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23SrDNA基因芯片对临床常见致病菌的检测 被引量:3

Detection of Clinical Infectious Bacteria by 23S Ribosomal DNA Microchips
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摘要 目的建立含有10种细菌探针的检测用基因芯片模型。方法使用合成的23SrDNA寡核苷酸探针,制备基因芯片。细菌核糖体DNA经过23SrDNA通用引物扩增后与芯片上的探针杂交,用荧光扫描仪检测信号。结果基因芯片检测临床致病菌具有较高的特异性和灵敏性。结论寡核苷酸探针基因芯片检测系统具有一定的种属鉴别能力,比常规培养法快速、准确。 Objective To develop a gene chip model containing 10 probes for infectious bacteria.Methods Ten synthesized oligonucleotide 23S rDNA probes were employed to make gene chips by spoter. The DNA of bacteria was amplified by 23S rDNA universal primers and the PCR product was then applied to the gene chips for hybridization. A fluorescent scanner was used to observe and record the hybridization signals.Results The sensitivity and specificity was high in detecting bacterial 23S rDNA by gene chips method.Conclusion The oligonucleotide microarray could determine most of the test strains at species level. It is more rapid and accurate than routine culture method.
出处 《华中科技大学学报(医学版)》 CAS CSCD 北大核心 2005年第3期356-358,362,共4页 Acta Medicinae Universitatis Scientiae et Technologiae Huazhong
基金 湖北省科技攻关计划资助项目(No.2003AA301C61)
关键词 23S RDNA 基因芯片 共同引物 细菌感染 23S rDNA gene chip universal primers bacteria infection
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  • 1Gurtler V, Stanisich V A. New approaches to typing and identification of bacteria using the 16S-23S rDNA spacer region. Microbiology,1996,142:3
  • 2Hall L M, Duke B, Urwin G. An approach to the identification of the pathogens of bacterial meningitis by the polymerase chain reaction. Eur J Clin Microbiol Infect Dis, 1995,14:1090
  • 3Bacot C M,Reeves R H. Novel tRNA gene organization in the 16S-23S intergenic spacer of the streptococcus pneumoniae rRNA gene cluster. J Bacteria,1991,173:4234
  • 4Roller C, Ludwig W, Schleifer K H. Gram-positive bacteria with a high DNA G+C content are characterized by a common insertion within their 23S rRNA genes. J General Microbiol,1992,138:1167
  • 5徐芸,杨瑞馥,郭兆彪,李继昌.PCR-Dotblot杂交法直接检测临床病原菌的报告[J].中华医院感染学杂志,1998,8(1):14-16. 被引量:11
  • 6Anthony R M, Brown T J, French G L. Rapid diagnosis of bacterimia by universal amplification of 23S ribosomal DNA followed by hybridization to an oligonucleotide array.J Clin Microbiol, 2000,38:781

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