Detection and association of <i>toxA</i> gene with antibiotic resistance in <i>Pseudomonas aeruginosa</i> strains isolated from different sources in Al Muthanna city

AbstractIntroductionExotoxin A (ETA) is a powerful chromosomal extracellular virulence factor produced by most of clinical P. aeruginosa isolates. P. aeruginosa is the most common respiratory pathogen in patients with cystic fibrosis (CF).PurposeIn this study, the <i>Pseudomonas aeruginosa</i> strains were isolated from patient's different sources and screened against the <i>toxA</i> gene in order to identify the association between the increase of antibiotics resistance and the toxin production.Methods and resultsOne hundred samples were collected from different cases included: 25 swabs otitis infection, 25 samples from urinary tract infections and 25 swabs from each wound and burn infections for isolation of <i>P. aeruginosa</i> and detection of <i>toxA</i> gene in during the period between July 2019 to January 2020. These samples were cultured firstly onto the Brain heart infusion for 24 h 37oC, followed by the re-streak single colony on the selective on chrome agar media and incubated for 18–24 h at 37oC. The <i>P. aeruginosa</i> isolates were confirmed isolation using VITEK-2 Compact system.The isolation percentage of <i>P. aeruginosa</i> was 80% in the total sample were collected. The highest percentage isolation of <i>P. aeruginosa</i> was from otitis infection at (92%), followed by in wound and burn was (80%), and urinary tract infection was (72%). The gDNA of these isolated was extracted and then subject to PCR technique, detection of the <i>toxA</i> gene as a chromosomal target for the <i>P. aeruginosa</i> infection. The <i>toxA</i> gene detection percentage was (35%) in all the <i>P. aeruginosa</i> isolates; the highest <i>toxA</i> amplification was among strains isolated from otitis at the percentage of 59%, followed by 27% among the strains isolated from urine and 25% of the strains isolated from each wound and burn infections. These isolates were tested against the antibiotic resistance showed the highest percentage of the resistance level, especially those strain associated with detection of <i>toxA</i> gene-positive PCR product. However, the meropenem showed the highest effect against all of <i>P. aeruginosa</i> except for six showed higher resistance than other strains. The PCR product of the strains among the <i>toxA</i> detection was digested with FoKI, yielding two-band at 152 bp and 118 bp, unless those strains resisted the meropenem were showed uncut PCR product by the FoKI, showing polymorphism in the <i>toxA</i> gene in those strains.<br>

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28188980.v1
Primary Topic
Bacterial biofilms and quorum sensing
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article
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article

Detection and association of toxA gene with antibiotic resistance in Pseudomonas aeruginosa strains isolated from different sources in Al Muthanna city

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Bacterial biofilms and quorum sensing
article

Detection and association of toxA gene with antibiotic resistance in Pseudomonas aeruginosa strains isolated from different sources in Al Muthanna city

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Abstract

AbstractIntroductionExotoxin A (ETA) is a powerful chromosomal extracellular virulence factor produced by most of clinical P. aeruginosa isolates. P. aeruginosa is the most common respiratory pathogen in patients with cystic fibrosis (CF).PurposeIn this study, the <i>Pseudomonas aeruginosa</i> strains were isolated from patient's different sources and screened against the <i>toxA</i> gene in order to identify the association between the increase of antibiotics resistance and the toxin production.Methods and resultsOne hundred samples were collected from different cases included: 25 swabs otitis infection, 25 samples from urinary tract infections and 25 swabs from each wound and burn infections for isolation of <i>P. aeruginosa</i> and detection of <i>toxA</i> gene in during the period between July 2019 to January 2020. These samples were cultured firstly onto the Brain heart infusion for 24 h 37oC, followed by the re-streak single colony on the selective on chrome agar media and incubated for 18–24 h at 37oC. The <i>P. aeruginosa</i> isolates were confirmed isolation using VITEK-2 Compact system.The isolation percentage of <i>P. aeruginosa</i> was 80% in the total sample were collected. The highest percentage isolation of <i>P. aeruginosa</i> was from otitis infection at (92%), followed by in wound and burn was (80%), and urinary tract infection was (72%). The gDNA of these isolated was extracted and then subject to PCR technique, detection of the <i>toxA</i> gene as a chromosomal target for the <i>P. aeruginosa</i> infection. The <i>toxA</i> gene detection percentage was (35%) in all the <i>P. aeruginosa</i> isolates; the highest <i>toxA</i> amplification was among strains isolated from otitis at the percentage of 59%, followed by 27% among the strains isolated from urine and 25% of the strains isolated from each wound and burn infections. These isolates were tested against the antibiotic resistance showed the highest percentage of the resistance level, especially those strain associated with detection of <i>toxA</i> gene-positive PCR product. However, the meropenem showed the highest effect against all of <i>P. aeruginosa</i> except for six showed higher resistance than other strains. The PCR product of the strains among the <i>toxA</i> detection was digested with FoKI, yielding two-band at 152 bp and 118 bp, unless those strains resisted the meropenem were showed uncut PCR product by the FoKI, showing polymorphism in the <i>toxA</i> gene in those strains.<br>

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