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Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt

PURPOSE: Ventilator-associated pneumonia caused by Pseudomonas aeruginosa (P. aeruginosa) is a major health-care problem. In this study, we explored the epidemiology of virulence determinants among multi-drug-resistant (MDR) clinical P. aeruginosa isolates from hospitalized patients with ventilator-...

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Autores principales: Hassuna, Noha A, Mandour, Sahar A, Mohamed, Ebtisam Samir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036984/
https://www.ncbi.nlm.nih.gov/pubmed/32110069
http://dx.doi.org/10.2147/IDR.S233694
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author Hassuna, Noha A
Mandour, Sahar A
Mohamed, Ebtisam Samir
author_facet Hassuna, Noha A
Mandour, Sahar A
Mohamed, Ebtisam Samir
author_sort Hassuna, Noha A
collection PubMed
description PURPOSE: Ventilator-associated pneumonia caused by Pseudomonas aeruginosa (P. aeruginosa) is a major health-care problem. In this study, we explored the epidemiology of virulence determinants among multi-drug-resistant (MDR) clinical P. aeruginosa isolates from hospitalized patients with ventilator-associated pneumonia in intensive care units in Upper Egypt. PATIENTS AND METHODS: MDR P. aeruginosa isolates were screened for the presence of eight virulence factors and typed by ERIC-PCR. RESULTS: A total of 39 clinical MDR isolates were selected out of 173 isolated P. aeruginosa showing a combination of adhesion and cytotoxicity virulence patterns, with the detection of aprA, exoU, exoS, lasB, algD, toxA in 74.3%, 58.9%, 46.1%, 41.2%, 30.7%, 20.5% of the isolates, respectively. The MDR isolates were grouped into 13 different virulence profiles according to the pattern of virulence gene distribution. exoU genotype was more predominant among the P. aeruginosa isolates with more than 48% of the isolates harboring this gene alone, 7% harboring both exoU and exoS and 43.5% harboring exoS gene. An intermediate degree of diversity was detected by ERIC-PCR typing where the isolates were clustered in 7 major groups, indicating possible cross-infection within the hospital. CONCLUSION: Our results highlight the increased frequency of virulent P. aeruginosa isolates with a shift to the more virulent cytotoxic exoU genotype. Further hospital infection-control measures are mandatory to control the hospital cross-transmission of these highly virulent isolates. This study could vastly be a help to develop efficient treatment policies against P. aeruginosa induced ventilator-associated pneumonia.
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spelling pubmed-70369842020-02-27 Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt Hassuna, Noha A Mandour, Sahar A Mohamed, Ebtisam Samir Infect Drug Resist Original Research PURPOSE: Ventilator-associated pneumonia caused by Pseudomonas aeruginosa (P. aeruginosa) is a major health-care problem. In this study, we explored the epidemiology of virulence determinants among multi-drug-resistant (MDR) clinical P. aeruginosa isolates from hospitalized patients with ventilator-associated pneumonia in intensive care units in Upper Egypt. PATIENTS AND METHODS: MDR P. aeruginosa isolates were screened for the presence of eight virulence factors and typed by ERIC-PCR. RESULTS: A total of 39 clinical MDR isolates were selected out of 173 isolated P. aeruginosa showing a combination of adhesion and cytotoxicity virulence patterns, with the detection of aprA, exoU, exoS, lasB, algD, toxA in 74.3%, 58.9%, 46.1%, 41.2%, 30.7%, 20.5% of the isolates, respectively. The MDR isolates were grouped into 13 different virulence profiles according to the pattern of virulence gene distribution. exoU genotype was more predominant among the P. aeruginosa isolates with more than 48% of the isolates harboring this gene alone, 7% harboring both exoU and exoS and 43.5% harboring exoS gene. An intermediate degree of diversity was detected by ERIC-PCR typing where the isolates were clustered in 7 major groups, indicating possible cross-infection within the hospital. CONCLUSION: Our results highlight the increased frequency of virulent P. aeruginosa isolates with a shift to the more virulent cytotoxic exoU genotype. Further hospital infection-control measures are mandatory to control the hospital cross-transmission of these highly virulent isolates. This study could vastly be a help to develop efficient treatment policies against P. aeruginosa induced ventilator-associated pneumonia. Dove 2020-02-19 /pmc/articles/PMC7036984/ /pubmed/32110069 http://dx.doi.org/10.2147/IDR.S233694 Text en © 2020 Hassuna et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Hassuna, Noha A
Mandour, Sahar A
Mohamed, Ebtisam Samir
Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt
title Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt
title_full Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt
title_fullStr Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt
title_full_unstemmed Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt
title_short Virulence Constitution of Multi-Drug-Resistant Pseudomonas aeruginosa in Upper Egypt
title_sort virulence constitution of multi-drug-resistant pseudomonas aeruginosa in upper egypt
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036984/
https://www.ncbi.nlm.nih.gov/pubmed/32110069
http://dx.doi.org/10.2147/IDR.S233694
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