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Bacterial Toxins as Pathogen Weapons Against Phagocytes
Bacterial toxins are virulence factors that manipulate host cell functions and take over the control of vital processes of living organisms to favor microbial infection. Some toxins directly target innate immune cells, thereby annihilating a major branch of the host immune response. In this review w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734073/ https://www.ncbi.nlm.nih.gov/pubmed/26870008 http://dx.doi.org/10.3389/fmicb.2016.00042 |
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author | do Vale, Ana Cabanes, Didier Sousa, Sandra |
author_facet | do Vale, Ana Cabanes, Didier Sousa, Sandra |
author_sort | do Vale, Ana |
collection | PubMed |
description | Bacterial toxins are virulence factors that manipulate host cell functions and take over the control of vital processes of living organisms to favor microbial infection. Some toxins directly target innate immune cells, thereby annihilating a major branch of the host immune response. In this review we will focus on bacterial toxins that act from the extracellular milieu and hinder the function of macrophages and neutrophils. In particular, we will concentrate on toxins from Gram-positive and Gram-negative bacteria that manipulate cell signaling or induce cell death by either imposing direct damage to the host cells cytoplasmic membrane or enzymatically modifying key eukaryotic targets. Outcomes regarding pathogen dissemination, host damage and disease progression will be discussed. |
format | Online Article Text |
id | pubmed-4734073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47340732016-02-11 Bacterial Toxins as Pathogen Weapons Against Phagocytes do Vale, Ana Cabanes, Didier Sousa, Sandra Front Microbiol Microbiology Bacterial toxins are virulence factors that manipulate host cell functions and take over the control of vital processes of living organisms to favor microbial infection. Some toxins directly target innate immune cells, thereby annihilating a major branch of the host immune response. In this review we will focus on bacterial toxins that act from the extracellular milieu and hinder the function of macrophages and neutrophils. In particular, we will concentrate on toxins from Gram-positive and Gram-negative bacteria that manipulate cell signaling or induce cell death by either imposing direct damage to the host cells cytoplasmic membrane or enzymatically modifying key eukaryotic targets. Outcomes regarding pathogen dissemination, host damage and disease progression will be discussed. Frontiers Media S.A. 2016-02-01 /pmc/articles/PMC4734073/ /pubmed/26870008 http://dx.doi.org/10.3389/fmicb.2016.00042 Text en Copyright © 2016 do Vale, Cabanes and Sousa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology do Vale, Ana Cabanes, Didier Sousa, Sandra Bacterial Toxins as Pathogen Weapons Against Phagocytes |
title | Bacterial Toxins as Pathogen Weapons Against Phagocytes |
title_full | Bacterial Toxins as Pathogen Weapons Against Phagocytes |
title_fullStr | Bacterial Toxins as Pathogen Weapons Against Phagocytes |
title_full_unstemmed | Bacterial Toxins as Pathogen Weapons Against Phagocytes |
title_short | Bacterial Toxins as Pathogen Weapons Against Phagocytes |
title_sort | bacterial toxins as pathogen weapons against phagocytes |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734073/ https://www.ncbi.nlm.nih.gov/pubmed/26870008 http://dx.doi.org/10.3389/fmicb.2016.00042 |
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