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Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword

Yersinia adhesin A (YadA) is an essential virulence factor for the food-borne pathogens Yersinia enterocolitica and Yersinia pseudotuberculosis. Suprisingly, it is a pseudogene in Yersinia pestis. Even more intriguing, the introduction of a functional yadA gene in Y. pestis EV76 was shown to correla...

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Autores principales: Casutt-Meyer, Salome, Renzi, Francesco, Schmaler, Mathias, Jann, Naja J., Amstutz, Marlise, Cornelis, Guy R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2999546/
https://www.ncbi.nlm.nih.gov/pubmed/21170337
http://dx.doi.org/10.1371/journal.pone.0015159
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author Casutt-Meyer, Salome
Renzi, Francesco
Schmaler, Mathias
Jann, Naja J.
Amstutz, Marlise
Cornelis, Guy R.
author_facet Casutt-Meyer, Salome
Renzi, Francesco
Schmaler, Mathias
Jann, Naja J.
Amstutz, Marlise
Cornelis, Guy R.
author_sort Casutt-Meyer, Salome
collection PubMed
description Yersinia adhesin A (YadA) is an essential virulence factor for the food-borne pathogens Yersinia enterocolitica and Yersinia pseudotuberculosis. Suprisingly, it is a pseudogene in Yersinia pestis. Even more intriguing, the introduction of a functional yadA gene in Y. pestis EV76 was shown to correlate with a decrease in virulence in a mouse model. Here, we report that wild type (wt) Y. enterocolitica E40, as well as YadA-deprived E40 induced the synthesis of neutrophil extracellular traps (NETs) upon contact with neutrophils, but only YadA-expressing Y. enterocolitica adhered to NETs and were killed. As binding seemed to be a prerequisite for killing, we searched for YadA-binding substrates and detected the presence of collagen within NETs. E40 bacteria expressing V98D,N99A mutant YadA with a severely reduced ability to bind collagen were found to be more resistant to killing, suggesting that collagen binding contributes significantly to sensitivity to NETs. Wt Y. pestis EV76 were resistant to killing by NETs, while recombinant EV76 expressing YadA from either Y. pseudotuberculosis or Y. enterocolitica were sensitive to killing by NETs, outlining the importance of YadA for susceptibility to NET-dependent killing. Recombinant EV76 endowed with YadA from Y. enterocolitica were also less virulent for the mouse than wt EV76, as shown before. In addition, EV76 carrying wt YadA were less virulent for the mouse than EV76 expressing YadA(V98D,N99A). The observation that YadA makes Yersinia sensitive to NETs provides an explanation as for why evolution selected for the inactivation of yadA in the flea-borne Y. pestis and clarifies an old enigma. Since YadA imposes the same cost to the food-borne Yersinia but was nevertheless conserved by evolution, this observation also illustrates the duality of some virulence functions.
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spelling pubmed-29995462010-12-17 Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword Casutt-Meyer, Salome Renzi, Francesco Schmaler, Mathias Jann, Naja J. Amstutz, Marlise Cornelis, Guy R. PLoS One Research Article Yersinia adhesin A (YadA) is an essential virulence factor for the food-borne pathogens Yersinia enterocolitica and Yersinia pseudotuberculosis. Suprisingly, it is a pseudogene in Yersinia pestis. Even more intriguing, the introduction of a functional yadA gene in Y. pestis EV76 was shown to correlate with a decrease in virulence in a mouse model. Here, we report that wild type (wt) Y. enterocolitica E40, as well as YadA-deprived E40 induced the synthesis of neutrophil extracellular traps (NETs) upon contact with neutrophils, but only YadA-expressing Y. enterocolitica adhered to NETs and were killed. As binding seemed to be a prerequisite for killing, we searched for YadA-binding substrates and detected the presence of collagen within NETs. E40 bacteria expressing V98D,N99A mutant YadA with a severely reduced ability to bind collagen were found to be more resistant to killing, suggesting that collagen binding contributes significantly to sensitivity to NETs. Wt Y. pestis EV76 were resistant to killing by NETs, while recombinant EV76 expressing YadA from either Y. pseudotuberculosis or Y. enterocolitica were sensitive to killing by NETs, outlining the importance of YadA for susceptibility to NET-dependent killing. Recombinant EV76 endowed with YadA from Y. enterocolitica were also less virulent for the mouse than wt EV76, as shown before. In addition, EV76 carrying wt YadA were less virulent for the mouse than EV76 expressing YadA(V98D,N99A). The observation that YadA makes Yersinia sensitive to NETs provides an explanation as for why evolution selected for the inactivation of yadA in the flea-borne Y. pestis and clarifies an old enigma. Since YadA imposes the same cost to the food-borne Yersinia but was nevertheless conserved by evolution, this observation also illustrates the duality of some virulence functions. Public Library of Science 2010-12-08 /pmc/articles/PMC2999546/ /pubmed/21170337 http://dx.doi.org/10.1371/journal.pone.0015159 Text en Casutt-Meyer et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Casutt-Meyer, Salome
Renzi, Francesco
Schmaler, Mathias
Jann, Naja J.
Amstutz, Marlise
Cornelis, Guy R.
Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword
title Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword
title_full Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword
title_fullStr Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword
title_full_unstemmed Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword
title_short Oligomeric Coiled-Coil Adhesin YadA Is a Double-Edged Sword
title_sort oligomeric coiled-coil adhesin yada is a double-edged sword
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2999546/
https://www.ncbi.nlm.nih.gov/pubmed/21170337
http://dx.doi.org/10.1371/journal.pone.0015159
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