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Showing 2 results for Pseudomonas Aeruginosa

Elham Ranjbar , Kumarss Amini,
Volume 11, Issue 6 (3-2018)
Abstract

Background and Aim: Pseudomonas aeruginosa is one of the most important factors in hospital infections, especially in patients with immune deficiency and Childhood diseases. The Virulence of bacteria are due to the presence of the Pyoverdine gene, which has many effects on the wild type of bacteria during the pathogenic pathway. Identification of different classes of PVD gene is necessary for the development of prevention and control Diseases program. In this research, the presence of PVD genes in the samples and their effect on pathogenicity was isolated and investigated.
Materials and Methods: In the present study 60 Species of P. aeruginosa was isolated from clinical samples of human and animal, after approval by diagnostic tests and differential, were studied. Finally, for every 60 Species, isolated, Multiplex PCR was performed to detect target genes. Multiplex PCR method is to be considered as the gold standard. Its results are more reliable.
Results: The results showed that the frequency of PVD gene in human isolates and livestock gene encoding the 3rd Pyoverdine was the highest frequency with 76.6% the lowest frequency is for Pyoverdine class 2 with 46%.
Conclusion: As a result, the identification of three type’s genes of PVD classes in all strains tested by Pseudomonas could help to identify human patients and livestock with Pseudomonas infection and, given the presence of the gene encoding PVDs, has a direct relation to important bacterial pathogenicity. 

Mona Konkuri, Yousef Erfani, Sharmin Kharrazi, Setareh Haghighat,
Volume 18, Issue 6 (2-2025)
Abstract

Background and Aim: Pseudomonas aeruginosa is a Gram-negative opportunistic pathogen that is often found in patients with cystic fibrosis, burn wounds, immunodeficiency, and chronic obstructive pulmonary disorder. In addition, P. aeruginosa is also considered one of the most important pathogens causing hospital infections, widely found in medical devices (ventilation), because they tend to grow on moist surfaces. Considering the importance of cystic fibrosis treatment and the ability of P. aeruginosa to form biofilms, this study examines the effect of nano zinc oxide particle on the expression of genes associated in biofilm formation in isolated P. aeruginosa from cystic fibrosis patients.
Materials and Methods: Sputum and throat samples from 150 patients with cystic fibrosis were cultured on MacConkey agar culture medium. After an overnight incubation, the grown colonies were determined and confirmed by biochemical tests. An antibiotic sensitivity test by disk diffusion method (Kirby –bauer) were used to determine the antibiotic susceptibility pattern. Zinc nanoparticles were synthesized following established protocols and evaluated using scanning electron microscopy (SEM). The multi-antibiotic-resistant strains were inoculated with 16 µg/ml of 2 nm ZnO nanoparticles and inhibition zone were meseared. The impact of these nanoparticles on the expression levels of gas, retS, lasR, and rhlR genes was assessed using Real-Time PCR. The relative gene expression level was determined using the gene expression method: (ΔΔCt-2).
Results: Of the total 150 samples, 73 (48.66%) isolates were identified as P. aeruginosa. All P. aeruginosa isolates were resistant to selected antibiotics. SEM evaluation indicated that the synthesized nanoparticles had an average size of approximately 4 ± 0.44 nm. The results from the Real-Time PCR tests showed a decrease in the expression of the gacA, retS, lasR, and rhlR genes in the presence of the zinc nanoparticles in P. aeruginosa strains. The most significant reduction in gene expression was observed for the rhlR gene, whereas the least reduction was noted for the retS gene.
Conclusion: The use of nano zinc oxide can eliminate Pseudomonas aeruginosa infection by preventing biofilm formation and providing better treatment results for cystic fibrosis patients with lung infection.


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