Khan Iman, Wu Sylvia, Hudson Anika, Hughes Clayton, Stryjniak Gabriel, Westblade Lars F, Satlin Michael J, Tedrow Nicholas, Uhlemann Anne-Catrin, Kraft Colleen, Dadhania Darshana M, Silberzweig Jeffrey, De Vlaminck Iwijn, Li Carol, Srivatana Vesh, Lee John Richard
Division of Nephrology and Hypertension, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
medRxiv. 2023 Feb 24:2023.02.23.23286379. doi: 10.1101/2023.02.23.23286379.
RATIONALE & OBJECTIVE: The nasal passages harbor both commensal and pathogenic bacteria. In this study, we sought to characterize the anterior nasal microbiota in PD patients using 16S rRNA gene sequencing.
Cross-sectional.
SETTING & PARTICIPANTS: We recruited 32 PD patients, 37 kidney transplant (KTx) recipients, 22 living donor/healthy control (HC) participants and collected anterior nasal swabs at a single point in time.
We performed 16S rRNA gene sequencing of the V4-V5 hypervariable region to determine the nasal microbiota.
Nasal microbiota profiles were determined at the genus level as well as the amplicon sequencing variant level.
We compared nasal abundance of common genera among the 3 groups using Wilcoxon rank sum testing with Benjamini-Hochberg adjustment. DESeq2 was also utilized to compare the groups at the ASV levels.
In the entire cohort, the most abundant genera in the nasal microbiota included: , and . Correlational analyses revealed a significant inverse relationship between the nasal abundance of and that of . PD patients have a higher nasal abundance of than KTx recipients and HC participants. PD patients have a more diverse representation of and than KTx recipients and HC participants. PD patients who concurrently have or who developed future peritonitis had a numerically higher nasal abundance of than PD patients who did not develop peritonitis.
16S RNA gene sequencing provides taxonomic information to the genus level.
We find a distinct nasal microbiota signature in PD patients compared to KTx recipients and HC participants. Given the potential relationship between the nasal pathogenic bacteria and infectious complications, further studies are needed to define the nasal microbiota associated with these infectious complications and to conduct studies on the manipulation of the nasal microbiota to prevent such complications.
鼻腔中既有共生菌也有致病菌。在本研究中,我们试图通过16S rRNA基因测序来描述帕金森病(PD)患者的前鼻微生物群特征。
横断面研究。
我们招募了32名PD患者、37名肾移植(KTx)受者、22名活体供者/健康对照(HC)参与者,并在单一时间点采集前鼻拭子。
我们对V4 - V5高变区进行16S rRNA基因测序以确定鼻腔微生物群。
在属水平以及扩增子测序变异水平上确定鼻腔微生物群谱。
我们使用经Benjamini - Hochberg校正的Wilcoxon秩和检验比较三组中常见属的鼻腔丰度。还利用DESeq2在ASV水平上比较各组。
在整个队列中,鼻腔微生物群中最丰富的属包括: 、 和 。相关性分析显示 的鼻腔丰度与 的鼻腔丰度之间存在显著负相关。PD患者的 鼻腔丰度高于KTx受者和HC参与者。与KTx受者和HC参与者相比,PD患者的 和 的表现更为多样。同时患有或未来发生腹膜炎的PD患者的 鼻腔丰度在数值上高于未发生腹膜炎的PD患者。
16S RNA基因测序提供属水平的分类信息。
与KTx受者和HC参与者相比,我们在PD患者中发现了独特的鼻腔微生物群特征。鉴于鼻腔致病菌与感染性并发症之间的潜在关系,需要进一步研究来确定与这些感染性并发症相关的鼻腔微生物群,并开展关于操纵鼻腔微生物群以预防此类并发症的研究。