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粪肠球菌efaA突变体的体内测试及利用efaA同源物进行菌种鉴定

In vivo testing of an Enterococcus faecalis efaA mutant and use of efaA homologs for species identification.

作者信息

Singh K V, Coque T M, Weinstock G M, Murray B E

机构信息

Center for the Study of Emerging and Re-emerging Pathogens, Department of Internal Medicine, The University of Texas Medical School, Houston 77030, USA.

出版信息

FEMS Immunol Med Microbiol. 1998 Aug;21(4):323-31. doi: 10.1111/j.1574-695X.1998.tb01180.x.

Abstract

Disruption of the previously described efaA (from Enterococcus faecalis antigen A) gene was generated in E. faecalis strain OG1RF and loss of an 37-kDa immunoreactive band from the mutant was demonstrated in Western blots. In a mouse peritonitis model, mice infected with the efaAfs (fs=from Enterococcus faecalis) mutant showed more prolonged survival than mice infected with the parent strain OG1RF. These results suggest that efaAfs encodes a function important for infection of mice by enterococci. An efaA-like gene was also identified in E. faecium DNA libraries and its deduced amino acid sequence showed 73% similarity to EfaA of E. faecalis and 42-63% similarities to a group of streptococcal virulence and adhesion associated proteins that are components of ATP-binding cassette transport systems. Intragenic probes representing efaAfs, recAfs, efaAfm (fm=from E. faecium) and gyrAfm were tested for their ability to identify E. faecalis and E. faecium using colony lysates of 133 enterococci and one Streptococcus sp. Probes of E. faecium and E. faecalis origin hybridized to all isolates of E. faecium and E. faecalis, respectively, regardless of their clinical source but not to any of 29 other enterococci. These results suggest that the use of gene probes may prove helpful in identification of isolates of E. faecium and E. faecalis.

摘要

在粪肠球菌菌株OG1RF中造成了先前所述的efaA(源自粪肠球菌抗原A)基因的破坏,并且在蛋白质免疫印迹中证实该突变体缺失了一条37 kDa的免疫反应条带。在小鼠腹膜炎模型中,感染efaAfs(fs = 源自粪肠球菌)突变体的小鼠比感染亲本菌株OG1RF的小鼠存活时间更长。这些结果表明,efaAfs编码一种对肠球菌感染小鼠很重要的功能。在屎肠球菌DNA文库中也鉴定出一个类似efaA的基因,其推导的氨基酸序列与粪肠球菌的EfaA有73%的相似性,与一组作为ATP结合盒转运系统组成部分的链球菌毒力和黏附相关蛋白有42 - 63%的相似性。使用133株肠球菌和1株链球菌属的菌落裂解物,测试了代表efaAfs、recAfs、efaAfm(fm = 源自屎肠球菌)和gyrAfm的基因内探针鉴定粪肠球菌和屎肠球菌的能力。源自屎肠球菌和粪肠球菌的探针分别与所有屎肠球菌和粪肠球菌分离株杂交,无论其临床来源如何,但不与其他29株肠球菌中的任何一株杂交。这些结果表明,基因探针的使用可能有助于鉴定屎肠球菌和粪肠球菌分离株。

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