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The feedstuffs used in dairy animals must be able to give consumers confidence about the wholesomeness of milk with regard to aflatoxin contamination. The aim of this study was to determine the excretion patterns of aflatoxin M1 (AFM1) in the milk of dairy goats fed a single dose of pure aflatoxin B1 (AFB1), which can occasionally occur if feeds are infected by hot-spot growth of molds that produce aflatoxins. Five dairy goats in midlactation were administered 0.8 mg of AFB1 orally. Individual milk samples were collected for 84 h after AFB1 dosage. Aflatoxin M1 was found in milk in the highest concentration. In all goats, AFM1 was not detected in milk before AFB1 administration, but was detected in the first milking following AFB1 administration. The excretion pattern of AFM1 concentration in milk was very similar in all goats even if the values of the concentration differed between animals. The peak values for AFM1 concentration in milk was observed in milk collected during the milking at 3 and 6 h. After the peak, the AFM1 in milk disappeared with a trend that fitted well a monoexponential decreasing function, and the toxin was not detected after 84 h. Only about 0.17% of the amount of AFB1 administered was detected as AFM1 in milk, and about 50% of this was excreted in the first liter of milk yielded after AFB1 intake. Correct procedures to prevent growth of molds, and consequent AFB1 contamination, on the feedstuffs for lactating goats represent the key to providing consumers a guarantee that milk is not contaminated by AFM1. [ABSTRACT FROM AUTHOR]

Dairy products offer an important source of iodine for humans, particularly infants and children. An adequate iodine content in the diet of lactating animals must guarantee a suitable milk iodine concentration. In this experiment, the effects of iodine supplementation of dairy goat diets on the iodine concentration, milk yield, and milk composition of goat milk were studied. Thirty crossbred dairy goats of the Sarda population were divided into 3 groups supplemented with 0 (control group), 0.45 (group 1), or 0.90 (group 2) mg of KI/d per goat. The dose of KI (76.5% of iodine) was dissolved in water and orally administered with a syringe every day for 10 wk. Mean milk iodine concentrations were 60.1 ± 50.5, 78.8 ± 55.4, and 130.2 ± 62.0 μg/L (mean ± SD) in the control group, group 1, and group 2, respectively. The extent of iodine enrichment in milk was approximately 31% in group 1 and 117% in group 2 compared with the control group. Milk yield was not influenced by KI supplementation and averaged 1,229, 1,227, and 1,179 g/d in groups 0, 1, and 2, respectively. Milk urea nitrogen concentration was significantly lower in the KI-supplemented groups (32 and 33 mg/dL in groups 1 and 2, respectively) than in the control group (37 mg/dL). Iodine supplementation of dairy goat diets can increase milk iodine content without adverse effects on milk production traits. [ABSTRACT FROM AUTHOR]

An experiment was carried out to investigate 1) the transfer of aflatoxin M1 (AFM1) into the milk of dairy ewes fed diets naturally contaminated with aflatoxin B1 (AFB1); 2) the effect of the addition of dried yeast culture in the diet on this transfer; and 3) the alteration of enzymatic activities in the liver of ewes fed diets contaminated with AFB1. Twenty-four Sarda dairy ewes were divided in 4 groups and fed a concentrate mix containing 4 amounts of wheat meal naturally contaminated with aflatoxins. The diet of the control group had no wheat meal, whereas that of treated groups had low, medium, or high amounts of contaminated wheat, which corresponded to 1.13, 2.30, and 5.03 μg of AFB1/kg of feed, respectively. The experiment lasted 14 d. On d 8 to 14 from the beginning of the trial, 12 g/d of a commercial dried yeast product (DYP) of Kluyveromyces lactis was added to the diet of each ewe. The AFM1 concentration in individual milk samples and the blood serum metabolites were measured periodically. The presence of AFM1 was first detected in milk on d 1 of administration, and then its concentration increased and approached a steady-state condition on d 3 simultaneously in all treated groups. The AFM1 in milk at the steady-state condition, which was linearly related to the AFB1 intake, was 39.72, 50.38, and 79.29 ng/L in the low-aflatoxin, medium-aflatoxin, and high-aflatoxin groups, respectively. The AFM1 concentration in milk of the high-aflatoxin group was approximately 1.5-fold greater than the European Commission maximum tolerance level (50 ng/kg). The addition of DYP to the diet did not affect the AFM1 concentration in milk. After the withdrawal of the contaminated concentrate mix, the AFM1 mean concentrations decreased quickly and were no longer detected after 3 d in all treated groups. Daily milk yield and composition did not differ because of aflatoxin treatment. Blood serum parameters (creatinine, glutamic oxalacetic transaminase, glutamic pyruvic transaminase, gamma glutamyl transferase, alkaline phosphatase, lactate dehydrogenase, cholesterol, protein, urea, calcium, and phosphorus) were not influenced by AFB1 intake. Therefore, the effect of DYP on certain blood parameters (gamma glutamyl transferase, urea, creatinine, and calcium) could not be attributed to amelioration of the aflatoxin-contaminated diet. In conclusion, diet contamination by AFB1 near the European Union tolerance level (0.005 mg/kg) in complete feed for dairy animals (e.g., high-aflatoxin group) can result in an AFM1 milk concentration higher than the European Commission maximum tolerance level. Transfer of aflatoxin from feed to milk was not affected by dietary addition of a commercial DYP. [ABSTRACT FROM AUTHOR]

The aim of this research was to determine the effect of adding extruded linseed cake to the dry diet of goats on the concentrations of conjugated linoleic acid (CLA) and vaccenic acid (VA) in milk fat. Thirty crossbreed dairy goats were divided into 3 groups. Their diet was supplemented with 0% (control group), 5% (low group), or 10% (high group) of extruded linseed cake (ELC), which supplied 0, 16, and 32 g/d of linseed fat, respectively. The milk fat percentage (overall mean 3.5%) and yield did not differ with the different diets, but fatty acid composition was affected by the ELC supplements. The inclusion of ELC in the diets did not influence the concentration of fatty acids from C6:0 to C12:0. The concentrations of C14:0 and C16:0 decreased as the quantity of ELC supplements increased. The concentrations (mg/100 mg of total fatty acid methyl esters) of VA (0.70, 1.23, and 1.39 in control, low, and high groups respectively) and cis-9,trans-11 CLA (0.63, 0.96, and 1.05 in control, low, and high groups, respectively) were increased by ELC supplements. The milk fat content of VA and cis- 9,trans-11 CLA were closely correlated (R² = 0.82). Desaturation of VA in the mammary gland to produce cis-9,trans-11 CLA was higher in the control group than in the groups with ELC diets. Extruded linseed cake supplementation to lactating goats may enhance the nutritional profile of milk lipids. [ABSTRACT FROM AUTHOR]

An experiment was carried out using dairy ewes to study the transfer of aflatoxin B1 (AFB1) from feed to milk and from milk to cheese. The effects of AFB1 on liver function and hematological parameters were also investigated. Fifteen ewes were assigned to treatments in replicated 3 x 3 Latin squares. The experimental groups received 32, 64, or 128 µg/d of pure AFB1 for 7 d followed by 5 d of clearance. On the sixth day of the first period, the total daily milk produced by each ewe was collected separately and processed into cheese. The results indicate that the level of AFB1 used did not adversely affect animal health and milk production traits. The aflatoxin M1 (AFM1) concentrations in milk approached a steady-state condition in all treated groups between 2 and 7 d after the start of treatment. The mean AFM1 concentrations of treated groups in steady-state condition (184.4, 324.7, and 596.9 ng/kg in ewes fed 32, 64, or 128 µg of AFB1, respectively) were significantly affected by the AFB1 doses. The AFM1 concentration was linearly related to the AFB1 intake/ kg of BW. The carry-over values of AFB 1 from feed into AFM1 in milk (0.26 to 0.33%) were not influenced by the AFB1 doses. The AFM1 concentrations in curd and whey were linearly related to the AFM1 concentrations in the unprocessed milk. [ABSTRACT FROM AUTHOR]

Focuses on a study which examined the amount of aflatoxin M2 in milk after feeding aflatoxin B1 to lactating dairy ewes. Materials and methods; Results and discussion; Conclusions.

Grape seed is a by-product of the winery and distillery industry which could be used in animal nutrition. To test the hypothesis that dietary supplementation with this by-product can decrease the biohydrogenation (BH) of healthy fatty acids (FA), the present study evaluated the effects of grape seed supplementation, alone or combined with linseed, on ruminal BH processes in dairy sheep. In this 60-d trial, 24 lactating Sarda dairy ewes were assigned to four homogeneous groups and fed as follows: (1) control diet (CON), (2) a diet supplemented with 300 g/d per head of grape seed (GS), (3) a diet supplemented with 220 g/d per head of extruded linseed (LIN), (4) and a diet supplemented with a mix of both grape seed and linseed (300 and 220 g/d per head, respectively) (MIX). Ammonia, pH, volatile fatty acids (VFA) and FA composition were determined in rumen liquor at three sampling dates (20, 40 and 60 d). Rumen pH was not influenced by diet (P>0.05). The ammonia content was increased (P<0.05) in GS and MIX compared with LIN and CON. The molar proportions of acetate and propionate and their ratio were not affected by the diet (P>0.05), whereas the molar proportion of butyrate was the lowest in MIX. Rumenic acid (RA; CLA cis- 9, trans- 11) concentration increased in GS compared with CON (0.78 vs. 0.45 mg/100 mg FA; P<0.05), whereas the percentage of vaccenic acid (VA; C18:1 trans- 11) tended to increase (P<0.10) in GS compared with CON. The concentration of VA was higher in MIX than in CON (8.18 vs. 3.77 mg/100 mg FA; P<0.05), whereas RA did not differ between the same groups. The concentration of linoleic acid (LA; C18:2 n –6) decreased and stearic acid (SA; C18:0) increased in all supplemented groups, whereas linolenic acid (LNA; C18:3 n –3) decreased in the two groups receiving grape seed compared with CON and LIN. The concentration of total odd- and branched-chain fatty acids (OBCFA) decreased in all supplemented groups compared with CON (P<0.05), evidencing that grape seed and linseed supplementation influenced the ruminal BH processes. Grape seed was able to increase the accumulation of RA when supplemented alone, and of VA when combined with linseed; however, the rumen accumulation of SA in both groups supplemented with grape seed evidenced that this by-product was not effective in decreasing the BH of dietary polyunsaturated fatty acids (PUFA). [ABSTRACT FROM AUTHOR]

The seasonal variation in conjugated linoleic acid (CLA) and vaccenic acid (VA) concentrations in sheep dairy products and the extent of their transfer from milk fat to cheese and ricotta fat were investigated. Samples were collected from 2 sheep milk processing plants in North Sardinia (Italy) every 2 wk from March through June. Concentrations of fatty acids (FA) in fresh cheese and ricotta fat were primarily dependent on the fatty acid content of the unprocessed raw milk. The content of c9,t11-CLA averaged 1.73, 1.69, and 1.75 mg/100 mg of FA methyl esters (FAME), respectively, for milk, cheese, and ricotta, and differed significantly between cheese and ricotta. The content of VA averaged 3.40, 3.33, and 3.43 mg/100 mg of FAME, respectively for milk, cheese, and ricotta. The FA composition of dairy products was markedly affected by period of sampling: the mean c9,t11-CLA and VA concentration decreased from March (2.20 and 4.52 mg/100 mg of FAME) to June (1.14 and 1.76 mg/100 mg of FAME) in all dairy products. No differences in c9,t11-CLA and VA concentration of dairy products were observed between the 2 dairy companies obtaining milk from the same geographical origin. The seasonal changes in CLA and VA in milk fat were probably related to changes in pasture quality. [ABSTRACT FROM AUTHOR]

The aim of this study was to test the effect of replacing soybean hulls with different doses of cocoa husk (CH) on milk production traits and the hematological profile of dairy ewes. Twenty-four mid-lactating Sarda dairy ewes were allotted to 3 homogeneous experimental groups (8 animals per group divided into 4 pens). Each group received a total mixed ration as a basal diet and a supplement that differed among groups. The first group was supplemented with 100 g of soybean hulls/d per head (SBH group). In the second group, soybean hulls were replaced with 50 g of CH/d (CH50 group). In the third group, soybean hulls were replaced with 100 g of CH/d per head (CH100 group). The study lasted 8 wk, with 3 wk of adaptation and 5 wk for the experimental period. The replacement of soybean hulls with 50 and 100 g of CH/d did not affect dry matter intake, milk production, and milk coagulation properties. Milk fat, protein, casein, and somatic cell count concentration and curd-firming time showed a significant interaction between treatment and sampling date. During the experiment, the somatic cell counts were lower in both the CH50 and CH100 groups than in the SBH group. Most of the hematological parameters were not affected by treatments except for basophiles, which were significantly higher in the SBH group than in the CH50 and CH100 groups. In conclusion, CH can be substituted for soybean hulls in the diet of dairy sheep without adverse effects on milk production or apparent negative effects on animal health conditions. [ABSTRACT FROM AUTHOR]

This study aimed to evaluate the effects of the dietary inclusion of grape seed, alone or in combination with linseed, on milk production traits, immune response, and liver and kidney metabolic activity of lactating ewes. Twenty-four Sarda dairy ewes were randomly assigned to 4 dietary treatments consisting of a control diet (CON), a diet containing 300 g/d per head of grape seed (GS), a diet containing 220 g/d per head of extruded linseed (LIN), and a diet containing a mix of 300 g/d per head of grape seed and 220 g/d per head of extruded linseed (MIX). The study lasted 10 wk, with 2 wk of adaptation period and 8 wk of experimental period. Milk yield was measured and samples were collected weekly and analyzed for fat, protein, casein, lactose, pH, milk urea nitrogen, and somatic cell count. Blood samples were collected every 2 wk by jugular vein puncture and analyzed for hematological parameters, for albumin, alkaline phosphatase, bilirubin, creatinine, gamma glutamyltransferase, aspartate aminotransferase, alanine aminotransferase, protein, blood urea nitrogen, and for anti-albumin IgG, IL-6, and lymphocyte T-helper (CD4+) and lymphocyte T-cytotoxic (CD8+) cells. On d 0, 45, and 60 of the trial, lymphocyte response to phytohemagglutinin was determined in vivo on each animal by measuring skinfold thickness (SFT) at the site of phytohemagglutinin injection. Humoral response to chicken egg albumin was stimulated by a subcutaneous injection with albumin. Dietary treatments did not affect milk yield and composition. Milk urea nitrogen and lactose were affected by diet x period. Diets did not influence hematological, kidney, and liver parameters, except for blood urea nitrogen, which decreased in LIN and increased in MIX compared with CON and GS. Dietary treatments did not alter CD4+, CD8+, and CD4+-to-CD8+ ratio. The SFT was reduced in GS and MIX and increased in LIN compared with CON. The IgG and IL-6 were affected by diet x period. The reduction in IgG on d 60 and SFT in ewes fed GS suggests an immunomodulatory effect of this residue. The limited variation in milk and hematological and metabolic parameters suggests that GS and LIN can be included, alone or in combination, in the diet of dairy ewes without adverse effects on milk production and health status. [ABSTRACT FROM AUTHOR]