Evaluation of Aspergillus flavus Growth and Detection of Aflatoxin B1 Content on Maize Agar Culture Medium Using Vis/NIR Hyperspectral Imaging

Abstract

The physiological and biochemical processes of Aspergillus flavus (A. flavus) are complex. Monitoring the metabolic evolution of products during the growth of A. flavus is critical to the overall understanding of the fungal and aflatoxin production detection mechanism. The dynamic growth process of A. flavus and the aflatoxin B1 (AFB1) accumulation in culture media was investigated with a visible/near-infrared hyperspectral imaging (Vis/NIR HSI) system in the range of 400 to 1000 nm. First, the growth of A. flavus and the synthesis pattern of AFB1 were monitored on maize agar medium (MAM) culture for 120 h with a 24-h time-lapse imaging interval. Second, to classify the A. flavus growth, a principal component analysis (PCA) was employed, and a support vector machine (SVM) model was established with the PC1–PC3 as inputs. The results suggested that the PCA-SVM method could distinguish the A. flavus growth time with a classification accuracy larger than 0.97, 0.91, and 0.92 for calibration, validation, and cross-validation, respectively. Third, regression models to predict the AFB1 accumulation using hyperspectral images were developed by comparing different pre-processing methods and key wavelengths. The successive projection algorithm (SPA) was adopted to distill the key wavelengths. The experimental results indicated that the standard normal variate transformation (SNV) with the partial least squares regression (PLSR) achieved the optimal regression performance with an RC value of 0.98–0.99 for calibration and RV values of 0.95–0.96 for validation. Finally, a spatial map of the AFB1 concentration was created using the PLSR model. The spatial regularity of the AFB1 concentration was comparable to the measurement performed. The study proved the potential of the Vis/NIR HSI to characterize the A. flavus growth and the concentration of AFB1 on the MAM over time.