z-logo
Premium
Differentiation of live, dead and treated cells of Escherichia coli O157:H7 using FT‐IR spectroscopy
Author(s) -
Davis R.,
Deering A.,
Burgula Y.,
Mauer L.J.,
Reuhs B.L.
Publication year - 2012
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/j.1365-2672.2011.05215.x
Subject(s) - escherichia coli , microbiology and biotechnology , enterobacteriaceae , bacteria , spectroscopy , chemistry , biology , biochemistry , genetics , gene , physics , quantum mechanics
Abstract Aims:  To apply specific collection techniques and spectroscopy to differentiate between live and dead Escherichia coli O157:H7 cells, as well as cells subjected to various inactivation treatments, including heat, salt, UV, antibiotics and alcohol. Methods and Results:  Fourier transform‐infrared (FT‐IR) spectroscopy was used to analyse E. coli O157:H7 cells, after filtration or immunomagnetic collection. Partial least squares analysis of the spectra quantified live E. coli O157:H7 in the presence of dead cells with an R 2  > 0·996. Canonical variate analysis (CVA) not only differentiated between spectra of 100% dead and 100% live cells but also between 1% live : 99% dead and 100% dead. CVA using principal components also differentiated between the spectra of the differentially treated cells at a 95% confidence level, and Cooman plots showed clear separation between clusters of spectra of bacteria exposed to the different inactivation treatments. Mahalanobis distances (MD) corroborated the results of CVA. Conclusions:  These results demonstrated the effectiveness of rapid cell collection and FT‐IR spectroscopy techniques to differentiate between live and dead E. coli O157:H7 cells. Significance and Impact of the Study:  This technique has potential applications for use with foods subjected to various inactivation treatments.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here