Use of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. Typhimurium

<p style="text-align:justify;"> This study describes the construction and analysis of three in vivo-inducible promoter expression plasmids, containing pnirB, ppagC, and pkatG, for the delivery of foreign antigens in the ΔaroAD mutant ofSalmonella enterica var. Typhimurium (hereafter...

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Main Authors: Dunstan, S, Simmons, C, Strugnell, R
Format: Journal article
Language:English
Published: American Society for Microbiology 1999
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author Dunstan, S
Simmons, C
Strugnell, R
author_facet Dunstan, S
Simmons, C
Strugnell, R
author_sort Dunstan, S
collection OXFORD
description <p style="text-align:justify;"> This study describes the construction and analysis of three in vivo-inducible promoter expression plasmids, containing pnirB, ppagC, and pkatG, for the delivery of foreign antigens in the ΔaroAD mutant ofSalmonella enterica var. Typhimurium (hereafter referred to as S. typhimurium). The reporter genes encoding β-galactosidase and firefly luciferase were used to assess the comparative levels of promoter activity in S. typhimuriumin vitro in response to different induction stimuli and in vivo in immunized mice. It was determined that the ppagC construct directed the expression of more β-galactosidase and luciferase inS. typhimurium than the pnirB and pkatG constructs, both in vitro and in vivo. The gene encoding the C fragment of tetanus toxin was expressed in thearoAD mutant of S. typhimurium (BRD509) under the control of the three promoters. Mice orally immunized with attenuated S. typhimurium expressing C fragment under control of the pagC promoter [BRD509(pKK/ppagC/C frag)] mounted the highest tetanus toxoid-specific serum antibody response. Levels of luciferase expression in vivo and C-fragment expression in vitro from thepagC promoter appeared to be equivalent to if not lower than the levels of expression detected with the constitutivetrc promoter. However, mice immunized with BRD509(pKK/ppagC/C frag) induced significantly higher levels of tetanus toxoid-specific antibody than BRD509(pKK/C frag)-immunized mice, suggesting that the specific location of foreign antigen expression may be important for immunogenicity. Mutagenesis of the ribosome binding sites (RBS) in the three promoter/C fragment expression plasmids was also performed. Despite optimization of the RBS in the three different promoter elements, the expression levels in vivo and overall immunogenicity of C fragment when delivered to mice by attenuated S. typhimurium were not affected. These studies suggest that in vivo-inducible promoters may give rise to enhanced immunogenicity and increase the efficacy of S. typhimuriumas a vaccine vector.</p>
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spelling oxford-uuid:9d865b37-ddd8-4f16-abed-4371ae4647442022-03-27T00:43:41ZUse of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. TyphimuriumJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9d865b37-ddd8-4f16-abed-4371ae464744EnglishSymplectic Elements at OxfordAmerican Society for Microbiology1999Dunstan, SSimmons, CStrugnell, R <p style="text-align:justify;"> This study describes the construction and analysis of three in vivo-inducible promoter expression plasmids, containing pnirB, ppagC, and pkatG, for the delivery of foreign antigens in the ΔaroAD mutant ofSalmonella enterica var. Typhimurium (hereafter referred to as S. typhimurium). The reporter genes encoding β-galactosidase and firefly luciferase were used to assess the comparative levels of promoter activity in S. typhimuriumin vitro in response to different induction stimuli and in vivo in immunized mice. It was determined that the ppagC construct directed the expression of more β-galactosidase and luciferase inS. typhimurium than the pnirB and pkatG constructs, both in vitro and in vivo. The gene encoding the C fragment of tetanus toxin was expressed in thearoAD mutant of S. typhimurium (BRD509) under the control of the three promoters. Mice orally immunized with attenuated S. typhimurium expressing C fragment under control of the pagC promoter [BRD509(pKK/ppagC/C frag)] mounted the highest tetanus toxoid-specific serum antibody response. Levels of luciferase expression in vivo and C-fragment expression in vitro from thepagC promoter appeared to be equivalent to if not lower than the levels of expression detected with the constitutivetrc promoter. However, mice immunized with BRD509(pKK/ppagC/C frag) induced significantly higher levels of tetanus toxoid-specific antibody than BRD509(pKK/C frag)-immunized mice, suggesting that the specific location of foreign antigen expression may be important for immunogenicity. Mutagenesis of the ribosome binding sites (RBS) in the three promoter/C fragment expression plasmids was also performed. Despite optimization of the RBS in the three different promoter elements, the expression levels in vivo and overall immunogenicity of C fragment when delivered to mice by attenuated S. typhimurium were not affected. These studies suggest that in vivo-inducible promoters may give rise to enhanced immunogenicity and increase the efficacy of S. typhimuriumas a vaccine vector.</p>
spellingShingle Dunstan, S
Simmons, C
Strugnell, R
Use of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. Typhimurium
title Use of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. Typhimurium
title_full Use of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. Typhimurium
title_fullStr Use of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. Typhimurium
title_full_unstemmed Use of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. Typhimurium
title_short Use of in vivo-regulated promoters to deliver antigens from attenuated salmonella enterica var. Typhimurium
title_sort use of in vivo regulated promoters to deliver antigens from attenuated salmonella enterica var typhimurium
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AT simmonsc useofinvivoregulatedpromoterstodeliverantigensfromattenuatedsalmonellaentericavartyphimurium
AT strugnellr useofinvivoregulatedpromoterstodeliverantigensfromattenuatedsalmonellaentericavartyphimurium