Wang Zhiqing, Liang Liping, Liu Le, Wang Zhi, Wang Ying, Yu Zonglin, Wu Baoping, Chen Ye
Department of Gastroenterology, State Key Laboratory of Organ Failure Research, Guangdong Provincial Key Laboratory of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Gastroenterology, Integrative Microecology Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Microbiol Spectr. 2023 Jan 31;11(2):e0281922. doi: 10.1128/spectrum.02819-22.
Peutz-Jeghers syndrome (PJS) is a rare hereditary disorder characterized by intestinal polyposis, and intestinal intussusception is one of the most urgent complications. While it is known that imbalance of the gut microbiota is highly associated with intestinal disorders, the role of the gut microbiome in the pathogenesis of PJS has not been reported. In this study, we performed 16S rRNA sequencing on stools from 168 patients and 68 healthy family members who lived together to determine the gut microbiome composition of PJS patients. Metagenomics sequencing was further performed on the representative samples (61 PJS patients and 27 healthy family members) to analyze the functional changes. We found that the fecal microbiome of patients with PJS showed a greater variation in β-diversity. An enhancement of Escherichia coli and a reduction of Faecalibacterium prausnitzii was identified in PJS patients. Further reduction of Faecalibacterium prausnitzii was the characteristic microbial change observed in patients with intussusception. Functional analysis revealed that the abundance of propanoate metabolism was enriched in PJS patients and further enriched in those with intussusception. Escherichia coli was the major contributor to the enrichment of this metabolism pathway, which was associated with the abnormal expression of methylglyoxal synthase (encoded by ) and phosphate acetyltransferase (encoded by ). Our findings showed a distinct gut microbiome signature in PJS patients and identified the connection between the gut microbiome and intussusception. Alterations in the gut microbiome might be involved in the pathogenesis of PJS and may serve as biomarkers for gastrointestinal surveillance. Recent research has established a link between the gut microbiome and polyps and neoplasia, and antibiotic use influences the microbiome and the development of colorectal polyps. Familial adenomatous polyposis (FAP), which is characterized by the early development of benign precursor lesions (polyps), is associated with enterotoxigenic Bacteroides fragilis and Escherichia coli biofilms. However, the relationship between the gut microbiome and the pathophysiology of PJS has not yet been established. In this study, we found that PJS patients had a distinct microbiome composition, with a greater variation in β-diversity, an increase in Escherichia coli, and a decrease in Faecalibacterium prausnitzii. A further reduction of Faecalibacterium prausnitzii was observed in patients with intussusception. Moreover, PJS involved increased propanoate metabolism as well as abnormal and expression. These findings may contribute to a better understanding of the etiology of PJS and improve disease control strategies.
黑斑息肉综合征(PJS)是一种罕见的遗传性疾病,其特征为肠道息肉病,肠套叠是最紧急的并发症之一。虽然已知肠道微生物群失衡与肠道疾病高度相关,但肠道微生物群在PJS发病机制中的作用尚未见报道。在本研究中,我们对168例患者和68名共同生活的健康家庭成员的粪便进行了16S rRNA测序,以确定PJS患者的肠道微生物群组成。对代表性样本(61例PJS患者和27名健康家庭成员)进一步进行宏基因组测序,以分析功能变化。我们发现,PJS患者的粪便微生物群在β多样性上表现出更大的差异。在PJS患者中,大肠杆菌增加,普拉梭菌减少。普拉梭菌的进一步减少是肠套叠患者观察到的特征性微生物变化。功能分析显示,丙酸代谢丰度在PJS患者中富集,并在肠套叠患者中进一步富集。大肠杆菌是该代谢途径富集的主要贡献者,这与甲基乙二醛合酶(由 编码)和磷酸乙酰转移酶(由 编码)的异常表达有关。我们的研究结果显示了PJS患者独特的肠道微生物群特征,并确定了肠道微生物群与肠套叠之间的联系。肠道微生物群的改变可能参与了PJS的发病机制,并可能作为胃肠道监测的生物标志物。最近的研究已经建立了肠道微生物群与息肉和肿瘤形成之间的联系,抗生素的使用会影响微生物群和结肠息肉的发展。家族性腺瘤性息肉病(FAP)以良性前体病变(息肉)的早期发展为特征,与产肠毒素脆弱拟杆菌和大肠杆菌生物膜有关。然而,肠道微生物群与PJS病理生理学之间的关系尚未确立。在本研究中,我们发现PJS患者具有独特的微生物群组成,β多样性差异更大,大肠杆菌增加,普拉梭菌减少。在肠套叠患者中观察到普拉梭菌进一步减少。此外,PJS涉及丙酸代谢增加以及 和 表达异常。这些发现可能有助于更好地理解PJS的病因,并改善疾病控制策略。