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The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD

Invading bacteria from the Neisseriaceae, Acinetobacteriaceae, Bordetellaceae and Moraxellaceae families express the conserved outer-membrane zinc transporter zinc-uptake component D (ZnuD) to overcome nutritional restriction imposed by the host organism during infection. Here we demonstrate that Zn...

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Autores principales: Calmettes, Charles, Ing, Christopher, Buckwalter, Carolyn M., El Bakkouri, Majida, Chieh-Lin Lai, Christine, Pogoutse, Anastassia, Gray-Owen, Scott D., Pomès, Régis, Moraes, Trevor F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557270/
https://www.ncbi.nlm.nih.gov/pubmed/26282243
http://dx.doi.org/10.1038/ncomms8996
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author Calmettes, Charles
Ing, Christopher
Buckwalter, Carolyn M.
El Bakkouri, Majida
Chieh-Lin Lai, Christine
Pogoutse, Anastassia
Gray-Owen, Scott D.
Pomès, Régis
Moraes, Trevor F.
author_facet Calmettes, Charles
Ing, Christopher
Buckwalter, Carolyn M.
El Bakkouri, Majida
Chieh-Lin Lai, Christine
Pogoutse, Anastassia
Gray-Owen, Scott D.
Pomès, Régis
Moraes, Trevor F.
author_sort Calmettes, Charles
collection PubMed
description Invading bacteria from the Neisseriaceae, Acinetobacteriaceae, Bordetellaceae and Moraxellaceae families express the conserved outer-membrane zinc transporter zinc-uptake component D (ZnuD) to overcome nutritional restriction imposed by the host organism during infection. Here we demonstrate that ZnuD is required for efficient systemic infections by the causative agent of bacterial meningitis, Neisseria meningitidis, in a mouse model. We also combine X-ray crystallography and molecular dynamics simulations to gain insight into the mechanism of zinc recognition and transport across the bacterial outer-membrane by ZnuD. Because ZnuD is also considered a promising vaccine candidate against N. meningitidis, we use several ZnuD structural intermediates to map potential antigenic epitopes, and propose a mechanism by which ZnuD can maintain high sequence conservation yet avoid immune recognition by altering the conformation of surface-exposed loops.
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spelling pubmed-45572702015-09-14 The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD Calmettes, Charles Ing, Christopher Buckwalter, Carolyn M. El Bakkouri, Majida Chieh-Lin Lai, Christine Pogoutse, Anastassia Gray-Owen, Scott D. Pomès, Régis Moraes, Trevor F. Nat Commun Article Invading bacteria from the Neisseriaceae, Acinetobacteriaceae, Bordetellaceae and Moraxellaceae families express the conserved outer-membrane zinc transporter zinc-uptake component D (ZnuD) to overcome nutritional restriction imposed by the host organism during infection. Here we demonstrate that ZnuD is required for efficient systemic infections by the causative agent of bacterial meningitis, Neisseria meningitidis, in a mouse model. We also combine X-ray crystallography and molecular dynamics simulations to gain insight into the mechanism of zinc recognition and transport across the bacterial outer-membrane by ZnuD. Because ZnuD is also considered a promising vaccine candidate against N. meningitidis, we use several ZnuD structural intermediates to map potential antigenic epitopes, and propose a mechanism by which ZnuD can maintain high sequence conservation yet avoid immune recognition by altering the conformation of surface-exposed loops. Nature Pub. Group 2015-08-18 /pmc/articles/PMC4557270/ /pubmed/26282243 http://dx.doi.org/10.1038/ncomms8996 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Calmettes, Charles
Ing, Christopher
Buckwalter, Carolyn M.
El Bakkouri, Majida
Chieh-Lin Lai, Christine
Pogoutse, Anastassia
Gray-Owen, Scott D.
Pomès, Régis
Moraes, Trevor F.
The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD
title The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD
title_full The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD
title_fullStr The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD
title_full_unstemmed The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD
title_short The molecular mechanism of Zinc acquisition by the neisserial outer-membrane transporter ZnuD
title_sort molecular mechanism of zinc acquisition by the neisserial outer-membrane transporter znud
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557270/
https://www.ncbi.nlm.nih.gov/pubmed/26282243
http://dx.doi.org/10.1038/ncomms8996
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