Hasegawa Satoru, Goto Sae, Tsuji Hirokazu, Okuno Tatsuya, Asahara Takashi, Nomoto Koji, Shibata Akihide, Fujisawa Yoshiro, Minato Tomomi, Okamoto Akira, Ohno Kinji, Hirayama Masaaki
Department of Pathophysiological Laboratory Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Division of Neurogenetics, Center for Neurological Diseases and Cancer, Nagoya University Graduate School of Medicine, Nagoya, Japan.
PLoS One. 2015 Nov 5;10(11):e0142164. doi: 10.1371/journal.pone.0142164. eCollection 2015.
The intestine is one of the first affected organs in Parkinson's disease (PD). PD subjects show abnormal staining for Escherichia coli and α-synuclein in the colon.
We recruited 52 PD patients and 36 healthy cohabitants. We measured serum markers and quantified the numbers of 19 fecal bacterial groups/genera/species by quantitative RT-PCR of 16S or 23S rRNA. Although the six most predominant bacterial groups/genera/species covered on average 71.3% of total intestinal bacteria, our analysis was not comprehensive compared to metagenome analysis or 16S rRNA amplicon sequencing.
In PD, the number of Lactobacillus was higher, while the sum of analyzed bacteria, Clostridium coccoides group, and Bacteroides fragilis group were lower than controls. Additionally, the sum of putative hydrogen-producing bacteria was lower in PD. A linear regression model to predict disease durations demonstrated that C. coccoides group and Lactobacillus gasseri subgroup had the largest negative and positive coefficients, respectively. As a linear regression model to predict stool frequencies showed that these bacteria were not associated with constipation, changes in these bacteria were unlikely to represent worsening of constipation in the course of progression of PD. In PD, the serum lipopolysaccharide (LPS)-binding protein levels were lower than controls, while the levels of serum diamine oxidase, a marker for intestinal mucosal integrity, remained unchanged in PD.
The permeability to LPS is likely to be increased without compromising the integrity of intestinal mucosa in PD. The increased intestinal permeability in PD may make the patients susceptible to intestinal dysbiosis. Conversely, intestinal dysbiosis may lead to the increased intestinal permeability. One or both of the two mechanisms may be operational in development and progression of PD.
肠道是帕金森病(PD)中最早受影响的器官之一。PD患者的结肠中大肠杆菌和α-突触核蛋白染色异常。
我们招募了52名PD患者和36名健康同居者。我们测量了血清标志物,并通过16S或23S rRNA的定量RT-PCR对19种粪便细菌群/属/种进行定量。尽管六个最主要的细菌群/属/种平均占肠道细菌总数的71.3%,但与宏基因组分析或16S rRNA扩增子测序相比,我们的分析并不全面。
在PD患者中,乳酸杆菌数量较高,而分析的细菌总数、球状梭菌属和脆弱拟杆菌属低于对照组。此外,PD患者中推定的产氢细菌总数较低。预测疾病持续时间的线性回归模型表明,球状梭菌属和加氏乳杆菌亚组的负系数和正系数分别最大。作为预测大便频率的线性回归模型表明,这些细菌与便秘无关,这些细菌的变化不太可能代表PD病程中便秘的恶化。在PD患者中,血清脂多糖(LPS)结合蛋白水平低于对照组,而作为肠道粘膜完整性标志物的血清二胺氧化酶水平在PD患者中保持不变。
在不损害PD患者肠道粘膜完整性的情况下,LPS的通透性可能会增加。PD患者肠道通透性增加可能使其易患肠道菌群失调。相反,肠道菌群失调可能导致肠道通透性增加。这两种机制中的一种或两种可能在PD的发生和发展中起作用。