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Colonizing multidrug-resistant bacteria and the longitudinal evolution of the intestinal microbiome after liver transplantation

机译:肝移植后肠道微生物组的殖民化多药细菌以及肠道微生物组的纵向演变

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Infections by multidrug-resistant bacteria (MDRB) remain a leading cause of morbidity and mortality after liver transplantation (LT). Gut dysbiosis characteristic of end-stage liver disease may predispose patients to intestinal MDRB colonization and infection, in turn exacerbating dysbiosis. However, relationships between MDRB colonization and dysbiosis after LT remain unclear. We prospectively recruited 177 adult patients undergoing LT at a single tertiary care center. 16?S V3-V4 rRNA sequencing was performed on 723 fecal samples collected pre-LT and periodically until one-year post-LT to test whether MDRB colonization was associated with decreased microbiome diversity. In multivariate linear mixed-effect models, MDRB colonization predicts reduced Shannon α-diversity, after controlling for underlying liver disease, antibiotic exposures, and clinical complications. Importantly, pre-LT microbial markers predict subsequent colonization by MDRB. Our results suggest MDRB colonization as a major, previously unrecognized, marker of persistent dysbiosis. Therapeutic approaches accounting for microbial and clinical factors are needed to address post-transplant microbiome health.
机译:多药细菌(MDRB)感染仍然是肝移植(LT)后发病率和死亡率的主要原因。肠道肝脏疾病的肠道功能性脱敏特征可以使患者倾向于肠道MDRB定植和感染,反过来加剧了消化不良。然而,在LT仍然不清楚的情况下MDRB定植与脱敏之间的关系。我们潜在招聘了177名成年患者在单个第三级护理中心进行的。在预先收集的723次粪便样品上进行16℃,并定期达到一年后,对测试MDRB定子是否与微生物组多样性降低有关。在多变量线性混合效果模型中,MDRB定植预测,在控制潜在的肝病,抗生素暴露和临床并发症后,减少了Shannonα-多样性。重要的是,Pre-LT微生物标记预测MDRB的后续定植。我们的结果表明,MDRB定植为主要,以前未被识别的持续失血症标记。需要治疗方法核算微生物和临床因素,以解决移植后的微生物组健康。

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