The use of molecular techniques for the diagnosis and epidemiologic study of sexually transmitted infections

被引:9
作者
Carolyn M. Black
Stephen A. Morse
机构
[1] Centers for Disease Control and Prevention,
关键词
Polymerase Chain Reaction Assay; Chlamydia Trachomatis; Genital Herpes; Neisseria Gonorrhoeae; Nucleic Acid Amplification;
D O I
10.1007/s11908-000-0085-x
中图分类号
学科分类号
摘要
Molecular diagnostic tests are more sensitive and, in many cases, more specific than conventional laboratory methods for the detection of sexually transmitted infections. Here, we review recently developed molecular methods for the diagnosis and subtyping of the most common sexually transmitted infections: infections caused by Chlamydia trachomatis, Neisseria gonorrhoeae, human papillomavirus, Trichomonas vaginalis, and the agents of genital ulcer disease (Haemophilus ducreyi, herpes simplex virus, Treponema pallidum, and Calymmatobacterium granulomatis). We also provide an overview of the laboratory diagnostic tests and clinical specimens to use when infection with these agents is suspected.
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页码:31 / 43
页数:12
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[1]  
Davis JD(1998)A comparison of ligase chain reaction to polymerase chain reaction in the detection of Chlamydia trachomatis endocervical infections Infect Dis Obstet Gynecol 6 57-60
[2]  
Riley PK(1997)Comparison of manual Amplicor PCR, Cobas Amplicor PCR, and LCx assays for detection of Chlamydia trachomatis infection in women by using urine specimens J Clin Microbiol 35 402-405
[3]  
Peters CW(1998)Comparison of performances of two commercially available tests, a PCR assay and ligase chain reaction test, in detection of urogenital Chlamydia trachomatis infection J Clin Microbiol 36 1489-1493
[4]  
Rand KH(1997)Comparison of three commercially available amplification assays, AMP CT, LCx, and COBAS AMPLICOR, for detection of Chlamydia trachomatis in first-void urine J Clin Microbiol 35 2628-2633
[5]  
Pasternack R(1998)Comparison of Roche Cobas Amplicor and Abbott LCx for the rapid detection of Chlamydia trachomatis in specimens from highrisk patients Sex Transm Dis 25 44-48
[6]  
Vuorinen P(1997)Ability of commercial ligase chain reaction and PCR assays to diagnose Chlamydia trachomatis infections in men by testing first-void urine J Clin Microbiol 35 982-984
[7]  
Pitkajarvi T(1998)Performance of transcription-mediated amplification and ligase chain reaction assays for detection of chlamydial infection in urogenital samples obtained by invasive and noninvasive methods J Clin Microbiol 36 2666-2670
[8]  
Puolakkainen M(1998)Inhibition of PCR in genital and urine specimens submitted for Chlamydia trachomatis testing J Clin Microbiol 36 2356-2358
[9]  
Hiltunen-Back E(1997)False-negative results of a ligase chain reaction assay to detect Chlamydia trachomatis due to inhibitors in urine Eur J Clin Microbiol Infect Dis 16 727-731
[10]  
Reunala T(1998)Urine specimens from pregnant and nonpregnant women inhibitory to amplification of Chlamydia trachomatis nucleic acid by PCR, ligase chain reaction, and transcription-mediated amplification: identification of urinary substances associated with inhibition and removal of inhibitory activity J Clin Microbiol 36 3122-3126