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本文引用的文献

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Molecular epidemiology of Mycobacterium bovis isolates from South America.来自南美洲的牛分枝杆菌分离株的分子流行病学
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Evaluation of four DNA typing techniques in epidemiological investigations of bovine tuberculosis.四种DNA分型技术在牛结核病流行病学调查中的评估
J Clin Microbiol. 1998 Jan;36(1):168-78. doi: 10.1128/JCM.36.1.168-178.1998.
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Identification by spoligotyping of a caprine genotype in Mycobacterium bovis strains causing human tuberculosis.通过间隔寡核苷酸分型鉴定引起人类结核病的牛分枝杆菌菌株中的一种山羊基因型
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Evaluation of spoligotyping in a study of the transmission of Mycobacterium tuberculosis.在一项关于结核分枝杆菌传播的研究中对间隔寡核苷酸分型技术的评估
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Transmission between HIV-infected patients of multidrug-resistant tuberculosis caused by Mycobacterium bovis.牛分枝杆菌引起的耐多药结核病在艾滋病毒感染患者之间的传播。
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Genetic characterization of multidrug-resistant Mycobacterium bovis strains from a hospital outbreak involving human immunodeficiency virus-positive patients.一起涉及人类免疫缺陷病毒阳性患者的医院感染暴发中多重耐药牛分枝杆菌菌株的基因特征分析
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Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology.同时检测结核分枝杆菌并进行菌株鉴别以用于诊断和流行病学研究。
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The insertion element IS 6110 is a useful tool for DNA fingerprinting of Mycobacterium bovis isolates from cattle and goats in Spain.插入元件IS 6110是用于对西班牙牛和山羊中分离出的牛分枝杆菌进行DNA指纹分析的有用工具。
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Spacer oligonucleotide typing of Mycobacterium bovis strains from cattle and other animals: a tool for studying epidemiology of tuberculosis.牛分枝杆菌菌株的间隔寡核苷酸分型:一种研究结核病流行病学的工具,来自牛和其他动物
J Clin Microbiol. 1996 Nov;34(11):2734-40. doi: 10.1128/jcm.34.11.2734-2740.1996.
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Differentiation of Mycobacterium bovis isolates from animals by DNA typing.通过DNA分型对动物源牛分枝杆菌分离株进行鉴别。
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间隔寡核苷酸分型法在南美洲牛分枝杆菌相关感染分子流行病学中的应用价值

Usefulness of spoligotyping in molecular epidemiology of Mycobacterium bovis-related infections in South America.

作者信息

Zumárraga M J, Martin C, Samper S, Alito A, Latini O, Bigi F, Roxo E, Cicuta M E, Errico F, Ramos M C, Cataldi A, van Soolingen D, Romano M I

机构信息

Instituto de Biotecnología, Centro de Investigación en Ciencias Veterinarias, INTA, Buenos Aires, Argentina.

出版信息

J Clin Microbiol. 1999 Feb;37(2):296-303. doi: 10.1128/JCM.37.2.296-303.1999.

DOI:10.1128/JCM.37.2.296-303.1999
PMID:9889207
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC84290/
Abstract

Two hundred twenty-four Mycobacterium bovis isolates, mainly from South American countries, were typed by spoligotyping, and 41 different spoligotypes were identified. A total of 202 M. bovis isolates (90%) were grouped into 19 different clusters. The largest cluster contained 96 isolates (42.8%) on the basis of the most frequently observed spoligotype, spoligotype 34. Nineteen M. bovis isolates from humans in Argentina had spoligotypes and polymorphic GC-rich repetitive sequence (PGRS) types that represented the most common types found among isolates from cattle. All five isolates from Uruguay and three of the six isolates from Paraguay had spoligotypes that were also detected for isolates from Argentina. The spoligotypes of isolates from Brazil, Costa Rica, and Mexico and of some of the isolates from Paraguay could not be found in Argentina. A total of 154 M. bovis isolates were selected in order to compare the discriminative power of spoligotyping and restriction fragment length polymorphism (RFLP) analysis with direct repeat (DR) and PGRS probes. By spoligotyping, 31 different types were found, while AluI-digested DR probe-associated RFLP analysis identified 42 types, and RFLP analysis with the PGRS probe also detected 42 types; these were partly independent of the DR types. By combining the results obtained by spoligotyping and by RFLP analysis with the DR and PGRS probes, 88 different types were obtained. Although the differentiation of M. bovis by spoligotyping was less discriminatory than differentiation by RFLP analysis with the DR and PGRS probes, spoligotyping is easier to perform and its results are easier to interpret. Therefore, for the purpose of typing of M. bovis isolates, spoligotyping could be performed first and the isolates could be grouped into clusters and then analyzed by RFLP analysis with the DR and PGRS probes.

摘要

对224株主要来自南美国家的牛分枝杆菌分离株进行了间隔寡核苷酸分型,共鉴定出41种不同的间隔寡核苷酸分型。共有202株牛分枝杆菌分离株(90%)被归入19个不同的簇。基于最常见的间隔寡核苷酸分型——间隔寡核苷酸分型34,最大的簇包含96株分离株(42.8%)。来自阿根廷人类的19株牛分枝杆菌分离株具有间隔寡核苷酸分型和富含GC的多态性重复序列(PGRS)类型,这些类型代表了在牛分离株中发现的最常见类型。来自乌拉圭的所有5株分离株以及来自巴拉圭的6株分离株中的3株,其间隔寡核苷酸分型在阿根廷的分离株中也被检测到。来自巴西、哥斯达黎加和墨西哥的分离株以及来自巴拉圭的一些分离株的间隔寡核苷酸分型在阿根廷未被发现。总共选择了154株牛分枝杆菌分离株,以比较间隔寡核苷酸分型和使用直接重复序列(DR)及PGRS探针的限制性片段长度多态性(RFLP)分析的鉴别能力。通过间隔寡核苷酸分型,发现了31种不同类型,而用AluI消化的DR探针相关RFLP分析鉴定出42种类型,用PGRS探针的RFLP分析也检测到42种类型;这些类型部分独立于DR类型。通过结合间隔寡核苷酸分型以及使用DR和PGRS探针的RFLP分析所获得的结果,得到了88种不同类型。尽管通过间隔寡核苷酸分型对牛分枝杆菌的区分能力不如使用DR和PGRS探针的RFLP分析,但间隔寡核苷酸分型操作更简便,结果也更易于解释。因此,为了对牛分枝杆菌分离株进行分型,可首先进行间隔寡核苷酸分型,将分离株归入簇中,然后使用DR和PGRS探针通过RFLP分析进行分析。