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源自恰加斯病患者的克氏锥虫株系和克隆的多样性。II. 同工酶和限制性片段长度多态性特征分析

Diversity of Trypanosoma cruzi stocks and clones derived from Chagas disease patients. II. Isozyme and RFLP characterizations.

作者信息

Lauria-Pires L, Bogliolo A R, Teixeira A R

机构信息

Departamento de Patologia, Faculdade de Ciências da Saúde, Universidade de Brasilia, DF Brazil.

出版信息

Exp Parasitol. 1996 Mar;82(2):182-90. doi: 10.1006/expr.1996.0023.

Abstract

Isoenzyme and RFLP analyses were carried on freshly isolated Trypanosoma cruzi stocks and subsequent clones derived from patients with chronic Chagas disease. The isoenzymes separated the parasite stocks and clones in two groups: The stock hSLU239 (group I), isolated from a heart disease patient, showed the zymodeme 3 (Z3) profile (M. A. Miles et al., 1977, Transactions of the Royal Society of Tropical Medicine and Hygiene 71, 217-225). The stock mSLU142 (group II), isolated from a digestive disease (megaesophagus) patient, showed the Z2 profile. The parasite clones m1, m2, m3, and m4, derived from mSLU142, and clones h1 and h2, derived from hSLU239, showed isoenzyme profiles similar to those of Z2 and ZA (Miles et al. 1977; J. A. Romanha, 1982, Thesis, Universidade Federal de Minas Gerais). Furthermore, the T. cruzi clones derived from the cardiac disease patient differed from those derived from the megacolon patient in 3 of the 13 enzymes analyzed. RFLP analysis showed polymorphism at the EcoRI and PstI restriction fragments of the DNA sequences coding the glycolytic enzymes ALD, GPI, GAPDH, and PYK and separated the T. cruzi stocks and clones in three groups: I, comprising the stock hSLU239 and clone m4, which was classified as homozygous CC, BB, AA, and AA for the ALD, GPI, PYK, and GAPDH genes, respectively; II, formed by the parasite stock mSLU142 and clones h1 and h2 (derived from hSLU239), which was classified as homozygous AA, AA, CC, and BB for ALD, GPI, PYK, and GAPDH genes, respectively . These findings show that the infection of each Chagas disease patient may be produced by genetically diverse mixed parasite populations.

摘要

对从慢性恰加斯病患者中分离出的新鲜克氏锥虫原种及其后续克隆进行了同工酶和限制性片段长度多态性(RFLP)分析。同工酶分析将寄生虫原种和克隆分为两组:从一名心脏病患者分离出的原种hSLU239(第一组)显示出酶谱型3(Z3)(M. A. 迈尔斯等人,1977年,《皇家热带医学与卫生学会会刊》71卷,217 - 225页)。从一名消化系统疾病(巨食管)患者分离出的原种mSLU142(第二组)显示出Z2谱型。源自mSLU142的寄生虫克隆m1、m2、m3和m4,以及源自hSLU239的克隆h1和h2,显示出与Z2和ZA相似的同工酶谱型(迈尔斯等人,1977年;J. A. 罗曼哈,1982年,论文,米纳斯吉拉斯联邦大学)。此外,在分析的13种酶中,源自心脏病患者的克氏锥虫克隆与源自巨结肠患者的克隆在3种酶上存在差异。RFLP分析显示,编码糖酵解酶ALD、GPI、GAPDH和PYK的DNA序列的EcoRI和PstI限制性片段存在多态性,并将克氏锥虫原种和克隆分为三组:第一组包括原种hSLU239和克隆m4,它们分别被分类为ALD、GPI、PYK和GAPDH基因的纯合子CC、BB、AA和AA;第二组由寄生虫原种mSLU142和克隆h1及h2(源自hSLU239)组成,它们分别被分类为ALD、GPI、PYK和GAPDH基因的纯合子AA、AA、CC和BB。这些发现表明,每位恰加斯病患者的感染可能是由基因多样的混合寄生虫群体引起的。

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