Ingrid Sousa

Mrs. Ingrid Sousa


Research Focus & Metrics

Academic Career Length

2Years (2025-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 June 2025 in Journal of Dairy Science
Verified
Journal Article
Open access
Gaia MeoniGaia Meoni
Gaia Meoni
ISIngrid Sousa
Ingrid Sousa
Leonardo TenoriLeonardo Tenori
Leonardo Tenori
GNGiovanni Niero
Giovanni Niero
MPMarta Pozza
Marta Pozza
CMCarmen L. Manuelian
Carmen L. Manuelian
The rising demand for nondairy and nonanimal protein sources has increased plant-based beverages (PBB) consumption. However, research on their functional properties, metabolic profile, and discrimination potential is limited. This study evaluated the potential of proton nuclear magnetic resonance (1H NMR) spectroscopy as an authentication method to discriminate milk (cow and goat) and PBB macro-groups, including soy-based, fruit-based (almond and coconut), and cereal-based (rice and oat) beverages, based on their metabolic profile. A total of 22 PBB (soy-, almond-, coconut-, rice-, and oat-based beverages), 4 cow milk, and 4 goat milk cartons were analyzed with 1H NMR spectroscopy to obtain their metabolic profile. Relevant metabolites to discriminate PBB macro-groups and cow and goat milk were identified through the Mann-Whitney U test and partial least squares-discriminant analysis. Results revealed that uridine diphosphate, glucose, and adenosine were key metabolites for the identification of goat and cow milk. At the same time, choline and guanosine emerged as important markers for different PBB macro-group detection. In addition, lactose played a significant role in differentiating milk from PBB. In conclusion, these findings represent an initial step toward applying 1H NMR spectroscopy for authentication and nutritional analysis of PBB, opening the door for further research into their authenticity and metabolic profiling.

1 January 2026 in JDS Communications
Verified
Journal Article
Open access
EVE. Visentin
E. Visentin
ISIngrid Sousa
Ingrid Sousa
SMSilvia Magro
Silvia Magro
SSS. Sabbadin
S. Sabbadin
GNGiovanni Niero
Giovanni Niero
MMMassimo De Marchi
Massimo De Marchi
Summary: The aim of this study was to validate a chromatographic method to detect and quantify allantoin, creatinine, and uric acid in cow urine samples. The method featured a simple chromatographic separation, yielding well-defined peaks. High repeatability and reproducibility were achieved, with optimal linearity performances. Excellent recovery rates were obtained, especially for allantoin and creatinine. The findings of this study confirm the effectiveness of the method in analyzing target compounds, laying the foundation for a better understanding of physiological responses to heat stress, one of the major challenges facing the future of the livestock sector.

28 November 2025 in Metabolites
Verified
Journal Article
Open access
PDF file
ISIngrid Sousa
Ingrid Sousa
Gaia MeoniGaia Meoni
Gaia Meoni
Leonardo TenoriLeonardo Tenori
Leonardo Tenori
MPMarta Pozza
Marta Pozza
MMMassimo De Marchi
Massimo De Marchi
GNGiovanni Niero
Giovanni Niero
Background/Objectives: Metabolites are low-molecular-weight organic compounds (<1 kDa) that act as intermediates and end products of cellular metabolism. Their characterization provides valuable information on the nutritional quality, functionality, and potential health impacts of food products. In the dairy sector, proton nuclear magnetic resonance (1H NMR) spectroscopy has emerged as a powerful tool for metabolite profiling, enabling the simultaneous identification and quantification of diverse compounds. In this study, 1H NMR was applied to characterize and compare the metabolic composition of whey, a major by-product of cheese and yogurt production, and whey protein concentrate (WPC-80), a whey derivative containing approximately 80% protein by weight and rich in essential amino acids. Methods: Five whey and four WPC-80 samples from a single Parmigiano Reggiano dairy plant were collected, each representing a biologically independent sample. Statistical evaluation was performed using Mann–Whitney U tests to identify significantly different metabolites between groups, while principal component analysis and partial least squares discriminant analysis were employed to assess group separation and determine discriminant metabolites. Results: The results revealed marked compositional differences: whey was higher in dimethyl sulfone, succinate, orotate, fumarate, and lactose (p < 0.05), whereas WPC-80 contained significantly higher levels of histidine, formate, glucose + glucose-6-phosphate, acetate, and choline (p < 0.05). Moreover, metabolites such as hippurate, valine, lactate + threonine, and uracil were exclusively found on whey and not in WPC-80, likely due to processing steps such as ultrafiltration. Conclusions: These findings highlight the metabolic distinctions introduced by WPC-80 processing from Parmigiano Reggiano whey and provide insights into the nutritional and functional characteristics of whey-derived products. Such knowledge can inform the design of innovative dairy ingredients and functional foods, with potential benefits for both industry applications and consumer health.