幽门螺杆菌
克拉霉素
甲硝唑
阿莫西林
抗菌剂
医学
微生物学
抗生素
23S核糖体RNA
抗生素耐药性
琼脂稀释
最小抑制浓度
生物
内科学
生物化学
基因
核糖体
核糖核酸
作者
Jung Won Lee,Nayoung Kim,Ryoung Hee Nam,Jeong Eun Yu,Joo Hee Son,Sun Min Lee,Dong Ho Lee
出处
期刊:Gut and Liver
[The Editorial Office of Gut and Liver]
日期:2020-11-16
卷期号:15 (1): 53-60
被引量:13
摘要
Background/Aims: Favorable outcomes of potassium-competitive acid blocker (PCAB)-containing eradication therapy have been reported. In fact, tegoprazan, a recently developed PCAB, was presumed to show good eradication efficacy even for resistant Helicobacter pylori. We aimed to investigate the anti-H. pylori efficacy of tegoprazan compared with that of vonoprazan.
Methods: A total of 220 resistant clinical H. pylori isolates were utilized. The anti-H. pylori efficacy of PCABs was determined by evaluating the minimum inhibitory concentrations (MICs) of clarithromycin, fluoroquinolone, metronidazole, and amoxicillin in combination with vonoprazan or tegoprazan by the agar dilution method. The impact of the mutations responsible for resistance development, such as 23S rRNA, gyrA, rdxA, frxA, and pbp1 mutations, was also analyzed.
Results: H. pylori growth was significantly inhibited in a medium containing 1 μg/mL clarithromycin with tegoprazan (128 μg/mL). The MICs of clarithromycin (46.3%), fluoroquinolone (46.7%), metronidazole (55.6%), and amoxicillin (34.5%) against resistant H. pylori isolates improved after tegoprazan administration. Tegoprazan demonstrated more frequent susceptibility acquisition with metronidazole than with vonoprazan (20.6% vs 4.7%, p=0.014). However, there were no significant differences depending on the mutational status of each antimicrobial agent.
Conclusions: Tegoprazan administration may improve the susceptibility of antimicrobial-resistant H. pylori, independent of acid suppression. (Gut Liver 2021;15:53-60)
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