Using Nanospray Liquid Chromatography and Mass Spectrometry to Quantitate Shiga Toxin Production in Environmental Escherichia coli Recovered from a Major Produce Production Region in California.
Christopher J SilvaBertram G LeeJaszemyn C YambaoMelissa L Erickson-BeltranBeatriz QuiñonesPublished in: Journal of agricultural and food chemistry (2018)
A set of 45 environmental strains of Shiga toxin producing Escherichia coli (STEC) from three California counties were analyzed for Shiga toxin production by nanospray liquid chromatography-mass spectrometry and Vero cell bioassay. The STEC in this set comprised six serotypes ((O113:H21, O121:H19, O157:H7, O6:H34, O177:H25, and O185:H7) each containing either the stx2a or stx2c operon. Six of the seven O113:H21 were found to contain two distinct stx2a operons. Eight strains of O157:H7 possessed a stx2c operon whose A subunit gene was interrupted by an insertion sequence (IS1203v). Shiga toxin production was induced by nutrient depletion and quantitated by mass spectrometry. The 37 strains produced Shiga toxins in a near 50-fold range (1.4-49 ng/mL). The IS-interrupted strains expressed low but measurable amounts of the B subunits (0.5-1.9 ng/mL). Another strain possessed an identical stx operon without an IS interruption and produced intact Stx2c (5.7 ng/mL).
Keyphrases
- escherichia coli
- mass spectrometry
- liquid chromatography
- high resolution mass spectrometry
- tandem mass spectrometry
- gas chromatography
- high performance liquid chromatography
- klebsiella pneumoniae
- biofilm formation
- simultaneous determination
- capillary electrophoresis
- high resolution
- solid phase extraction
- single cell
- dna methylation
- gene expression
- cell therapy
- pseudomonas aeruginosa
- mesenchymal stem cells
- staphylococcus aureus
- genome wide identification
- genome wide analysis