Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier
<p>Abstract</p> <p>Background</p> <p>Multi-drug resistant <it>Pseudomonas aeruginosa </it>nosocomial infections are increasingly recognized worldwide. In this study, we focused on the virulence of multi-drug resistant clinical strains <it>P. aeruginosa...
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doaj-0e94a13f4c12431c9b6e99b85b1d89f52020-11-24T22:21:50ZengBMCAnnals of Clinical Microbiology and Antimicrobials1476-07112006-06-01511410.1186/1476-0711-5-14Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrierShevchenko OlgaBethel CindyWang YingminKohler Jonathan EZaborina OlgaWu LichengTurner Jerrold RAlverdy John C<p>Abstract</p> <p>Background</p> <p>Multi-drug resistant <it>Pseudomonas aeruginosa </it>nosocomial infections are increasingly recognized worldwide. In this study, we focused on the virulence of multi-drug resistant clinical strains <it>P. aeruginosa </it>against the intestinal epithelial barrier, since <it>P. aeruginosa </it>can cause lethal sepsis from within the intestinal tract of critically ill and immuno-compromised patients via mechanisms involving disruption of epithelial barrier function.</p> <p>Methods</p> <p>We screened consecutively isolated multi-drug resistant <it>P. aeruginosa </it>clinical strains for their ability to disrupt the integrity of human cultured intestinal epithelial cells (Caco-2) and correlated these finding to related virulence phenotypes such as adhesiveness, motility, biofilm formation, and cytotoxicity.</p> <p>Results</p> <p>Results demonstrated that the majority of the multi-drug resistant <it>P. aeruginosa </it>clinical strains were attenuated in their ability to disrupt the barrier function of cultured intestinal epithelial cells. Three distinct genotypes were found that displayed an extreme epithelial barrier-disrupting phenotype. These strains were characterized and found to harbor the <it>exoU </it>gene and to display high swimming motility and adhesiveness.</p> <p>Conclusion</p> <p>These data suggest that detailed phenotypic analysis of the behavior of multi-drug resistant <it>P. aeruginosa </it>against the intestinal epithelium has the potential to identify strains most likely to place patients at risk for lethal gut-derived sepsis. Surveillance of colonizing strains of <it>P. aeruginosa </it>in critically ill patients beyond antibiotic sensitivity is warranted.</p> http://www.ann-clinmicrob.com/content/5/1/14 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shevchenko Olga Bethel Cindy Wang Yingmin Kohler Jonathan E Zaborina Olga Wu Licheng Turner Jerrold R Alverdy John C |
spellingShingle |
Shevchenko Olga Bethel Cindy Wang Yingmin Kohler Jonathan E Zaborina Olga Wu Licheng Turner Jerrold R Alverdy John C Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier Annals of Clinical Microbiology and Antimicrobials |
author_facet |
Shevchenko Olga Bethel Cindy Wang Yingmin Kohler Jonathan E Zaborina Olga Wu Licheng Turner Jerrold R Alverdy John C |
author_sort |
Shevchenko Olga |
title |
Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier |
title_short |
Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier |
title_full |
Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier |
title_fullStr |
Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier |
title_full_unstemmed |
Identification of multi-drug resistant <it>Pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier |
title_sort |
identification of multi-drug resistant <it>pseudomonas aeruginosa </it>clinical isolates that are highly disruptive to the intestinal epithelial barrier |
publisher |
BMC |
series |
Annals of Clinical Microbiology and Antimicrobials |
issn |
1476-0711 |
publishDate |
2006-06-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Multi-drug resistant <it>Pseudomonas aeruginosa </it>nosocomial infections are increasingly recognized worldwide. In this study, we focused on the virulence of multi-drug resistant clinical strains <it>P. aeruginosa </it>against the intestinal epithelial barrier, since <it>P. aeruginosa </it>can cause lethal sepsis from within the intestinal tract of critically ill and immuno-compromised patients via mechanisms involving disruption of epithelial barrier function.</p> <p>Methods</p> <p>We screened consecutively isolated multi-drug resistant <it>P. aeruginosa </it>clinical strains for their ability to disrupt the integrity of human cultured intestinal epithelial cells (Caco-2) and correlated these finding to related virulence phenotypes such as adhesiveness, motility, biofilm formation, and cytotoxicity.</p> <p>Results</p> <p>Results demonstrated that the majority of the multi-drug resistant <it>P. aeruginosa </it>clinical strains were attenuated in their ability to disrupt the barrier function of cultured intestinal epithelial cells. Three distinct genotypes were found that displayed an extreme epithelial barrier-disrupting phenotype. These strains were characterized and found to harbor the <it>exoU </it>gene and to display high swimming motility and adhesiveness.</p> <p>Conclusion</p> <p>These data suggest that detailed phenotypic analysis of the behavior of multi-drug resistant <it>P. aeruginosa </it>against the intestinal epithelium has the potential to identify strains most likely to place patients at risk for lethal gut-derived sepsis. Surveillance of colonizing strains of <it>P. aeruginosa </it>in critically ill patients beyond antibiotic sensitivity is warranted.</p> |
url |
http://www.ann-clinmicrob.com/content/5/1/14 |
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