Showing 6 results for Esbl
Mana Shojapour, Laleh Shariati, Ali Karimi, Behnam Zamanzad,
Volume 14, Issue 1 (3-2011)
Abstract
Background: Existence of extended spectrum B-lactamase (ESBL) genes plays an important role in spreading B-lactam antibiotic resistance in the producing strains of these enzymes. The resistance of gram-negative bacteria, such as Pseudomonas aeruginosa, to different antimicrobial agents, especially B-lactam and carbapenem, has increasingly been reported. This study was conducted to determine the prevalence of TEM-1 beta-lactamases in Pseudomonas aeruginosa isolates through Duplex PCR. Materials and Methods: In this descriptive-analytic study, 175 Pseudomonas aeruginosa isolates collected from burn patients were subjected to bacteriological tests. The samples were cultured and identified according to standard methods. Then the frequency of ESBL producing strains was determined via the combined disk method. Using boiling method, DNA was extracted and examined for the existence of TEM-1 gene by Duplex PCR. Results: Out of the 175 Pseudomonas aeruginosa isolates, 66 (37.7%) were ESBL positive, 15.15% of which were positive for TEM-1 B-lactamases resistance gene. Conclusion: Noticing the increasing rate of the ESBLs producing strains, using the appropriate treatment protocol based on the antibiogram pattern of the strains is highly recommended.
Ali Hashemi, Saeed Shams, Mohammad Barati, Azizeh Samedani,
Volume 14, Issue 4 (9-2011)
Abstract
Background: Pseudomonas aeruginosa is one of the most important causes of nosocomial infection which due to extended spectrum-beta lactamases (ESBLs) and metallo-beta lactamase (MBL) producing strains is resistant to a wide range of antibiotics. The aim of this study was to detect ESBL and MBL producing P.aeruginosa isolated from patients and investigate the effects of methanol extracts of Zataria multiflora, Myrtus communis, and Peganum harmala on them.
Materials and Methods: In this experimental study, samples were obtained from 245 patients, referring to Shafa Hospital, Kerman, Iran. ESBLs producing strains were detected by double disk synergy test and phenotypic confirmatory test. In addition, E-test strips were used for MBL detection. P.aeruginosa MIC was determined for cefotaxime, ceftazidime, azteronam, imipenem, and meropenem. Methanol extracts of Zataria multiflora, Peganum harmala, and Myrtus communis plants were prepared by Agar perculation method.
Results: Out of 245 patients referring to the burn unit, 120 P.aeruginosa isolates were detected from which 41 contained ESBL but they lacked MBL. 60% of isolates were resistant to cefotaxime, 66% to ceftazidime, 42% to azteronam, 3% to imipenem, and 5% to meropenem. Among the extracts, Zataria multiflora had the highest antibacterial effect on standard strains of P.aeruginosa in comparison with Peganum harmala and Myrtus communis.
Conclusion: The prevalence of ESBL producing P.aeruginosa strains is high. In addition, noticing their high antibiotic resistance, utilization of herbs, such as Zataria multiflora may be considered an appropriate alternative for treatment however, more investigations are needed.
Majid Eslami, Shahin Najar Peerayeh,
Volume 15, Issue 1 (4-2012)
Abstract
Background: TEM, PER, and VEB are extended-spectrum betalactamase (ESBL) enzymes that are capable of hydrolyzing penicillins, cephalosporins, and aztreonam. The aim of this study was to determine the prevalence of ESBL producing E.coli and molecular evaluation of TEM, PER, and VEB β-lactamases among E.coli strains.
Materials and Methods: A total of 200 clinical strains of E.coli were isolated from clinical specimens and their antibiotic susceptibility was determined by disk diffusion method. ESBL production was determined using the combined disk method with CAZ and CTX with clavulanic acid and alone. Minimum concentration inhibition (MIC) for CAZ and CTX with clavulanic acid and alone was determined by agar dilution method. Finally, PCR with specific primers was used for determining the presence of blaTEM, blaPER, and blaVEB genes.
Results: Combined disk method confirmed 94 strains (47%) to be ESBL producing E.coli. Of the 94 ESBL producing strains, 36 samples had MIC=16, 44 samples had MIC between 32-256, and 10 samples had MIC≥512 for ceftazidime, whereas 8 samples had MIC=16, 68 samples had MIC between 32-256, and 21 samples had MIC≥512 for cefotaxime. The frequency of TEM was 44% however, blaPER and blaVEB genes were not detected by PCR among ESBL producing isolates.
Conclusion:The results indicated that the high percentage of ESBL producing E.coli is 47% and PCR method showed a high frequency of TEM enzyme, but PER and VEB betalactamase were not found among them.
Mohammad Hosein Feiz Sarshar, Alisha Akya,
Volume 19, Issue 2 (5-2016)
Abstract
Background: The dissemination of extended-spectrum β-lactamases (ESBL) in Klebsiella pneumoniae isolates has resulted in the increase of antibiotic resistance and mortality among patients. The aim of this study was to determine the prevalence of ESBL and SHV-2a, SHV-5 and SHV-12 genes in K. pneumoniae isolates from Kermanshah.
Materials and Methods: In this descriptive – analytical study, from 112 clinical samples of patients admitted at Kermanshah medical centers in 2014, 60 K. pneumoniae isolates were recognized by standard methods of bacteriology and API Kit. Antibiotic susceptibility of isolates was determined by disk diffusion method and the isolates were screened for ESBL-producerig using the combination disc method. The SHV-2a, SHV-5 and SHV-12 genes were determined among isolates using PCR method. Primers were designed in this study.
Results: Of 60 isolates tested, the highest and the lowest resistance was for ampicillin and carbapenem antibiotics, respectively. Forty-five percent of isolates were ESBL-producer. Among 60 isolates tested, 5 (8.3%), 57 (95%) and 43 (71.7%) isolates contained SHV-2a, SHV-5 and SHV-12 genes, respectively. Five isolates contained all the three genes of SHV-2a, SHV-5 and SHV-12.
Conclusion: The results indicate the relatively high prevalence of SHV type beta-lactamase genes in K. pneumoniae isolates in Kermanshah. Given this high prevalence, the surveillance of antibiotic resistant patterns and relevant genes is necessary among gram-negative bacilli in Kermanshah region. Due to the high resistance of K. pneumoniae isolates to antibiotics and to reduce the dissemination of resistant genes, susceptibility testing to choose more affective antibiotics is recommended even for isolates from outpatients.
Sare Karimi, Azam Haddadi, Parvin Torabzadeh,
Volume 21, Issue 2 (5-2018)
Abstract
Abstract
Background: In recent years, increasingly antibiotic resistance problem among Klebsiella isolates and side effects of antibiotics overuse have made researchers to study the antimicrobial activity of medicinal plants. The aim of this study was to study the inhibitory effect of ethanolic and aqueous extract of Vaccinium arctostaphylos on ESBLs producing Klebsiella strains.
Materials and Methods: Among 143 isolates of Klebsiella collected from some hospitals and clinical laboratories in Karaj, ESBLs producer were screened by phenotypic confirmatory test (PCT). One of them was identified based on 16S rRNA gene sequencing. MIC and MBC of ethanol and aqueous extracts of Vaccinium arctostaphylos were determined using microdilution method on selected ESBLs producing Klebsiella strains.
Results: Resistance to ceftazidime, ceftriaxon and cefotaxime was observed in 14.7% of the isolates. 32 isolates (22%) were detected as ESBL producers. Results of MIC and MBC tests showed that ethanolic and aqueous extract of Vaccinium arctostaphylos have inhibitory effect on ESBLs producing Klebsiella strains,
Conclusion: The presence of antibacterial activity could be confirmed in most plant species used in traditional medicine in Iran and we should focus on combining traditional medicines and modern drugs.
Maryam Sadrnia, Ghasem Habibi, Mohammad Arjomandzadegan,
Volume 21, Issue 3 (6-2018)
Abstract
Background and Aim: In this study, the effect of Myrtus extracts on 25 methicillin resistant Staphylococcus aureus (MRSA) and Escherichia coli ESBL strains isolated from patients were compared by two methods.
Materials and Methods: 15 methicillin-resistant Staphylococcus aureus (MRSA) and 10 Escherichia coli ESBL isolates were used in this study. Fresh Leaves of Myrtus were collected from the herbal medicine farm. Extraction was performed using a reflux distillation. The effect of concentrations 0.195-100 micrograms per ml of Myrtus extract on clinical isolates was analyzed in disk diffusion method compared with micro broth dilution method and with MTT in 545 nm on an ELISA reader apparatus.
Findings: Inhibition zone diameter for the minimum effective concentration of 50 micrograms per milliliter in all isolates of ESBL and MRSA were as 8±1 mm and 11±1. Minimum Inhibitory Concentration (MIC) was 6.25mic/ml and Minimum Bactericidal Concentration (MBC) was determined 12.5mic/ml for E. coli ESBL. Furthermore, the amounts for MIC and MBC was determined as 12.5 and 25 mic/ml, respectively for Staphylococcus aureus.
Conclusion: The results of this study showed compliance of two methods in evaluation of drug-resistant clinical isolates. It was proved that the disk diffusion method could be determining range of effective concentration but micro broth method determines the effective concentration carefully. It is recommended that results obtained from disk diffusion not to be basis for final decisions in traditional medicine studies. Bacterial behavior in the broth and determination of the point of death greatly increases the accuracy of the results.
