移植对肾脏受者和供者口腔微生物群的影响

Paul M. Campbell, Thomas Willmott, Gavin J. Humphreys, Oana Piscoran, Houda Chea, Angela M. Summers, Joanne E. Konkel, Christopher G. Knight, Titus Augustine, Andrew J. McBain
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摘要

慢性肾脏疾病(CKD)可能通过尿素和肌酐等尿毒症毒素浓度的增加影响人体微生物群。方法我们对肾脏移植前和移植后一周CKD患者的口腔微生物群进行了分析。活体肾脏供者也在类似的时间内进行了纵向跟踪,允许直接比较单独接受移植手术的组(供者)(n=13)和另外接受免疫抑制剂和CKD解决的组(受体)(n=45)。通过Kruskal-Wallis测试,移植与受体和供体在移植后一周内口腔微生物组α多样性下降的相似模式相关。与副流感嗜血杆菌、segnis聚集菌、Peptostreptococcus和放线杆菌s相关的扩增子序列变异(asv)在移植后一周内显著减少。这些属asv的减少可能影响细菌性心内膜炎的风险,细菌性心内膜炎是一种罕见但高死亡率的肾移植并发症。一系列因素可能驱动观察到的口腔微生物组的变化,包括手术本身和唾液尿素减少、大环内酯类抗生素免疫抑制剂的施用以及肾移植特征的免疫功能破坏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transplantation impacts on the oral microbiome of kidney recipients and donors
Introduction Chronic kidney disease (CKD) may affect the human microbiome via increased concentrations of uremic toxins such as urea and creatinine. Methods We have profiled the oral microbiota in patients with CKD before and one week after kidney transplantation. Living kidney donors were also longitudinally tracked over a similar period, allowing direct comparison between a group undergoing transplant surgery alone (donors) (n=13) and a group additionally undergoing the introduction of immunosuppressive agents and the resolution of CKD (recipients) (n=45). Results Transplantation was associated with a similar pattern of decreasing alpha diversity in the oral microbiome in recipients and donors via Kruskal-Wallis testing, within one week of transplantation. Amplicon sequence variants (ASVs) associated with Haemophilus parainfluenzae , Aggregatibacteria segnis , Peptostreptococcus and Actinobacillu s were significantly decreased in recipients within a week of transplantation. Discussion A reduction in ASVs in these genera could influence the risk of bacterial endocarditis, a rare but high-mortality kidney transplantation complication. A range of factors may drive the observed changes in oral microbiome including both factors associated with surgery itself and the decreases in salivary urea, administration of macrolide antibiotic immunosuppressants, and disruption to immune function that characterise kidney transplant.
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