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Showing 2 results for Multidrug Resistance
Dissemination of Class 1 Integron among Different Multidrug Resistant Pseudomonas aeruginosa Strains
Zahra Salimizadeh, Seyed Masoud Hashemi Karouei , Farzaneh Hosseini,
Volume 12, Issue 4 (7-2018)
Abstract
ABSTRACT
            Background and objectives: The present study was conducted to detect class 1 integrons and evaluate antibiotic susceptibility patterns among clinical isolates of P. aeruginosa.
            Methods: Sixty clinical samples from blood, tracheal wounds, burns and urinary tract infections were collected from three general hospitals in Tehran, Iran. Culture of specimens was performed on common bacteriological culture media. Bacteria were  identified based on mobility, pigment production, growth at 42 oC, and oxidase and catalase tests. Overall, 21 P.  aeruginosa strains were isolated. Antimicrobial susceptibility of was evaluated via the disk diffusion method (Kirby-Bauer) according to the CLSI guidelines. Presence of the intI1, sul1, aadA2 and aadB gene cassettes was investigated using PCR. The collected data were analyzed using SPSS software (version 21).
            Results: The most effective antimicrobial agents against P. aeruginosa isolates were tetracycline and gentamicin. All P. aeruginosa isolates were multidrug re­sistant. Moreover, the intI1, sul1, aadA2 and aadB genes were found in 90.5%, 90.5%, 47.6% and 19% of the P. aeruginosa isolates, respectively.
            Conclusion: The results indicate that the presence of aadB, aadA2 and sul1 gene cassetes may play an important role in the dissemination of antimicrobial resistance determinants.
          Keywords: Pseu­domonas aeruginosa, integron, multidrug resistance.
ABSTRACT
            Background and objectives: The present study was conducted to detect class 1 integrons and evaluate antibiotic susceptibility patterns among clinical isolates of P. aeruginosa.
            Methods: Sixty clinical samples from blood, tracheal wounds, burns and urinary tract infections were collected from three general hospitals in Tehran, Iran. Culture of specimens was performed on common bacteriological culture media. Bacteria were  identified based on mobility, pigment production, growth at 42 oC, and oxidase and catalase tests. Overall, 21 P.  aeruginosa strains were isolated. Antimicrobial susceptibility of was evaluated via the disk diffusion method (Kirby-Bauer) according to the CLSI guidelines. Presence of the intI1, sul1, aadA2 and aadB gene cassettes was investigated using PCR. The collected data were analyzed using SPSS software (version 21).
            Results: The most effective antimicrobial agents against P. aeruginosa isolates were tetracycline and gentamicin. All P. aeruginosa isolates were multidrug re­sistant. Moreover, the intI1, sul1, aadA2 and aadB genes were found in 90.5%, 90.5%, 47.6% and 19% of the P. aeruginosa isolates, respectively.
            Conclusion: The results indicate that the presence of aadB, aadA2 and sul1 gene cassetes may play an important role in the dissemination of antimicrobial resistance determinants.
          Keywords: Pseu­domonas aeruginosa, integron, multidrug resistance.
ABSTRACT
            Background and objectives: The present study was conducted to detect class 1 integrons and evaluate antibiotic susceptibility patterns among clinical isolates of P. aeruginosa.
            Methods: Sixty clinical samples from blood, tracheal wounds, burns and urinary tract infections were collected from three general hospitals in Tehran, Iran. Culture of specimens was performed on common bacteriological culture media. Bacteria were  identified based on mobility, pigment production, growth at 42 oC, and oxidase and catalase tests. Overall, 21 P.  aeruginosa strains were isolated. Antimicrobial susceptibility of was evaluated via the disk diffusion method (Kirby-Bauer) according to the CLSI guidelines. Presence of the intI1, sul1, aadA2 and aadB gene cassettes was investigated using PCR. The collected data were analyzed using SPSS software (version 21).
            Results: The most effective antimicrobial agents against P. aeruginosa isolates were tetracycline and gentamicin. All P. aeruginosa isolates were multidrug re­sistant. Moreover, the intI1, sul1, aadA2 and aadB genes were found in 90.5%, 90.5%, 47.6% and 19% of the P. aeruginosa isolates, respectively.
            Conclusion: The results indicate that the presence of aadB, aadA2 and sul1 gene cassetes may play an important role in the dissemination of antimicrobial resistance determinants.
          Keywords: Pseu­domonas aeruginosa, integron, multidrug resistance.

The Spread of Antibiotic Resistance in Iran: A Review of Multidrug-Resistant Pathogens, Resistance Mechanisms, and National Challenges
Behin Omidi, Sana Zarrin, Yasaman Ghazzagh, Yasin Sarveahrabi,
Volume 20, Issue 4 (9-2026)
Abstract
Background: Antimicrobial resistance (AMR) represents one of the most significant global health threats of the 21st century, undermining advances in modern medicine. Iran, as a geographically and demographically strategic nation, faces a severe and escalating AMR crisis. This review synthesizes current evidence on the epidemiology, molecular mechanisms, and systemic drivers of AMR in Iran, while outlining priorities for effective national response.
Methods: A structured review was conducted of studies published between January 2015 and November 2025 in PubMed, Scopus, and Web of Science, supplemented by national and Persian-language databases. Eligible studies investigated the prevalence, molecular characteristics, and clinical outcomes of antibiotic-resistant bacteria in Iran. Data were extracted and narratively synthesized.
Results: Iran faces an alarming burden of MDR and drug resistant (XDR) Gram negative pathogens, notably Acinetobacter baumannii, Pseudomonas aeruginosa and carbapenem resistant Enterobacteriaceae, with carbapenem resistance rates exceeding 80-90%. Widespread dissemination of key carbapenemase genes (blaNDM, blaOXA-48, blaVIM) has been documented. Gram positive pathogens, including methicillin resistant Staphylococcus aureus and vancomycin resistant Enterococci, also remain highly prevalent. The crisis is driven by unregulated over the antibiotic use, weak infection prevention and control measures, fragmented surveillance, and limited diagnostic capacity.
Conclusion: AMR in Iran has reached critical levels, constituting a national public health emergency. Urgent, coordinated reforms across integrated surveillance, mandatory antimicrobial stewardship, strengthened infection prevention and control, One Health integration, expanded research, and public engagement are required. Without decisive national action, Iran risks a post antibiotic era in which routine infections and medical procedures become life threatening.
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