Bart Aldert, van der Heijden Harold M, Greve Sophie, Speijer Dave, Landman Wil J, van Gool Tom
Section Parasitology, Department of Medical Microbiology, Academic Medical Center, University of Amsterdam, Meibergdreef 9, Amsterdam 1105 AZ, The Netherlands.
J Clin Microbiol. 2008 Oct;46(10):3270-5. doi: 10.1128/JCM.00680-08. Epub 2008 Jul 23.
Dientamoeba fragilis is a parasite that has been recognized to be a causative agent of gastrointestinal symptoms. Because in most studies only some infected persons experience symptoms, it is possible that D. fragilis is a heterogeneous species with variants that display similar morphologies but different pathogenicities. The search for genetic variation in D. fragilis was based on the small-subunit rRNA gene, which was not found to be useful for molecular epidemiology. In this report, we describe the isolation and characterization of additional rRNA gene cluster sequences, the internal transcribed spacer 1 (ITS-1)-5.8S rRNA gene-ITS-2 region. For comparative purposes, we also isolated the ITS-1-5.8S rRNA gene-ITS-2 region of Histomonas meleagridis, a protozoan parasite of birds and a close relative of D. fragilis. This region was found to be highly variable, and 11 different alleles of the ITS-1 sequence could be identified. Variation in the ITS-1 region was found to be intragenomic, with up to four different alleles in a single isolate. So-called C profiles were produced from the ITS-1 repertoire of single isolates. Analysis of the C profiles of isolates from nonrelated patients identified several clearly distinguishable strains of D. fragilis. Within families, it was shown that members can be infected with the same or different strains of D. fragilis. In conclusion, the ITS-1 region can serve as a molecular epidemiological tool for the subtyping of D. fragilis directly from feces. This may serve as a means of studying the transmission, geographical distribution, and relationships between strains and the pathogenicity of this parasite.
脆弱双核阿米巴是一种已被确认为胃肠道症状病原体的寄生虫。由于在大多数研究中只有部分感染者出现症状,因此脆弱双核阿米巴可能是一个异质物种,其变种具有相似的形态但不同的致病性。对脆弱双核阿米巴遗传变异的研究基于小亚基rRNA基因,但发现该基因对分子流行病学无用。在本报告中,我们描述了额外的rRNA基因簇序列(内部转录间隔区1(ITS-1)-5.8S rRNA基因-ITS-2区域)的分离和特征。为了进行比较,我们还分离了火鸡组织滴虫(一种鸟类原生动物寄生虫,也是脆弱双核阿米巴的近亲)的ITS-1-5.8S rRNA基因-ITS-2区域。发现该区域高度可变,可识别出11种不同等位基因的ITS-1序列。发现ITS-1区域的变异是基因组内变异,单个分离株中存在多达四种不同的等位基因。从单个分离株的ITS-1库中产生了所谓的C图谱。对来自非相关患者分离株的C图谱分析确定了几种明显可区分的脆弱双核阿米巴菌株。在家庭内部,研究表明家庭成员可能感染相同或不同菌株的脆弱双核阿米巴。总之,ITS-1区域可作为直接从粪便中对脆弱双核阿米巴进行亚型分型的分子流行病学工具。这可作为研究该寄生虫的传播、地理分布、菌株间关系及致病性的一种手段。