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在爱迪生海山(巴布亚新几内亚利希尔岛以南)冷泉沉积物中鉴定出的TEM型β-内酰胺酶的分子特征

Molecular characterization of TEM-type beta-lactamases identified in cold-seep sediments of Edison Seamount (south of Lihir Island, Papua New Guinea).

作者信息

Song Jae Seok, Jeon Jeong Ho, Lee Jung Hun, Jeong Seok Hoon, Jeong Byeong Chul, Kim Sang-Jin, Lee Jung-Hyun, Lee Sang Hee

机构信息

Department of Biological Sciences, Myongji University, San 38-2 Namdong, Yongin, Kyunggido, 449-728, Republic of Korea.

出版信息

J Microbiol. 2005 Apr;43(2):172-8.

Abstract

To determine the prevalence and genotypes of beta-lactamases among clones of a metagenomic library from the cold-seep sediments of Edison seamount (10,000 years old), we performed pulse-field gel electrophoresis, antibiotic susceptibility testing, pI determination, and DNA sequencing analysis. Among the 8,823 clones of the library, thirty clones produced beta-lactamases and had high levels of genetic diversity. Consistent with minimum inhibitory concentration patterns, we found that five (16.7%) of thirty clones produced an extended-spectrum beta-lactamase. 837- and 259-bp fragments specific to blaTEM genes were amplified, as determined by banding patterns of PCR amplification with designed primers. TEM-1 was the most prevalent beta-lactamase and conferred resistance to ampicillin, piperacillin, and cephalothin. TEM-116 had a spectrum that was extended to ceftazidime, cefotaxime, and aztreonam. The resistance levels conferred by the pre-antibiotic era alleles of TEM-type beta-lactamases were essentially the same as the resistance levels conferred by the TEM-type alleles which had been isolated from clinically resistant strains of bacteria of the antibiotic era. Our first report on TEM-type beta-lactamases of the pre-antibiotic era indicates that TEM-type beta-lactamases paint a picture in which most of the diversity of the enzymes may not be the result of recent evolution, but that of ancient evolution.

摘要

为了确定来自爱迪生海山冷泉沉积物宏基因组文库(有10000年历史)的克隆中β-内酰胺酶的流行情况和基因型,我们进行了脉冲场凝胶电泳、抗生素敏感性测试、等电点测定和DNA测序分析。在该文库的8823个克隆中,有30个克隆产生β-内酰胺酶,并且具有高度的遗传多样性。与最低抑菌浓度模式一致,我们发现30个克隆中有5个(16.7%)产生超广谱β-内酰胺酶。通过用设计引物进行PCR扩增的条带模式确定,扩增出了blaTEM基因特异性的837和259bp片段。TEM-1是最常见的β-内酰胺酶,对氨苄西林、哌拉西林和头孢噻吩具有抗性。TEM-116的谱带扩展到了头孢他啶、头孢噻肟和氨曲南。TEM型β-内酰胺酶的抗生素前时代等位基因赋予的抗性水平与从抗生素时代临床耐药菌株中分离出的TEM型等位基因赋予的抗性水平基本相同。我们关于抗生素前时代TEM型β-内酰胺酶的首次报告表明,TEM型β-内酰胺酶呈现出这样一种情况:大多数酶的多样性可能不是近期进化的结果,而是古代进化的结果。

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