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...

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Veröffentlicht in:PloS one 2012-11, Vol.7 (11), p.e49625
Hauptverfasser: Ambrosi, Cecilia, Pompili, Monica, Scribano, Daniela, Zagaglia, Carlo, Ripa, Sandro, Nicoletti, Mauro
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Pompili, Monica
Scribano, Daniela
Zagaglia, Carlo
Ripa, Sandro
Nicoletti, Mauro
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.
doi_str_mv 10.1371/journal.pone.0049625
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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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23166731</pmid><doi>10.1371/journal.pone.0049625</doi><oa>free_for_read</oa></addata></record>
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subjects Aberration
Actin
Actins - metabolism
Antigens
Bacteria
Bacterial infections
Bacterial Outer Membrane Proteins - genetics
Bacterial Outer Membrane Proteins - metabolism
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Biology
Cell Membrane Permeability - genetics
Cell spreading
Cell Surface Extensions - genetics
Cell Surface Extensions - metabolism
Comet tails
Complementation
Cytoplasm
DNA-Binding Proteins - genetics
DNA-Binding Proteins - metabolism
E coli
Enzyme Activation
Escherichia coli
Exposure
Gene Expression Regulation, Bacterial
Group IV Phospholipases A2 - metabolism
Health aspects
HeLa Cells
Hostages
Humans
Infection
Kinases
Lipopolysaccharides - metabolism
Membrane proteins
Monolayers
Monomolecular films
Muscle proteins
Mutants
Mutation
OmpA protein
Pathogenesis
Pathogens
Phenotype
Physics
Plasmids
Polymerization
Protein A
Proteins
Shigella
Shigella flexneri - genetics
Shigella flexneri - metabolism
Shigella flexneri - pathogenicity
Spreading
Transcription Factors - genetics
Transcription Factors - metabolism
Virulence
Virulence (Microbiology)
Virulence - genetics
title Outer membrane protein A (OmpA): a new player in shigella flexneri protrusion formation and inter-cellular spreading
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