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解脲脲原体的系统发育分析——支持建立一个新物种,微小脲原体。

Phylogenetic analysis of Ureaplasma urealyticum--support for the establishment of a new species, Ureaplasma parvum.

作者信息

kong F, James G, Ma Z, Gordon S, Bin W, Gilbert G L

机构信息

Centre for Infectious Diseases and Microbiology, Institute of Clinical Pathology and Medical Research, Westmead, New South Wales, Australia.

出版信息

Int J Syst Bacteriol. 1999 Oct;49 Pt 4:1879-89. doi: 10.1099/00207713-49-4-1879.

Abstract

In this study, the phylogenetic relationships between the two biovars and 14 serovars of Ureaplasma urealyticum were studied using the sequences of four different genes or genetic regions, namely: 16S rRNA genes; 16S-23S rRNA gene spacer regions; urease gene subunits ureA, ureB, partial ureC and adjoining regions upstream of ureA, ureA-ureB spacer and ureB-ureC spacer; the 5'-ends of the multiple-banded antigen (MBA) genes. U. urealyticum genotypes, based on all four genomic sequences, could be clearly separated into two clusters corresponding with currently recognized biovars 1 and 2. Sequences were generally conserved within each biovar. However, there was heterogeneity within the 5'-end regions of the MBA genes of the four serovars of biovar 1; the sequence of serovar 3 was identical with the previously published sequence and differed by only three bases from that of serovar 14; but there were significant differences between the sequences of serovars 3 and 14 and those of serovars 1 and 6. Based on the phylogenetic analysis, support is given to previous recommendations that the two biovars of U. urealyticum be classified as distinct species, namely U. parvum and U. urealyticum for biovars 1 and 2, respectively. In the future, the relationship between the new species and clinical manifestations of ureaplasma infections should be studied.

摘要

在本研究中,利用四个不同基因或基因区域的序列,即16S rRNA基因、16S - 23S rRNA基因间隔区、脲酶基因亚基ureA、ureB、部分ureC以及ureA上游毗邻区域、ureA - ureB间隔区和ureB - ureC间隔区、多带抗原(MBA)基因的5′端,研究了解脲脲原体两个生物变种和14个血清型之间的系统发育关系。基于所有这四个基因组序列,解脲脲原体基因型可清晰地分为两个簇,分别对应目前公认的生物变种1和生物变种2。各生物变种内的序列通常是保守的。然而,生物变种1的四个血清型的MBA基因5′端区域存在异质性;血清型3的序列与先前发表的序列相同,与血清型14的序列仅相差三个碱基;但血清型3和14与血清型1和6的序列之间存在显著差异。基于系统发育分析,支持了先前的建议,即将解脲脲原体的两个生物变种分别归类为不同的物种,即生物变种1为微小脲原体,生物变种2为解脲脲原体。未来,应研究这些新物种与脲原体感染临床表现之间的关系。

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