Unit of Human Microbiome, Bambino Gesù Children's Hospital, IRCCS, Viale San Paolo 15, 00146 Rome, Italy.
Unit of Gastroenterology, Hepatology and Nutrition, Bambino Gesù Children's Hospital, IRCCS, Piazza Sant' Onofrio 4, 00165 Rome, Italy.
Int J Mol Sci. 2018 Apr 25;19(5):1280. doi: 10.3390/ijms19051280.
The increase of microorganisms multi-drug resistant (MDR) to antibiotics (ATBs) is becoming a global emergency, especially in frail subjects. In chronic liver disease (LD) with indications for liver transplantation (LT), MDR colonization can significantly affect the LT outcome. However, no clear guidelines for microbial management are available. A novel approach toward MDR-colonized patients undergoing LT was developed at our Center refraining from ATBs use during the transplant waiting list, and use of an intensive perioperative prophylaxis cycle. This study aimed to couple clinical evaluation with monitoring of gut microbiota in a pediatric LD patient colonized with MDR (KP) who underwent LT. No peri-transplant complications were reported, and a decontamination from the MDR bacteria occurred during follow-up. Significant changes in gut microbiota, especially during ATB treatment, were reported by microbiota profiling. Patterns of predominance and microbiota diversity revealed opposite temporal trends, with ecological microbiota niches linked to ATB-driven selection. Our infection control program appeared to control complications following LT in an MDR-KP-colonized patient. The perioperative ATB regimen, acting as LT prophylaxis, triggered MDR-KP overgrowth and gut dysbiosis, but buffered infectious processes. Mechanisms modulating the gut ecosystem should be taken into account in MDR colonization clinical management.
微生物对抗生素(ATBs)的多药耐药性(MDR)的增加正在成为全球紧急情况,尤其是在体弱的患者中。在有肝移植(LT)指征的慢性肝病(LD)中,MDR 定植可显著影响 LT 结果。然而,目前尚无针对微生物管理的明确指南。我们中心开发了一种针对 MDR 定植患者的新方法,即在 LT 等待名单期间避免使用 ATBs,并使用强化围手术期预防方案。本研究旨在将临床评估与监测胃肠道微生物群结合起来,对一名接受 LT 的患有 MDR 定植的儿科 LD 患者(KP)进行研究。未报告移植前并发症,并且在随访期间发生了 MDR 细菌的清除。通过微生物组谱分析报告了胃肠道微生物群的显著变化,特别是在 ATB 治疗期间。优势模式和微生物多样性揭示了相反的时间趋势,与 ATB 驱动的选择相关的生态微生物生态位。我们的感染控制计划似乎控制了 MDR-KP 定植患者 LT 后的并发症。作为 LT 预防的围手术期 ATB 方案引发了 MDR-KP 过度生长和肠道菌群失调,但缓冲了感染过程。在 MDR 定植的临床管理中,应考虑调节肠道生态系统的机制。