2018
DOI: 10.12688/f1000research.15316.1
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Molecular characterization of Pseudomonas aeruginosa isolates from Sudanese patients: A cross-sectional study

Abstract: Abstract16S rRNA gene sequence analysis is a robust tool for Background: characterization of new pathogens in clinical specimens with suspected bacterial disease. The aim of this study was to characterize Pseudomonas isolated from clinical specimens by sequencing the 16S rRNA aeruginosa gene.Forty bacterial isolates were obtained from different clinical Methods: specimens (wound, urine and sputum) using enrichment selective media and biochemical tests to characterize and identify the bacteria as P. aeruginosa.… Show more

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Cited by 5 publications
(7 citation statements)
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“…It can be used for reproducible and reliable bacterial identification, and also to define the species and for useful distinction between the bacterial strains. The same results obtained by [58][59]. transcribed spacer (ITS) region of the rRNA gene was selected as a target sequence because it is the most reliable gene for iden differentiation between Candida species Silver nanoparticles have been employed in the medical industry, especially for wound dressings, heart valves, medical face masks, bandages, and water filtration systems [61 biosynthesis of new nanostructured materials with high adsorption has been attracting significant interest lately [64][65][66].…”
Section: Discussionmentioning
confidence: 99%
“…It can be used for reproducible and reliable bacterial identification, and also to define the species and for useful distinction between the bacterial strains. The same results obtained by [58][59]. transcribed spacer (ITS) region of the rRNA gene was selected as a target sequence because it is the most reliable gene for iden differentiation between Candida species Silver nanoparticles have been employed in the medical industry, especially for wound dressings, heart valves, medical face masks, bandages, and water filtration systems [61 biosynthesis of new nanostructured materials with high adsorption has been attracting significant interest lately [64][65][66].…”
Section: Discussionmentioning
confidence: 99%
“…All bacterial genomic DNA were used as templates for PCR amplification of the 16S rDNA gene for the confirmation of P. aeruginosa. The two primers used were 27F (5′ AGAGTTTGATCCTGGCTCAG-3ʹ) and 1495R (5′ CTACGGCTACCTTGTTACGA- 3ʹ) for forward primer and reverse primer, respectively [ 44 ]. According to the phenotypic resistance profile, each isolate was screened using PCR for the presence of the following antimicrobial resistance genes: bla TEM , bla SHV , bla CTX , bla PER , bla SME , bla KPC , bla Smp , bla Vim , bla Vim-2 , bla NDM , bla OXA , aac (6′)-Ie- aph (2″)-Ia, aph (3′)-IIIa, acc3I, aac3II, aacIII, aac3IV, ant (4′)-Ia, and ant (2′)-Ia.…”
Section: Methodsmentioning
confidence: 99%
“…The two primers used were 27F (5′ AGAGTTTGATCCTGGCTCAG-3′) and 1495R (5′ CTACGGCTACCTTGTTACGA-3′). These functions as forward primer and reverse primer, respectively [ 30 ]. Based on their phenotypic resistance profile, each isolate underwent PCR screening for the presence of the following antimicrobial resistance genes: bla TEM , bla SHV , bla CTX , bla PER , bla SME , bla KPC , bla IMP bla Smp , bla Vim , bla Vim-2 , bla NDM , bla OXA , aac (6′)-Ie- aph (2″)-Ia, aph (3′)-IIIa, aac(3)-I, aac(3)-II, aac(3)-III, aac(3)-IV, ant (4′)-Ia and ant (2′)-Ia.…”
Section: Methodsmentioning
confidence: 99%