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白色念珠菌在合成培养基中继代培养过程中丢失的细胞壁抗原的鉴定。

Identification of Candida albicans cell wall antigens lost during subculture in synthetic media.

作者信息

Hernando F L, Estevez J J, Cebrian M, Poulain D, Ponton J

机构信息

Departamento de Microbiologia e Inmunologia, Facultad de Ciencias, Universidad del Pais Vasco, Bilbao, Spain.

出版信息

J Med Vet Mycol. 1993;31(3):227-37.

PMID:8360814
Abstract

A high variability in reactivity was observed when Candida albicans strains freshly isolated from both patients with candidiasis and asymptomatic carriers were tested against different human sera. The highest reactivity was observed in C. albicans strains isolated from blood cultures. This high reactivity was observed when the isolates were tested against sera from patients with Candida oesophagitis, patients with vulvovaginal candidiasis, or asymptomatic carriers but not against sera from blood donors. The antigenic reactivity of the strongly reactive strains, but not that of the weakly reactive strains, decreased during subculture in synthetic media. Five major components of an apparent molecular mass of > 200, 67-70, 49-52, 33-35 and 29-31 kDa were observed in alpha-mannosidase extracts from C. albicans strains from both blood cultures (Group I) and patients with Candida oesophagitis (Group II) subcultured in synthetic media for different times. Changes in staining intensity through the different subcultures were observed for some bands. Group I strains showed a decrease in staining intensity for bands of > 200 and 67-70 kDa, an increase for bands of 33-35 and 29-31 kDa, but no changes were observed for the band of 49-52 kDa. Group II strains showed opposite changes in banding intensity. A decrease in staining intensity was observed for the proteins of 33-35 and 29-31 kDa, an increase for the protein of 49-52 kDa, and no change in intensity was observed for the band of 67-70 kDa. A component of > 200 kDa showed an irregular expression through the subcultures. The main antigen present in extracts from the first subculture of isolates from Group I and II had a molecular mass of 67-70 kDa. It could be related to the P antigens since it disappeared following subculture of the strains in synthetic media.

摘要

当对从念珠菌病患者和无症状携带者中新鲜分离出的白色念珠菌菌株与不同的人血清进行测试时,观察到反应性存在高度变异性。在从血培养物中分离出的白色念珠菌菌株中观察到最高反应性。当分离株与念珠菌食管炎患者、外阴阴道念珠菌病患者或无症状携带者的血清进行测试时,观察到这种高反应性,但与献血者的血清测试时未观察到。强反应性菌株的抗原反应性在合成培养基中继代培养期间降低,而弱反应性菌株则没有。在分别在合成培养基中继代培养不同时间的来自血培养物(第一组)和念珠菌食管炎患者(第二组)的白色念珠菌菌株的α-甘露糖苷酶提取物中,观察到表观分子量>200、67-70、49-52、33-35和29-31 kDa的五个主要成分。在不同的继代培养中观察到一些条带的染色强度变化。第一组菌株中>200和67-70 kDa条带的染色强度降低,33-35和29-31 kDa条带的染色强度增加,但49-52 kDa条带未观察到变化。第二组菌株的条带强度变化相反。观察到33-35和29-31 kDa蛋白质的染色强度降低,49-52 kDa蛋白质的染色强度增加,67-70 kDa条带的强度没有变化。>200 kDa的一个成分在继代培养中表现出不规则表达。第一组和第二组分离株第一次继代培养提取物中的主要抗原分子量为67-70 kDa。它可能与P抗原有关,因为菌株在合成培养基中继代培养后它消失了。

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