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从感染人类免疫缺陷病毒患者口腔分离出的白色念珠菌菌株基因不同亚组的特征分析

Characterization of genetically distinct subgroup of Candida albicans strains isolated from oral cavities of patients infected with human immunodeficiency virus.

作者信息

McCullough M, Ross B, Reade P

机构信息

School of Dental Science, Faculty of Medicine, Dentistry, and Health Science, University of Melbourne, Victoria, Australia.

出版信息

J Clin Microbiol. 1995 Mar;33(3):696-700. doi: 10.1128/jcm.33.3.696-700.1995.

Abstract

During the course of a study of oral Candida albicans strains from 60 human immunodeficiency virus-infected patients over a 2.5-year period, 18 of the 295 C. albicans isolates had genomes that failed to hybridize with a C. albicans-specific DNA probe (27A). These strains were germ tube positive and chlamydospore positive and were identified as C. albicans by the ID 32C test (API Systems, Montlieu, France). These strains were analyzed for the presence of two other C. albicans-specific DNA segments by PCR. The first was a C. albicans 1,348-bp species-specific sequence, and the second was a 1,059-bp C. albicans repetitive element. The probe 27A-hybridizing strains yielded PCR products which differed from those of the nonhybridizing strains. Five of these genetically atypical C. albicans strains and 98 of the C. albicans strains were then analyzed for purported virulence factors. The genetically atypical C. albicans strains, in comparison with typical C. albicans strains, produced greater amounts of extracellular proteinase (P = 0.038, Student's t test), adhered to a greater degree to buccal epithelial cells (P = 0.018, Student's t test), and were less susceptible to the antifungal drug 5-flucytosine (P = 0.0003, Mann-Whitney test). Analysis of these strains with other common antifungal drugs showed no statistically significant variation in susceptibility. The results of this study indicated that these genetically atypical C. albicans strains possess increased virulence in comparison with typical C. albicans strains.

摘要

在一项对60名人类免疫缺陷病毒感染患者的口腔白色念珠菌菌株进行的为期2.5年的研究过程中,295株白色念珠菌分离株中有18株的基因组未能与白色念珠菌特异性DNA探针(27A)杂交。这些菌株芽管阳性、厚壁孢子阳性,通过ID 32C试验(法国蒙利厄的API系统公司)鉴定为白色念珠菌。通过聚合酶链反应(PCR)分析这些菌株中其他两个白色念珠菌特异性DNA片段的存在情况。第一个是1348bp的白色念珠菌物种特异性序列,第二个是1059bp的白色念珠菌重复元件。与未杂交菌株相比,与探针27A杂交的菌株产生的PCR产物不同。然后分析了其中5株遗传非典型白色念珠菌菌株和98株白色念珠菌菌株的假定毒力因子。与典型白色念珠菌菌株相比,遗传非典型白色念珠菌菌株产生更多的细胞外蛋白酶(学生t检验,P = 0.038),对颊上皮细胞的黏附程度更高(学生t检验,P = 0.018),并且对抗真菌药物5-氟胞嘧啶的敏感性较低(曼-惠特尼检验,P = 0.0003)。用其他常见抗真菌药物对这些菌株进行分析,结果显示敏感性无统计学显著差异。这项研究的结果表明,与典型白色念珠菌菌株相比,这些遗传非典型白色念珠菌菌株具有更强的毒力。

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