Ghaly Timothy M, Chow Louise, Asher Amy J, Waldron Liette S, Gillings Michael R
Department of Biological Sciences, Macquarie University, Sydney, New South Wales, Australia.
PLoS One. 2017 Jun 6;12(6):e0179169. doi: 10.1371/journal.pone.0179169. eCollection 2017.
Class 1 integrons have played a major role in the global dissemination of antibiotic resistance. Reconstructing the history of class 1 integrons might help us control further spread of antibiotic resistance by understanding how human activities influence microbial evolution. Here we describe a class 1 integron that represents an intermediate stage in the evolutionary history of clinical integrons. It was embedded in a series of nested transposons, carried on an IncP plasmid resident in Enterobacter, isolated from the surface of baby spinach leaves. Based on the structure of this integron, we present a modified hypothesis for integron assembly, where the ancestral clinical class 1 integron was captured from a betaproteobacterial chromosome to form a Tn402-like transposon. This transposon then inserted into a plasmid-borne Tn21-like ancestor while in an environmental setting, possibly a bacterium resident in the phyllosphere. We suggest that the qacE gene cassette, conferring resistance to biocides, together with the mercury resistance operon carried by Tn21, provided a selective advantage when this bacterium made its way into the human commensal flora via food. The integron characterized here was located in Tn6007, which along with Tn6008, forms part of the larger Tn6006 transposon, itself inserted into another transposable element to form the Tn21-like transposon, Tn6005. This element has previously been described from the human microbiota, but with a promoter mutation that upregulates integron cassette expression. This element we describe here is from an environmental bacterium, and supports the hypothesis that the ancestral class 1 integron migrated into anthropogenic settings via foodstuffs. Selection pressures brought about by early antimicrobial agents, including mercury, arsenic and disinfectants, promoted its initial fixation, the acquisition of promoter mutations, and subsequent dissemination into various species and pathogens.
1类整合子在抗生素耐药性的全球传播中发挥了重要作用。重建1类整合子的历史可能有助于我们通过了解人类活动如何影响微生物进化来控制抗生素耐药性的进一步传播。在这里,我们描述了一个1类整合子,它代表了临床整合子进化历史中的一个中间阶段。它嵌入在一系列嵌套转座子中,位于一个IncP质粒上,该质粒存在于从婴儿菠菜叶表面分离的肠杆菌中。基于这个整合子的结构,我们提出了一个关于整合子组装的修正假说,即祖先临床1类整合子是从β-变形菌染色体捕获而来,形成一个Tn402样转座子。然后这个转座子在环境中,可能是叶际中的一种细菌,插入到一个质粒携带的Tn21样祖先中。我们认为,赋予对杀生物剂耐药性的qacE基因盒,与Tn21携带的汞抗性操纵子一起,当这种细菌通过食物进入人类共生菌群时提供了选择优势。这里表征的整合子位于Tn6007中,它与Tn6008一起构成了更大的Tn6006转座子的一部分,Tn6006本身插入到另一个转座元件中形成Tn21样转座子Tn6005。这个元件先前已在人类微生物群中被描述,但存在一个上调整合子盒表达的启动子突变。我们这里描述的这个元件来自一种环境细菌,并支持祖先1类整合子通过食品迁移到人为环境中的假说。早期抗菌剂,包括汞、砷和消毒剂带来的选择压力促进了它的最初固定、启动子突变的获得以及随后向各种物种和病原体的传播。