Abstract

Histamine poisoning is the most common cause of human foodborne illness due to the consumption of fish products. An enzyme-based amperometric biosensor was developed to be used as a screening tool to detect histamine and histamine-producing bacteria (HPB) in tuna. It was developed by immobilizing histidine decarboxylase and horseradish peroxidase on the surface of screen-printed electrodes through a cross-linking procedure employing glutaraldehyde and bovine serum albumin. The signal generated in presence of histamine at the surface of the electrode was measured by chronoamperometry at in presence of a soluble redox mediator. The sensitivity of the electrode was 1.31–1.59 μA/mM, with a linear range from 2 to 20 μg/ml and detection limit of 0.11 μg/ml. In this study fresh tuna filets purchased in supermarkets in different days (n = 8) were analyzed to detect HPB. Samples with different concentration of histamine were analyzed with culture-based counting methods, biosensor and HPLC and also a challenge test was made. Recovery of histamine from cultures and tuna samples was also assessed. The presence of Morganella psychrotolerans, Photobacterium phosphoreum, P. damselae and Hafnia alvei was detected using culture- and PCR-based methods. At the time of purchase these tuna samples had histamine concentrations from below the limit of detection (LOD) to 60 μg/g. HPLC and biosensor methods provided similar results in the range from zero to 432 μg/g (correlation coefficient, R2 = 0.990) and the recovery of histamine from cultures and tuna samples was very high (mean bias −12.69 to 1.63%, with root-mean-square error <12%). These results clearly show that fresh tuna is commonly contaminated with strong HPB. The histamine biosensor can be used by the Food Business Operators as a screening tool to detect their presence and to determine whether their process controls are adequate or not.

Highlights

  • Histamine poisoning is the most common cause of human foodborne illness due to the consumption of fish products

  • With this aim single colonies isolated from the fish samples were cultured in duplicate in 10 ml HD broth at 4◦C for 5 days (P. phosphoreum) or 20◦C for 2 days (M. psychrotolerans and other histamine-producing bacteria (HPB)) and histamine was extracted as described in the section “Extraction of Histamine From Bacterial Cultures and Recovery Tests” and detected by the enzyme-based amperometric biosensor, as described in the section “Histamine Biosensor Calibration and Assay Procedure.”

  • Histamine-producing bacteria were detected in the eight lots of tuna analyzed (Table 1)

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Summary

Introduction

Histamine poisoning is the most common cause of human foodborne illness due to the consumption of fish products. During the period 2010–2015, 12 EU Member States reported 176 food-borne outbreaks caused by histamine associated with the consumption of fish and fish products. These outbreaks involved 961 human cases and 104 of hospitalizations (European Food Safety Authority [EFSA], 2017). The U.S Food & Drug Administration have a 50 mg/kg defect action level for histamine in tuna, mahi-mahi and related fish (FDA, 2011). These limits concern fish and fish products placed on the market during their shelf life

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