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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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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. |
format | Online Article Text |
id | pubmed-4557270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
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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