Jo Sungyang, Kang Woorim, Hwang Yun Su, Lee Seung Hyun, Park Kye Won, Kim Mi Sun, Lee Hyunna, Yoon Hyung Jeong, Park Yoo Kyoung, Chalita Mauricio, Lee Je Hee, Sung Hojun, Lee Jae-Yun, Bae Jin-Woo, Chung Sun Ju
Department of Neurology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, 05505, South Korea.
Department of Biology and Department of Life and Nanopharmaceutical Sciences, Kyung Hee University, Seoul, 02447, South Korea.
NPJ Parkinsons Dis. 2022 Jul 7;8(1):87. doi: 10.1038/s41531-022-00351-6.
Although several studies have identified a distinct gut microbial composition in Parkinson's disease (PD), few studies have investigated the oral microbiome or functional alteration of the microbiome in PD. We aimed to investigate the connection between the oral and gut microbiome and the functional changes in the PD-specific gut microbiome using shotgun metagenomic sequencing. The taxonomic composition of the oral and gut microbiome was significantly different between PD patients and healthy controls (P = 0.003 and 0.001, respectively). Oral Lactobacillus was more abundant in PD patients and was associated with opportunistic pathogens in the gut (FDR-adjusted P < 0.038). Functional analysis revealed that microbial gene markers for glutamate and arginine biosynthesis were downregulated, while antimicrobial resistance gene markers were upregulated in PD patients than healthy controls (all P < 0.001). We identified a connection between the oral and gut microbiota in PD, which might lead to functional alteration of the microbiome in PD.
尽管多项研究已确定帕金森病(PD)患者有独特的肠道微生物组成,但很少有研究调查PD患者的口腔微生物群或微生物群的功能改变。我们旨在通过鸟枪法宏基因组测序研究口腔和肠道微生物群之间的联系以及PD特异性肠道微生物群的功能变化。PD患者与健康对照者的口腔和肠道微生物群的分类组成存在显著差异(分别为P = 0.003和0.001)。PD患者口腔中的乳酸杆菌更为丰富,且与肠道中的机会性病原体有关(经FDR校正,P < 0.038)。功能分析显示,与健康对照者相比,PD患者中谷氨酸和精氨酸生物合成的微生物基因标记物下调,而抗菌抗性基因标记物上调(所有P < 0.001)。我们确定了PD患者口腔和肠道微生物群之间的联系,这可能导致PD患者微生物群的功能改变。