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首页> 外文期刊>Advances in Microbiology >Ultrastructural Analysis of in Vitro Adherence and Production of Acid Proteases by Clinical Isolates of Candida parapsilosis Sensu Stricto Following Growth in the Presence of Keratinous Substrates from Human Source
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Ultrastructural Analysis of in Vitro Adherence and Production of Acid Proteases by Clinical Isolates of Candida parapsilosis Sensu Stricto Following Growth in the Presence of Keratinous Substrates from Human Source

机译:人源角蛋白底物生长后,临床副产物假丝酵母念珠菌的临床分离株对酸性蛋白酶的体外粘附和产生的超微结构分析

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Candida parapsilosis is an increasingly important human pathogen. However, little is known about its potential to cause disease. The aims of the present study were to analyse the production of acid proteinases by clinical isolates of C. parapsilosis in the presence of different keratinous substrates from human sources (stratum corneum, nail and hair) and to verify the capability of yeast cells to adhere and grow as biofilm on these substrates. By scanning electron microscopy, it was observed that all C. parapsilosis sensu stricto isolates adhered to the keratinous substrates. For the isolate recovered from onychomycosis, the cell population attached to stratum corneum and hair keratin consisted mainly of blastoconidia. Differently, on nail keratin, pseudohyphae production was observed. Overall, there was a loose association between yeast cells and keratinous substrates. However, on stratum corneum, flocculent extracellular material was seen evolving cells from the onychomycosis isolate by forming a biofilm-like structure. The isolates recovered from onychomycosis and cutaneous lesion produced higher amount of acid proteinases in medium supplemented with nail keratin and stratum corneum keratin, respectively, than that in salt medium (absence of keratin). Furthermore, no differences were observed in the amount of acid proteinases produced by the isolate recovered from tracheal secretion in the media tested (absence and presence of keratin substrates). The information derived from this study will further our understanding of acid proteinase production by C. parapsilosis isolates and provide an insight into pathogenic mechanisms in C. parapsilosis particularly from isolates recovered from superficial mycoses.
机译:副念珠菌是越来越重要的人类病原体。但是,人们对其潜在的疾病知之甚少。本研究的目的是在人源(角质层,指甲和头发)存在不同角蛋白底物的情况下,通过副猪破囊菌的临床分离物分析酸性蛋白酶的产生,并验证酵母细胞粘附和分离酵母的能力。在这些底物上以生物膜的形式生长。通过扫描电子显微镜观察,观察到所有的C. parapsilosis sensu stricto分离株都粘附在角质基质上。对于从甲癣中回收的分离株,附着在角质层和毛发角蛋白上的细胞群主要由破乳杆菌组成。不同地,在指甲角蛋白上,观察到假菌丝的产生。总体而言,酵母细胞和角质基质之间存在松散的联系。然而,在角质层上,看到絮凝的细胞外物质通过形成生物膜样结构而从灰指甲分离物中分离出细胞。从甲癣和皮肤病灶中回收的分离株分别在添加了指甲角蛋白和角质层角蛋白的培养基中比在盐培养基(不存在角蛋白)中产生更多的酸性蛋白酶。此外,在所测试的培养基中(不存在和存在角蛋白底物),从气管分泌物中回收的分离物产生的酸性蛋白酶的量没有观察到差异。从这项研究中获得的信息将使我们进一步了解副寄生念珠菌分离株产生的酸性蛋白酶,并深入了解副寄生念珠菌的致病机制,特别是从表皮霉菌中回收的分离株。

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