Food adulteration and fraudulent practices are widely observed in the food industry worldwide and are of great concern for Balkan countries. This study aims at investigating the level of undeclared pork meat in commercial beef and chicken meat products sold in Kosovo by implying one commercial enzyme-linked immunosorbent assay (ELISA) and two confirmatory real-time polymerase chain reaction (PCR) approaches [ready-to-use real-time PCR and real-time PCR with primers specific for pork mitochondrial deoxyribonucleic acid (DNA)]. In supermarkets in the capital city, Prishtina, 62 meat products were randomly sampled, and the three methods were applied. Additionally, these three approaches were evaluated for their practicability, reproducibility, and cost. The results showed that pork was present in 32% of beef- and 8% chicken-based products. ELISA and real-time PCR with pork specific primers showed 100% of reproducibility for beef- and chicken-based products. In contrast, the ready-to-use real-time PCR kit showed 100% reproducibility in chicken-, but only 75% in beef-based samples. ELISA was more rapid than both real-time PCR approaches, but it was more challenging when large numbers of samples were processed. The real-time PCR approach with pork specific primers was the cheapest, while the ready-to-use real-time PCR was the most practical method. Commercial ELISA, in combination with real-time PCR with pork specific primers, provides a reliable and affordable testing methodology that can be implemented for rapid detection and monitoring of pork adulteration in diverse commercial foods.
An 8-week experiment was conducted to study the effect of added Natuphos® 5000 phytase in corn–soybean meal-based diets on laying hens fed different levels of crude protein (CP) (14 and 17%). Two levels of phytase enzyme were used: 0 and 600 Phytase Units (FTU)/kg feed. The experiment used 144 Hisex Brown laying hens in a 2 × 2 factorial design. Four treatments and three replicates per treatment with 12 hens per replicate were used. Egg production was recorded daily while egg weight was assessed on 13th and 14th day of each two-week period to calculate total egg mass. Total excreta were collected and approximately 10% of the amount was used for analysis after drying in a forced draft oven. The results showed no significant effect of added phytase on excreta Calcium (Ca) content, but significantly lower Magnesium (Mg) content was observed with phytase (3.54, 2.48, 3.13 and 2.75 % for hens fed 14% CP no phytase, 14% CP + phytase, 17% CP no phytase, and 17% CP + phytase, respectively). Added phytase also significantly decreased Mg excretion measured as grams/kg of egg mass (21.43, 12.47, 16.76 and 14.75 g/kg egg mass for hens of respective dietary treatments. Phytase had a strong effect on Zink (Zn) levels with 438.96, 369.17, 434.38 and 374.58 mg Zn/kg dry excreta of hens. Similar results were observed with Cu. Added phytase significantly reduced the excreta content and the excretion of Cu. The results of this experiment indicate that adding 600 FTU to laying hen diets containing 14% CP decreases the excretion of Mg, Zn and Cu without any adverse effects on the egg mass produced of laying hens.
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