Abstract

Near infrared hyperspectral imaging (NIR-HSI) and multivariate image analysis were used to distinguish between foodborne pathogenic bacteria, Bacillus cereus, Escherichia coli, Salmonella Enteritidis, Staphylococcus aureus and a non- pathogenic bacterium, Staphylococcus epidermidis. Hyperspectral images of bacteria, streaked out on Luria—Bertani agar, were acquired after 20 h, 40 h and 60 h growth at 37 °C using a SisuCHEMA hyperspectral pushbroom imaging system with a spectral range of 920–2514 nm. Three different pre-processing methods: standard normal variate (SNV), Savitzky—Golay (1stderivative, 2nd order polynomial, 15-point smoothing) and Savitzky—Golay (2nd derivative, 3rd order polynomial, 15-point smoothing) were evaluated. SNV provided the most distinct clustering in the principal component score plots and was thus used as the sole pre-processing method. Partial least squares discriminant analysis (PLS-DA) models were developed for each growth period and was tested on a second set of plates, to determine the effect the age of the colony has on classification accuracies. The highest overall prediction accuracies where test plates required the least amount of growth time, was found with models built after 60 h growth and tested on plates after 20 h growth. Predictions for bacteria differentiation within these models ranged from 83.1 % to 98.8 % correctly predicted pixels.

Highlights

  • The widespread occurrence of foodborne diseases in developed and developing countries indicate underlying food safety flaws in adequate pathogen detection.[1]

  • We decided to refrain from using selective media as these could result in the production of substances that would interfere with near infrared (NIR) hyperspectral imaging measurements

  • When studying the Principal component analysis (PCA) score plots (Figures 3a–d), it was found that standard normal variate (SNV)-pretreated data produced the best clustering for all groups over the three growth periods

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Summary

Introduction

The widespread occurrence of foodborne diseases in developed and developing countries indicate underlying food safety flaws in adequate pathogen detection.[1] Conventional methods for pathogen detection and identification are labour intensive and time consuming—often taking two to three days for initial results (enrichment and growth on specialised media) and up to a week for species identification. Pure culture identifications are typically required for regulatory and legal purposes.[2] rapid methods for pathogen detection and improvements on existing methods are constantly being investigated. Near infrared (NIR) hyperspectral imaging (HSI) has been explored as a tool to differentiate pathogenic bacteria from each other as well as from non-pathogenic bacteria.[3,4,5,6] Barbin et al.[7] determined total viable count (TVC) and psychrotrophic plate count (PPC) on porcine meat over 21 days.

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