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Showing 3 results for E. Coli

Bahareh Khodashenas, Hamid Reza Ghorbani, Ehsan Binaeian,
Volume 22, Issue 136 (10-2015)
Abstract

Background: Today, the synthesis of silver nanoparticles is very common due to their many applications in various fields. The synthesis of these nanoparticles is done by means of physical, chemical, or biological methods. However, due to its inexpensive and environmentally friendly features, the biological method is more preferable than the other two methods. Previous research has shown that nitrate reductase enzyme released by microorganisms, is a major factor in the synthesis of silver nanoparticles. In the present paper the effects of nitrate reductase enzyme amount and silver nitrate concentration on nanoparticles synthesis were studied.

Methods: Silver nanoparticles obtained from biosynthesis using E. coli supernatant were synthesized. Finally, to be more accurate, Uv-VIS spectrophotometer and dynamic light scattering DLS were applied.

Results: Using Uv-Vis spectrophotometer, wavelengths for silver nanoparticles in concentrations of 0.001M silver nitrate, one with 5 and the other with 20 cc of the bacterial supernatant containing the soluble nitrate reductase enzyme was calculated as 415, and 405 nm, respectively. Also, the climax was seen in 435 nm for 0.01M silver nitrate with 20 cc of the bacterial supernatant. The spectrophotometer determined the silver nanoparticles’ sizes for 0.001M containing 5 and 20 cc bacterial supernatant as 74.47, and 45.73 nm, respectively.

Conclusion: The results showed that by increasing the amount of bacterial supernatant  containing the soluble nitrate reductase enzyme, the size of produced silver nanoparticles will be smaller. Also, it was found that by increasing the concentration of silver nitrate the size of produced nanoparticles increases.


Amin Norouzi, Hossien Hossieni Nave, Samane Mohebi, Mohammadreza Kandekar Ghareman, Majid Taati Moghadam,
Volume 23, Issue 148 (10-2016)
Abstract

Background: Plasmid-mediated quinolone resistance, which complicates treatment, has been increasingly identified in Escherichia coli isolates worldwide. The purpose of this study was to investigate the frequency of plasmid-mediated qnrA, qnrB, and qnrS genes among quinolones resistant E.coli isolated from Kerman hospitals, Iran.
Methods: In the current study, 80 E. coli isolates were collected from urine, blood, and wound from Kerman hospitals. Then antibiotic susceptibility test was carried out by using disc diffusion method. Detection of qnrA, qnrB, and qnrS genes were carried out by polymerase chain reaction. Data were evaluated through SPSS v.22.
Results: Effective antibiotic against E. coli isolates was imipenem (93.7%) but 58 isolates (72.5%) were resistance to ampicillin which more than others antibiotics. 33 (41.2%) and 15 (18.7%) of 80 Escherichia coli isolates were nalidixic acid and ciprofloxacin-resistant, respectively. Detection of qnr genes demonstrated that 5 (6.2%) isolates were observed qnrS
and one (1.2%) were identified qnrA genes isolates. No qnrA gene was identified in our study.
Conclusion: Because of different antibiotic resistance patterns in various geographical regions, antimicrobial treatment should be based on local experience. Therefore, prescribing correct antibiotics can prevent the extension of antibiotic resistance through qnr borne bacteria in the future.


Sina Mashaiekhi, Babak Kheirkhah, Kumarss Amini,
Volume 25, Issue 1 (3-2018)
Abstract

Background: Escherichia coli (E.coli) bacteria are member of Enterobacteriaceae which are one of the common causes of urinary tract infections. Beta-lactamase enzymes are important factors for antibiotic resistance of beta-lactam family in gram-negative bacteria. According to increasing rate of urinary tract infections due to antibiotic resistant E. coli, the aim of this study was to study the antibiotic sensitivity pattern relative to beta-lactam antibiotics and the presence of SHV and TEM beta-lactamase genes in E. coli specimens isolated from patients with urinary tract infections.
Methods: In a descriptive study, 181 E.coli strains are collected from urine of patients with urinary tract infections and then the sensitivity of the antibiotic is measured by Disk diffusion method. Combined Disk test is used for confirming ESBL-producing E. coli phenotype and finally, the presence of SHV and TEM beta-lactamase genes in ESBL positive isolates were analyzed by multiplex PCR.
Results: From 181 isolates, 66 strains (36.46%) were resistant to cefotaxime and 82 strains (45.30%) were resistant to ceftazidime. Also, 58 percent of isolates were ESBL positive, 16 strains (33%) of them were the carrier of SHV gene and 28 strains (58%) were the carrier of TEM gene and also 3 isolates (6%) were the carrier of both TEM and SHV genes.
Conclusion: According to the production of ESBL which is considered as a great threat to society, it seems it is essential to use suitable molecular methods along with other phenotypic methods to identify this type of resistance.
 



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