Kwon D H, Kato M, El-Zaatari F A, Osato M S, Graham D Y
Department of Medicine and Division of Molecular Virology of Baylor College of Medicine and Veterans Affairs Medical Center, Rm 3A-320 (111D), 2002 Holcombe Blvd., 77030, Houston, TX 77030, USA.
FEMS Microbiol Lett. 2000 Jul 15;188(2):197-202. doi: 10.1111/j.1574-6968.2000.tb09193.x.
Metronidazole is a critical ingredient for combination therapies of Helicobacter pylori infection, the major cause of peptic ulcer and gastric cancer. It has been recently reported that metronidazole resistance from H. pylori ATCC43504 is caused by the insertion of a mini-IS605 sequence and deletion of sequences in an oxygen insensitive NAD(P)H nitroreductase encoding gene (rdxA). We also found that an additional gene (frxA) encoding NAD(P)H flavin oxidoreductase in the same strain was truncated by frame-shift mutations. To assess whether the frxA truncation is also involved in metronidazole resistance, metronidazole sensitive H. pylori strains ATCC43629 and SS1 were transformed by the truncated frxA gene cloned from strain ATCC43504. All transformed cells grew on agar plates containing 16 microg ml(-1) of metronidazole. The involvement of the frxA gene in metronidazole resistance was also confirmed by insertion inactivation of frxA and/or rdxA genes from strain ATCC43629 and one metronidazole sensitive clinical isolate H. pylori 2600. In addition, the frxA gene cloned from the H. pylori 2600 showed metronidazole nitroreductase activity in Escherichia coli and rendered ordinary metronidazole resistant E. coli to metronidazole sensitive cell. These results indicate that the frxA gene may also be involved in metronidazole resistance among clinical H. pylori isolates.
甲硝唑是幽门螺杆菌感染联合治疗的关键成分,幽门螺杆菌感染是消化性溃疡和胃癌的主要病因。最近有报道称,幽门螺杆菌ATCC43504对甲硝唑产生耐药性是由于插入了一个mini-IS605序列以及编码氧不敏感型NAD(P)H硝基还原酶的基因(rdxA)中的序列缺失所致。我们还发现,同一菌株中另一个编码NAD(P)H黄素氧化还原酶的基因(frxA)因移码突变而被截断。为了评估frxA基因截断是否也与甲硝唑耐药性有关,我们用从ATCC43504菌株克隆的截断型frxA基因转化了对甲硝唑敏感的幽门螺杆菌菌株ATCC43629和SS1。所有转化细胞都能在含有16微克/毫升甲硝唑的琼脂平板上生长。通过对ATCC43629菌株和一株对甲硝唑敏感的临床分离株幽门螺杆菌2600的frxA和/或rdxA基因进行插入失活,也证实了frxA基因与甲硝唑耐药性有关。此外,从幽门螺杆菌2,600克隆的frxA基因在大肠杆菌中显示出甲硝唑硝基还原酶活性,并使普通的甲硝唑耐药大肠杆菌对甲硝唑敏感。这些结果表明,frxA基因可能也与临床幽门螺杆菌分离株的甲硝唑耐药性有关。