Paul G. Allen School for Global Health, Washington State Universitygrid.30064.31, Pullman, Washington, USA.
Department of Chemistry, Washington State Universitygrid.30064.31, Pullman, Washington, USA.
Appl Environ Microbiol. 2022 Aug 9;88(15):e0079122. doi: 10.1128/aem.00791-22. Epub 2022 Jul 14.
At a time when antibiotic resistance is seemingly ubiquitous worldwide, understanding the mechanisms responsible for successful emergence of new resistance genes may provide insights into the persistence and pathways of dissemination for antibiotic-resistant organisms in general. For example, Escherichia coli strains harboring a class A β-lactamase-encoding gene () appear to be displacing strains that harbor a class C β-lactamase gene () in Washington State dairy cattle. We cloned these genes with native promoters into low-copy-number plasmids that were then transformed into isogenic strains of E. coli, and growth curves were generated for two commonly administered antibiotics (ampicillin and ceftiofur). Both strains met the definition of resistance for ampicillin (≥32 μg/mL) and ceftiofur (≥16 μg/mL). Growth of the CMY-2-producing strain was compromised at 1,000 μg/mL ampicillin, whereas the CTX-M-15-producing strain was not inhibited in the presence of 3,000 μg/mL ampicillin or with most concentrations of ceftiofur, although there were mixed outcomes with ceftiofur metabolites. Consequently, in the absence of competing genes, E. coli harboring either gene would experience a selective advantage if exposed to these antibiotics. Successful emergence of CTX-M-15-producing strains where CMY-2-producing strains are already established, however, requires high concentrations of antibiotics that can only be found in the urine of treated animals (e.g., >2,000 μg/mL for ampicillin, based on literature). This selection pressure may be important for the emergence of new and more efficient antibiotic resistance genes and likely for persistence of antibiotic-resistant bacteria in food animal populations. We studied the relative fitness benefits of a cephalosporin resistance enzyme (CTX-M-15) that is displacing a similar enzyme (CMY-2), which is extant in E. coli from dairy cattle in Washington State. experiments demonstrated that CTX-M-15 provides a significant fitness advantage, but only in the presence of very high concentrations of antibiotic that are only found when the antibiotic ampicillin, and to a lesser extent ceftiofur, is excreted in urine from treated animals. As such, the increasing prevalence of bacteria with is likely occurring . Interventions should focus on controlling waste from treated animals and, when possible, selecting antibiotics that are less likely to impact the proximal environment of treated animals.
在全球范围内,抗生素耐药性似乎无处不在的情况下,了解导致新的耐药基因成功出现的机制,可能有助于深入了解抗生素耐药生物体在一般情况下的持续存在和传播途径。例如,在华盛顿州的奶牛场,携带 A 类β-内酰胺酶编码基因 ()的大肠杆菌菌株似乎正在取代携带 C 类β-内酰胺酶基因 ()的菌株。我们将这些带有天然启动子的基因克隆到低拷贝数质粒中,然后转化为大肠杆菌的同源菌株,并生成两种常用抗生素(氨苄西林和头孢噻呋)的生长曲线。两种菌株对氨苄西林(≥32μg/mL)和头孢噻呋(≥16μg/mL)的耐药性均符合定义。CMY-2 产生菌的生长在 1000μg/mL 氨苄西林时受到抑制,而 CTX-M-15 产生菌在 3000μg/mL 氨苄西林或大多数头孢噻呋浓度下均不受抑制,尽管头孢噻呋代谢物的结果存在差异。因此,如果暴露于这些抗生素,携带这两种基因中的任何一种的大肠杆菌都将具有选择性优势。然而,CTX-M-15 产生菌的成功出现需要高浓度的抗生素,这些抗生素只能在接受治疗的动物尿液中找到(例如,氨苄西林的浓度大于 2000μg/mL,这是基于文献的结果)。这种选择压力对于新的和更有效的抗生素耐药基因的出现以及抗生素耐药细菌在食用动物种群中的持续存在可能非常重要。我们研究了正在取代在华盛顿州奶牛场的大肠杆菌中已存在的类似酶(CMY-2)的头孢菌素耐药酶(CTX-M-15)的相对适应优势。实验表明,CTX-M-15 提供了显著的适应优势,但仅在抗生素氨苄西林和在较小程度上头孢噻呋排泄在接受治疗动物的尿液中时,才会出现非常高浓度的抗生素的情况下才会出现。因此,具有 的细菌的日益流行很可能正在发生。干预措施应侧重于控制来自接受治疗动物的废物,并在可能的情况下选择不太可能影响接受治疗动物的近端环境的抗生素。