Volume 2, Issue 1 (2016)
IEM 2016, 2(1): 18-21 |
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Boustanshenas M, Akbari M, Rezaie N. Evaluation of two different laboratory methods for the identification of Aeromonas spp. in stool sample of patients with diarrhea. IEM 2016; 2 (1) :18-21
URL: http://iem.modares.ac.ir/article-4-10573-en.html
URL: http://iem.modares.ac.ir/article-4-10573-en.html
1- Antimicrobial Resistance Research Center, Rasul-e-Akram Hospital, Iran University of Medical Sciences, Tehran, Iran
2- Department of Microbiology, School of Nursing and midwifery, Arak University of Medical Sciences, Arak, Iran
3- Department of Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
2- Department of Microbiology, School of Nursing and midwifery, Arak University of Medical Sciences, Arak, Iran
3- Department of Bacteriology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
Abstract: (6841 Views)
Background: Aeromonas spp. can cause diarrhea and various infections in humans. Access to rapid techniques with a high sensitivity and specificity is strongly needed for the identification of Aeromonas species. The aim of this study was to evaluate two different methods including API 20E bacterial identification tests and the molecular detection using PCR primers specific for 16s-rRNA and 23S-rRNA genes sequences for identification of Aeromonas spp. in stool samples from patients with diarrhea. Materials and Methods: One hundred stool samples from diarrheal patients were collected. All isolates were subjected toAPI 20 E strip tests and PCR using specific primers for identification of Aeromonas spp. Results: The API 20E analysis identified 2 (2.2%) isolates as Aeromonas spp. Molecular identification by aero-23S-rRNA gene confirmed the same 2 isolates as identified by the API 20E strips. Conclusion: Both API 20E system and PCR method using Aero 23S-rRNA primer were found to be accurate in identification of Aeromonas spp. isolates with highconfidence.
Received: 2016/01/16 | Accepted: 2016/01/1 | Published: 2016/01/16
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