The National Food Institute, Technical University of Denmark, Kongens Lyngby, Denmark.
Department of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Appl Environ Microbiol. 2022 Jul 26;88(14):e0073422. doi: 10.1128/aem.00734-22. Epub 2022 Jun 27.
Oral antibiotic treatment is often applied in animal studies in order to allow establishment of an introduced antibiotic-resistant bacterium in the gut. Here, we compared the application of streptomycin dosed orally in microcontainers to dosage through drinking water. The selective effect on a resistant bacterial strain, as well as the effects on fecal, luminal, and mucosal microbiota composition, were investigated. Three groups of rats ( = 10 per group) were orally dosed with microcontainers daily for 3 days. One of these groups (STR-M) received streptomycin-loaded microcontainers designed for release in the distal ileum, while the other two groups (controls [CTR] and STR-W) received empty microcontainers. The STR-W group was additionally dosed with streptomycin through the drinking water. A streptomycin-resistant Escherichia coli strain was orally inoculated into all animals. Three days after inoculation, the resistant E. coli was found only in the cecum and colon of animals receiving streptomycin in microcontainers but in all intestinal compartments of animals receiving streptomycin in the drinking water. 16S rRNA amplicon sequencing revealed significant changes in the fecal microbiota of both groups of streptomycin-treated animals. Investigation of the inner colonic mucus layer by confocal laser scanning microscopy and laser capture microdissection revealed no significant effect of streptomycin treatment on the mucus-inhabiting microbiota or on E. coli encroachment into the inner mucus. Streptomycin-loaded microcontainers thus enhanced proliferation of an introduced streptomycin-resistant E. coli in the cecum and colon without affecting the small intestine environment. While improvements of the drug delivery system are needed to facilitate optimal local concentration and release of streptomycin, the application of microcontainers provides new prospects for antibiotic treatment. Delivery of antibiotics in microcontainer devices designed for release at specific sites of the gut represents a novel approach which might reduce the amount of antibiotic needed to obtain a local selective effect. We propose that the application of microcontainers may have the potential to open novel opportunities for antibiotic treatment of humans and animals with fewer side effects on nontarget bacterial populations. In the current study, we therefore elucidated the effects of streptomycin, delivered in microcontainers coated with pH-sensitive lids, on the selective effect on a resistant bacterium, as well as on the surrounding intestinal microbiota in rats.
口服抗生素治疗常用于动物研究中,以便在肠道中建立引入的抗生素耐药菌。在这里,我们比较了通过微容器口服给予链霉素和通过饮用水给予链霉素的效果。研究了对耐药菌株的选择作用,以及对粪便、腔和黏膜微生物群落组成的影响。三组大鼠(每组 10 只)连续 3 天每天口服微容器给药。其中一组(STR-M)接受设计用于在回肠远端释放的载有链霉素的微容器,而另外两组(对照组 [CTR]和 STR-W)接受空微容器。STR-W 组还通过饮用水给予链霉素。所有动物均口服接种一株链霉素耐药大肠杆菌。接种后 3 天,仅在接受微容器中链霉素治疗的动物的盲肠和结肠中发现耐药大肠杆菌,但在接受饮用水中链霉素治疗的动物的所有肠道部位均发现耐药大肠杆菌。16S rRNA 扩增子测序显示,两组接受链霉素治疗的动物的粪便微生物群均发生显著变化。通过共聚焦激光扫描显微镜和激光捕获显微切割研究结肠内层黏液层发现,链霉素处理对黏液栖息微生物群或大肠杆菌侵入内层黏液没有显著影响。因此,载有链霉素的微容器增强了引入的耐链霉素大肠杆菌在盲肠和结肠中的增殖,而不会影响小肠环境。虽然需要改进药物输送系统以促进链霉素的最佳局部浓度和释放,但微容器的应用为抗生素治疗提供了新的前景。在肠道特定部位释放的微容器装置中递送抗生素代表了一种新的方法,可能减少获得局部选择性效果所需的抗生素量。我们提出,微容器的应用有可能为人类和动物的抗生素治疗开辟新的机会,减少对非目标细菌群体的副作用。在本研究中,我们因此阐明了用 pH 敏感盖涂覆的微容器递送链霉素对耐药菌的选择性作用以及对大鼠周围肠道微生物群的影响。