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多种硝基还原酶可能参与幽门螺杆菌对甲硝唑的耐药性。

Potential involvement of several nitroreductases in metronidazole resistance in Helicobacter pylori.

作者信息

Jorgensen M A, Trend M A, Hazell S L, Mendz G L

机构信息

School of Microbiology and Immunology, The University of New South Wales, Sydney, NSW 2052, Australia.

出版信息

Arch Biochem Biophys. 2001 Aug 15;392(2):180-91. doi: 10.1006/abbi.2001.2427.

Abstract

Susceptibility of Helicobacter pylori to the antibiotic metronidazole has been attributed to the activity of an oxygen-insensitive NADPH-dependent nitroreductase (RdxA), with resistance to this antimicrobial arising from null mutations in rdxA. To obtain a better understanding of the factors involved in resistance, nitroreductase and metronidazole reduction activities were investigated in matched pairs of clinical and laboratory-derived sensitive and resistant H. pylori strains. Significant differences in enzyme activities were observed between sensitive and resistant strains, suggesting that metronidazole susceptibility in H. pylori was associated with more than one enzyme activity. To establish the mutations occurring in rdxA, the genes from seventeen bacterial strains, including matched pairs were sequenced. To assess whether metronidazole was responsible for inducing random mutations in this gene, the complete nucleotide sequence of gene hp0630, encoding an NAD(P)H-quinone reductase which also has NADPH-dependent nitroreductase activity, was determined in the same strains. All resistant strains showed nonsense, missense, or frameshift mutations randomly throughout rdxA. In contrast, no mutations were observed in hp0630. The results confirmed the presence of rdxA null mutations in resistant strains and suggested that other factors involved in the metabolism of metronidazole contributed to the resistant phenotype.

摘要

幽门螺杆菌对甲硝唑的敏感性归因于一种对氧不敏感的NADPH依赖性硝基还原酶(RdxA)的活性,而对这种抗菌药物的耐药性则源于rdxA中的无效突变。为了更好地了解参与耐药性的因素,我们对临床和实验室来源的敏感及耐药幽门螺杆菌菌株的配对菌株进行了硝基还原酶和甲硝唑还原活性的研究。在敏感菌株和耐药菌株之间观察到酶活性存在显著差异,这表明幽门螺杆菌对甲硝唑的敏感性与多种酶活性有关。为了确定rdxA中发生的突变,我们对包括配对菌株在内的17株细菌的基因进行了测序。为了评估甲硝唑是否负责诱导该基因中的随机突变,我们在相同菌株中测定了编码NAD(P)H-醌还原酶(该酶也具有NADPH依赖性硝基还原酶活性)的基因hp0630的完整核苷酸序列。所有耐药菌株在整个rdxA中均显示出无义、错义或移码突变。相比之下,在hp0630中未观察到突变。结果证实了耐药菌株中存在rdxA无效突变,并表明参与甲硝唑代谢的其他因素导致了耐药表型。

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