Literature DB >> 9891781

Intracellular pathogens and the actin cytoskeleton.

S Dramsi1, P Cossart.   

Abstract

Many pathogens actively exploit the actin cytoskeleton during infection. This exploitation may take place during entry into mammalian cells after engagement of a receptor and/or as series of signaling events culminating in the engulfment of the microorganism. Although actin rearrangements are a common feature of most internalization events (e.g. entry of Listeria, Salmonella, Shigella, Yersinia, Neisseria, and Bartonella), bacterial and other cellular factors involved in entry are specific to each bacterium. Another step during which pathogens harness the actin cytoskeleton takes place in the cytosol, within which some bacteria (Listeria, Shigella, Rickettsia) or viruses (vaccinia virus) are able to move. Movement is coupled to a polarized actin polymerization process, with the formation of characteristic actin tails. Increasing attention has focused on this phenomenon due to its striking similarity to cellular events occurring at the leading edge of locomoting cells. Thus pathogens are convenient systems in which to study actin cytoskeleton rearrangements in response to stimuli at the plasma membrane or inside cells.

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Year:  1998        PMID: 9891781     DOI: 10.1146/annurev.cellbio.14.1.137

Source DB:  PubMed          Journal:  Annu Rev Cell Dev Biol        ISSN: 1081-0706            Impact factor:   13.827


  69 in total

1.  Entry of the two infectious forms of vaccinia virus at the plasma membane is signaling-dependent for the IMV but not the EEV.

Authors:  J K Locker; A Kuehn; S Schleich; G Rutter; H Hohenberg; R Wepf; G Griffiths
Journal:  Mol Biol Cell       Date:  2000-07       Impact factor: 4.138

Review 2.  Polarity in action: asymmetric protein localization in bacteria.

Authors:  S R Lybarger; J R Maddock
Journal:  J Bacteriol       Date:  2001-06       Impact factor: 3.490

3.  Dual epitope recognition by the VASP EVH1 domain modulates polyproline ligand specificity and binding affinity.

Authors:  L J Ball; R Kühne; B Hoffmann; A Häfner; P Schmieder; R Volkmer-Engert; M Hof; M Wahl; J Schneider-Mergener; U Walter; H Oschkinat; T Jarchau
Journal:  EMBO J       Date:  2000-09-15       Impact factor: 11.598

4.  Growth velocities of branched actin networks.

Authors:  A E Carlsson
Journal:  Biophys J       Date:  2003-05       Impact factor: 4.033

5.  Identification of profilin and src homology 3 domains as binding partners for Drosophila enabled.

Authors:  S M Ahern-Djamali; C Bachmann; P Hua; S K Reddy; A S Kastenmeier; U Walter; F M Hoffmann
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

6.  Role of actin filament network in Burkholderia multivorans invasion in well-differentiated human airway epithelia.

Authors:  Ute E Schwab; Carla M P Ribeiro; Heiner Neubauer; Richard C Boucher
Journal:  Infect Immun       Date:  2003-11       Impact factor: 3.441

7.  Probing polymerization forces by using actin-propelled lipid vesicles.

Authors:  Arpita Upadhyaya; Jeffrey R Chabot; Albina Andreeva; Azadeh Samadani; Alexander van Oudenaarden
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-25       Impact factor: 11.205

8.  OHMS**: Phytoplasmas dictate changes in sieve-element ultrastructure to accommodate their requirements for nutrition, multiplication and translocation.

Authors:  Rita Musetti; Laura Pagliari; Stefanie V Buxa; Francesca Degola; Federica De Marco; Alberto Loschi; Karl-Heinz Kogel; Aart J E van Bel
Journal:  Plant Signal Behav       Date:  2016

9.  Multinucleated giant cell formation and apoptosis in infected host cells is mediated by Burkholderia pseudomallei type III secretion protein BipB.

Authors:  Supaporn Suparak; Wannapa Kespichayawattana; Ashraful Haque; Anna Easton; Suwat Damnin; Ganjana Lertmemongkolchai; Gregory J Bancroft; Sunee Korbsrisate
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

10.  Kaposi's sarcoma-associated herpesvirus modulates microtubule dynamics via RhoA-GTP-diaphanous 2 signaling and utilizes the dynein motors to deliver its DNA to the nucleus.

Authors:  Pramod P Naranatt; Harinivas H Krishnan; Marilyn S Smith; Bala Chandran
Journal:  J Virol       Date:  2005-01       Impact factor: 5.103

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