OSA's Digital Library

Virtual Journal for Biomedical Optics

Virtual Journal for Biomedical Optics


  • Editor: Gregory W. Faris
  • Vol. 4, Iss. 13 — Dec. 2, 2009

Fluorescence Spectroscopy for Rapid Detection and Classification of Bacterial Pathogens

Miryeong Sohn, David S. Himmelsbach, Franklin E. Barton, and Paula J. Fedorka-Cray

Applied Spectroscopy, Vol. 63, Issue 11, pp. 1251-1255 (2009)

View Full Text Article

Acrobat PDF (391 KB)

Browse Journals / Lookup Meetings

Browse by Journal and Year


Lookup Conference Papers

Close Browse Journals / Lookup Meetings

Article Tools

  • Export Citation/Save Click for help


This study deals with the rapid detection and differentiation of Escherichia coli, Salmonella, and Campylobacter, which are the most commonly identified commensal and pathogenic bacteria in foods, using fluorescence spectroscopy and multivariate analysis. Each bacterial sample cultured under controlled conditions was diluted in physiologic saline for analysis. Fluorescence spectra were collected over a range of 200–700 nm with 0.5 nm intervals on the PerkinElmer Fluorescence Spectrometer. The synchronous scan technique was employed to find the optimum excitation (λex) and emission (λem) wavelengths for individual bacteria with the wavelength interval (Δλ) being varied from 10 to 200 nm. The synchronous spectra and two-dimensional plots showed two maximum λex values at 225 nm and 280 nm and one maximum λem at 335–345 nm (λem = λex + Δλ), which correspond to the λex = 225 nm, Δλ = 110–120 nm, and λex = 280 nm, Δλ = 60–65 nm. For all three bacterial genera, the same synchronous scan results were obtained. The emission spectra from the three bacteria groups were very similar, creating difficulty in classification. However, the application of principal component analysis (PCA) to the fluorescence spectra resulted in successful classification of the bacteria by their genus as well as determining their concentration. The detection limit was approximately 103–104 cells/mL for each bacterial sample. These results demonstrated that fluorescence spectroscopy, when coupled with PCA processing, has the potential to detect and to classify bacterial pathogens in liquids. The methology is rapid (>10 min), inexpensive, and requires minimal sample preparation compared to standard analytical methods for bacterial detection.

Virtual Issues
Vol. 4, Iss. 13 Virtual Journal for Biomedical Optics

Miryeong Sohn, David S. Himmelsbach, Franklin E. Barton, and Paula J. Fedorka-Cray, "Fluorescence Spectroscopy for Rapid Detection and Classification of Bacterial Pathogens," Appl. Spectrosc. 63, 1251-1255 (2009)

Sort:  Journal  |  Reset


References are not available for this paper.

Cited By

OSA is able to provide readers links to articles that cite this paper by participating in CrossRef's Cited-By Linking service. CrossRef includes content from more than 3000 publishers and societies. In addition to listing OSA journal articles that cite this paper, citing articles from other participating publishers will also be listed.

« Previous Article  |  Next Article »

OSA is a member of CrossRef.

CrossCheck Deposited