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Composite mobile genetic elements disseminating macrolide resistance in Streptococcus pneumoniae

机译:传播肺炎链球菌大环内酯类耐药性的复合移动遗传元件

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Macrolide resistance in Streptococcus pneumoniae emerged in the U.S. and globally during the early 1990's. The RNA methylase encoded by erm(B) and the macrolide efflux genes mef(E) and mel were identified as the resistance determining factors. These genes are disseminated in the pneumococcus on mobile, often chimeric elements consisting of multiple smaller elements. To better understand the variety of elements encoding macrolide resistance and how they have evolved in the pre- and post-conjugate vaccine eras, the genomes of 121 invasive and ten carriage isolates from Atlanta from 1994 to 2011 were analyzed for mobile elements involved in the dissemination of macrolide resistance. The isolates were selected to provide broad coverage of the genetic variability of antibiotic resistant pneumococci and included 100 invasive isolates resistant to macrolides. Tn916-like elements carrying mef(E) and mel on the Macrolide Genetic Assembly (Mega) and erm(B) on the erm(B) element and Tn917 were integrated into the pneumococcal chromosome backbone and into larger Tn5253-like composite elements. The results reported here include identification of novel insertion sites for Mega and characterization of the insertion sites of Tn916-like elements in the pneumococcal chromosome and in larger composite elements. The data indicate that integration of elements by conjugation was infrequent compared to recombination. Thus, it appears that conjugative mobile elements allow the pneumococcus to acquire DNA from distantly related bacteria, but once integrated into a pneumococcal genome, transformation and recombination is the primary mechanism for transmission of novel DNA throughout the pneumococcal population.
机译:肺炎链球菌对大环内酯类药物的耐药性在1990年代初期在美国和全球范围内出现。由erm(B)和大环内酯外排基因mef(E)和mel编码的RNA甲基化酶被确定为耐药性决定因素。这些基因在由多个较小元件组成的可移动的,常为嵌合的元件上散布在肺炎球菌中。为了更好地理解编码大环内酯类抗药性的元素的种类以及它们在结合前后的时代如何演变,分析了1994年至2011年亚特兰大的121种侵入性和十种运输分离株的基因组,分析了传播中涉及的移动元素大环内酯的抗药性。选择这些分离株以提供广泛的抗生素抗性肺炎链球菌遗传变异性,并包括100个对大环内酯类耐药的侵入性分离株。大环内酯遗传大会(Mega)上带有mef(E)和mel的Tn916样元件,以及erm(B)元件上的erm(B)和Tn917的erm(B)被整合到肺炎球菌的染色体骨架和更大的Tn5253样复合元件中。此处报道的结果包括鉴定Mega的新插入位点以及表征肺炎球菌染色体和较大复合元件中Tn916样元件的插入位点。数据表明与重组相比,通过缀合整合元件的频率很少。因此,似乎结合的移动元件允许肺炎球菌从远缘的细菌中获取DNA,但是一旦整合入肺炎球菌基因组,转化和重组是新的DNA在整个肺炎球菌种群中传播的主要机制。

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