Starikova Irina, Al-Haroni Mohammed, Werner Guido, Roberts Adam P, Sørum Vidar, Nielsen Kaare M, Johnsen Pål J
Department of Pharmacy, Faculty of Health Sciences, University of Tromsø, Tromsø, Norway.
J Antimicrob Chemother. 2013 Dec;68(12):2755-65. doi: 10.1093/jac/dkt270. Epub 2013 Jul 5.
To determine the fitness effects of various mobile genetic elements (MGEs) in Enterococcus faecium and Enterococcus faecalis when newly acquired. We also tested the hypothesis that the biological cost of vancomycin resistance plasmids could be mitigated during continuous growth in the laboratory.
Different MGEs, including two conjugative transposons (CTns) of the Tn916 family (18 and 33 kb), a pathogenicity island (PAI) of 200 kb and vancomycin-resistance (vanA) plasmids (80-200 kb) of various origins and classes, were transferred into common ancestral E. faecium and E. faecalis strains by conjugation assays and experimentally evolved (vanA plasmids only). Transconjugants were characterized by PFGE, S1 nuclease assays and Southern blotting hybridization analyses. Single specific primer PCR was performed to determine the target sites for the insertion of the CTns. The fitness costs of various MGEs in E. faecium and E. faecalis were estimated in head-to-head competition experiments, and evolved populations were generated in serial transfer assays.
The biological cost of a newly acquired PAI and two CTns were both host- and insertion-locus-dependent. Newly acquired vanA plasmids may severely reduce host fitness (25%-27%), but these costs were rapidly mitigated after only 400 generations of continuous growth in the absence of antibiotic selection.
Newly acquired MGEs may impose an immediate biological cost in E. faecium. However, as demonstrated for vanA plasmids, the initial costs of MGE carriage may be mitigated during growth and beneficial plasmid-host association can rapidly emerge.
确定粪肠球菌和屎肠球菌中新获得的各种可移动遗传元件(MGEs)的适应性影响。我们还检验了以下假设:在实验室持续传代培养过程中,耐万古霉素质粒的生物学代价可能会降低。
通过接合试验将不同的MGEs,包括Tn916家族的两个接合转座子(CTns)(18和33 kb)、一个200 kb的致病岛(PAI)以及各种来源和类型的耐万古霉素(vanA)质粒(80 - 200 kb),转移到常见的粪肠球菌和屎肠球菌祖先菌株中,并进行实验进化(仅针对vanA质粒)。通过脉冲场凝胶电泳(PFGE)、S1核酸酶分析和Southern印迹杂交分析对接合子进行表征。进行单特异性引物PCR以确定CTns的插入靶点。在直接竞争实验中估计各种MGEs在粪肠球菌和屎肠球菌中的适应性代价,并通过连续传代试验产生进化群体。
新获得的PAI和两个CTns的生物学代价均取决于宿主和插入位点。新获得的vanA质粒可能会严重降低宿主适应性(25% - 27%),但在无抗生素选择的情况下仅连续传代400代后,这些代价就迅速降低。
新获得的MGEs可能会给粪肠球菌带来直接的生物学代价。然而,正如vanA质粒所示,携带MGEs的初始代价在生长过程中可能会降低,并且有益的质粒 - 宿主关联可以迅速出现。