Alterations of ileal mucosa-associated microbiota in hypercholesterolemia patients

被引:0
|
作者
Li, Jia [1 ,2 ,3 ]
Ma, Jinxia [2 ,3 ]
Wang, Weihua [2 ,3 ]
Du, Haitao [2 ,3 ]
Tang, Shuai [2 ,3 ]
Li, Yi [2 ,3 ]
Zhu, Wenya [2 ,3 ]
Zhang, Ru [2 ,3 ]
Wan, Jun [2 ,3 ]
机构
[1] 983rd Hosp Joint Logist Support Force PLA, Dept Gastroenterol, 60 Huangwei Rd, Tianjin 300142, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr, Dept Gastroenterol, 28 Fuxing Rd, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Natl Clin Res Ctr Geriatr Dis, 28 Fuxing Rd, Beijing 100853, Peoples R China
关键词
Hypercholesterolemia; Microbiota; Mucosa; Small intestine; 16S rRNA gene sequencing; CHAIN FATTY-ACIDS; GUT MICROBIOTA; NONALCOHOLIC STEATOHEPATITIS; BILE-ACIDS; CHOLESTEROL; DIVERSITY; SEQUENCES; COLITIS; DISEASE; OBESITY;
D O I
10.1016/j.heliyon.2023.e22116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many metabolic diseases have been demonstrated to be associated with changes in the microbiome. However, no studies have yet been conducted to examine the characteristics of the mucosal microbiota of patients with hypercholesterolemia. We aimed to examine mucosaassociated microbiota in subjects with hypercholesterolemia. We conducted a case-control study, in which ileal mucosal samples were collected from 13 hypercholesterolemia patients and 13 controls for 16S rRNA gene sequencing. There were differences in the composition of ileal mucosal microbiota based on beta diversity between the hypercholesterolemia and control groups (P < 0.05). Compared with the control group, the phylum Bacteroidetes and the genera Bacteroides, Butyricicoccus, Parasutterella, Candidatus_Soleaferrea, and norank_f__norank_o__Izemoplasmatales were less abundant in the hypercholesterolemia group (P < 0.05), while the genus Anaerovibrio was enriched in the hypercholesterolemia group (P < 0.05). The relative abundance of Bacteroides was negatively correlated with total cholesterol and low-density lipoprotein cholesterol (P < 0.01). The relative abundance of Coprococcus was negatively correlated with triglycerides and body mass index (all P < 0.05). PICRUSt functional prediction analysis showed that pathways related to Glycerophospholipid metabolism, ABC transporters, Phosphotransferase system, and Biofilm formation - Escherichia coli, and infectious diseases of pathogenic Escherichia coli were enriched in the hypercholesterolemia group. This work suggests a potential role of ileal mucosal microbiota in the development of hypercholesterolemia.
引用
收藏
页数:13
相关论文
共 50 条
  • [21] Fungal Dysbiosis in Mucosa-associated Microbiota of Crohn's Disease Patients
    Liguori, Giuseppina
    Lamas, Bruno
    Richard, Mathias L.
    Brandi, Giovanni
    da Costa, Gregory
    Hoffmann, Thomas W.
    Di Simone, Massimo Pierluigi
    Calabrese, Carlo
    Poggioli, Gilberto
    Langella, Philippe
    Campieri, Massimo
    Sokol, Harry
    JOURNAL OF CROHNS & COLITIS, 2016, 10 (03): : 296 - 305
  • [22] Mucosa-Associated Microbiota in Patients with Irritable Bowel Syndrome: A Comparison of Subtypes
    Matsumoto, Hiroshi
    Shiotani, Akiko
    Katsumata, Ryo
    Fukushima, Shinya
    Handa, Yukiko
    Osawa, Motoyasu
    Murao, Takahisa
    Handa, Osamu
    Umegaki, Eiji
    Inoue, Ryo
    Naito, Yuji
    DIGESTION, 2021, 102 (01) : 49 - 56
  • [23] Human Intestinal Lumen and Mucosa-Associated Microbiota in Patients with Colorectal Cancer
    Chen, Weiguang
    Liu, Fanlong
    Ling, Zongxin
    Tong, Xiaojuan
    Xiang, Charlie
    PLOS ONE, 2012, 7 (06):
  • [24] Comparison of brush and biopsy sampling methods of the ileal pouch for assessment of mucosa-associated microbiota of human subjects
    Susan M Huse
    Vincent B Young
    Hilary G Morrison
    Dionysios A Antonopoulos
    John Kwon
    Sushila Dalal
    Rose Arrieta
    Nathaniel A Hubert
    Lici Shen
    Joseph H Vineis
    Jason C Koval
    Mitchell L Sogin
    Eugene B Chang
    Laura E Raffals
    Microbiome, 2
  • [25] Comparison of brush and biopsy sampling methods of the ileal pouch for assessment of mucosa-associated microbiota of human subjects
    Huse, Susan M.
    Young, Vincent B.
    Morrison, Hilary G.
    Antonopoulos, Dionysios A.
    Kwon, John
    Dalal, Sushila
    Arrieta, Rose
    Hubert, Nathaniel A.
    Shen, Lici
    Vineis, Joseph H.
    Koval, Jason C.
    Sogin, Mitchell L.
    Chang, Eugene B.
    Raffals, Laura E.
    MICROBIOME, 2014, 2
  • [26] Reduction of butyric acid-producing bacteria in the ileal mucosa-associated microbiota is associated with the history of abdominal surgery in patients with Crohn's disease
    Handa, Osamu
    Miura, Hiroto
    Gu, Tingting
    Osawa, Motoyasu
    Matsumoto, Hiroshi
    Umegaki, Eiji
    Inoue, Ryo
    Naito, Yuji
    Shiotani, Akiko
    REDOX REPORT, 2023, 28 (01)
  • [27] The dysbiosis of mucosa-associated gastric microbiota during aging
    He, C.
    Peng, C.
    Ouyang, Y.
    Yang, X.
    Zhu, Z.
    Shu, X.
    Zhu, Y.
    Lu, N.
    HELICOBACTER, 2019, 24
  • [28] Dominant Intestinal Mucosa-Associated Microbiota in Pediatric Patients With Inflammatory Bowel Disease
    Iebba, Valerio
    Checchi, Monica Proietti
    Totino, Valentina
    Longhi, Catia
    Conte, Maria P.
    Schippa, Serena
    Cucchiara, Salvatore
    GASTROENTEROLOGY, 2010, 138 (05) : S583 - S584
  • [29] Probiotics modify human intestinal mucosa-associated microbiota in patients with colorectal cancer
    Gao, Zhiguang
    Guo, Bomin
    Gao, Renyuan
    Zhu, Qingchao
    Wu, Wen
    Qin, Huanlong
    MOLECULAR MEDICINE REPORTS, 2015, 12 (04) : 6119 - 6127
  • [30] Effects of Proton Pump Inhibitors on the Gastric Mucosa-Associated Microbiota in Dyspeptic Patients
    Sterbini, Francesco Paroni
    Palladini, Alessandra
    Masucci, Luca
    Cannistraci, Carlo Vittorio
    Pastorino, Roberta
    Ianiro, Gianluca
    Bugli, Francesca
    Martini, Cecilia
    Ricciardi, Walter
    Gasbarrini, Antonio
    Sanguinetti, Maurizio
    Cammarota, Giovanni
    Posteraro, Brunella
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2016, 82 (22) : 6633 - 6644