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Dive into the research topics where Carlo Brera is active.

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Featured researches published by Carlo Brera.


Food and Chemical Toxicology | 2009

Climate change and food safety: An emerging issue with special focus on Europe

M. Miraglia; Hans J.P. Marvin; Gijs Kleter; Paola Battilani; Carlo Brera; E. Coni; F. Cubadda; L. Croci; B. De Santis; S. Dekkers; L. Filippi; R.W.A. Hutjes; M.Y. Noordam; M. Pisante; Gianfranco Piva; Aldo Prandini; L. Toti; G.J. van den Born; A. Vespermann

According to general consensus, the global climate is changing, which may also affect agricultural and livestock production. The potential impact of climate change on food security is a widely debated and investigated issue. Nonetheless, the specific impact on safety of food and feed for consumers has remained a less studied topic. This review therefore identifies the various food safety issues that are likely to be affected by changes in climate, particularly in Europe. Amongst the issues identified are mycotoxins formed on plant products in the field or during storage; residues of pesticides in plant products affected by changes in pest pressure; trace elements and/or heavy metals in plant products depending on changes in their abundance and availability in soils; polycyclic aromatic hydrocarbons in foods following changes in long-range atmospheric transport and deposition into the environment; marine biotoxins in seafood following production of phycotoxins by harmful algal blooms; and the presence of pathogenic bacteria in foods following more frequent extreme weather conditions, such as flooding and heat waves. Research topics that are amenable to further research are highlighted.


Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment | 1989

A study of the contamination by ochratoxin A of green and roasted coffee beans

C. Micco; M. Grossi; Marina Miraglia; Carlo Brera

A study was performed to evaluate the contamination by ochratoxin A in coffee beans. Twenty-nine samples of green coffee were collected from large lots of material by representative sampling. The analyses of green coffee samples showed a significantly high contamination percentage (58%) ranging from 0.2 to 15 micrograms/kg. Naturally and artificially contaminated samples were roasted at different operation times (5-6 min) to verify the percentage of destruction of the mycotoxin. The percentage ranged from 48% to 87% and from 90% to 100% in artificially and naturally contaminated samples respectively. The beverages prepared from artificially contaminated coffee using the most common types of coffee makers showed no residues of ochratoxin A.


Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment | 1995

Evaluation of ochratoxin A level in human milk in Italy

C. Micco; Marina Miraglia; Carlo Brera; S. Corneli; A. Ambruzzi

In order to estimate the incidence of ochratoxin A (OA) in biological fluids, a study was carried out to determine the concentration of OA in breast milk of donor mothers in Italy. Out of 111 samples, 22 were contaminated in the range 0.1-12 micrograms/kg.


Journal of Food Protection | 2004

Effect of industrial processing on the distribution of fumonisin B1 in dry milling corn fractions.

Carlo Brera; Francesca Debegnach; Silvana Grossi; Marina Miraglia

The aim of this study was to investigate the distribution of fumonisin B1 in various corn milling fractions processed by an industrial plant. Corn kernels and six derived milling fractions (germ, bran, large and small grits, animal feed flour, and flour) were sampled. In addition, in order to evaluate the effect of cooking, samples of polenta were prepared starting from naturally contaminated flour obtained from the industrial processing cycle. The industrial plant worked continuously at a rate of 60 tons per day. Two sublots of 5 tons each were investigated with samples of derived products taken at regular time intervals. Due to a similar heterogeneous distribution of fumonisin B1 with other mycotoxins, such as aflatoxins, the sampling scheme was derived from the European Directive 98/53 for aflatoxins. Both lots of kernels showed fumonisin contamination at 4.54 and 5.09 mg/kg, respectively. Germ, bran, and animal feed flour showed contamination levels, namely 8.92 mg/kg (lot 1) and 9.56 mg/kg (lot 2), 7.08 mg/kg (lot 1) and 8.08 mg/kg (lot 2), and 9.36 mg/kg (lot 1) and 6.86 mg/kg (lot 2) higher than large and small grits and flour (0.39 mg/kg [lot 1] and 0.42 mg/kg [lot 2], 0.60 mg/kg [lot 1] and 1.01 mg/kg [lot 2], and 0.40 mg/kg [lot 1] and 0.45 mg/kg [lot 2], respectively). These results seem to account both for the industrial yields of the derived products and the distribution of fumonisin contamination in a kernel. The cooking of polenta in a domestic pressure cooker did not affect fumonisin contamination because the mycotoxin concentrations were similar to those of the starting flour (0.40 and 0.45 mg/kg).


Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment | 2005

The role of sampling in mycotoxin contamination: An holistic view

Marina Miraglia; B. De Santis; V. Minardi; Francesca Debegnach; Carlo Brera

The need to obtain a representative sample deserves particular consideration since a wrong sampling plan can greatly affect the reliability of the measured levels of mycotoxins. This can even result in legal disputes and barriers to trade. Reported here is an holistic view for an ideal sampling plan, which is based on two consecutive steps: (i) To establish ‘why, where and when’ sampling has to be performed by assessing the purpose, the appropriate time and the site for collecting the samples; (ii) To establish ‘how’ to draw samples by assessing practical ad hoc guidelines, considering that, for bulk goods in particular, mycotoxins are not at all homogeneously distributed in a lot. So far, step 1 is not yet covered by specific guidelines while for step 2, European regulations establish the procedures for the sampling of bulk and retail products potentially contaminated by mycotoxins.


Journal of Agricultural and Food Chemistry | 2008

Ochratoxin a contamination in italian wine samples and evaluation of the exposure in the italian population.

Carlo Brera; Francesca Debegnach; V. Minardi; Elisabetta Prantera; Elena Pannunzi; Silvia Faleo; Barbara De Santis; Marina Miraglia

The scope of this study was to evaluate the exposure of the Italian population to ochratoxin A (OTA) attributable to wine consumption. With this aim 1166 wine samples (773 red wines, 290 white, 75 rose, and 28 dessert wines), collected in 19 different Italian regions and mostly produced between 1988 and 2004, were analyzed for OTA content. The obtained results are reported by year of harvest, geographical area of production, and type of wine. Red wine showed the highest maximum level of contamination (7.50 ng/mL), even though rose wines were characterized by a higher mean value (0.01 ng/mL). A gradually increasing mean concentration was also observed from the north (0.05 ng/mL) to south of Italy (0.54 ng/mL). Exposure calculations, performed using two different consumption databases, indicate a daily intake for consumer only of 0.59 up to 1.24 ng/(kg of b.w.)/day and of 0.33 up to 0.90 ng/(kg of b.w.)/day for the total population. Even in the worst case, corresponding to the calculation of the intake for consumers only in southern Italy and Islands and considering the mean consumption data increased by 1 standard deviation, a quite low exposure (1.68 ng/(kg of b.w.)/day, accounting for 9.8% of TDI) was obtained. Considering the overall OTA dietary exposure, obtained exposure rates indicate that wine did not pose a risk to the Italian population health.


Food Additives and Contaminants Part A-chemistry Analysis Control Exposure & Risk Assessment | 1988

Long-term administration of low doses of mycotoxins to poultry. 1. Residues of aflatoxin B1 and its metabolites in broilers and laying hens.

C. Micco; Marina Miraglia; R. Onori; Carlo Brera; A. Mantovani; A. Ioppolo; D. Stasolla

A study was performed to determine aflatoxin residues in tissues and organs of male broilers and hens that had been fed a diet contaminated with 50 micrograms/kg aflatoxin B1 (AFB1). Residue levels of AFB1, aflatoxicol (Ro), aflatoxin M1 (AFM1) and aflatoxin B2a (AFB2a) were determined by an HPLC method and, with the exception of AFB2a, were detected in the liver, kidney and thigh of both male broilers and hens. The highest levels found were for Ro in liver (1.10 and 0.60 micrograms/kg for male broilers and hens, respectively). On the other hand no detectable amounts of aflatoxins were found in any tissue after withdrawal periods of 14 and 33 days for male broilers and laying hens respectively.


Talanta | 2011

Simultaneous determination of aflatoxins and ochratoxin A in baby foods and paprika by HPLC with fluorescence detection: A single-laboratory validation study

Carlo Brera; F. Debegnach; B. De Santis; Elena Pannunzi; C. Berdini; E. Prantera; E. Gregori; M. Miraglia

Mycotoxins are toxic secondary metabolites of fungal origin, the major mycotoxins of food concern are aflatoxins and ochratoxin A. Due to the wide range of matrices susceptible to mycotoxin contamination, the possible co-occurrence, and the very wide range of concentration, validated versatile multi-mycotoxin and multi-matrix methods are strongly requested. A reversed phase HPLC method for the simultaneous determination of aflatoxins and ochratoxin A in baby foods and paprika was set up. Three bulk samples were prepared according to commercial availability, one for paprika and for baby foods, two different bulks were set, a corn based and a multi-cereal based baby food. A single-laboratory validation was performed, for each investigated level ten analyses were performed, relative standard deviations of repeatability (RSD(r)) and recovery factors were calculated; RSD(r) values ranged from 2% to 10% for AFB(1) and from 3% to 10% for OTA, while the recovery factors ranged from 86% to 96% for AFB(1) and from 77% to 96% for OTA. The checked compliance of the RSD(r) and recovery with the values reported in the current EU Regulations confirmed the fitting for purpose of the method. Limit of detection and LoQ values of the method were respectively 0.002 and 0.020 μg/kg for AFB(1) and 0.012 and 0.080 μg/kg for OTA in baby foods; and 0.002 and 0.200 μg/kg for AFB(1) and 0.012 and 0.660 μg/kg for OTA in paprika. The current method represents a good example of the possibility of a multi-mycotoxin and/or a multi-matrix analysis depending on the laboratory research or official control purposes.


Nutritional Neuroscience | 2015

Environment, dysbiosis, immunity and sex-specific susceptibility: A translational hypothesis for regressive autism pathogenesis

Alessandra Mezzelani; Martina Landini; Francesco Facchiano; Maria Elisabetta Raggi; Laura Villa; Massimo Molteni; Barbara De Santis; Carlo Brera; Anna Maria Caroli; Luciano Milanesi; Anna Marabotti

Abstract Background Autism is an increasing neurodevelopmental disease that appears by 3 years of age, has genetic and/or environmental etiology, and often shows comorbid situations, such as gastrointestinal (GI) disorders. Autism has also a striking sex-bias, not fully genetically explainable. Objective Our goal was to explain how and in which predisposing conditions some compounds can impair neurodevelopment, why this occurs in the first years of age, and, primarily, why more in males than females. Methods We reviewed articles regarding the genetic and environmental etiology of autism and toxins effects on animal models selected from PubMed and databases about autism and toxicology. Discussion Our hypothesis proposes that in the first year of life, the decreasing of maternal immune protection and child immune-system immaturity create an immune vulnerability to infection diseases that, especially if treated with antibiotics, could facilitate dysbiosis and GI disorders. This condition triggers a vicious circle between immune system impairment and increasing dysbiosis that leads to leaky gut and neurochemical compounds and/or neurotoxic xenobiotics production and absorption. This alteration affects the ‘gut-brain axis’ communication that connects gut with central nervous system via immune system. Thus, metabolic pathways impaired in autistic children can be affected by genetic alterations or by environment–xenobiotics interference. In addition, in animal models many xenobiotics exert their neurotoxicity in a sex-dependent manner. Conclusions We integrate fragmented and multi-disciplinary information in a unique hypothesis and first disclose a possible environmental origin for the imbalance of male:female distribution of autism, reinforcing the idea that exogenous factors are related to the recent rise of this disease.


Journal of Liquid Chromatography & Related Technologies | 2003

Automated HPLC method for the determination of ochratoxin A in wine samples

Carlo Brera; Silvana Grossi; Barbara De Santis; Marina Miraglia

Abstract Recently food safety issues received increasing attention and they will be more and more the matter of interest of risk assessors. Among the others, Ochratoxin A (OTA) contamination in wine resulted in an emerging risk for consumers. Recently, both monitoring programs and researches have been performed, aimed at individuating the status of contamination world‐wide and critical control points in the wine‐making chain. At the moment, all studies confirmed that red wines resulted in contamination more frequently and at higher levels than white wines. This paper describes a study to carry out an automated method of analysis for the determination of OTA in wine samples, in order to process a high number of samples for Hazard Analysis Critical Control Points (HACCP) purposes. Method performance characteristics, such as repeatability, internal reproducibility, and accuracy, showed good performance and reliability of the method, adequately matching with the criteria suggested by Comité Européen de Normalisation (CEN) for the analysis of mycotoxins. The advantages coming out from this method are, therefore, the saving of time of analysis, the possibility to analyze large amounts of samples, the reduction of the employment of personnel, and the obtaining of all the requirements requested by the national legislation dealing with the official control of foodstuffs.

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Marina Miraglia

Istituto Superiore di Sanità

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Francesca Debegnach

Istituto Superiore di Sanità

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Barbara De Santis

Istituto Superiore di Sanità

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Emanuela Gregori

Istituto Superiore di Sanità

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R. Onori

Istituto Superiore di Sanità

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Elena Pannunzi

National Institutes of Health

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B. De Santis

National Institutes of Health

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Elisabetta Prantera

Istituto Superiore di Sanità

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Brunella Miano

Istituto Superiore di Sanità

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C. Micco

Istituto Superiore di Sanità

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