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抗生素耐药性的演变与传播

Evolution and spread of antibiotic resistance.

作者信息

Normark B Henriques, Normark S

机构信息

Swedish Institute of Infectious Disease Control and the Microbiology and Tumor Biology Center, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Intern Med. 2002 Aug;252(2):91-106. doi: 10.1046/j.1365-2796.2002.01026.x.

DOI:10.1046/j.1365-2796.2002.01026.x
PMID:12190884
Abstract

Antibiotic resistance is a clinical and socioeconomical problem that is here to stay. Resistance can be natural or acquired. Some bacterial species, such as Pseudomonas aeruginosa, show a high intrinsic resistance to a number of antibiotics whereas others are normally highly antibiotic susceptible such as group A streptococci. Acquired resistance evolve via genetic alterations in the microbes own genome or by horizontal transfer of resistance genes located on various types of mobile DNA elements. Mutation frequencies to resistance can vary dramatically depending on the mechanism of resistance and whether or not the organism exhibits a mutator phenotype. Resistance usually has a biological cost for the microorganism, but compensatory mutations accumulate rapidly that abolish this fitness cost, explaining why many types of resistances may never disappear in a bacterial population. Resistance frequently occurs stepwise making it important to identify organisms with low level resistance that otherwise may constitute the genetic platform for development of higher resistance levels. Self-replicating plasmids, prophages, transposons, integrons and resistance islands all represent DNA elements that frequently carry resistance genes into sensitive organisms. These elements add DNA to the microbe and utilize site-specific recombinases/integrases for their integration into the genome. However, resistance may also be created by homologous recombination events creating mosaic genes where each piece of the gene may come from a different microbe. The selection with antibiotics have informed us much about the various genetic mechanisms that are responsible for microbial evolution.

摘要

抗生素耐药性是一个持续存在的临床和社会经济问题。耐药性可以是天然的,也可以是后天获得的。一些细菌物种,如铜绿假单胞菌,对多种抗生素表现出高度的固有耐药性,而其他一些细菌,如A组链球菌,通常对抗生素高度敏感。获得性耐药性是通过微生物自身基因组的基因改变或位于各种类型移动DNA元件上的耐药基因的水平转移而产生的。耐药性的突变频率可能因耐药机制以及生物体是否表现出突变表型而有很大差异。耐药性通常对微生物具有生物学成本,但补偿性突变会迅速积累,从而消除这种适应性成本,这就解释了为什么许多类型的耐药性在细菌种群中可能永远不会消失。耐药性通常是逐步发生的,因此识别低水平耐药的生物体很重要,否则它们可能构成更高耐药水平发展的遗传平台。自我复制质粒、原噬菌体、转座子、整合子和耐药岛都代表了经常将耐药基因带入敏感生物体的DNA元件。这些元件将DNA添加到微生物中,并利用位点特异性重组酶/整合酶将其整合到基因组中。然而,耐药性也可能由同源重组事件产生镶嵌基因而产生,其中基因的每一部分可能来自不同的微生物。抗生素的选择让我们对负责微生物进化的各种遗传机制有了很多了解。

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