Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1

Host cell entry by the foodborne pathogen Campylobacter jejuni has been reported as one of the primary reasons of tissue damage in infected humans, however, molecular invasion mechanisms and cellular factors involved in this process are widely unclear. Here we used knockout cell lines derived from f...

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Main Authors: Manja eBoehm, Malgorzata eKrause-Gruszczynska, Manfred eRohde, Nicole eTegtmeyer, Seiichiro eTakahashi, Omar A. Oyarzabal, Steffen eBackert
Format: Article
Language:English
Published: Frontiers Media S.A. 2011-12-01
Series:Frontiers in Cellular and Infection Microbiology
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fcimb.2011.00017/full
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spelling doaj-8dad077f84bd477d9ded5c55722c6fb82020-11-24T21:18:30ZengFrontiers Media S.A.Frontiers in Cellular and Infection Microbiology2235-29882011-12-01110.3389/fcimb.2011.0001716829Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1Manja eBoehm0Manja eBoehm1Malgorzata eKrause-Gruszczynska2Manfred eRohde3Nicole eTegtmeyer4Seiichiro eTakahashi5Omar A. Oyarzabal6Steffen eBackert7Steffen eBackert8Universtiy College DublinOtto von Guericke University,Otto von Guericke University,Helmholtz Center for Infection ResearchUniverstiy College DublinMax-Planck-Institute for BiochemistryAlabama State UniversityUniverstiy College DublinOtto von Guericke University,Host cell entry by the foodborne pathogen Campylobacter jejuni has been reported as one of the primary reasons of tissue damage in infected humans, however, molecular invasion mechanisms and cellular factors involved in this process are widely unclear. Here we used knockout cell lines derived from fibronectin-/-, integrin-beta1-/- and focal adhesion kinase (FAK)-/- deficient mice and corresponding wild-type controls, to study C. jejuni-induced signalling cascades involved in the bacterial invasion process. Using high-resolution scanning electron microscopy, GTPase pulldowns, G-Lisa and gentamicin protection assays we found that each of these host cell factors is indeed required for activation of the small Rho GTPase member Rac1 and maximal host cell invasion of this pathogen. Interestingly, membrane ruffling, tight engulfment of bacteria and invasion were only seen during infection of wild-type control cells, but not in fibronectin-/-, integrin-beta1-/- and FAK-/- knockout cell lines. We also demonstrate that C. jejuni activates FAK autophosphorylation activity at Y-397 and phosphorylation of Y-925, which is required for stimulating two downstream guanine exchange factors, DOCK180 and Tiam-1, which are upstream of Rac1. Small interfering (si) RNA studies further show that DOCK180 and Tiam-1 act cooperatively to trigger Rac1 activation and C. jejuni invasion. Moreover, mutagenesis data indicate that the bacterial fibronectin-binding protein CadF and the intact flagellum are involved in Rho GTPase activation and host cell invasion. Collectively, our results suggest that C. jejuni infection of host epithelial target cells hijacks a major fibronectin>integrin beta1>FAK>DOCK180/Tiam-1 signalling cascade, which has a crucial role for Rac1 GTPase activity and bacterial entry into host target cells.http://journal.frontiersin.org/Journal/10.3389/fcimb.2011.00017/fullVirulencesignallingcellular invasionmolecular pathogenesisRho family GTPases
collection DOAJ
language English
format Article
sources DOAJ
author Manja eBoehm
Manja eBoehm
Malgorzata eKrause-Gruszczynska
Manfred eRohde
Nicole eTegtmeyer
Seiichiro eTakahashi
Omar A. Oyarzabal
Steffen eBackert
Steffen eBackert
spellingShingle Manja eBoehm
Manja eBoehm
Malgorzata eKrause-Gruszczynska
Manfred eRohde
Nicole eTegtmeyer
Seiichiro eTakahashi
Omar A. Oyarzabal
Steffen eBackert
Steffen eBackert
Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1
Frontiers in Cellular and Infection Microbiology
Virulence
signalling
cellular invasion
molecular pathogenesis
Rho family GTPases
author_facet Manja eBoehm
Manja eBoehm
Malgorzata eKrause-Gruszczynska
Manfred eRohde
Nicole eTegtmeyer
Seiichiro eTakahashi
Omar A. Oyarzabal
Steffen eBackert
Steffen eBackert
author_sort Manja eBoehm
title Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1
title_short Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1
title_full Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1
title_fullStr Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1
title_full_unstemmed Major host factors involved in epithelial cell invasion of Campylobacter jejuni: Role of fibronectin, integrin beta1, FAK, Tiam-1 and DOCK180 in activating Rho GTPase Rac1
title_sort major host factors involved in epithelial cell invasion of campylobacter jejuni: role of fibronectin, integrin beta1, fak, tiam-1 and dock180 in activating rho gtpase rac1
publisher Frontiers Media S.A.
series Frontiers in Cellular and Infection Microbiology
issn 2235-2988
publishDate 2011-12-01
description Host cell entry by the foodborne pathogen Campylobacter jejuni has been reported as one of the primary reasons of tissue damage in infected humans, however, molecular invasion mechanisms and cellular factors involved in this process are widely unclear. Here we used knockout cell lines derived from fibronectin-/-, integrin-beta1-/- and focal adhesion kinase (FAK)-/- deficient mice and corresponding wild-type controls, to study C. jejuni-induced signalling cascades involved in the bacterial invasion process. Using high-resolution scanning electron microscopy, GTPase pulldowns, G-Lisa and gentamicin protection assays we found that each of these host cell factors is indeed required for activation of the small Rho GTPase member Rac1 and maximal host cell invasion of this pathogen. Interestingly, membrane ruffling, tight engulfment of bacteria and invasion were only seen during infection of wild-type control cells, but not in fibronectin-/-, integrin-beta1-/- and FAK-/- knockout cell lines. We also demonstrate that C. jejuni activates FAK autophosphorylation activity at Y-397 and phosphorylation of Y-925, which is required for stimulating two downstream guanine exchange factors, DOCK180 and Tiam-1, which are upstream of Rac1. Small interfering (si) RNA studies further show that DOCK180 and Tiam-1 act cooperatively to trigger Rac1 activation and C. jejuni invasion. Moreover, mutagenesis data indicate that the bacterial fibronectin-binding protein CadF and the intact flagellum are involved in Rho GTPase activation and host cell invasion. Collectively, our results suggest that C. jejuni infection of host epithelial target cells hijacks a major fibronectin>integrin beta1>FAK>DOCK180/Tiam-1 signalling cascade, which has a crucial role for Rac1 GTPase activity and bacterial entry into host target cells.
topic Virulence
signalling
cellular invasion
molecular pathogenesis
Rho family GTPases
url http://journal.frontiersin.org/Journal/10.3389/fcimb.2011.00017/full
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