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新种猫脲原体和新种猫口脲原体,从猫口腔中分离得到。

Ureaplasma felinum sp. nov. and Ureaplasma cati sp. nov. isolated from the oral cavities of cats.

作者信息

Harasawa R, Imada Y, Ito M, Koshimizu K, Cassell G H, Barile M F

机构信息

Department of Veterinary Microbiology, Faculty of Agriculture, Miyazaki University, Japan.

出版信息

Int J Syst Bacteriol. 1990 Jan;40(1):45-51. doi: 10.1099/00207713-40-1-45.

Abstract

Seven ureaplasma strains isolated from the oral cavities of domestic cats (Felis domestica) were characterized and compared with the type strains of the three previously established species of this genus, Ureaplasma urealyticum (humans), Ureaplasma diversum (cattle), and Ureaplasma gallorale (chickens). The feline strains hydrolyzed urea but not arginine or glucose, were membrane bound, lacked cell walls, passed through 0.45-micron membrane filters, required cholesterol for growth, and formed minute (15- to 140-microns) colonies on agar medium. The seven feline strains fell into two distinct groups based on (i) their antigenic properties (determined by using the metabolism and growth inhibition and indirect immunoperoxidase procedures), (ii) their genomic properties (determined by using DNA-DNA hybridization and DNA cleavage pattern procedures), and (iii) their polypeptide profiles (determined by using sodium dodecyl sulfate-polyacrylamide gel electrophoresis analyses). Based on these properties, the two feline groups were unrelated to each other or to the three previously established species, and each group represents a distinct Ureaplasma species. Thus, we propose that ureaplasmas with these phylogenetic and genomic properties be given taxonomic status as Ureaplasma felinum and Ureaplasma cati, with strain FT2-B (= ATCC 49229 = NCTC 11709) and strain F2 (= ATCC 49228 = NCTC 11710) as the type strains, respectively.

摘要

对从家猫口腔中分离出的7株脲原体菌株进行了特性鉴定,并与该属之前已确立的3个种的模式菌株进行了比较,这3个种分别是解脲脲原体(人源)、差异脲原体(牛源)和鸡源脲原体。猫源菌株能水解尿素,但不能水解精氨酸或葡萄糖,具有膜结合性,无细胞壁,能通过0.45微米的滤膜,生长需要胆固醇,且在琼脂培养基上形成微小(15至140微米)的菌落。基于以下几点,这7株猫源菌株分为两个不同的组:(i)它们的抗原特性(通过代谢、生长抑制和间接免疫过氧化物酶方法确定);(ii)它们的基因组特性(通过DNA-DNA杂交和DNA酶切图谱方法确定);(iii)它们的多肽谱(通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析确定)。基于这些特性,这两个猫源组彼此之间以及与之前确立的3个种均无关联,且每组代表一个独特的脲原体种。因此,我们建议将具有这些系统发育和基因组特性的脲原体分别归类为猫脲原体和猫源脲原体,菌株FT2-B(=ATCC 49229=NCTC 11709)和菌株F2(=ATCC 49228=NCTC 11710)分别作为它们的模式菌株。

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