Literature DB >> 2548211

Cloning and molecular characterization of genes whose products allow Salmonella typhimurium to penetrate tissue culture cells.

J E Galán1, R Curtiss.   

Abstract

Invasion of the intestinal epithelium is thought to be an important step in the pathogenesis of Salmonella infections. Using an in vitro system, we have isolated a genetic locus, inv, that confers to a noninvasive strain of Salmonella typhimurium the ability to penetrate tissue culture cells. Highly virulent S. typhimurium strains carrying inv mutations were defective for entry into Henle-407 cells while remaining unaffected in their ability to attach to cultured cells. When administered perorally to BALB/c mice, inv mutants of S. typhimurium had higher 50% lethal doses (LD50) than their wild-type parent strains. To the contrary, there were no differences in the observed LD50 when strains were administered intraperitoneally. In addition, inv mutants presented decreased ability to colonize the Peyer's patches, the small intestinal wall, and the spleen when administered perorally, although when administered intraperitoneally, they showed no difference in their ability to colonize the spleen compared to the wild-type parent strain.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2548211      PMCID: PMC297844          DOI: 10.1073/pnas.86.16.6383

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  37 in total

1.  Increased virulence of Yersinia pseudotuberculosis by two independent mutations.

Authors:  R Rosqvist; M Skurnik; H Wolf-Watz
Journal:  Nature       Date:  1988-08-11       Impact factor: 49.962

2.  Site-directed insertion and deletion mutagenesis with cloned fragments in Escherichia coli.

Authors:  S C Winans; S J Elledge; J H Krueger; G C Walker
Journal:  J Bacteriol       Date:  1985-03       Impact factor: 3.490

3.  A single genetic locus encoded by Yersinia pseudotuberculosis permits invasion of cultured animal cells by Escherichia coli K-12.

Authors:  R R Isberg; S Falkow
Journal:  Nature       Date:  1985 Sep 19-25       Impact factor: 49.962

4.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

5.  Enhancement of invasiveness of Yersinia enterocolitica and Escherichia coli in HEp-2 cells by centrifugation.

Authors:  T Vesikari; J Bromirska; M Mäki
Journal:  Infect Immun       Date:  1982-05       Impact factor: 3.441

6.  Polarity of Tn5 insertion mutations in Escherichia coli.

Authors:  D E Berg; A Weiss; L Crossland
Journal:  J Bacteriol       Date:  1980-05       Impact factor: 3.490

7.  Ingestion and survival of Y. pseudotuberculosis in HeLa cells.

Authors:  A Bovallius; G Nilsson
Journal:  Can J Microbiol       Date:  1975-12       Impact factor: 2.419

8.  Identification of invasin: a protein that allows enteric bacteria to penetrate cultured mammalian cells.

Authors:  R R Isberg; D L Voorhis; S Falkow
Journal:  Cell       Date:  1987-08-28       Impact factor: 41.582

9.  Intestinal colonization and virulence of Salmonella in mice.

Authors:  A W Hohmann; G Schmidt; D Rowley
Journal:  Infect Immun       Date:  1978-12       Impact factor: 3.441

10.  Cosmid cloning and transposon mutagenesis in Salmonella typhimurium using phage lambda vehicles.

Authors:  E T Palva; P Liljeström; S Harayama
Journal:  Mol Gen Genet       Date:  1981
View more
  421 in total

1.  Type III secretion chaperone-dependent regulation: activation of virulence genes by SicA and InvF in Salmonella typhimurium.

Authors:  K H Darwin; V L Miller
Journal:  EMBO J       Date:  2001-04-17       Impact factor: 11.598

Review 2.  Molecular basis of the interaction of Salmonella with the intestinal mucosa.

Authors:  K H Darwin; V L Miller
Journal:  Clin Microbiol Rev       Date:  1999-07       Impact factor: 26.132

3.  DNA adenine methylase mutants of Salmonella typhimurium show defects in protein secretion, cell invasion, and M cell cytotoxicity.

Authors:  F García-Del Portillo; M G Pucciarelli; J Casadesús
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

4.  OmpR regulates the two-component system SsrA-ssrB in Salmonella pathogenicity island 2.

Authors:  A K Lee; C S Detweiler; S Falkow
Journal:  J Bacteriol       Date:  2000-02       Impact factor: 3.490

5.  Molecular characterization and assembly of the needle complex of the Salmonella typhimurium type III protein secretion system.

Authors:  T Kubori; A Sukhan; S I Aizawa; J E Galán
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-29       Impact factor: 11.205

6.  SrfJ, a Salmonella type III secretion system effector regulated by PhoP, RcsB, and IolR.

Authors:  Mar Cordero-Alba; Joaquín Bernal-Bayard; Francisco Ramos-Morales
Journal:  J Bacteriol       Date:  2012-06-01       Impact factor: 3.490

7.  Salmonella type III secretion-associated protein InvE controls translocation of effector proteins into host cells.

Authors:  Tomoko Kubori; Jorge E Galán
Journal:  J Bacteriol       Date:  2002-09       Impact factor: 3.490

8.  Poultry body temperature contributes to invasion control through reduced expression of Salmonella pathogenicity island 1 genes in Salmonella enterica serovars Typhimurium and Enteritidis.

Authors:  Bryan Troxell; Nicholas Petri; Caitlyn Daron; Rafaela Pereira; Mary Mendoza; Hosni M Hassan; Matthew D Koci
Journal:  Appl Environ Microbiol       Date:  2015-09-18       Impact factor: 4.792

9.  The Salmonella effector SteA contributes to the control of membrane dynamics of Salmonella-containing vacuoles.

Authors:  Lia Domingues; David W Holden; Luís Jaime Mota
Journal:  Infect Immun       Date:  2014-04-28       Impact factor: 3.441

10.  Leucine-responsive regulatory protein (Lrp) acts as a virulence repressor in Salmonella enterica serovar Typhimurium.

Authors:  Chang-Ho Baek; Shifeng Wang; Kenneth L Roland; Roy Curtiss
Journal:  J Bacteriol       Date:  2008-12-12       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.