幽门螺杆菌对甲硝唑的耐药机制

Jiang Kui, Zhang Jianzhong, Pan Guozong
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引用次数: 2

摘要

目的:幽门螺杆菌耐药是导致抗幽门螺杆菌治疗失败的重要原因之一。螺杆菌治疗。甲硝唑是消除幽门螺杆菌的首选药物。然而,单独使用这种药物很容易导致耐药性。本研究旨在探讨幽门螺旋杆菌对甲硝唑的耐药机制。方法:采用国际标准菌株NCTC11639。硝酸还原试验以4株为阳性对照,2株为大肠杆菌,2株为霍乱弧菌。以甲硝唑为片剂,0.2 g /片。使用了以下技术:(i)使用甲硝唑施加选择性压力;(ii)十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE);(iii)硝酸盐还原试验;(iv)检测与革兰氏阴性菌95种不同底物相关的酶活性。结果:在甲硝唑选择性压力作用下,幽门螺杆菌存活20个菌落;这些菌落的抑菌区直径为0 mm,而原NCTC11639的抑菌区直径为25 mm。18株耐药幽门螺杆菌与原菌株NCTC11639蛋白电泳条带间差异无统计学意义。在硝酸盐还原试验中,敏感和耐药幽门螺杆菌均为阴性,对照菌株大肠杆菌和霍乱弧菌均为阳性。幽门螺杆菌由敏感突变为抗性突变后,与琥珀酸单甲基、琥珀酸和d -丙氨酸代谢相关的酶活性降低,与L-聚焦和6-磷酸糖代谢相关的酶活性升高。结论:幽门螺杆菌对甲硝唑的耐药与硝基还原酶无关。耐药菌株的膜蛋白可能没有明显变化。幽门螺杆菌对甲硝唑的耐药性与其代谢和酶活性的变化有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanism of metronidazole resistance in Helicobacter pylori
OBJECTIVE: Drug resistance to Helicobacter pylori is one of the most important reasons for the failure of anti-H. pylori treatment. Metronidazole is a preferred drug for the elimination of H. pylori. However, using this drug alone can easily lead to resistance. The aim of the present study was to investigate the mechanism of metronidazole resistance in H. pylori. METHODS: International standard strain NCTC11639 was used. For the nitrate reduction test, four strains were used as positive controls, two strains of Bacillus coli and two strains of Vibrio cholerae. Metronidazole was used as tablets (0.2 g per tablet). The following techniques were used: (i) metronidazole used to apply selective pressure; (ii) sodium dodecylsulfate–polyacrylamide gel electrophoresis (SDS-PAGE); (iii) nitrate reduction test; and (iv) test to detect the enzyme activities associated with 95 different substrates for Gram-negative bacteria. RESULTS: As a result of the selective pressure of metronidazole, 20 H. pylori colonies survived; the bacteriostatic zones of these colonies were 0 mm in diameter, whereas the original NCTC11639 bacteriostatic zones were 25 mm in diameter. There was no significant difference seen among the 18 strains of drug-resistant H. pylori and the original NCTC11639 strain protein electrophoresis strips. In the nitrate reduction test, both sensitive and resistant H. pylori all tested negative and the control strains of Bacillus coli and Vibrio cholerae tested positive. After the mutation of H. pylori from sensitive to resistant, the activities of enzymes associated with mono-methyl succinate, succinic acid and D-alanine metabolism were decreased, and those associated with L-fucose and 6-phosphate glucose metabolism were increased. CONCLUSIONS: The resistance of H. pylori to metronidazole is not related to nitroreductase. There may be no obvious changes in membrane protein in the drug-resistant strain. The metronidazole resistance of H. pylori is associated with its metabolism and a change in enzyme activities.
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