Snipes L J, Gamard P M, Narcisi E M, Beard C B, Lehmann T, Secor W E
Immunology Branch, Division of Parasitic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Public Health Service, U.S. Department of Health and Human Services, Atlanta, Georgia 30341-3724, USA.
J Clin Microbiol. 2000 Aug;38(8):3004-9. doi: 10.1128/JCM.38.8.3004-3009.2000.
Trichomonas vaginalis, the causative agent for human trichomoniasis, is a problematic sexually transmitted disease mainly in women, where it may be asymptomatic or cause severe vaginitis and cervicitis. Despite its high prevalence, the genetic variability and drug resistance characteristics of this organism are poorly understood. To address these issues, genetic analyses were performed on 109 clinical isolates using three approaches. First, two internal transcribed spacer (ITS) regions flanking the 5.8S subunit of the ribosomal DNA gene were sequenced. The only variation was a point mutation at nucleotide position 66 of the ITS1 region found in 16 isolates (14.7%). Second, the presence of a 5.5-kb double-stranded RNA T. vaginalis virus (TVV) was assessed. TVV was detected in 55 isolates (50%). Finally, a phylogenetic analysis was performed based on random amplified polymorphic DNA data. The resulting phylogeny indicated at least two distinct lineages that correlate with the presence of TVV. A band-sharing index indicating relatedness was created for different groups of isolates. It demonstrated that isolates harboring the virus are significantly more closely related to each other than to the rest of the population, and it indicated a high level of relatedness among isolates with in vitro metronidazole resistance. This finding is consistent with the hypothesis that drug resistance to T. vaginalis resulted from a single or very few mutational events. Permutation tests and nonparametric analyses showed associations between metronidazole resistance and phylogeny, the ITS mutation, and TVV presence. These results suggest the existence of genetic markers with clinical implications for T. vaginalis infections.
阴道毛滴虫是人类滴虫病的病原体,是一种主要困扰女性的性传播疾病,在女性中可能无症状,也可能引起严重的阴道炎和宫颈炎。尽管其患病率很高,但对这种生物体的遗传变异性和耐药性特征了解甚少。为了解决这些问题,使用三种方法对109株临床分离株进行了遗传分析。首先,对核糖体DNA基因5.8S亚基两侧的两个内部转录间隔区(ITS)进行测序。唯一的变异是在16株分离株(14.7%)中发现的ITS1区域核苷酸位置66处的点突变。其次,评估5.5 kb双链RNA阴道毛滴虫病毒(TVV)的存在情况。在55株分离株(50%)中检测到TVV。最后,基于随机扩增多态性DNA数据进行系统发育分析。所得系统发育结果表明至少有两个不同的谱系与TVV的存在相关。为不同组的分离株创建了一个表示相关性的条带共享指数。结果表明,携带病毒的分离株彼此之间的关系比与其他群体的关系更为密切,并且表明体外对甲硝唑耐药的分离株之间存在高度相关性。这一发现与阴道毛滴虫耐药性是由单个或极少数突变事件导致的假设一致。置换检验和非参数分析表明甲硝唑耐药性与系统发育、ITS突变和TVV存在之间存在关联。这些结果表明存在对阴道毛滴虫感染具有临床意义的遗传标记。