Grossgebauer, H Rolly","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The newer DNA-binding fluorochromes DAPI (4',6-diamidino-2-phenylindole) and fluorochrome 33258 H (Hoechst) (2-[2-(4-hydroxy-phenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazyl)-benzimidazole . 3 HCl) proved useful in identifying genital strains of Chlamydia trachomatis in McCoy cells. For practical purposes, e.g. to analyse patient specimens, we recommend this technique using the fluorochromes at pH 2.0 in a final concentration of 3 micrograms/ml and non-replicative McCoy cells after fixation with alcohol-acetic acid. The application of the fluorochrome technique in demonstrating Chlamydia trachomatis-infections is recommendable because it is a) simple to perform, b) a rapid procedure, c) it corresponded well with the Giemsa staining in identifying mature inclusions, and d) it facilitates the detection of the RNA-rich early stages of chlamydial growth. For this reasons the fluorochrome technique with DAPI or 33258 H at pH 2.0 can be considered a highly specific and sensitive method for identifying Chlamydia trachomatis.</p>","PeriodicalId":76158,"journal":{"name":"Microscopica acta","volume":"86 1","pages":"1-11"},"PeriodicalIF":0.0000,"publicationDate":"1982-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Fluorescent, DNA-binding dyes for rapid detection of Chlamydia trachomatis.\",\"authors\":\"K Grossgebauer, H Rolly\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The newer DNA-binding fluorochromes DAPI (4',6-diamidino-2-phenylindole) and fluorochrome 33258 H (Hoechst) (2-[2-(4-hydroxy-phenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazyl)-benzimidazole . 3 HCl) proved useful in identifying genital strains of Chlamydia trachomatis in McCoy cells. For practical purposes, e.g. to analyse patient specimens, we recommend this technique using the fluorochromes at pH 2.0 in a final concentration of 3 micrograms/ml and non-replicative McCoy cells after fixation with alcohol-acetic acid. The application of the fluorochrome technique in demonstrating Chlamydia trachomatis-infections is recommendable because it is a) simple to perform, b) a rapid procedure, c) it corresponded well with the Giemsa staining in identifying mature inclusions, and d) it facilitates the detection of the RNA-rich early stages of chlamydial growth. For this reasons the fluorochrome technique with DAPI or 33258 H at pH 2.0 can be considered a highly specific and sensitive method for identifying Chlamydia trachomatis.</p>\",\"PeriodicalId\":76158,\"journal\":{\"name\":\"Microscopica acta\",\"volume\":\"86 1\",\"pages\":\"1-11\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1982-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microscopica acta\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microscopica acta","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
新的dna结合荧光染料DAPI(4′,6-二氨基-2-苯基吲哚)和荧光染料33258 H (Hoechst)(2-[2-(4-羟基苯基)-6-苯并咪唑]-6-(1-甲基-4-哌嗪基)-苯并咪唑。事实证明,3hcl)可用于鉴定McCoy细胞中的沙眼衣原体生殖器菌株。出于实际目的,例如分析患者标本,我们推荐使用pH为2.0的荧光染料,最终浓度为3微克/毫升,并使用酒精-乙酸固定后的非复制McCoy细胞。荧光技术在沙眼衣原体感染诊断中的应用是值得推荐的,因为它a)操作简单,b)过程快速,c)在鉴定成熟包裹体时与吉姆萨染色相吻合,d)它有助于检测衣原体生长的富含rna的早期阶段。因此,使用DAPI或33258 H在pH 2.0下的荧光技术可以被认为是一种高度特异和敏感的沙眼衣原体鉴定方法。
Fluorescent, DNA-binding dyes for rapid detection of Chlamydia trachomatis.
The newer DNA-binding fluorochromes DAPI (4',6-diamidino-2-phenylindole) and fluorochrome 33258 H (Hoechst) (2-[2-(4-hydroxy-phenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazyl)-benzimidazole . 3 HCl) proved useful in identifying genital strains of Chlamydia trachomatis in McCoy cells. For practical purposes, e.g. to analyse patient specimens, we recommend this technique using the fluorochromes at pH 2.0 in a final concentration of 3 micrograms/ml and non-replicative McCoy cells after fixation with alcohol-acetic acid. The application of the fluorochrome technique in demonstrating Chlamydia trachomatis-infections is recommendable because it is a) simple to perform, b) a rapid procedure, c) it corresponded well with the Giemsa staining in identifying mature inclusions, and d) it facilitates the detection of the RNA-rich early stages of chlamydial growth. For this reasons the fluorochrome technique with DAPI or 33258 H at pH 2.0 can be considered a highly specific and sensitive method for identifying Chlamydia trachomatis.