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The aim of this study was to estimate the aflatoxin M1 (AFM1) contamination in raw milk and processed milk (pasteurized or UHT) collected from two regions in Italy (Puglia and Basilicata) during a 12-year period: 2012–2023. A total of 1017 milk samples were analyzed first proceeding with screening analysis by enzyme-linked immunosorbent assay (ELISA), and suspected non-compliant samples (AFM1 concentration higher than 0.042 µg/kg) were then analyzed by high performance liquid chromatographic with fluorimetric detection (HPLC/FLD) confirmation method. AFM1 concentration ≥ 0.005 µg/kg (ELISA limit of quantitation) was detected in 553 of the 1017 milk samples (54.4%). AFM1 levels exceeding the European Union maximum limit (ML) of 0.050 µg/kg were detected in 70 samples, 49 of which were determined as non-compliant samples (4.8%). Particularly high concentrations of AFM1, exceeding 200 µg/kg, were found in four samples, three raw milk and one pasteurized. Regarding this risk exposure study, only the MOE values obtained under "high exposure scenario" were lower than 10,000, while those calculated from the overall mean values resulted as not of concern. [ABSTRACT FROM AUTHOR]

Water basins with low hydrodynamic activities can promote the growth and increase in algal biomass due to eutrophication, and toxic cyanobacteria species might then produce metabolites hazardous to human health. Over the last decade, a neurotoxic non-protein amino acid, (2S)-2-amino-3-(methylamino) propanoic acid, known as β-N-methylamino-L-alanine (BMAA), has become of particular interest because it has been hypothesised to be involved in progressive human neurodegenerative pathologies. This toxin can be found both in algal cells and free in water, as well as in some foods of aquatic and terrestrial origin. Analytical methods used for BMAA are often based on chromatography coupled with mass spectrometry, although these techniques involve long and expensive analysis. As the availability of a faster and cheaper screening method would be useful, we tested the only available Enzyme-Linked Immunosorbent Assay kit for BMAA evaluation and validated methods to verify their reliability for the analysis of water and fish muscle. For both matrices, we determined adequate selectivity and repeatability (relative standard deviation < 6%), with recoveries from 70% to 83% at the tested spiking levels; the methods were also robust. These data appear in contrast to a previous evaluation carried out on the same kit in 2013, although this might depend on an improvement to the kit performance. We can conclude that a preliminary determination of BMAA in water, and also in fish tissue after an adequate extraction procedure, can be performed efficiently with the tested kit, which provides for easier monitoring of this dangerous toxin. [ABSTRACT FROM AUTHOR]

The occurrence of harmful cyanobacterial blooms in surface waters is often accompanied by the production of a variety of cyanotoxins, and these toxins are designed to target in humans specific organs on which they act. When introduced into the soil ecosystem by spray irrigation of crops, they may affect the same molecular pathways in plants having identical or similar target organs, tissues, cells, or biomolecules. There are also several indications that terrestrial plants, including crops, can bioaccumulate cyanotoxins and present, therefore, potential health hazards for humans. During this project, for monitoring purposes, water samples were collected from lake Occhito, in which there was an algal bloom ( Planktothrix rubescens) in 2009, and from three tanks which acted as hydraulic junctions. In addition, crop samples irrigated with water from the three tanks mentioned above were also picked. Finally, the characterization of principal cyanobacteria was performed, to determine the presence of cyanotoxins such as microcystins and validate a method of screening ELISA for the determination of microcystins in vegetable samples and a confirmatory method by HPLC-ESI-MS/MS. [ABSTRACT FROM AUTHOR]