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YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization
BACKGROUND: Salmonella enterica serovar Typhimurium is an intracellular bacterial pathogen which can colonize a variety of hosts, including human, causing syndromes that vary from gastroenteritis and diarrhea to systemic disease. RESULTS: In this work we present structural information as well as ins...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107778/ https://www.ncbi.nlm.nih.gov/pubmed/21554724 http://dx.doi.org/10.1186/1471-2180-11-95 |
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author | Carrica, Mariela C Craig, Patricio O García-Angulo, Víctor A Aguirre, Andes García-Véscovi, Eleonora Goldbaum, Fernando A Cravero, Silvio L |
author_facet | Carrica, Mariela C Craig, Patricio O García-Angulo, Víctor A Aguirre, Andes García-Véscovi, Eleonora Goldbaum, Fernando A Cravero, Silvio L |
author_sort | Carrica, Mariela C |
collection | PubMed |
description | BACKGROUND: Salmonella enterica serovar Typhimurium is an intracellular bacterial pathogen which can colonize a variety of hosts, including human, causing syndromes that vary from gastroenteritis and diarrhea to systemic disease. RESULTS: In this work we present structural information as well as insights into the in vivo function of YqiC, a 99-residue protein of S. Typhimurium, which belongs to the cluster of the orthologous group 2960 (COG2960). We found that YqiC shares biophysical and biochemical properties with Brucella abortus BMFP, the only previously characterized member of this group, such as a high alpha helix content, a coiled-coil domain involved in trimerization and a membrane fusogenic activity in vitro. In addition, we demonstrated that YqiC localizes at cytoplasmic and membrane subcellular fractions, that a S. Typhimurium yqiC deficient strain had a severe attenuation in virulence in the murine model when inoculated both orally and intraperitoneally, and was impaired to replicate at physiological and high temperatures in vitro, although it was still able to invade and replicate inside epithelial and macrophages cell lines. CONCLUSION: This work firstly demonstrates the importance of a COG2960 member for pathogen-host interaction, and suggests a common function conserved among members of this group. |
format | Online Article Text |
id | pubmed-3107778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31077782011-06-04 YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization Carrica, Mariela C Craig, Patricio O García-Angulo, Víctor A Aguirre, Andes García-Véscovi, Eleonora Goldbaum, Fernando A Cravero, Silvio L BMC Microbiol Research Article BACKGROUND: Salmonella enterica serovar Typhimurium is an intracellular bacterial pathogen which can colonize a variety of hosts, including human, causing syndromes that vary from gastroenteritis and diarrhea to systemic disease. RESULTS: In this work we present structural information as well as insights into the in vivo function of YqiC, a 99-residue protein of S. Typhimurium, which belongs to the cluster of the orthologous group 2960 (COG2960). We found that YqiC shares biophysical and biochemical properties with Brucella abortus BMFP, the only previously characterized member of this group, such as a high alpha helix content, a coiled-coil domain involved in trimerization and a membrane fusogenic activity in vitro. In addition, we demonstrated that YqiC localizes at cytoplasmic and membrane subcellular fractions, that a S. Typhimurium yqiC deficient strain had a severe attenuation in virulence in the murine model when inoculated both orally and intraperitoneally, and was impaired to replicate at physiological and high temperatures in vitro, although it was still able to invade and replicate inside epithelial and macrophages cell lines. CONCLUSION: This work firstly demonstrates the importance of a COG2960 member for pathogen-host interaction, and suggests a common function conserved among members of this group. BioMed Central 2011-05-09 /pmc/articles/PMC3107778/ /pubmed/21554724 http://dx.doi.org/10.1186/1471-2180-11-95 Text en Copyright ©2011 Carrica et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Carrica, Mariela C Craig, Patricio O García-Angulo, Víctor A Aguirre, Andes García-Véscovi, Eleonora Goldbaum, Fernando A Cravero, Silvio L YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization |
title | YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization |
title_full | YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization |
title_fullStr | YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization |
title_full_unstemmed | YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization |
title_short | YqiC of Salmonella enterica serovar Typhimurium is a membrane fusogenic protein required for mice colonization |
title_sort | yqic of salmonella enterica serovar typhimurium is a membrane fusogenic protein required for mice colonization |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107778/ https://www.ncbi.nlm.nih.gov/pubmed/21554724 http://dx.doi.org/10.1186/1471-2180-11-95 |
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