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首页> 外文期刊>Journal of Microbiological Methods >Disparity between multilocus enzyme electrophoresis, microsatellite markers and pulsed-field gel electrophoresis in epidemiological tracking of Candida albicans.
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Disparity between multilocus enzyme electrophoresis, microsatellite markers and pulsed-field gel electrophoresis in epidemiological tracking of Candida albicans.

机译:多点念珠菌流行病学追踪中多位点酶电泳,微卫星标记和脉冲场凝胶电泳之间的差异。

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摘要

Various molecular systems are available for epidemiological, genetic, evolutionary, taxonomic and systematic studies of innumerable fungal infections, especially those caused by the opportunistic pathogen C. albicans. A total of 75 independent oral isolates were selected in order to compare Multilocus Enzyme Electrophoresis (MLEE), Electrophoretic Karyotyping (EK) and Microsatellite Markers (Simple Sequence Repeats - SSRs), in their abilities to differentiate and group C. albicans isolates (discriminatory power), and also, to evaluate the concordance and similarity of the groups of strains determined by cluster analysis for each fingerprinting method. Isoenzyme typing was performed using eleven enzyme systems: Adh, Sdh, M1p, Mdh, Idh, Gdh, G6pdh, Asd, Cat, Po, and Lap (data previously published). The EK method consisted of chromosomal DNA separation by pulsed-field gel electrophoresis using a CHEF system. The microsatellite markers were investigated by PCR using three polymorphic loci: EF3, CDC3, and HIS3. Dendrograms were generated by the SAHN method and UPGMA algorithm based on similarity matrices (SSM). The discriminatory power of the three methods was over 95%, however a paired analysis among them showed a parity of 19.7-22.4% in the identification of strains. Weak correlation was also observed among the genetic similarity matrices (SSMMLEE x SSMEK x SSMSSRs). Clustering analyses showed a mean of 9+or-12.4 isolates per cluster (3.8+or-8 isolates/taxon) for MLEE, 6.2+or-4.9 isolates per cluster (4+or-4.5 isolates/taxon) for SSRs, and 4.1+or-2.3 isolates per cluster (2.6+or-2.3 isolates/taxon) for EK. A total of 45 (13%), 39 (11.2%), 5 (1.4%) and 3 (0.9%) clusters pairs from 347 showed similarity (SJ) of 0.1-10%, 10.1-20%, 20.1-30% and 30.1-40%, respectively. Clinical and molecular epidemiological correlation involving the opportunistic pathogen C. albicans may be attributed dependently of each method of genotyping (i.e., MLEE, EK, and SSRs) supplemented with similarity and grouping analysis. Therefore, the use of genotyping systems that give results which offer minimum disparity, or the combination of the results of these systems, can provide greater security and consistency in the determination of strains and their genetic relationships.
机译:各种分子系统可用于无数真菌感染的流行病学,遗传,进化,分类学和系统研究,特别是机会性病原体C引起的那些。白色的。总共选择了75个独立的口腔分离株,以比较多基因座酶电泳(MLEE),电泳核型分析(EK)和微卫星标记(简单序列重复-SSR)在区分和分组iC方面的能力。白色念珠菌的隔离(区分能力),并评估通过聚类分析针对每种指纹方法确定的菌株组的一致性和相似性。使用11种酶系统进行同工酶分型: Adh , Sdh , M1p , Mdh , Idh < / i>, Gdh , G6pdh , Asd , Cat , Po 和 Lap (以前发布的数据)。 EK方法包括使用CHEF系统通过脉冲场凝胶电泳分离染色体DNA。使用三个多态性位点: EF3 , CDC3 和 HIS3 ,通过PCR研究了微卫星标记。通过SAHN方法和UPGMA算法基于相似性矩阵( S SM )生成树状图。三种方法的辨别力均超过95%,但是在它们之间的配对分析显示,在菌株鉴定中的均等值为19.7-22.4%。在遗传相似性矩阵( S SM MLEE x S 之间也观察到弱相关性> SM EK x S SM SSR )。聚类分析显示,对于MLEE,每簇平均有9+或-12.4菌株(3.8+或-8菌株/ 紫杉类),每簇6.2+或-4.9菌株(4+或-4.5菌株/ SSR的 taxon ),EK的每个集群为4.1+或-2.3分离株(2.6+或2.3分离株/ 紫杉)。来自347个的总共45个(13%),39个(11.2%),5个(1.4%)和3个(0.9%)集群对显示出相似性( S J )分别为0.1-10%,10.1-20%,20.1-30%和30.1-40%。临床和分子流行病学相关性涉及机会病原体 C。可能会根据每种基因分型方法(例如MLEE,EK和SSR)以及相似性和分组分析来归因于白色念珠菌。因此,使用提供最小差异结果的基因分型系统或这些系统结果的组合,可以在确定菌株及其遗传关系时提供更大的安全性和一致性。

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