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迟缓真杆菌的细胞脂肪酸组成、可溶性蛋白谱及抗菌耐药模式

Cellular fatty acid composition, soluble-protein profile, and antimicrobial resistance pattern of Eubacterium lentum.

作者信息

Mosca A, Summanen P, Finegold S M, De Michele G, Miragliotta G

机构信息

Institute of Medical Microbiology, University of Bari, Policlinico, Italy.

出版信息

J Clin Microbiol. 1998 Mar;36(3):752-5. doi: 10.1128/JCM.36.3.752-755.1998.

Abstract

Phenotypic heterogeneity among isolates of Eubacterium lentum has been recognized for many years. To better delineate their taxonomic relatedness, 29 clinical isolates of E. lentum were examined for soluble-protein content, cellular fatty acid profile, and antimicrobial resistance pattern in order to ascertain whether differences in these characteristics could be correlated with differences in biochemical activities. Among 29 isolates we could identify 6 that were different from all the others. These strains were coccobacilli with translucent colonies; they were catalase and H2S negative, not fluorescent under UV light, and susceptible to beta-lactam drugs; growth was not stimulated by arginine; and fatty acid analysis revealed the presence of straight-chain fatty acids. The remainder of the strains, including the type species, were pleomorphic bacilli with speckled colonies and were catalase and H2S positive; all but two were fluorescent under UV light; they were resistant to beta-lactam antibiotics; growth was greatly stimulated by arginine; and they demonstrated saturated branched-chain fatty acids. Our data suggest that E. lentum can be further differentiated into different types.

摘要

迟缓真杆菌分离株之间的表型异质性多年来已为人所知。为了更好地描述它们的分类学相关性,对29株迟缓真杆菌临床分离株进行了可溶性蛋白含量、细胞脂肪酸谱和抗菌药物耐药模式检测,以确定这些特征的差异是否与生化活性的差异相关。在29株分离株中,我们鉴定出6株与其他所有菌株不同。这些菌株为球杆菌,菌落半透明;它们过氧化氢酶和H2S阴性,在紫外线下不发荧光,对β-内酰胺类药物敏感;精氨酸不能刺激其生长;脂肪酸分析显示存在直链脂肪酸。其余菌株,包括模式种,为多形性杆菌,菌落有斑点,过氧化氢酶和H2S阳性;除两株外,所有菌株在紫外线下均发荧光;它们对β-内酰胺类抗生素耐药;精氨酸能极大地刺激其生长;并且它们显示出饱和支链脂肪酸。我们的数据表明,迟缓真杆菌可进一步分为不同类型。

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本文引用的文献

1
UV red fluorescence of Eubacterium lentum.迟缓真杆菌的紫外线红色荧光。
J Clin Microbiol. 1993 Apr;31(4):1001-2. doi: 10.1128/jcm.31.4.1001-1002.1993.

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