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Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP

Pasteurella pneumotropica is an opportunist Gram negative bacterium responsible for rodent pasteurellosis that affects upper respiratory, reproductive and digestive tracts of mammals. In animal care facilities the presence of P. pneumotropica causes severe to lethal infection in immunodeficient mice...

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Autores principales: Sahagún-Ruiz, Alfredo, Granados Martinez, Adriana Patricia, Breda, Leandro Carvalho Dantas, Fraga, Tatiana Rodrigues, Castiblanco Valencia, Mónica Marcela, Barbosa, Angela Silva, Isaac, Lourdes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210218/
https://www.ncbi.nlm.nih.gov/pubmed/25347183
http://dx.doi.org/10.1371/journal.pone.0111194
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author Sahagún-Ruiz, Alfredo
Granados Martinez, Adriana Patricia
Breda, Leandro Carvalho Dantas
Fraga, Tatiana Rodrigues
Castiblanco Valencia, Mónica Marcela
Barbosa, Angela Silva
Isaac, Lourdes
author_facet Sahagún-Ruiz, Alfredo
Granados Martinez, Adriana Patricia
Breda, Leandro Carvalho Dantas
Fraga, Tatiana Rodrigues
Castiblanco Valencia, Mónica Marcela
Barbosa, Angela Silva
Isaac, Lourdes
author_sort Sahagún-Ruiz, Alfredo
collection PubMed
description Pasteurella pneumotropica is an opportunist Gram negative bacterium responsible for rodent pasteurellosis that affects upper respiratory, reproductive and digestive tracts of mammals. In animal care facilities the presence of P. pneumotropica causes severe to lethal infection in immunodeficient mice, being also a potential source for human contamination. Indeed, occupational exposure is one of the main causes of human infection by P. pneumotropica. The clinical presentation of the disease includes subcutaneous abscesses, respiratory tract colonization and systemic infections. Given the ability of P. pneumotropica to fully disseminate in the organism, it is quite relevant to study the role of the complement system to control the infection as well as the possible evasion mechanisms involved in bacterial survival. Here, we show for the first time that P. pneumotropica is able to survive the bactericidal activity of the human complement system. We observed that host regulatory complement C4BP and Factor H bind to the surface of P. pneumotropica, controlling the activation pathways regulating the formation and maintenance of C3-convertases. These results show that P. pneumotropica has evolved mechanisms to evade the human complement system that may increase the efficiency by which this pathogen is able to gain access to and colonize inner tissues where it may cause severe infections.
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spelling pubmed-42102182014-10-30 Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP Sahagún-Ruiz, Alfredo Granados Martinez, Adriana Patricia Breda, Leandro Carvalho Dantas Fraga, Tatiana Rodrigues Castiblanco Valencia, Mónica Marcela Barbosa, Angela Silva Isaac, Lourdes PLoS One Research Article Pasteurella pneumotropica is an opportunist Gram negative bacterium responsible for rodent pasteurellosis that affects upper respiratory, reproductive and digestive tracts of mammals. In animal care facilities the presence of P. pneumotropica causes severe to lethal infection in immunodeficient mice, being also a potential source for human contamination. Indeed, occupational exposure is one of the main causes of human infection by P. pneumotropica. The clinical presentation of the disease includes subcutaneous abscesses, respiratory tract colonization and systemic infections. Given the ability of P. pneumotropica to fully disseminate in the organism, it is quite relevant to study the role of the complement system to control the infection as well as the possible evasion mechanisms involved in bacterial survival. Here, we show for the first time that P. pneumotropica is able to survive the bactericidal activity of the human complement system. We observed that host regulatory complement C4BP and Factor H bind to the surface of P. pneumotropica, controlling the activation pathways regulating the formation and maintenance of C3-convertases. These results show that P. pneumotropica has evolved mechanisms to evade the human complement system that may increase the efficiency by which this pathogen is able to gain access to and colonize inner tissues where it may cause severe infections. Public Library of Science 2014-10-27 /pmc/articles/PMC4210218/ /pubmed/25347183 http://dx.doi.org/10.1371/journal.pone.0111194 Text en © 2014 Sahagún-Ruiz 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
Sahagún-Ruiz, Alfredo
Granados Martinez, Adriana Patricia
Breda, Leandro Carvalho Dantas
Fraga, Tatiana Rodrigues
Castiblanco Valencia, Mónica Marcela
Barbosa, Angela Silva
Isaac, Lourdes
Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP
title Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP
title_full Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP
title_fullStr Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP
title_full_unstemmed Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP
title_short Pasteurella pneumotropica Evades the Human Complement System by Acquisition of the Complement Regulators Factor H and C4BP
title_sort pasteurella pneumotropica evades the human complement system by acquisition of the complement regulators factor h and c4bp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210218/
https://www.ncbi.nlm.nih.gov/pubmed/25347183
http://dx.doi.org/10.1371/journal.pone.0111194
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