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Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms

Burkholderia pathogenicity relies on protein virulence factors to control and promote bacterial internalization, survival, and replication within eukaryotic host cells. We recently used yeast two-hybrid (Y2H) screening to identify a small set of novel Burkholderia proteins that were shown to attenua...

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Autores principales: Memišević, Vesna, Zavaljevski, Nela, Rajagopala, Seesandra V., Kwon, Keehwan, Pieper, Rembert, DeShazer, David, Reifman, Jaques, Wallqvist, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349708/
https://www.ncbi.nlm.nih.gov/pubmed/25738731
http://dx.doi.org/10.1371/journal.pcbi.1004088
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author Memišević, Vesna
Zavaljevski, Nela
Rajagopala, Seesandra V.
Kwon, Keehwan
Pieper, Rembert
DeShazer, David
Reifman, Jaques
Wallqvist, Anders
author_facet Memišević, Vesna
Zavaljevski, Nela
Rajagopala, Seesandra V.
Kwon, Keehwan
Pieper, Rembert
DeShazer, David
Reifman, Jaques
Wallqvist, Anders
author_sort Memišević, Vesna
collection PubMed
description Burkholderia pathogenicity relies on protein virulence factors to control and promote bacterial internalization, survival, and replication within eukaryotic host cells. We recently used yeast two-hybrid (Y2H) screening to identify a small set of novel Burkholderia proteins that were shown to attenuate disease progression in an aerosol infection animal model using the virulent Burkholderia mallei ATCC 23344 strain. Here, we performed an extended analysis of primarily nine B. mallei virulence factors and their interactions with human proteins to map out how the bacteria can influence and alter host processes and pathways. Specifically, we employed topological analyses to assess the connectivity patterns of targeted host proteins, identify modules of pathogen-interacting host proteins linked to processes promoting infectivity, and evaluate the effect of crosstalk among the identified host protein modules. Overall, our analysis showed that the targeted host proteins generally had a large number of interacting partners and interacted with other host proteins that were also targeted by B. mallei proteins. We also introduced a novel Host-Pathogen Interaction Alignment (HPIA) algorithm and used it to explore similarities between host-pathogen interactions of B. mallei, Yersinia pestis, and Salmonella enterica. We inferred putative roles of B. mallei proteins based on the roles of their aligned Y. pestis and S. enterica partners and showed that up to 73% of the predicted roles matched existing annotations. A key insight into Burkholderia pathogenicity derived from these analyses of Y2H host-pathogen interactions is the identification of eukaryotic-specific targeted cellular mechanisms, including the ubiquitination degradation system and the use of the focal adhesion pathway as a fulcrum for transmitting mechanical forces and regulatory signals. This provides the mechanisms to modulate and adapt the host-cell environment for the successful establishment of host infections and intracellular spread.
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spelling pubmed-43497082015-03-17 Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms Memišević, Vesna Zavaljevski, Nela Rajagopala, Seesandra V. Kwon, Keehwan Pieper, Rembert DeShazer, David Reifman, Jaques Wallqvist, Anders PLoS Comput Biol Research Article Burkholderia pathogenicity relies on protein virulence factors to control and promote bacterial internalization, survival, and replication within eukaryotic host cells. We recently used yeast two-hybrid (Y2H) screening to identify a small set of novel Burkholderia proteins that were shown to attenuate disease progression in an aerosol infection animal model using the virulent Burkholderia mallei ATCC 23344 strain. Here, we performed an extended analysis of primarily nine B. mallei virulence factors and their interactions with human proteins to map out how the bacteria can influence and alter host processes and pathways. Specifically, we employed topological analyses to assess the connectivity patterns of targeted host proteins, identify modules of pathogen-interacting host proteins linked to processes promoting infectivity, and evaluate the effect of crosstalk among the identified host protein modules. Overall, our analysis showed that the targeted host proteins generally had a large number of interacting partners and interacted with other host proteins that were also targeted by B. mallei proteins. We also introduced a novel Host-Pathogen Interaction Alignment (HPIA) algorithm and used it to explore similarities between host-pathogen interactions of B. mallei, Yersinia pestis, and Salmonella enterica. We inferred putative roles of B. mallei proteins based on the roles of their aligned Y. pestis and S. enterica partners and showed that up to 73% of the predicted roles matched existing annotations. A key insight into Burkholderia pathogenicity derived from these analyses of Y2H host-pathogen interactions is the identification of eukaryotic-specific targeted cellular mechanisms, including the ubiquitination degradation system and the use of the focal adhesion pathway as a fulcrum for transmitting mechanical forces and regulatory signals. This provides the mechanisms to modulate and adapt the host-cell environment for the successful establishment of host infections and intracellular spread. Public Library of Science 2015-03-04 /pmc/articles/PMC4349708/ /pubmed/25738731 http://dx.doi.org/10.1371/journal.pcbi.1004088 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Memišević, Vesna
Zavaljevski, Nela
Rajagopala, Seesandra V.
Kwon, Keehwan
Pieper, Rembert
DeShazer, David
Reifman, Jaques
Wallqvist, Anders
Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms
title Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms
title_full Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms
title_fullStr Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms
title_full_unstemmed Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms
title_short Mining Host-Pathogen Protein Interactions to Characterize Burkholderia mallei Infectivity Mechanisms
title_sort mining host-pathogen protein interactions to characterize burkholderia mallei infectivity mechanisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4349708/
https://www.ncbi.nlm.nih.gov/pubmed/25738731
http://dx.doi.org/10.1371/journal.pcbi.1004088
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