Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells

Staphylococcus epidermidis biofilm formation on indwelling medical devices is frequently associated with the development of chronic infections. Nevertheless, it has been suggested that cells released from these biofilms may induce severe acute infections with bacteraemia as one of its major associat...

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Main Authors: Ângela França, Begoña Pérez-Cabezas, Alexandra Correia, Gerald B. Pier, Nuno Cerca, Manuel Vilanova
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-09-01
Series:Frontiers in Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01530/full
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spelling doaj-aecd2f73c95047c0ab1c6b522dcd82ab2020-11-24T23:58:52ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2016-09-01710.3389/fmicb.2016.01530209296Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cellsÂngela França0Ângela França1Begoña Pérez-Cabezas2Alexandra Correia3Gerald B. Pier4Nuno Cerca5Manuel Vilanova6Manuel Vilanova7Universidade do MinhoUniversidade do PortoUniversidade do PortoUniversidade do PortoBrigham and Women's Hospital/Harvard Medical SchoolUniversidade do MinhoUniversidade do PortoUniversidade do PortoStaphylococcus epidermidis biofilm formation on indwelling medical devices is frequently associated with the development of chronic infections. Nevertheless, it has been suggested that cells released from these biofilms may induce severe acute infections with bacteraemia as one of its major associated clinical manifestations. However, how biofilm-released cells interact with the host remains unclear. Here, using a murine model of hematogenously disseminated infection, we characterized the interaction of cells released from S. epidermidis biofilms with the immune system. Gene expression analysis of mouse splenocytes suggested that biofilm-released cells might be particularly effective at activating inflammatory and antigen presenting cells and inducing cellular apoptosis. Furthermore, biofilm-released cells induced a higher production of pro-inflammatory cytokines, in contrast to mice infected with planktonic cells, even though these had a similar bacterial load in livers and spleens. Overall, these results not only provide insights into the understanding of the role of biofilm-released cells in S. epidermidis biofilm-related infections and pathogenesis, but may also help explain the relapsing character of these infections.http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01530/fullS. epidermidis biofilmsTissue colonizationBiofilm-released cellsmice spleen microarraySerum pro-inflammatory cytokines
collection DOAJ
language English
format Article
sources DOAJ
author Ângela França
Ângela França
Begoña Pérez-Cabezas
Alexandra Correia
Gerald B. Pier
Nuno Cerca
Manuel Vilanova
Manuel Vilanova
spellingShingle Ângela França
Ângela França
Begoña Pérez-Cabezas
Alexandra Correia
Gerald B. Pier
Nuno Cerca
Manuel Vilanova
Manuel Vilanova
Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells
Frontiers in Microbiology
S. epidermidis biofilms
Tissue colonization
Biofilm-released cells
mice spleen microarray
Serum pro-inflammatory cytokines
author_facet Ângela França
Ângela França
Begoña Pérez-Cabezas
Alexandra Correia
Gerald B. Pier
Nuno Cerca
Manuel Vilanova
Manuel Vilanova
author_sort Ângela França
title Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells
title_short Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells
title_full Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells
title_fullStr Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells
title_full_unstemmed Staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells
title_sort staphylococcus epidermidis biofilm-released cells induce a prompt and more marked in vivo inflammatory-type response than planktonic or biofilm cells
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2016-09-01
description Staphylococcus epidermidis biofilm formation on indwelling medical devices is frequently associated with the development of chronic infections. Nevertheless, it has been suggested that cells released from these biofilms may induce severe acute infections with bacteraemia as one of its major associated clinical manifestations. However, how biofilm-released cells interact with the host remains unclear. Here, using a murine model of hematogenously disseminated infection, we characterized the interaction of cells released from S. epidermidis biofilms with the immune system. Gene expression analysis of mouse splenocytes suggested that biofilm-released cells might be particularly effective at activating inflammatory and antigen presenting cells and inducing cellular apoptosis. Furthermore, biofilm-released cells induced a higher production of pro-inflammatory cytokines, in contrast to mice infected with planktonic cells, even though these had a similar bacterial load in livers and spleens. Overall, these results not only provide insights into the understanding of the role of biofilm-released cells in S. epidermidis biofilm-related infections and pathogenesis, but may also help explain the relapsing character of these infections.
topic S. epidermidis biofilms
Tissue colonization
Biofilm-released cells
mice spleen microarray
Serum pro-inflammatory cytokines
url http://journal.frontiersin.org/Journal/10.3389/fmicb.2016.01530/full
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