Literature DB >> 8866478

The use of differential display-PCR to isolate and characterize a Legionella pneumophila locus induced during the intracellular infection of macrophages.

Y Abu Kwaik1, L L Pederson.   

Abstract

The differential display (DD)-PCR technique has been modified to identify prokaryotic cDNA fragments that are differentially induced by facultative intracellular bacteria in response to the intracellular environment of eukaryotic cells. Several DD-PCR fragments identified from the intracellular bacterium Legionella pneumophila were induced at 4 h post-infection of the U937 macrophage-like cells. From these, a 700 bp fragment was cloned and sequenced. Neither the DNA sequence nor the predicted protein sequence from the open reading frame has similarity to other sequences in genetic databases. Transcription of the chromosomal locus containing the 700 bp fragment (eml, for early stage macrophage-induced locus) was induced by intracellular bacteria during the first few hours post-infection of macrophages but the expression was downregulated by 12 h post-infection. Transcription of eml was not growth phase-related in vitro, and was not affected by in vitro stress stimuli. A 3.7 kb EcoRI genomic fragment containing the 700 bp DD-PCR product was cloned. Six mini-Tn 10 insertions in the 3.7 kb EcoRI fragment were recombined into the L. pneumophila chromosome. Compared to the wild-type strain, five of the eml isogenic mutants had a similar phenotype of reduced cytopathicity to the U937 cells, showed a 100-fold increase in killing by macrophages during the first 5 h of the intracellular infection, and showed a 100-fold increase in killing during the first 24h of infection of the amoeba Hartmanella vermiformis. The 6th mutant had a phenotype indistinguishable from the wild-type strain. The cytopathicity defect of the mutants to the U937 cells was restored to wild-type levels by complementation of the mutants with a plasmid containing the 3.7 kb EcoRI fragment. These data showed that the 3.7 kb fragment containing eml is a novel L. pneumophila locus whose expression is uniquely induced by non-stress stimuli during early stages of the intracellular infection of phagocytic cells. Expression of this locus is required for survival of L. pneumophila within macrophages and within amoebae during early stages of the infection.

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Year:  1996        PMID: 8866478     DOI: 10.1111/j.1365-2958.1996.tb02563.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  42 in total

1.  HtrA homologue of Legionella pneumophila: an indispensable element for intracellular infection of mammalian but not protozoan cells.

Authors:  L L Pedersen; M Radulic; M Doric; Y Abu Kwaik
Journal:  Infect Immun       Date:  2001-04       Impact factor: 3.441

2.  Activation of caspase 3 during Legionella pneumophila-induced apoptosis.

Authors:  L Y Gao; Y Abu Kwaik
Journal:  Infect Immun       Date:  1999-09       Impact factor: 3.441

3.  Temporal pore formation-mediated egress from macrophages and alveolar epithelial cells by Legionella pneumophila.

Authors:  O A Alli; L Y Gao; L L Pedersen; S Zink; M Radulic; M Doric; Y Abu Kwaik
Journal:  Infect Immun       Date:  2000-11       Impact factor: 3.441

4.  Simultaneous identification of two cyclohexanone oxidation genes from an environmental Brevibacterium isolate using mRNA differential display.

Authors:  P C Brzostowicz; K L Gibson; S M Thomas; M S Blasko; P E Rouvière
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

Review 5.  Measurement of bacterial gene expression in vivo.

Authors:  I Hautefort; J C Hinton
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-05-29       Impact factor: 6.237

6.  icmT is essential for pore formation-mediated egress of Legionella pneumophila from mammalian and protozoan cells.

Authors:  Maelle Molmeret; O A Terry Alli; Steven Zink; Antje Flieger; Nicholas P Cianciotto; Yousef Abu Kwaik
Journal:  Infect Immun       Date:  2002-01       Impact factor: 3.441

7.  Identification of genes induced in vivo during Klebsiella pneumoniae CG43 infection.

Authors:  Y C Lai; H L Peng; H Y Chang
Journal:  Infect Immun       Date:  2001-11       Impact factor: 3.441

8.  Isolation of regulated genes of the cyanobacterium Synechocystis sp. strain PCC 6803 by differential display.

Authors:  D Bhaya; D Vaulot; P Amin; A W Takahashi; A R Grossman
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

9.  Identification of aerobically and anaerobically induced genes in Enterococcus faecalis by random arbitrarily primed PCR.

Authors:  B D Shepard; M S Gilmore
Journal:  Appl Environ Microbiol       Date:  1999-04       Impact factor: 4.792

10.  Identification of genes in Xanthomonas campestris pv. vesicatoria induced during its interaction with tomato.

Authors:  Dafna Tamir-Ariel; Naama Navon; Saul Burdman
Journal:  J Bacteriol       Date:  2007-06-15       Impact factor: 3.490

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