Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene Studies

Pathogenic microbes influence gene regulation in eukaryotic hosts. Reporter gene studies can define the roles of promoter regulatory sequences. The effect of pathogenic bacteria on reporter genes has not been examined. The aim of this study was to identify which reporter genes are reliable in studie...

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Main Authors: Suzana D. Savkovic, Athanasia Koutsouris, Gary Wu, Gail Hecht
Format: Article
Language:English
Published: Taylor & Francis Group 2000-09-01
Series:BioTechniques
Online Access:https://www.future-science.com/doi/10.2144/00293st03
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author Suzana D. Savkovic
Athanasia Koutsouris
Gary Wu
Gail Hecht
author_facet Suzana D. Savkovic
Athanasia Koutsouris
Gary Wu
Gail Hecht
author_sort Suzana D. Savkovic
collection DOAJ
description Pathogenic microbes influence gene regulation in eukaryotic hosts. Reporter gene studies can define the roles of promoter regulatory sequences. The effect of pathogenic bacteria on reporter genes has not been examined. The aim of this study was to identify which reporter genes are reliable in studies concerning host gene regulation by bacterial pathogens expressing type III secretory systems. Human intestinal epithelial cells, T84, Caco-2 and HT-29, were transfected with plasmids containing luciferase (luc), chloramphenicol acetyltransferase (CAT) or β-galactosidase (β-gal) as reporter genes driven by the inducible interleukin-8 (IL-8) or constitutively active simian virus 40 (SV40) promoter. Cells were infected with enteropathogenic E. coli or Salmonella typhimurium, and the reporter activity was assessed. Luc activity significantly decreased following infection, regardless of the promoter. The activity of recombinant luc was nearly ablated by incubation with either EPEC or Salmonella in a cell-free system. Activity was partially preserved by protease inhibitors, and immunoblot analysis showed a decreased amount and molecular weight of recombinant luc, suggesting protein degradation. Neither β-gal nor CAT activity was altered by infection. Disruption of type III secretion prevented the loss of luc activity. We conclude that CAT or β-gal, but not luc, can be used as reliable reporter genes to assess the impact of pathogenic microbes, especially those expressing type III secretion on host cell gene regulation.
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spelling doaj-art-4d028f1e74dc4dcdb925393f6b9556432025-08-20T02:26:06ZengTaylor & Francis GroupBioTechniques0736-62051940-98182000-09-0129351452210.2144/00293st03Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene StudiesSuzana D. Savkovic0Athanasia Koutsouris1Gary Wu2Gail Hecht31University of Illinois, West Side VA Medical Center, Chicago, IL, USA1University of Illinois, West Side VA Medical Center, Chicago, IL, USA1University of Illinois, West Side VA Medical Center, Chicago, IL, USA1University of Illinois, West Side VA Medical Center, Chicago, IL, USAPathogenic microbes influence gene regulation in eukaryotic hosts. Reporter gene studies can define the roles of promoter regulatory sequences. The effect of pathogenic bacteria on reporter genes has not been examined. The aim of this study was to identify which reporter genes are reliable in studies concerning host gene regulation by bacterial pathogens expressing type III secretory systems. Human intestinal epithelial cells, T84, Caco-2 and HT-29, were transfected with plasmids containing luciferase (luc), chloramphenicol acetyltransferase (CAT) or β-galactosidase (β-gal) as reporter genes driven by the inducible interleukin-8 (IL-8) or constitutively active simian virus 40 (SV40) promoter. Cells were infected with enteropathogenic E. coli or Salmonella typhimurium, and the reporter activity was assessed. Luc activity significantly decreased following infection, regardless of the promoter. The activity of recombinant luc was nearly ablated by incubation with either EPEC or Salmonella in a cell-free system. Activity was partially preserved by protease inhibitors, and immunoblot analysis showed a decreased amount and molecular weight of recombinant luc, suggesting protein degradation. Neither β-gal nor CAT activity was altered by infection. Disruption of type III secretion prevented the loss of luc activity. We conclude that CAT or β-gal, but not luc, can be used as reliable reporter genes to assess the impact of pathogenic microbes, especially those expressing type III secretion on host cell gene regulation.https://www.future-science.com/doi/10.2144/00293st03
spellingShingle Suzana D. Savkovic
Athanasia Koutsouris
Gary Wu
Gail Hecht
Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene Studies
BioTechniques
title Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene Studies
title_full Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene Studies
title_fullStr Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene Studies
title_full_unstemmed Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene Studies
title_short Infection by Bacterial Pathogens Expressing Type III Secretion Decreases Luciferase Activity: Ramifications for Reporter Gene Studies
title_sort infection by bacterial pathogens expressing type iii secretion decreases luciferase activity ramifications for reporter gene studies
url https://www.future-science.com/doi/10.2144/00293st03
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AT garywu infectionbybacterialpathogensexpressingtypeiiisecretiondecreasesluciferaseactivityramificationsforreportergenestudies
AT gailhecht infectionbybacterialpathogensexpressingtypeiiisecretiondecreasesluciferaseactivityramificationsforreportergenestudies