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A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development
Bacterial pathogens must overcome host immune mechanisms to acquire micronutrients for successful replication and infection. Streptococcus pyogenes, also known as group A streptococcus (GAS), is a human pathogen that causes a variety of clinical manifestations, and disease prevention is hampered by...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514391/ https://www.ncbi.nlm.nih.gov/pubmed/28596134 http://dx.doi.org/10.1016/j.ebiom.2017.05.030 |
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author | Makthal, Nishanth Nguyen, Kimberly Do, Hackwon Gavagan, Maire Chandrangsu, Pete Helmann, John D. Olsen, Randall J. Kumaraswami, Muthiah |
author_facet | Makthal, Nishanth Nguyen, Kimberly Do, Hackwon Gavagan, Maire Chandrangsu, Pete Helmann, John D. Olsen, Randall J. Kumaraswami, Muthiah |
author_sort | Makthal, Nishanth |
collection | PubMed |
description | Bacterial pathogens must overcome host immune mechanisms to acquire micronutrients for successful replication and infection. Streptococcus pyogenes, also known as group A streptococcus (GAS), is a human pathogen that causes a variety of clinical manifestations, and disease prevention is hampered by lack of a human GAS vaccine. Herein, we report that the mammalian host recruits calprotectin (CP) to GAS infection sites and retards bacterial growth by zinc limitation. However, a GAS-encoded zinc importer and a nuanced zinc sensor aid bacterial defense against CP-mediated growth inhibition and contribute to GAS virulence. Immunization of mice with the extracellular component of the zinc importer confers protection against systemic GAS challenge. Together, we identified a key early stage host-GAS interaction and translated that knowledge into a novel vaccine strategy against GAS infection. Furthermore, we provided evidence that a similar struggle for zinc may occur during other streptococcal infections, which raises the possibility of a broad-spectrum prophylactic strategy against multiple streptococcal pathogens. |
format | Online Article Text |
id | pubmed-5514391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55143912017-07-27 A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development Makthal, Nishanth Nguyen, Kimberly Do, Hackwon Gavagan, Maire Chandrangsu, Pete Helmann, John D. Olsen, Randall J. Kumaraswami, Muthiah EBioMedicine Research Paper Bacterial pathogens must overcome host immune mechanisms to acquire micronutrients for successful replication and infection. Streptococcus pyogenes, also known as group A streptococcus (GAS), is a human pathogen that causes a variety of clinical manifestations, and disease prevention is hampered by lack of a human GAS vaccine. Herein, we report that the mammalian host recruits calprotectin (CP) to GAS infection sites and retards bacterial growth by zinc limitation. However, a GAS-encoded zinc importer and a nuanced zinc sensor aid bacterial defense against CP-mediated growth inhibition and contribute to GAS virulence. Immunization of mice with the extracellular component of the zinc importer confers protection against systemic GAS challenge. Together, we identified a key early stage host-GAS interaction and translated that knowledge into a novel vaccine strategy against GAS infection. Furthermore, we provided evidence that a similar struggle for zinc may occur during other streptococcal infections, which raises the possibility of a broad-spectrum prophylactic strategy against multiple streptococcal pathogens. Elsevier 2017-06-02 /pmc/articles/PMC5514391/ /pubmed/28596134 http://dx.doi.org/10.1016/j.ebiom.2017.05.030 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Makthal, Nishanth Nguyen, Kimberly Do, Hackwon Gavagan, Maire Chandrangsu, Pete Helmann, John D. Olsen, Randall J. Kumaraswami, Muthiah A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development |
title | A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development |
title_full | A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development |
title_fullStr | A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development |
title_full_unstemmed | A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development |
title_short | A Critical Role of Zinc Importer AdcABC in Group A Streptococcus-Host Interactions During Infection and Its Implications for Vaccine Development |
title_sort | critical role of zinc importer adcabc in group a streptococcus-host interactions during infection and its implications for vaccine development |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514391/ https://www.ncbi.nlm.nih.gov/pubmed/28596134 http://dx.doi.org/10.1016/j.ebiom.2017.05.030 |
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