Microfiltration method of removal of bacterial contaminants and their monitoring by nitric oxide and Limulus assays
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22981390
DOI
10.1016/j.niox.2012.08.078
PII: S1089-8603(12)00375-8
Knihovny.cz E-resources
- MeSH
- Bacillus subtilis chemistry isolation & purification MeSH
- Cell Line MeSH
- Centrifugation MeSH
- Escherichia coli chemistry isolation & purification MeSH
- Filtration * MeSH
- Rats MeSH
- Teichoic Acids analysis MeSH
- Limulus Test * MeSH
- Lipopolysaccharides analysis MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Nitric Oxide biosynthesis metabolism MeSH
- Peptidoglycan analysis MeSH
- Rats, Wistar MeSH
- Cell Survival MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Teichoic Acids MeSH
- Lipopolysaccharides MeSH
- lipoteichoic acid MeSH Browser
- Nitric Oxide MeSH
- Peptidoglycan MeSH
Similar to lipopolysaccharide (LPS), a product of Gram-negative bacteria, the signal macromolecules of Gram-positive bacteria lipoteichoic acid (LTA) and peptidoglycan (PGN) possess multiple biological activities. They may be a source of misinterpretation of experimental findings. We have found that not only LPS but also LTA and PGN can be detected by the Limulus amebocyte lysate (LAL) assay. All of them stimulate the high output in vitro nitric oxide (NO) production of in rat peritoneal cells. The onset of the NO enhancement was observed with 25-100pg/ml of LPS and 25-100ng/ml of PGN and LTA. Polymyxin B (PMX), if applied at concentration 10,000-fold higher than that of LPS, can completely inhibit the NO and LAL binding responses of LPS. The NO-stimulatory and LAL-binding properties of LTA and PGN are not eliminated by PMX. Handling of LPS contamination with PMX may be associated with serious problems because it possesses intrinsic biological activity and becomes cytotoxic at concentration >25μg/ml. The present findings suggest a convenient alternative avoiding these issues. As monitored by the NO and LAL assays, even high amounts of LPS as well as PGN and LTA can be removed by molecular mass cutoff microfiltration. All types of the filters (3kDa to 100kDa) are equally effective. It is suggested that the microfiltration procedure may be considered as a preferable, general and easy method of sample decontamination.
References provided by Crossref.org