Clostridium difficile spore-macrophage interactions: spore survival.

BACKGROUND: Clostridium difficile is the main cause of nosocomial infections including antibiotic associated diarrhea, pseudomembranous colitis and toxic megacolon. During the course of Clostridium difficile infections (CDI), C. difficile undergoes sporulation and releases spores to the colonic envi...

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Main Authors: Daniel Paredes-Sabja, Glenda Cofre-Araneda, Christian Brito-Silva, Marjorie Pizarro-Guajardo, Mahfuzur R Sarker
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3428350?pdf=render
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author Daniel Paredes-Sabja
Glenda Cofre-Araneda
Christian Brito-Silva
Marjorie Pizarro-Guajardo
Mahfuzur R Sarker
author_facet Daniel Paredes-Sabja
Glenda Cofre-Araneda
Christian Brito-Silva
Marjorie Pizarro-Guajardo
Mahfuzur R Sarker
author_sort Daniel Paredes-Sabja
collection DOAJ
description BACKGROUND: Clostridium difficile is the main cause of nosocomial infections including antibiotic associated diarrhea, pseudomembranous colitis and toxic megacolon. During the course of Clostridium difficile infections (CDI), C. difficile undergoes sporulation and releases spores to the colonic environment. The elevated relapse rates of CDI suggest that C. difficile spores has a mechanism(s) to efficiently persist in the host colonic environment. METHODOLOGY/PRINCIPAL FINDINGS: In this work, we provide evidence that C. difficile spores are well suited to survive the host's innate immune system. Electron microscopy results show that C. difficile spores are recognized by discrete patchy regions on the surface of macrophage Raw 264.7 cells, and phagocytosis was actin polymerization dependent. Fluorescence microscopy results show that >80% of Raw 264.7 cells had at least one C. difficile spore adhered, and that ∼60% of C. difficile spores were phagocytosed by Raw 264.7 cells. Strikingly, presence of complement decreased Raw 264.7 cells' ability to phagocytose C. difficile spores. Due to the ability of C. difficile spores to remain dormant inside Raw 264.7 cells, they were able to survive up to 72 h of macrophage infection. Interestingly, transmission electron micrographs showed interactions between the surface proteins of C. difficile spores and the phagosome membrane of Raw 264.7 cells. In addition, infection of Raw 264.7 cells with C. difficile spores for 48 h produced significant Raw 264.7 cell death as demonstrated by trypan blue assay, and nuclei staining by ethidium homodimer-1. CONCLUSIONS/SIGNIFICANCE: These results demonstrate that despite efficient recognition and phagocytosis of C. difficile spores by Raw 264.7 cells, spores remain dormant and are able to survive and produce cytotoxic effects on Raw 264.7 cells.
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spelling doaj.art-71d8a6caf9b445358819d841e98da8ab2022-12-22T01:37:16ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0178e4363510.1371/journal.pone.0043635Clostridium difficile spore-macrophage interactions: spore survival.Daniel Paredes-SabjaGlenda Cofre-AranedaChristian Brito-SilvaMarjorie Pizarro-GuajardoMahfuzur R SarkerBACKGROUND: Clostridium difficile is the main cause of nosocomial infections including antibiotic associated diarrhea, pseudomembranous colitis and toxic megacolon. During the course of Clostridium difficile infections (CDI), C. difficile undergoes sporulation and releases spores to the colonic environment. The elevated relapse rates of CDI suggest that C. difficile spores has a mechanism(s) to efficiently persist in the host colonic environment. METHODOLOGY/PRINCIPAL FINDINGS: In this work, we provide evidence that C. difficile spores are well suited to survive the host's innate immune system. Electron microscopy results show that C. difficile spores are recognized by discrete patchy regions on the surface of macrophage Raw 264.7 cells, and phagocytosis was actin polymerization dependent. Fluorescence microscopy results show that >80% of Raw 264.7 cells had at least one C. difficile spore adhered, and that ∼60% of C. difficile spores were phagocytosed by Raw 264.7 cells. Strikingly, presence of complement decreased Raw 264.7 cells' ability to phagocytose C. difficile spores. Due to the ability of C. difficile spores to remain dormant inside Raw 264.7 cells, they were able to survive up to 72 h of macrophage infection. Interestingly, transmission electron micrographs showed interactions between the surface proteins of C. difficile spores and the phagosome membrane of Raw 264.7 cells. In addition, infection of Raw 264.7 cells with C. difficile spores for 48 h produced significant Raw 264.7 cell death as demonstrated by trypan blue assay, and nuclei staining by ethidium homodimer-1. CONCLUSIONS/SIGNIFICANCE: These results demonstrate that despite efficient recognition and phagocytosis of C. difficile spores by Raw 264.7 cells, spores remain dormant and are able to survive and produce cytotoxic effects on Raw 264.7 cells.http://europepmc.org/articles/PMC3428350?pdf=render
spellingShingle Daniel Paredes-Sabja
Glenda Cofre-Araneda
Christian Brito-Silva
Marjorie Pizarro-Guajardo
Mahfuzur R Sarker
Clostridium difficile spore-macrophage interactions: spore survival.
PLoS ONE
title Clostridium difficile spore-macrophage interactions: spore survival.
title_full Clostridium difficile spore-macrophage interactions: spore survival.
title_fullStr Clostridium difficile spore-macrophage interactions: spore survival.
title_full_unstemmed Clostridium difficile spore-macrophage interactions: spore survival.
title_short Clostridium difficile spore-macrophage interactions: spore survival.
title_sort clostridium difficile spore macrophage interactions spore survival
url http://europepmc.org/articles/PMC3428350?pdf=render
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AT christianbritosilva clostridiumdifficilesporemacrophageinteractionssporesurvival
AT marjoriepizarroguajardo clostridiumdifficilesporemacrophageinteractionssporesurvival
AT mahfuzurrsarker clostridiumdifficilesporemacrophageinteractionssporesurvival