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首页> 外文期刊>Journal of Clinical Microbiology >Variability of Kinetoplast DNA Gene Signatures of Trypanosoma cruzi II Strains from Patients with Different Clinical Forms of Chagas' Disease in Brazil
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Variability of Kinetoplast DNA Gene Signatures of Trypanosoma cruzi II Strains from Patients with Different Clinical Forms of Chagas' Disease in Brazil

机译:巴西恰加斯氏病不同临床形式患者的克鲁氏锥虫II菌株运动塑料DNA基因签名的变异性

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The clinical course of Chagas' disease varies widely among different patients and geographic regions. For reasons that are not completely understood but involve host and parasite factors, some patients never develop the disease while others present cardiac and/or gastrointestinal symptoms. Many studies have been conducted in order to correlate the genetic variability of the parasites with the clinical forms of the disease, but no conclusive data have been obtained. Our research aims at characterizing the genetic profiles of Trypanosoma cruzi isolates recently obtained from 70 chagasic patients who either showed pathological lesions with symptoms of various intensities or were asymptomatic. All patients came from an area where Chagas' disease is endemic in southeast Brazil where vectorial transmission has been controlled and different clinical forms of the disease can be found. The molecular characterization of parasites evaluated the polymorphisms of the 3′ region of the 24Sα rRNA gene and the variability of kinetoplast DNA (kDNA) minicircles of T. cruzi populations by low-stringency single specific primer PCR. Data presented here provide a strong correlation between T. cruzi II and human infection in this region. However, a high degree of variability was observed within T. cruzi II, as demonstrated by intense kDNA polymorphism among all clinical forms and also within each of them, irrespective of the intensity of pathological processes.
机译:恰加斯病的临床病程在不同患者和地理区域之间差异很大。由于尚未完全了解但涉及宿主和寄生虫因素的原因,一些患者从未发展成该疾病,而其他患者则表现出心脏和/或胃肠道症状。为了使寄生虫的遗传变异性与疾病的临床形式相关联,已经进行了许多研究,但是尚未获得确凿的数据。我们的研究旨在表征最近从70例脱发性哮喘患者中分离出的克鲁姆氏锥虫分离株的遗传特征,这些患者表现出各种强度的病理性病变或无症状。所有患者均来自巴西东南部恰加斯病流行的地区,该地区已控制了媒介传播,可发现该疾病的不同临床形式。寄生虫的分子特征评估了24SαrRNA基因3'区域的多态性和 T的运动塑料DNA(kDNA)小圆的变异性。低严格性单特异性引物PCR技术检测cruzi种群。此处提供的数据在 T之间提供了很强的相关性。 Cruzi II和该地区的人类感染。然而,在 T内观察到高度的可变性。不论病理过程的强度如何,所有临床形式之间以及每种临床形式之间都存在强烈的kDNA多态性,这证明了cruzi II。

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