Literature DB >> 2182715

The primary effect of the Ity locus is on the rate of growth of Salmonella typhimurium that are relatively protected from killing.

W H Benjamin1, P Hall, S J Roberts, D E Briles.   

Abstract

The Ity locus affects the net increase in numbers of Salmonella typhimurium in the liver and spleen of infected mice. There has been controversy, however, about whether the effects of this locus are due to differential killing of S. typhimurium or differential growth rates of S. typhimurium in mice. Our studies using S. typhimurium aroA mutants, which do not grow in vivo, demonstrate that growth of the infecting salmonella is necessary for the observation of the Ity phenotype. To examine the effects of the Ity locus on the growth and killing of fully virulent salmonella, we infected Ity-congenic mice i.v. with stationary phase S. typhimurium containing a single copy of the plasmid pHSG422. This plasmid exhibits defective replication at body temperature and is diluted out during salmonella growth in vivo. Thus, the frequency of plasmid-containing salmonella recovered from mice provides a measure of salmonella cell divisions in vivo. Inasmuch as the numbers of plasmid-containing salmonella are only slightly affected by bacterial division, any decline in the numbers of plasmid-containing salmonella is an unbiased measure of killing. By infecting mice with these plasmid-containing salmonella we observed that: 1) during the first four h post infection (during blood clearance of injected salmonella) there is about 3-fold more killing of salmonella in Ityr mice than in Itys mice; 2) from 4 to 44 h postinfection (after blood clearance is completed) there is little if any additional killing in either Itys or Ityr mice; and 3) during the first 48 h postinfection there is about 18-fold more growth of salmonella in Itys mice than in Ityr mice. Thus, the major effect of the Ity locus on resistance to salmonella, is the regulation of growth within a "safe" (relatively nonbactericidal) site in the liver and spleen.

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Year:  1990        PMID: 2182715

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  37 in total

1.  Human C-reactive protein is protective against fatal Salmonella enterica serovar typhimurium infection in transgenic mice.

Authors:  A J Szalai; J L VanCott; J R McGhee; J E Volanakis; W H Benjamin
Journal:  Infect Immun       Date:  2000-10       Impact factor: 3.441

2.  Influence of the Salmonella typhimurium pathogenicity island 2 type III secretion system on bacterial growth in the mouse.

Authors:  J E Shea; C R Beuzon; C Gleeson; R Mundy; D W Holden
Journal:  Infect Immun       Date:  1999-01       Impact factor: 3.441

3.  The full expression of the ity phenotype in ityr mice requires C3 activation by Salmonella lipopolysaccharide.

Authors:  F Nishikawa; S Yoshikawa; H Harada; M Kita; E Kita
Journal:  Immunology       Date:  1998-12       Impact factor: 7.397

4.  Acid shock induction of RpoS is mediated by the mouse virulence gene mviA of Salmonella typhimurium.

Authors:  S M Bearson; W H Benjamin; W E Swords; J W Foster
Journal:  J Bacteriol       Date:  1996-05       Impact factor: 3.490

Review 5.  Identification and analysis of bacterial virulence genes in vivo.

Authors:  K E Unsworth; D W Holden
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-05-29       Impact factor: 6.237

6.  In vivo visualization of bacterial colonization, antigen expression, and specific T-cell induction following oral administration of live recombinant Salmonella enterica serovar Typhimurium.

Authors:  D Bumann
Journal:  Infect Immun       Date:  2001-07       Impact factor: 3.441

7.  Exogenous tumor necrosis factor alpha and interleukin-1 alpha increase resistance to Salmonella typhimurium: efficacy is influenced by the Ity and Lps loci.

Authors:  P J Morrissey; K Charrier; S N Vogel
Journal:  Infect Immun       Date:  1995-08       Impact factor: 3.441

8.  Mouse hepatitis virus strain UAB infection enhances resistance to Salmonella typhimurium in mice by inducing suppression of bacterial growth.

Authors:  M T Fallon; W H Benjamin; T R Schoeb; D E Briles
Journal:  Infect Immun       Date:  1991-03       Impact factor: 3.441

9.  Gamma interferon and interleukin-10 gene expression in innately susceptible and resistant mice during the early phase of Salmonella typhimurium infection.

Authors:  S Pie; P Matsiota-Bernard; P Truffa-Bachi; C Nauciel
Journal:  Infect Immun       Date:  1996-03       Impact factor: 3.441

10.  Role of gamma interferon in late stages of murine salmonellosis.

Authors:  A Muotiala; P H Mäkelä
Journal:  Infect Immun       Date:  1993-10       Impact factor: 3.441

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