Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes

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spelling 15029 https://intelek.unisza.edu.my/intelek/pages/view.php?ref=15029 https://intelek.unisza.edu.my/intelek/pages/search.php?search=!collection407072 Restricted Document Conference Conference Paper application/pdf 4 1.6 Adobe Acrobat Pro DC 20 Paper Capture Plug-in fadlina ismail 2024-08-28 13:59:57 4581-01-FH03-FBIM-21-52813.pdf UniSZA Private Access Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes Pseudomonas aeruginosa is an opportunistic and versatile pathogenic bacterium that can adapt in various environmental condition, which play a role in multiple virulence factor and resistance to antibiotics. Moreover, molecular identification techniques using single target gene is more susceptible to error and false positive. Thus, the detection of this strain with high specificity and sensitivity is crucial in order to control this pathogenic bacterium. The aim of this study was to evaluate six bacteria strains isolated from Dorper sheep milk’s samples (13-1, 66-1, 00-1, 46-1, 10-R and 67-1) and two P. aeruginosa ATCC strains (ATCC BAA-2108 and ATCC27853) for prompt identification of the strains based on uniplex polymerase chain reaction which targeting PA-SS, PA-GS, lasI/R, gyrB and ecfX genes. In the present study, the Dorper sheep milk’s samples (n = 32) were collected and tested with California mastitis test (CMT). Out of 32 samples, six of the samples were detected with strong mastitis, and thus were continued with inoculation process on selective media Pseudomonas Agar P (for pyocyanin) or F (fluorescein) and MacConkey agar for differentiation. After extraction of the bacteria chromosomal DNA, uniplex PCR amplification were carried out by using 16S rRNA (PA-SS and PA-GS) primers and specific P. aeruginosa genes (lasI/R, gyrB and ecfX) primers. The specificity of the primers was also examined by non-Pseudomonas species as a control for data comparison. Sequence analysis has revealed that six of the isolated strains were confirmed as P. aeruginosa strains with the respective genes sequence confirmed by BLAST and Clustal Omega. From this study, lasI/R, gyrB and ecfX were highly reliable primers with the percentage of identification of more than 95-100% as compared to PA-SS and PAGS which were less than 90%. This study concludes that highly specific and sensitive assay has been developed using lasI/R, gyrB and ecfX targeted genes for the detection of P. aeruginosa strains isolated from fresh sheep milk samples. ICAFT 2021 Universiti Sultan Zainal Abidin
spellingShingle Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes
summary Pseudomonas aeruginosa is an opportunistic and versatile pathogenic bacterium that can adapt in various environmental condition, which play a role in multiple virulence factor and resistance to antibiotics. Moreover, molecular identification techniques using single target gene is more susceptible to error and false positive. Thus, the detection of this strain with high specificity and sensitivity is crucial in order to control this pathogenic bacterium. The aim of this study was to evaluate six bacteria strains isolated from Dorper sheep milk’s samples (13-1, 66-1, 00-1, 46-1, 10-R and 67-1) and two P. aeruginosa ATCC strains (ATCC BAA-2108 and ATCC27853) for prompt identification of the strains based on uniplex polymerase chain reaction which targeting PA-SS, PA-GS, lasI/R, gyrB and ecfX genes. In the present study, the Dorper sheep milk’s samples (n = 32) were collected and tested with California mastitis test (CMT). Out of 32 samples, six of the samples were detected with strong mastitis, and thus were continued with inoculation process on selective media Pseudomonas Agar P (for pyocyanin) or F (fluorescein) and MacConkey agar for differentiation. After extraction of the bacteria chromosomal DNA, uniplex PCR amplification were carried out by using 16S rRNA (PA-SS and PA-GS) primers and specific P. aeruginosa genes (lasI/R, gyrB and ecfX) primers. The specificity of the primers was also examined by non-Pseudomonas species as a control for data comparison. Sequence analysis has revealed that six of the isolated strains were confirmed as P. aeruginosa strains with the respective genes sequence confirmed by BLAST and Clustal Omega. From this study, lasI/R, gyrB and ecfX were highly reliable primers with the percentage of identification of more than 95-100% as compared to PA-SS and PAGS which were less than 90%. This study concludes that highly specific and sensitive assay has been developed using lasI/R, gyrB and ecfX targeted genes for the detection of P. aeruginosa strains isolated from fresh sheep milk samples.
title Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes
title_full Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes
title_fullStr Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes
title_full_unstemmed Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes
title_short Identification of Pseudomonas aeruginosa strains isolated from Dorper sheep milk with subclinical-mastitis infection by a uniplex PCR using 16S rRNA, lasI/R, gyrB and ecfX genes
title_sort identification of pseudomonas aeruginosa strains isolated from dorper sheep milk with subclinical-mastitis infection by a uniplex pcr using 16s rrna, lasi/r, gyrb and ecfx genes