Literature DB >> 7960150

Regulation of surface presentation of IcsA, a Shigella protein essential to intracellular movement and spread, is growth phase dependent.

M B Goldberg1, J A Theriot, P J Sansonetti.   

Abstract

After lysing the phagocytic vacuole, Shigella spp. accumulate filaments of polymerized actin on their surface at one pole, leading to the formation of actin tails that enable them to move through the cytoplasm. We have recently demonstrated that the Shigella protein IcsA is located at the pole that is adjacent to the growing end of the actin tail (M. B. Goldberg, O. Barzu, C. Parsot, and P. J. Sansonetti, J. Bacteriol. 175:2189-2196, 1993). Not every bacterium that is observed within the cytoplasm has an actin tail. The factors that determine when a bacterium will form a tail are unknown. Here we demonstrate that at the moment of initiation of movement, Shigella spp. are frequently in the process of division. Furthermore, the expression of IcsA on the surface of the bacteria occurs in a growth phase-dependent fashion, suggesting that the surface expression of IcsA per se determines the observed association of bacterial division with movement.

Mesh:

Substances:

Year:  1994        PMID: 7960150      PMCID: PMC303317          DOI: 10.1128/iai.62.12.5664-5668.1994

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  22 in total

1.  The transfer RNA binding site of the 30 S ribosome and the site of tetracycline inhibition.

Authors:  G R Craven; R Gavin; T Fanning
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1969

2.  A genetic determinant required for continuous reinfection of adjacent cells on large plasmid in S. flexneri 2a.

Authors:  S Makino; C Sasakawa; K Kamata; T Kurata; M Yoshikawa
Journal:  Cell       Date:  1986-08-15       Impact factor: 41.582

3.  Distinct penicillin binding proteins involved in the division, elongation, and shape of Escherichia coli K12.

Authors:  B G Spratt
Journal:  Proc Natl Acad Sci U S A       Date:  1975-08       Impact factor: 11.205

4.  Cadherin expression is required for the spread of Shigella flexneri between epithelial cells.

Authors:  P J Sansonetti; J Mounier; M C Prévost; R M Mège
Journal:  Cell       Date:  1994-03-11       Impact factor: 41.582

5.  Unipolar localization and ATPase activity of IcsA, a Shigella flexneri protein involved in intracellular movement.

Authors:  M B Goldberg; O Bârzu; C Parsot; P J Sansonetti
Journal:  J Bacteriol       Date:  1993-04       Impact factor: 3.490

6.  Multiplication of Shigella flexneri within HeLa cells: lysis of the phagocytic vacuole and plasmid-mediated contact hemolysis.

Authors:  P J Sansonetti; A Ryter; P Clerc; A T Maurelli; J Mounier
Journal:  Infect Immun       Date:  1986-02       Impact factor: 3.441

7.  Involvement of a plasmid in the invasive ability of Shigella flexneri.

Authors:  P J Sansonetti; D J Kopecko; S B Formal
Journal:  Infect Immun       Date:  1982-03       Impact factor: 3.441

8.  Intracellular spread of Shigella flexneri associated with the kcpA locus and a 140-kilodalton protein.

Authors:  T Pál; J W Newland; B D Tall; S B Formal; T L Hale
Journal:  Infect Immun       Date:  1989-02       Impact factor: 3.441

9.  Differential expression and positioning of chemotaxis methylation proteins in Caulobacter.

Authors:  S L Gomes; L Shapiro
Journal:  J Mol Biol       Date:  1984-09-25       Impact factor: 5.469

10.  Transcription of ftsZ oscillates during the cell cycle of Escherichia coli.

Authors:  T Garrido; M Sánchez; P Palacios; M Aldea; M Vicente
Journal:  EMBO J       Date:  1993-10       Impact factor: 11.598

View more
  21 in total

1.  Changing views on the nature of the bacterial cell: from biochemistry to cytology.

Authors:  R Losick; L Shapiro
Journal:  J Bacteriol       Date:  1999-07       Impact factor: 3.490

2.  Regulation of IcsP, the outer membrane protease of the Shigella actin tail assembly protein IcsA, by virulence plasmid regulators VirF and VirB.

Authors:  Helen J Wing; Arthur W Yan; Seth R Goldman; Marcia B Goldberg
Journal:  J Bacteriol       Date:  2004-02       Impact factor: 3.490

3.  An elastic analysis of Listeria monocytogenes propulsion.

Authors:  F Gerbal; P Chaikin; Y Rabin; J Prost
Journal:  Biophys J       Date:  2000-11       Impact factor: 4.033

4.  Bruton's tyrosine kinase regulates Shigella flexneri dissemination in HT-29 intestinal cells.

Authors:  Ana-Maria Dragoi; Arthur M Talman; Hervé Agaisse
Journal:  Infect Immun       Date:  2012-12-10       Impact factor: 3.441

5.  Two promoters and two translation start sites control the expression of the Shigella flexneri outer membrane protease IcsP.

Authors:  Christopher T Hensley; Olga K Kamneva; Karen M Levy; Stephanie K Labahn; Lia A Africa; Helen J Wing
Journal:  Arch Microbiol       Date:  2011-01-12       Impact factor: 2.552

6.  The iron-responsive Fur/RyhB regulatory cascade modulates the Shigella outer membrane protease IcsP.

Authors:  Lia A A Africa; Erin R Murphy; Nicholas R Egan; Amanda F Wigley; Helen J Wing
Journal:  Infect Immun       Date:  2011-08-22       Impact factor: 3.441

7.  Shigella flexneri DegP facilitates IcsA surface expression and is required for efficient intercellular spread.

Authors:  Georgiana E Purdy; Mei Hong; Shelley M Payne
Journal:  Infect Immun       Date:  2002-11       Impact factor: 3.441

8.  Intracellular multiplication and virulence of Shigella flexneri auxotrophic mutants.

Authors:  A Cersini; A M Salvia; M L Bernardini
Journal:  Infect Immun       Date:  1998-02       Impact factor: 3.441

Review 9.  Molecular and cellular mechanisms of invasion of the intestinal barrier by enteric pathogens. The paradigm of Shigella.

Authors:  P J Sansonetti
Journal:  Folia Microbiol (Praha)       Date:  1998       Impact factor: 2.099

10.  Shigella flexneri surface protein IcsA is sufficient to direct actin-based motility.

Authors:  M B Goldberg; J A Theriot
Journal:  Proc Natl Acad Sci U S A       Date:  1995-07-03       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.