Flow cytometry characterisation of Salmonella typhimurium mutants defective in proton translocating proteins and stationary-phase growth phenotype
Language English Country Netherlands Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
11044569
DOI
10.1016/s0167-7012(00)00199-8
PII: S0167701200001998
Knihovny.cz E-resources
- MeSH
- Acridine Orange MeSH
- Genes, Bacterial MeSH
- Coloring Agents MeSH
- Cytochrome b Group MeSH
- Cytochromes genetics metabolism MeSH
- Electron Transport Chain Complex Proteins * MeSH
- Phenotype MeSH
- Fluorescent Dyes MeSH
- Mutation * MeSH
- NADH, NADPH Oxidoreductases genetics metabolism MeSH
- Oxidoreductases genetics metabolism MeSH
- Propidium MeSH
- Escherichia coli Proteins * MeSH
- Flow Cytometry * MeSH
- Electron Transport Complex I MeSH
- Rhodamine 123 MeSH
- Salmonella typhimurium genetics growth & development physiology MeSH
- Oxygen Consumption MeSH
- DNA Transposable Elements MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Acridine Orange MeSH
- Coloring Agents MeSH
- cytochrome bd terminal oxidase complex, E coli MeSH Browser
- Cytochrome b Group MeSH
- Cytochromes MeSH
- Electron Transport Chain Complex Proteins * MeSH
- Fluorescent Dyes MeSH
- NADH, NADPH Oxidoreductases MeSH
- Oxidoreductases MeSH
- Propidium MeSH
- Escherichia coli Proteins * MeSH
- Electron Transport Complex I MeSH
- Rhodamine 123 MeSH
- DNA Transposable Elements MeSH
We have shown that the growth, starvation and population heterogeneity of Salmonella typhimurium and its isogenic nuoG and cydA mutants can be monitored by flow cytometry. Bacterial cells were analysed unstained, and after staining with rhodamine 123, propidium iodide and acridine orange. In unstained cultures it was possible to distinguish flagellated and non-flagellated cells. nuoG and cydA mutants were less stained with rhodamine confirming their defects in generating membrane potential. Increase in propidium iodide staining associated with reduced membrane integrity was seen between day 4 and 14 in all the strains. Acridine orange staining showed that there was retarded development in stationary phase in nuoG and cydA mutants. Furthermore, up to day 28, a small portion of cells showed high RNA and DNA levels. To determine whether these cells represent a sub-population better adapted for long term survival, we measured the growth of the population by both OD values and viable counts. Because the OD values increased throughout the whole study in both wild-type and mutant strains, while the viable counts gradually decreased, we propose that even in very old cultures there must be a population of cells undergoing replication.
References provided by Crossref.org
aro mutations in Salmonella enterica cause defects in cell wall and outer membrane integrity