Nicola Costanzo

Dr. Nicola Costanzo

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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1 January 2020 in Journal of Proteomics
Verified
Journal Article
Closed access
BTBruno Tilocca
Bruno Tilocca
NCNicola Costanzo
Nicola Costanzo
VMValeria Maria Morittu
Valeria Maria Morittu
ASANNA ANTONELLA SPINA
ANNA ANTONELLA SPINA
ASalessio soggiu
alessio soggiu
CPCristian Piras
Cristian Piras

1 July 2019 in Journal of Dairy Science
Verified
Journal Article
Closed access
FTFrancesca Trimboli
Francesca Trimboli
NCNicola Costanzo
Nicola Costanzo
VLVincenzo Lopreiato
Vincenzo Lopreiato
CCCarlotta Ceniti
Carlotta Ceniti
VMValeria Maria Morittu
Valeria Maria Morittu
DBDomenico Britti
Domenico Britti
The addition of cow milk during the production of buffalo mozzarella is a common fraud in dairy industries because of the lower price and greater availability of cow milk throughout the year. The aim of this study was to develop a new, rapid, and robust capillary electrophoresis method for detecting and quantifying cow milk in buffalo milk by exploiting cow α-lactalbumin as a marker of adulteration. In particular, a linear calibration curve was generated, using a training set of calibrators consisting of 7 series of 17 buffalo/bovine whey mixtures, obtained after casein precipitation, with increasing percentages of cow whey. The capillary electrophoresis method showed high linearity (R2 = 0.968), repeatability [relative standard deviation (RSD) = 2.11, 3.02, 4.38, and 1.18%, respectively for 5, 10, 20, and 50% of buffalo/bovine whey mixtures], and intermediate precision (RSD = 2.18, 2.49, 5.09, and 3.19%, respectively, for 5, 10, 20, and 50% buffalo/bovine whey mixtures). Moreover, the minimum amount of detectable fraudulent cow milk was 1%, and the limit of quantification was 3.1%.

22 January 2020 in International Journal of Food Science
Verified
Journal Article
Open access
PDF file
NCNicola Costanzo
Nicola Costanzo
CCCarlotta Ceniti
Carlotta Ceniti
ASAdriano Santoro
Adriano Santoro
MCMaria Teresa Clausi
Maria Teresa Clausi
FCFrancesco Casalinuovo
Francesco Casalinuovo
General hygienic parameters and selected foodborne pathogens in raw milk cheeses at the retail level were evaluated. A total of 245 raw milk cheese samples were analysed for total bacterial count, Enterobacteriaceae, E. coli, Salmonella spp., Listeria monocytogenes, coagulase-positive Staphylococci, and staphylococcal enterotoxin. Results showed only 3 samples that were not compliant with European rules on staphylococcal enterotoxin, but coagulase-positive Staphylococci were evidenced in all samples tested. Salmonella spp. and Listeria monocytogenes were never detected whereas E. coli was evidenced in 20 samples. Results suggest a need for improvement of good manufacturing practice and milking operation.

1 January 2012 in Italian Journal of Animal Science
Verified
Journal Article
Open access
ESEleonora Sarno
Eleonora Sarno
ASAdriano M.L. Santoro
Adriano M.L. Santoro
ROSSELLA DI PALOROSSELLA DI PALO
ROSSELLA DI PALO
NCNicola Costanzo
Nicola Costanzo
Microbiological quality of raw milk from eight healthy donkeys reared in Campania Region was investigated. A total of 152 samples were analyzed in order to evaluate the milk safety status trough monitoring mesophilic total bacterial count (TBC) at 32°C and 20°C, psychrophilic TBC at 5°C, Enterobacteriaceae, Salmonella spp., Listeria monocytogenes, Staphylococcus aureus and somatic cell count (SCC). The ranges for mesophilic bacteria at 32°C, 20°C and psy- chrophilic bacteria at 5°C were, respectively, 2.80–4.00 Log CFU/mL, 2.84–3.92 Log CFU/mL and 1.27–2.12 Log CFU/ml. Enterobacteriaceae showed a load ranging between 0.68–1.93 Log CFU/mL. No pathogenic bacteria were isolated. Estimated SCC values were always under 50.000 cells/mL. Additionally quantitative changes of bacterial population in raw bulk milk during eight storing days at 8°C and 3°C, were evaluated. Firstly, fresh bulk milk was contaminated by bacteria with a mean TBC at 32°C and 20°C of 2.71 Log CFU/mL and 2.64 Log CFU/mL, respectively, where...

12 February 2021 in Microbiology Research
Verified
Journal Article
Open access
PDF file
CCCarlotta Ceniti
Carlotta Ceniti
BTBruno Tilocca
Bruno Tilocca
Domenico BrittiDomenico Britti
Domenico Britti
ASAdriano Santoro
Adriano Santoro
NCNicola Costanzo
Nicola Costanzo
In March 2020, the World Health Organization (WHO) declared that the COVID-19 outbreak can be characterized as a pandemic. Human-to-human transmission of the SARS-CoV-2 virus may initially be blamed as the first cause of spread, but can an infection be contracted by ingestion of contaminated food or touching contaminated food surfaces? Recently cold-chain food contamination has been indicated as a possible source of many human cases in China. However, the risk of a food-related COVID-19 infection is still debated since the virus may reach people through a fresh product or packaging, which have been touched/sneezed on by infected people. This review summarizes the most recent evidence on the zoonotic origin of the pandemic, reports the main results regarding the transmission of SARS-CoV-2 through food or a food chain, as well as the persistence of the virus at different environmental conditions and surfaces. Emphasis is also posed on how to manage the risk of food-related COVID-19 spread and potential approaches that can reduce the risk of SARS-CoV-2 contamination.

1 November 2015 in Journal of Food Protection
Verified
Journal Article
Closed access
NCNicola Costanzo
Nicola Costanzo
ESEleonora Sarno
Eleonora Sarno
VPVincenzo Peretti
Vincenzo Peretti
LCLucia Ciambrone
Lucia Ciambrone
FCFrancesco Casalinuovo
Francesco Casalinuovo
ASAdriano Santoro
Adriano Santoro
Hepatitis E virus (HEV) infection is a common acute hepatitis transmitted by the fecal-oral route. In developed countries, the virus has a zoonotic potential, and domestic pigs and wild boars are considered main reservoirs. To assess the prevalence of HEV-positive animals in the Calabria region (southern Italy) on a serological and molecular level, a total of 216 autochthonous healthy pigs (Apulo-Calabrese breed) were sampled. Both sera and feces were collected. Pigs were grouped based on age: 117 pigs 6 months. By using a commercial enzyme-linked immunosorbent assay system, a total of 173 (80%) of the 216 pigs tested seropositive. In all sampled farms (n = 8), pigs with antibodies (immunoglobulin G) against HEV were detected at a level higher than 60%, with a significant difference among age groups (P < 0.0001). Moreover, 16 fattening pigs were found to be nested reverse transcription PCR positive and thus to shed viral genomes in their feces. These positive findings resulted in a prevalence of 48.4% on the farm level (16 of 35 pigs) and an overall prevalence of 7.4% at the animal level (16 of 216 pigs). Based on the present study, HEV seems to circulate among the autochthonous domestic pig population of southern Italy with a low sharing rate. Further studies exploring the origin of infection are needed to minimize the risk of human exposure and to reduce consequences for public health.