Cargando…
Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading
Outer membrane protein A (OmpA) is a multifaceted predominant outer membrane protein of Escherichia coli and other Enterobacteriaceae whose role in the pathogenesis of various bacterial infections has recently been recognized. Here, the role of OmpA on the virulence of Shigella flexneri has been inv...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498225/ https://www.ncbi.nlm.nih.gov/pubmed/23166731 http://dx.doi.org/10.1371/journal.pone.0049625 |
_version_ | 1782249805970407424 |
---|---|
author | Ambrosi, Cecilia Pompili, Monica Scribano, Daniela Zagaglia, Carlo Ripa, Sandro Nicoletti, Mauro |
author_facet | Ambrosi, Cecilia Pompili, Monica Scribano, Daniela Zagaglia, Carlo Ripa, Sandro Nicoletti, Mauro |
author_sort | Ambrosi, Cecilia |
collection | PubMed |
description | Outer membrane protein A (OmpA) is a multifaceted predominant outer membrane protein of Escherichia coli and other Enterobacteriaceae whose role in the pathogenesis of various bacterial infections has recently been recognized. Here, the role of OmpA on the virulence of Shigella flexneri has been investigated. An ompA mutant of wild-type S. flexneri 5a strain M90T was constructed (strain HND92) and it was shown to be severely impaired in cell-to-cell spreading since it failed to plaque on HeLa cell monolayers. The lack of OmpA significantly reduced the levels of IcsA while the levels of cell associated and released IcsP-cleaved 95 kDa amino-terminal portion of the mature protein were similar. Nevertheless, the ompA mutant displayed IcsA exposed across the entire bacterial surface. Surprisingly, the ompA mutant produced proper F-actin comet tails, indicating that the aberrant IcsA exposition at bacterial lateral surface did not affect proper activation of actin-nucleating proteins, suggesting that the absence of OmpA likely unmasks mature or cell associated IcsA at bacterial lateral surface. Moreover, the ompA mutant was able to invade and to multiply within HeLa cell monolayers, although internalized bacteria were found to be entrapped within the host cell cytoplasm. We found that the ompA mutant produced significantly less protrusions than the wild-type strain, indicating that this defect could be responsible of its inability to plaque. Although we could not definitely rule out that the ompA mutation might exert pleiotropic effects on other S. flexneri genes, complementation of the ompA mutation with a recombinant plasmid carrying the S. flexneri ompA gene clearly indicated that a functional OmpA protein is required and sufficient for proper IcsA exposition, plaque and protrusion formation. Moreover, an independent ompA mutant was generated. Since we found that both mutants displayed identical virulence profile, these results further supported the findings presented in this study. |
format | Online Article Text |
id | pubmed-3498225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34982252012-11-19 Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading Ambrosi, Cecilia Pompili, Monica Scribano, Daniela Zagaglia, Carlo Ripa, Sandro Nicoletti, Mauro PLoS One Research Article Outer membrane protein A (OmpA) is a multifaceted predominant outer membrane protein of Escherichia coli and other Enterobacteriaceae whose role in the pathogenesis of various bacterial infections has recently been recognized. Here, the role of OmpA on the virulence of Shigella flexneri has been investigated. An ompA mutant of wild-type S. flexneri 5a strain M90T was constructed (strain HND92) and it was shown to be severely impaired in cell-to-cell spreading since it failed to plaque on HeLa cell monolayers. The lack of OmpA significantly reduced the levels of IcsA while the levels of cell associated and released IcsP-cleaved 95 kDa amino-terminal portion of the mature protein were similar. Nevertheless, the ompA mutant displayed IcsA exposed across the entire bacterial surface. Surprisingly, the ompA mutant produced proper F-actin comet tails, indicating that the aberrant IcsA exposition at bacterial lateral surface did not affect proper activation of actin-nucleating proteins, suggesting that the absence of OmpA likely unmasks mature or cell associated IcsA at bacterial lateral surface. Moreover, the ompA mutant was able to invade and to multiply within HeLa cell monolayers, although internalized bacteria were found to be entrapped within the host cell cytoplasm. We found that the ompA mutant produced significantly less protrusions than the wild-type strain, indicating that this defect could be responsible of its inability to plaque. Although we could not definitely rule out that the ompA mutation might exert pleiotropic effects on other S. flexneri genes, complementation of the ompA mutation with a recombinant plasmid carrying the S. flexneri ompA gene clearly indicated that a functional OmpA protein is required and sufficient for proper IcsA exposition, plaque and protrusion formation. Moreover, an independent ompA mutant was generated. Since we found that both mutants displayed identical virulence profile, these results further supported the findings presented in this study. Public Library of Science 2012-11-14 /pmc/articles/PMC3498225/ /pubmed/23166731 http://dx.doi.org/10.1371/journal.pone.0049625 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Ambrosi, Cecilia Pompili, Monica Scribano, Daniela Zagaglia, Carlo Ripa, Sandro Nicoletti, Mauro Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading |
title | Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading |
title_full | Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading |
title_fullStr | Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading |
title_full_unstemmed | Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading |
title_short | Outer Membrane Protein A (OmpA): A New Player in Shigella flexneri Protrusion Formation and Inter-Cellular Spreading |
title_sort | outer membrane protein a (ompa): a new player in shigella flexneri protrusion formation and inter-cellular spreading |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498225/ https://www.ncbi.nlm.nih.gov/pubmed/23166731 http://dx.doi.org/10.1371/journal.pone.0049625 |
work_keys_str_mv | AT ambrosicecilia outermembraneproteinaompaanewplayerinshigellaflexneriprotrusionformationandintercellularspreading AT pompilimonica outermembraneproteinaompaanewplayerinshigellaflexneriprotrusionformationandintercellularspreading AT scribanodaniela outermembraneproteinaompaanewplayerinshigellaflexneriprotrusionformationandintercellularspreading AT zagagliacarlo outermembraneproteinaompaanewplayerinshigellaflexneriprotrusionformationandintercellularspreading AT ripasandro outermembraneproteinaompaanewplayerinshigellaflexneriprotrusionformationandintercellularspreading AT nicolettimauro outermembraneproteinaompaanewplayerinshigellaflexneriprotrusionformationandintercellularspreading |