The sustainability of food systems is of growing concern worldwide, so insects are a growing source of animal proteins for food and feed. Among insect species, the house cricket, Acheta domesticus, is a promising option from a sustainability point of view. This study aimed at evaluating both microbiological and chemical stability of A. domesticus powders during one year of storage at room temperature. Our study was conducted on cricket powders obtained by three different processes: drying at 80°C (P80), drying at 120°C (P120), and lyophilization (PL). Regarding microbiological profile, the pathogens Listeria monocytogenes and Salmonella were not detected, while total viable count and lactic acid bacteria tended to decrease during the storage period. Bacillus cereus was detected at low counts during the entire storage period, but only one replicate of P80 exceeded the limit set for A. domesticus by the European Commission Implementing Regulation 2017/2470. The measured protein contents of the cricket powders immediately after production ranged between 60.6 and 64.3%. The peroxide values were far higher than the limit established by the EU Regulation in all samples. Higher amounts of hexanal and pentanal were detected in P80 and P120 than in PL, indicating that oven drying could enhance lipid oxidation. In conclusion, a one year shelf-life can suitably be ascribed to the analyzed cricket powders from a microbiological point of view, but lacked chemical stability and had a clear early tendency toward rancidity. The samples dried at 120°C and lyophilized never exceeded the limit set by European Commission for B. cereus count in A. domesticus powder. In addition, lyophilized samples showed the lowest values of hexanal and pentanal, the aldehydes that are primarily responsible for the rancid smell. The oxidative status of the final products could be strongly influenced by the powder processing, so for this reason, edible insect species-specific post-rearing protocols should be implemented. These results open an interesting scenario for a long period of storage of insect powder in the absence of a cold chain, making the insect market an increasingly sustainable sector.

Thermal desorption direct analysis in real‐time high‐resolution mass spectrometry (TD‐DART‐HRMS) approaches have gained popularity for fast screening of a variety of samples. With rapid volatilization of the sample at increasing temperatures outside the mass spectrometer, this technique can provide a direct readout of the sample content with no sample preparation. In this study, TD‐DART‐HRMS's utility for establishing spice authenticity was examined. To this aim, we directly analyzed authentic (typical) and adulterated (atypical) samples of ground black pepper and dried oregano in positive and negative ion modes. We analyzed a set of authentic ground black pepper samples (n = 14) originating from Brazil, Sri Lanka, Madagascar, Ecuador, Vietnam, Costa Rica, Indonesia, Cambodia, and adulterated samples (n = 25) consisting of mixtures of ground black pepper with this spice's nonfunctional by‐products (pinheads or spent) or with different exogenous materials (olive kernel, green lentils, black mustard seeds, red beans, gypsum plaster, garlic, papaya seeds, chili, green aniseed, or coriander seeds). TD‐DART‐HRMS facilitated the capture of informative fingerprinting of authentic dried oregano (n = 12) originating from Albania, Turkey, and Italy and those spiked (n = 12) with increasing percentages of olive leaves, sumac, strawberry tree leaves, myrtle, and rock rose. A predictive LASSO classifier was built, after merging by low‐level data fusion, the positive and negative datasets for ground black pepper. Fusing multimodal data allowed retrieval of more comprehensive information from both datasets. The resultant classifier achieved on the withheld test set accuracy, sensitivity, and specificity of 100%, 75%, and 90%, respectively. On the contrary, the sole TD‐(+)DART‐HRMS spectra of the oregano samples allowed construction of a LASSO classifier that predicted the adulteration of the oregano with excellent statistical indicators. This classifier achieved, on the withheld test set, 100% each for accuracy, sensitivity, and specificity.

The study aimed to assess the seasonal variation in raw milk volatile organic compounds (VOCs) from three indoor feeding systems based on maize silage (n = 31), silages/hay (n = 19) or hay (n = 16). After headspace solid-phase microextraction (HS-SPME), VOC profiles were determined by gas chromatography (GC). Chemical and VOC (log₁₀ transformations of the peak areas) data were submitted to a two-way ANOVA to assess the feeding system (FS) and season (S) effects; an interactive principal component analysis (iPCA) was also performed. The interaction FS × S was never significant. The FS showed the highest (p < 0.05) protein and casein content for hay-milk samples, while it did not affect any VOCs. Winter milk had higher (p < 0.05) proportions of protein, casein, fat and some carboxylic acids, while summer milk was higher (p < 0.05) in urea and 2-pentanol and methyl aldehydes. The iPCA confirmed a seasonal spatial separation. Carboxylic acids might generate from incomplete esterification in the mammary gland and/or milk lipolytic activity, while aldehydes seemed to be correlated with endogenous lipid or amino acid oxidation and/or feed transfer. The outcomes suggested that VOCs could be an operative support to trace raw milk for further mild processing.

Raw milk cheeses harbor complex microbial communities. Some of these microorganisms are technologically essential, but undesirable microorganisms can also be present. While most of the microbial dynamics and cross-talking studies involving interaction between food-derived bacteria have been carried out on agar plates in laboratory-controlled conditions, the present study evaluated the modulation of the resident microbiota and the changes of metabolite production directly in ripening raw milk cheese inoculated with Listeria innocua strains. Using a proxy of the pathogenic Listeria monocytogenes, we aimed to establish the key microbiota players and chemical signals that characterize Latteria raw milk cheese over 60 days of ripening time. The microbiota of both the control and Listeria-inoculated cheeses was analyzed using 16S rRNA targeted amplicon sequencing, while direct analysis in real time mass spectrometry (DART-HRMS) was applied to investigate the differences in the metabolic profiles of the cheeses. The diversity analysis showed the same microbial diversity trend in both the control cheese and the inoculated cheese, while the taxonomic analysis highlighted the most representative genera of bacteria in both the control and inoculated cheese: Lactobacillus and Streptococcus. On the other hand, the metabolic fingerprints revealed that the complex interactions between resident microbiota and L. innocua were governed by continuously changing chemical signals. Changes in the amounts of small organic acids, hydroxyl fatty acids, and antimicrobial compounds, including pyroglutamic acid, hydroxy-isocaproic acid, malic acid, phenyllactic acid, and lactic acid, were observed over time in the L. innocua-inoculated cheese. In cheese that was inoculated with L. innocua, Streptococcus was significantly correlated with the volatile compounds carboxylbenzaldheyde and cyclohexanecarboxylic acid, while Lactobacillus was positively correlated with some volatile and flavor compounds (cyclohexanecarboxylic acid, pyroxidal acid, aminobenzoic acid, and vanillic acid). Therefore, we determined the metabolic markers that characterize a raw milk cheese inoculated with L. innocua, the changes in these markers with the ripening time, and the positive correlation of flavor and volatile compounds with the resident microbiota. This multi-omics approach could suggest innovative food safety strategies based on the enhanced management of undesirable microorganisms by means of strain selection in raw matrices and the addition of specific antimicrobial metabolites to prevent the growth of undesirable microorganisms.

Differential mobility spectrometry (DMS) enables the detection and separation of volatile organic compounds, exploiting differences in ion mobility under varying electric fields, which enhance the resolution of complex mixtures. In this study, DMS, upon integration with chemometrics, enabled the differentiation of the botanical origins of Italian honeys. Utilizing a benchtop differential mobility spectrometer connected to pure air, 219 monofloral honeys of five different botanical origins (acacia, chestnut, citrus, eucalyptus, and linden) were simultaneously analyzed in positive and negative ion modes and with the analysis duration of less than 2 min. Repeatability of the resultant volatilomic fingerprints was verified by cosine similarity with the subsequent elimination of the nonrepeatable data. Afterward, the data for both polarities were concatenated, and an exploratory investigation was carried out into the discrimination capabilities of DMS by principal component analysis. The merged data were then submitted to a statistical analysis for classification. The performance of the resultant random forest (RF) classifier was evaluated by repeated cross-validation and resubstitution into the training set, and finally, this classifier was validated on a withheld subset of data. The performances of the classification model for each test were evaluated by calculating the contingency table-derived parameters of accuracy, Matthew's correlation coefficient (MCC), sensitivity, and specificity. The RF classifier produced high-performance values when predicting the botanical origin of the honey in both training (MCC 84.8%, accuracy 88.0%, sensitivity 87.5%, and specificity 96.9%) and validation subsets (MCC 82.6%, accuracy 86.3%, sensitivity 85.7%, and specificity 96.5%). Some limitations, expected to be mitigated by further research, were encountered in the correct classification of acacia honey.