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慢性前列腺炎患者前列腺液细菌16S rRNA基因的检测 被引量:1

Detection of 16S ribosomal RNA gene of bacteria in prostatic secretion of patients with chronic prostatitis
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摘要 目的通过采用聚合酶链反应(PCR)技术对慢性前列腺炎患者前列腺液中细菌16S rRNA基因检测,探讨PCR方法诊断慢性前列腺炎细菌学病因的价值。方法收集102例慢性前列腺炎患者的前列腺液进行细菌培养,同时采用PCR法检测前列腺液中细菌16S rRNA基因,并测定和分析所得片段的DNA序列。对培养结果与PCR法检测结果进行了比较。结果102份前列腺液标本中,细菌培养法18例阳性,84例阴性,阳性率17.7%;PCR法71例阳性,31例阴性,阳性率69.6%。细菌培养法与PCR法检测结果比较,其差异有统计学意义(P<0.05)。测序结果显示DNA序列与GenBank公布的16S rRNA基因序列具有很高的同源性。结论PCR技术对慢性前列腺炎的临床诊断具有重要意义。 Objective To explore the role of bacteria in chronic prostatitis by detecting the bacterial 16S ribosomal RNA gene of the expressed prostatic secretion (EPS) using polymerase chain reaction (PCR). Methods EPS from 102 patients with chronic prostatitis were performed bacteria culture and analyzed by PCR for bacterial 16S ribosomal RNA gene. The DNA fragments were directly sequenced and compared with the 16S ribosomal RNA sequences reported in GenBank. At the same time, the results of two methods were compared. Results Among 102 EPS specimens, there were 18 positive and 84 negative analyzed by culture, and the positive rate of bacteria culture wasl7.7%. There were 71 positive in 16S ribosomal RNA gene and 31 negative analyzed by PCR, and the positive rate was 69.6%. There were sig- nificant difference between the result of bacteria culture and PCR (P 〈 O. 05 ). The DNA sequences had significantly ho- mology with 16S ribosomal RNA gene. Conclusions PCR technique plays an important part in clinical diagnosis of chronic prostatitis.
出处 《检验医学》 CAS 北大核心 2009年第3期165-168,共4页 Laboratory Medicine
关键词 慢性前列腺炎 前列腺液 16S RRNA基因 聚合酶链反应 Chronic prostatitis Prostatic secretion 16S ribosomal RNA gene Polymerase chain reaction
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  • 1夏同礼,孔祥田,宓培,王静华,苏晋伟.我国成人前列腺非特异性炎[J].中华泌尿外科杂志,1995,16(12):711-712. 被引量:82
  • 2Krieger JN,Ross SO,Riley DE,et al.Chronic prostatitis:epidemi-ology and role of infection.Urology ,2002,60:8~13.
  • 3Krieger JN, Nyberg L Jr, Nickel JC. NIH consensus definition and classification of prostatitis [ letter ] [ J ]. JAMA, 1999, 282(3) :236-237.
  • 4Tanner MA, Shoskes D, Shahed A, et al. Prevalence of corynebacterial 16S rRNA sequences in Patients with bacterial and "nonbacterial" prostatitis [J]. J Clin Micro, 1999, 37(6) :1863 -1870.
  • 5Nickel JC. Prostratitis. In: MulbollandG (ED) [A]. Antibiotics in Urology. Philadelphia: Lippincott, 1996. 57-70.
  • 6Nickel JC, Downey J, Johnston B, et al. Predictors of patient response to antibiotic therapy for the chronic prostatitis/chronic pelvic pain syndrome : a prospective multicenter clinical trial [ J ]. J Urol, 2001, 165(5) : 1539-1544.
  • 7Meier A, Persing DH, Finken M, et al. Elimination of contaminating DNA within polymerase chain reaction reagents : implications for a general approach to detection of uncultured pathogens[J]. J Clin Micro, 1993, 31(3) : 646-652.
  • 8Krieger JN, Riley DE, Robert MC, et al. Prokarotic DNA sequences in patients with chronic idiopathic prostatitis[J]. J Clin Micro, 1996, 34(12), 3120-3128.
  • 9Hochreiter WW, Duncan JL, Schaeffer AJ. Evaluation of the bacterial flora of the prostate using a 16S rRNA gone based polymerase chain reaction[J]. J Urol, 2000, 163(1) : 127-130.
  • 10Riley DE, Berger RE, Miner DC, et al. Diverse and related 16S rRNA-encoding DNA sequences in prostate tissues of men with chronic prostatitis [ J ]. J Clin Microbiol, 1998, 36(6) : 1646-1652.

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