Anti-Helicobacter pylori activity of crude N-acetylneuraminic acid isolated from glycomacropeptide of whey

被引:3
|
作者
Kim D.-J. [1 ]
Kang M.-J. [2 ]
Choi J.-A. [3 ]
Na D.-S. [4 ]
Kim J.-B. [4 ]
Na C.-S. [4 ]
Park J.-H. [2 ,5 ]
机构
[1] Laboratory Animal Resource Center, Daegu Gyeongbuk Institute of Science & Technology (DGIST, Daegu
[2] Laboratory Animal Medicine and Brain Korea 21 PLUS Project, College of Veterinary Medicine, Chonnam National University, Gwangju
[3] Department of Biochemistry, College of Medicine, Konyang University, Daejeon
[4] Lifetree Biotechnology Institute, Lifetree Bitotech Co. Ltd., Gyeonggi
[5] Laboratory Animal Medicine, College of Veterinary Medicine, Chonnam National University, 77 Yongbongro, Buk-gu, Gwangju
关键词
antibacterial activity; glycomacropeptide; Helicobacter; N-neuraminic acid;
D O I
10.5625/lar.2016.32.2.99
中图分类号
学科分类号
摘要
Helicobacter pylori colonizes the gastric mucosa of about half of the world’s population, causing chronic gastritis and gastric cancer. An increasing emergence of antibiotic-resistant H. pylori arouses demand on alternative non-antibiotic-based therapies. In this study, we freshly prepared crude N-acetylneuraminic acid obtained from glycomacropeptide (G-NANA) of whey through a neuraminidase-mediated reaction and evaluated its antibacterial ability against H. pylori and H. felis. Overnight cultures of the H. pylori were diluted with fresh media and different concentrations (1-150 mg/mL) of crude G-NANA were added directly to the culture tube. Bacterial growth was evaluated by measuring the optical density of the culture medium and the number of viable bacteria was determined by a direct count of the colony forming units (CFU) on agar plates. For the in vivo study, mice were orally infected with 100 μL (5×108 cfu/mL) of H. felis four times at a day’s interval, accompanied by a daily administration of crude G-NANA or vehicle. A day after the last infection, the mice were daily administered the crude G-NANA (0, 75, and 300 mg/mL) for 10 days and euthanized. Their stomachs were collected and bacterial colonization was determined by quantitative real-time PCR. Crude G-NANA inhibited H. pylori’s growth and reduced the number of viable bacteria in a dose-dependent manner. Furthermore, crude G-NANA inhibited bacterial colonization in the mice. These results showed that crude G-NANA has antibacterial activity against Helicobacter and demonstrated its therapeutic potential for the prevention of chronic gastritis and gastric carcinogenesis induced by Helicobacter infection in humans. © 2019, The Author(s).
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页码:99 / 104
页数:5
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