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首页> 外文期刊>Journal of Clinical Microbiology >Multiplex PCR Testing Detection of Higher-than-Expected Rates of Cervical Mycoplasma, Ureaplasma, and Trichomonas and Viral Agent Infections in Sexually Active Australian Women
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Multiplex PCR Testing Detection of Higher-than-Expected Rates of Cervical Mycoplasma, Ureaplasma, and Trichomonas and Viral Agent Infections in Sexually Active Australian Women

机译:多重PCR检测检测到性活跃的澳大利亚女性宫颈支原体,脲原体和滴虫和病毒的感染率高于预期

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Knowing the prevalence of potential etiologic agents of nongonococcal and nonchlamydial cervicitis is important for improving the efficacy of empirical treatments for this commonly encountered condition. We describe four multiplex PCRs (mPCRs), designated VDL05, VDL06, VDL07, and VDL09, which facilitate the detection of a wide range of agents either known to be or putatively associated with cervicitis, including cytomegalovirus (CMV), enterovirus (EV), Epstein-Barr virus (EBV), varicella-zoster virus (VZV), herpes simplex virus type 1 (HSV-1), and herpes simplex virus type 2 (HSV-2) (VDL05); Ureaplasma parvum, Ureaplasma urealyticum, Mycoplasma genitalium, and Mycoplasma hominis (VDL06); Chlamydia trachomatis, Trichomonas vaginalis, Treponema pallidum, and group B streptococci (VDL07); and adenovirus species A to E (VDL09). The mPCRs were used to test 233 cervical swabs from 175 women attending a sexual-health clinic in Sydney, Australia, during 2006 and 2007. The agents detected alone or in combination in all cervical swabs (percentage of total swabs) included CMV (6.0), EV (2.1), EBV (2.6), VZV (4.7), HSV-1 (2.6), HSV-2 (0.8), HSV-2 and VZV (0.4), U. parvum (57.0), U. urealyticum (6.1), M. genitalium (1.3), M. hominis (13.7), C. trachomatis (0.4), T. vaginalis (3.4), and group B streptococci (0.4). Adenovirus species A to E and T. pallidum were not detected. These assays are adaptable for routine diagnostic laboratories and provide an opportunity to measure the true prevalence of microorganisms potentially associated with cervicitis and other genital infections.
机译:了解非淋球菌和非衣原体宫颈炎的潜在病原体的流行对于提高针对这种常见疾病的经验治疗的有效性非常重要。我们描述了四个多重PCR(mPCR),分别命名为VDL05,VDL06,VDL07和VDL09,它们有助于检测多种与宫颈炎有关的试剂,包括巨细胞病毒(CMV),肠病毒(EV),爱泼斯坦巴尔病毒(EBV),水痘带状疱疹病毒(VZV),1型单纯疱疹病毒(HSV-1)和2型单纯疱疹病毒(HSV-2)(VDL05); Ureaplasma parvum Ureaplasma Ur解霉菌生殖器支原体人支原体(VDL06); 沙眼衣原体,阴道毛滴虫,梅毒螺旋体和B组链球菌(VDL07);和腺病毒种A至E(VDL09)。 mPCR用于测试2006年至2007年间在澳大利亚悉尼性健康诊所就诊的175名妇女的233例宫颈拭子。在所有宫颈拭子中(单独或联合检测)的试剂(总拭子百分比)包括CMV(6.0) ,EV(2.1),EBV(2.6),VZV(4.7),HSV-1(2.6),HSV-2(0.8),HSV-2和VZV(0.4), U。 parvum (57.0), U。解脲酶(6.1), M。生殖器(1.3), M。 Hominis (13.7), C。沙眼(0.4), T。 (3.4)和B组链球菌(0.4)。腺病毒种A至E和T。未检测到苍白子。这些测定适用于常规诊断实验室,并提供了一个机会来测量可能与宫颈炎和其他生殖器感染有关的微生物的真实流行率。

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