Are molecular methods appropriate substitutions for traditional antimicrobial assays in detecting Helicobacter pylori antibiotic resistance in Iranian clinical trials?

سال انتشار: 1384
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 2,062

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شناسه ملی سند علمی:

NBCI04_417

تاریخ نمایه سازی: 30 دی 1386

چکیده مقاله:

Metronidazole and clarithromycin are usually used for Hp eradication therapy with good rates of. Resistance to one or both of these antibiotics reduces the effectiveness of the designed therapy. The rate of resistance to these antibiotics among Iranian Hp strains was determined according to modified disc diffusion test and PCR-RFLP methods. According to modified disc diffusion test, 16.7% of the studied strains were resistant to clarithromycin and 57.5% to metronidazole. Of the Clarithromycin resistant strains, 73.68% had the A2143G mutation in the 23srRNA gene, 21.05% A2142C and 5.26% A2142G. None of the sensitive strains were positive for any of the three point mutations. Of the metronidazole resistant strains, deletion in rdxA gene was studied and detected in only 6 (5%) of the antibiogram-based resistant strains. None of the metronidazole sensitive strains possessed rdxA gene deletion. These data show that despite the fact that molecular methods believe to be consistent and time-consuming methods, they are not reliable for the detection of metronidazloe resistance in a highly infected population as the results of microbial and molecular tests for resistance to this antibiotic are in accordance. The scenario is opposite for clarithromycin, if a diagnostic laboratory is mobilized to the molecular assay equipments these methods are preferred.

نویسندگان

Delaram Doroud

Biotechnology Research Center, Pasteur Institute of Iran

Nazanin Mohajerani

Biotechnology Research Center, Pasteur Institute of Iran

Sadegh Massarrat

Gastroenterology Department, Shariati Hospital

Marjan Mohammadi

Biotechnology Research Center, Pasteur Institute of Iran

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  • _ کرهان مردادماه 1384 _ _ قی ...
  • Perri F et al. 2003. Hel icobacter. 8:53-60. ...
  • Taylor D E et al. 1997. Antimicrob. Agents Chemother. 41:2621-2628 ...
  • Versalovic J et al. 1996. Antimicrob Agents Chemother. 40: 477-80. ...
  • Hao Q et al. 2004. World J Gas troenterol. 1:1075-7. ...
  • Chisholm SA et al. 2001. J Clin Microbiol. 39: 1217-20. ...
  • Occhialini A et al. 1997. Antimicrob. Agents Chemother. 41:2724-2728 ...
  • Menard A et al. 2002. Antimicrob Agents Chemother. 46:1156-7. ...
  • Alarcon T et al. 2000. J Clin Microbiol. 38: 923-5. ...
  • Marais A et al. 2003. Res Microbiol. 154: 137-44. ...
  • Chisholm SA et al. 2004. J Med Microbiol. 53:135-40. ...
  • Grignon B et al. 2002. Microb Drug Resist. 8:61-6. ...
  • Midolo PD et al. 1995. Diagn Micr Infec Dis. 21:135-40. ...
  • Eltahawy AT et al. 2002. Med Princ Pract. 11: 65-8. ...
  • McNulty C et al. 2002. J Antimicrob Chemother. 49: 601-9. ...
  • Debets- Ossenkopp YJ et al. 1999. J Antimicrob Chemother. 43: ...
  • Chaves S et al. 1999. J Clin Microbiol. 37: 1628-31. ...
  • Debets- Ossenkopp YJ et al. 1999. Antimicrob. Agents Chemother. 43 ...
  • Van der Wouden EJ et al. 1999. Antimicrob Agents Chemother. ...
  • Parsons HK et al. 2001. Aliment Pharmacol Ther. 15: 1473-8. ...
  • Dai N et al. 2003. Zhejiang Da Xue Xue Bao ...
  • Bereswil] S et al. 2003. FEMS Immunol Med Microbiol. 36: ...
  • Yang YJ et al. 2004. Helicobacter. 9: 400-7. ...
  • Massarrat S et al. 1995. Eur J Gastroenterol Hepatol. 7:427-33. ...
  • Perri F et al. 2001. Aliment Pharmacol Ther. 15:1023-9. Furuta ...
  • نمایش کامل مراجع