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aro mutations in Salmonella enterica cause defects in cell wall and outer membrane integrity
A Sebkova, D Karasova, M Crhanova, E Budinska, I Rychlik
Language English Country United States
NLK
Free Medical Journals
from 1916 to 6 months ago
Freely Accessible Science Journals
from 1916 to 6 months ago
PubMed Central
from 1916 to 1 year ago
Europe PubMed Central
from 1916 to 6 months ago
Open Access Digital Library
from 1916-01-01
Open Access Digital Library
from 1916-01-01
- MeSH
- Albumins pharmacology MeSH
- Alkyl and Aryl Transferases genetics MeSH
- Amino Acids, Aromatic biosynthesis genetics MeSH
- Anti-Bacterial Agents pharmacology MeSH
- Genes, Bacterial MeSH
- Drug Resistance, Bacterial genetics MeSH
- Cell Membrane genetics drug effects MeSH
- Cell Wall genetics drug effects MeSH
- Edetic Acid pharmacology MeSH
- Financing, Organized MeSH
- Phosphoenolpyruvate metabolism MeSH
- Cloning, Molecular MeSH
- Complement System Proteins pharmacology MeSH
- Mutation MeSH
- Conalbumin pharmacology MeSH
- Plasmids genetics MeSH
- Salmonella enteritidis enzymology genetics drug effects MeSH
- Salmonella typhimurium enzymology genetics drug effects MeSH
- Oligonucleotide Array Sequence Analysis MeSH
- Serum MeSH
- Genetic Complementation Test MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
In this study we characterized aro mutants of Salmonella enterica serovars Enteritidis and Typhimurium, which are frequently used as live oral vaccines. We found that the aroA, aroD, and aroC mutants were sensitive to blood serum, albumen, EDTA, and ovotransferrin, and this defect could be complemented by an appropriate aro gene cloned in a plasmid. Subsequent microarray analysis of gene expression in the aroD mutant in serovar Typhimurium indicated that the reason for this sensitivity might be the upregulation of murA. To confirm this, we artificially overexpressed murA from a multicopy plasmid, and this overexpression caused sensitivity of the strain to albumen and EDTA but not to serum and ovotransferrin. We concluded that attenuation of aro mutants is caused not only by their inability to synthesize aromatic metabolites but also by their defect in cell wall and outer membrane functions associated with decreased resistance to components of innate immune response.
References provided by Crossref.org
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- $a In this study we characterized aro mutants of Salmonella enterica serovars Enteritidis and Typhimurium, which are frequently used as live oral vaccines. We found that the aroA, aroD, and aroC mutants were sensitive to blood serum, albumen, EDTA, and ovotransferrin, and this defect could be complemented by an appropriate aro gene cloned in a plasmid. Subsequent microarray analysis of gene expression in the aroD mutant in serovar Typhimurium indicated that the reason for this sensitivity might be the upregulation of murA. To confirm this, we artificially overexpressed murA from a multicopy plasmid, and this overexpression caused sensitivity of the strain to albumen and EDTA but not to serum and ovotransferrin. We concluded that attenuation of aro mutants is caused not only by their inability to synthesize aromatic metabolites but also by their defect in cell wall and outer membrane functions associated with decreased resistance to components of innate immune response.
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