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

机译:肝移植后定殖的耐多药细菌和肠道微生物组的纵向演变

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摘要

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:耐多药细菌(MDRB)感染仍然是肝移植(LT)后发病率和死亡率的主要原因。终末期肝病的肠道消化不良特征可能使患者易于肠道MDRB定植和感染,进而加剧消化不良。但是,LT术后MDRB定植与营养不良之间的关系仍不清楚。我们前瞻性地在一个三级护理中心招募了177名接受LT的成年患者。对LT前收集的723份粪便样品进行16 andS V3-V4 rRNA测序,并定期进行,直到LT后一年,以检测MDRB定植是否与微生物组多样性降低有关。在多变量线性混合效应模型中,在控制了潜在的肝脏疾病,抗生素暴露和临床并发症后,MDRB定殖预测了香农α多样性降低。重要的是,LT前的微生物标记可预测随后通过MDRB定殖。我们的结果表明,MDRB定殖是持续性营养不良的主要标志,以前未被认识。需要考虑微生物和临床因素的治疗方法来解决移植后微生物组的健康问题。

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