外阴阴道念珠菌病念珠菌分离株形态、毒力标记物及药敏检测

R. Yoganand, P. Mahadevaiah, S. M. Rudresh, Ravi G S
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引用次数: 0

摘要

属的物种在自然界中无处不在,其中许多形成了人体和动物体内正常的微生物菌群。在一定条件下,粘膜表面的多种感染可由sp引起:从476例临床疑似VVC患者的阴道拭子中分离出40株念珠菌。氟康唑和伏立康唑抗真菌药敏试验。采用标准方法检测毒力指标磷脂酶活性、蛋白酶活性、生物膜产量。在40株分离株中,从阴道拭子中分离出的菌种最多,为52.5%。分离种分别为(27.5%)、(15%)、(5%)。12份(30%)样品有较强的磷脂酶活性,18份(45%)样品无活性。6株(15%)样品的磷脂酶活性中等,4株(10%)样品的磷脂酶活性较差。33株分离株的蛋白酶活性呈强阳性,经鉴定为和。生物膜形成强9株,中等8株,弱11株,阴性12株。40株分离株均对氟康唑和伏立康唑敏感。从本研究中观察到,和是引起VVC的主要物种。毒力标记分析,如磷脂酶、蛋白酶和生物膜的形成,将有助于分析致病性和进一步研究阐明这些途径所涉及的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Speciation of Candida isolates from vulvovaginal candidiasis cases, detection of virulence markers of Candida and antifungal susceptibility by disc diffusion method
: Species belonging to the genus are ubiquitous in nature and many of them form the normal microbial flora in human and animal bodies. A wide variety of infections on mucosal surfaces under certain conditions can be caused due to the sp: A total of 40 isolates of Candida, isolated from vaginal swabs among 476 patients with clinically suspected VVC. Antifungal susceptibility testing done using Fluconazole and Voriconazole. Virulence markers Phospholipase activity, Proteinase activity, Biofilm Productionwere detected by standard methods.: Out of 40 isolates, the following species were isolated, (52.5%) was the most common species isolated from vaginal swabs. The species isolated were (27.5%), (15%), (5%).Intense phospholipase activity was observed in 12 (30%) samples, there was no activity in 18 (45%) samples. A moderate phospholipase activity was observed in 6 (15%) isolates, poor activity in 4 (10%) samples.Proteinase activity was strongly positive in 33 isolates which was identified as and. Strong biofilm formation was observed in 9 isolates, moderate in 8, weak in 11 and negative in 12 isolates. All 40 isolates are susceptible to Fluconazole and Voriconazole.From this study it is observed that and are the major species of causing VVC. Virulence marker analysis such as that for phospholipase, proteinase and biofilm formation will help to analyse the pathogenicity and further research required to elucidate the mechanisms involved in these pathways.
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