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与抗生素抗性酶SME-1β-内酰胺酶相关的适合度代价。

A fitness cost associated with the antibiotic resistance enzyme SME-1 beta-lactamase.

作者信息

Marciano David C, Karkouti Omid Y, Palzkill Timothy

机构信息

Department of Molecular Virology and Microbiology, Baylor College of Medicine, 1 Baylor Plaza, Houston, TX 77030, USA.

出版信息

Genetics. 2007 Aug;176(4):2381-92. doi: 10.1534/genetics.106.069443. Epub 2007 Jun 11.

Abstract

The bla(TEM-1) beta-lactamase gene has become widespread due to the selective pressure of beta-lactam use and its stable maintenance on transferable DNA elements. In contrast, bla(SME-1) is rarely isolated and is confined to the chromosome of carbapenem-resistant Serratia marcescens strains. Dissemination of bla(SME-1) via transfer to a mobile DNA element could hinder the use of carbapenems. In this study, bla(SME-1) was determined to impart a fitness cost upon Escherichia coli in multiple genetic contexts and assays. Genetic screens and designed SME-1 mutants were utilized to identify the source of this fitness cost. These experiments established that the SME-1 protein was required for the fitness cost but also that the enzyme activity of SME-1 was not associated with the fitness cost. The genetic screens suggested that the SME-1 signal sequence was involved in the fitness cost. Consistent with these findings, exchange of the SME-1 signal sequence for the TEM-1 signal sequence alleviated the fitness cost while replacing the TEM-1 signal sequence with the SME-1 signal sequence imparted a fitness cost to TEM-1 beta-lactamase. Taken together, these results suggest that fitness costs associated with some beta-lactamases may limit their dissemination.

摘要

由于β-内酰胺类药物使用的选择压力及其在可转移DNA元件上的稳定维持,bla(TEM-1)β-内酰胺酶基因已广泛传播。相比之下,bla(SME-1)很少被分离出来,并且局限于耐碳青霉烯类粘质沙雷氏菌菌株的染色体上。bla(SME-1)通过转移到移动DNA元件上进行传播可能会阻碍碳青霉烯类药物的使用。在本研究中,通过多种遗传背景和试验确定bla(SME-1)会给大肠杆菌带来适应性代价。利用遗传筛选和设计的SME-1突变体来确定这种适应性代价的来源。这些实验证实SME-1蛋白是适应性代价所必需的,但SME-1的酶活性与适应性代价无关。遗传筛选表明SME-1信号序列与适应性代价有关。与这些发现一致,将SME-1信号序列替换为TEM-1信号序列可减轻适应性代价,而用SME-1信号序列替换TEM-1信号序列则会给TEM-1β-内酰胺酶带来适应性代价。综上所述,这些结果表明与某些β-内酰胺酶相关的适应性代价可能会限制它们的传播。

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