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首页> 外文期刊>Journal de mycologie medicale >Aspergillus tubingensis and Aspergillus niger as the dominant black Aspergillus, use of simple PCR-RFLP for preliminary differentiation
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Aspergillus tubingensis and Aspergillus niger as the dominant black Aspergillus, use of simple PCR-RFLP for preliminary differentiation

机译:油曲霉和黑曲霉为主要黑曲霉,使用简单的PCR-RFLP进行初步分化

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This work aimed to identify the species distribution of common clinical and environmental isolates of black Aspergilli based on simple restriction fragment length polymorphism (RFLP) analysis of the P-tubulin gene. A total of 149 clinical and environmental strains of black Aspergilli were collected and subjected to preliminary morphological examination. Total genomic DNAs were extracted, and PCR was performed to amplify part of the beta-tubulin gene. At first, 52 randomly selected samples were species-delineated by sequence analysis. In order to distinguish the most common species, PCR amplicons of 117 black Aspergillus strains were identified by simple PCR-RFLP analysis using the enzyme Tasl. Among 52 sequenced isolates, 28 were Aspergillus tubingensis, 21 Aspergillus niger, and the three remaining isolates included Aspergillus uvarum, Aspergillus awamori, and Aspergillus acidus. All 100 environmental and 17 BAL samples subjected to Tasl-RFLP analysis of the beta-tubulin gene, fell into two groups, consisting of about 59% (n = 69) A. tubingensis and 41% (n = 48) A. niger. Therefore, the method successfully and rapidly distinguished A. tubingensis and A. niger as the most common species among the clinical and environmental isolates. Although tardy, the Ehrlich test was also able to differentiate A. tubingensis and A. niger according to the yellow color reaction specific to A. niger. A. tubingensis and A. niger are the most common black Aspergillus in both clinical and environmental isolates in Iran. PCR-RFLP using Tasl digestion of B-tubulin DNA enables rapid screening for these common species. (C) 2016 Elsevier Masson SAS. All rights reserved.
机译:这项工作旨在基于对P-微管蛋白基因的简单限制性片段长度多态性(RFLP)分析,确定黑曲霉的常见临床和环境分离株的物种分布。总共收集了149株黑曲霉的临床和环境菌株,并进行了初步形态学检查。提取总基因组DNA,并进行PCR以扩增部分β-微管蛋白基因。首先,通过序列分析对52个随机选择的样本进行物种描述。为了区分最常见的物种,使用酶Tasl通过简单的PCR-RFLP分析鉴定了117个黑色曲霉菌株的PCR扩增子。在52个测序的分离株中,有28个是曲霉曲霉,21个黑曲霉,其余三个分离株包括曲霉,泡盛曲霉和酸曲霉。对β-微管蛋白基因进行Tasl-RFLP分析的所有100个环境样品和17个BAL样品均分为两组,分别由约59%(n = 69)的油曲霉和41%(n = 48)的黑曲霉组成。因此,该方法成功并迅速地将油曲霉和黑曲霉区分为临床和环境分离物中最常见的物种。尽管迟钝,但是根据黑曲霉特有的黄色反应,Ehrlich试验也能够区分油曲霉和黑曲霉。伊朗的临床和环境分离物中,油曲霉和黑曲霉是最常见的黑色曲霉。使用B-微管蛋白DNA的Tasl消化进行PCR-RFLP,可以快速筛选这些常见物种。 (C)2016 Elsevier Masson SAS。版权所有。

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