Fumonisin B1, T-2 toxin, and deoxynivalenol are frequently detected in feed materials. The mycotoxins induce free radical formation and, thereby, lipid peroxidation. The effects of mycotoxin exposure at the EU recommended limit (T-2/HT-2 toxin: 0.25 mg/kg; DON = 3AcDON/15-AScDON: 5 mg/kg; fumonisin B1: 20 mg/kg) and double dose (T-2/HT-2 toxin: 0.5 mg/kg, DON/3-AcDON/15-AcDON: 10 mg, and FB1: 40 mg/kg feed) were investigated during short-term (3 days) per os exposure in the liver of laying hens. On day 1 higher while on day 3 lower MDA concentrations were found in the low-dose group compared to the control. Fatty acid composition also changed: the proportion of monounsaturated fatty acids increased (p < 0.05) and the proportion of polyunsaturated fatty acids decreased by day 3. These alterations resulted in a decrease in the index of unsaturation and average fatty acid chain length. Histopathological alterations suggested that the incidence and severity of liver lesions were higher in the mycotoxin-treated laying hens, and the symptoms correlated with the fatty acid profile of total phospholipids. Overall, the findings revealed that mycotoxin exposure, even at the EU-recommended limits, induced lipid peroxidation in the liver, which led to changes in fatty acid composition, matched with tissue damage.

Male weaned piglets n = 6/group were fed Fumonisin B₁₊₂₊₃ (FBs) mycotoxins at 0, 15, or 30 mg/kg diet for 3 weeks to assess the fatty acid (FA) composition of membrane lipid classes, lipid peroxidation, and histomorphological changes in the liver and lung. Growth performance and lipid peroxidation were unaltered, but histomorphological lesion scores increased in the liver. Linear dose–response was detected in liver phosphatidylcholines for C16:1n7, C18:1n9, and total monounsaturation and in lungs for C22:6n3, total n-3 and n-3:n-6, in pulmonary phosphatidylserines C20:0 and C24:0. Alterations associated with the highest FBs dose were detected in sphingomyelins (liver: total saturation ↓, total monounsaturation ↑), phosphatidylcholines (liver: total n-6 ↓, n-6:n-3 ↑; in lungs: total monounsaturation ↑, total polyunsaturation ↑), phosphatidylethanolamines (liver: total n-3 ↓; in lungs: total monounsaturation ↑ and n-6:n-3 ↑), phosphatidylserines (liver: n-6:n-3 ↑; in lungs: total saturation ↓, total polyunsatuartion ↑, and total n-6 and its ratio to n-3 ↑), and phosphatidylinositol (n-6:n-3 ↑; lungs: C22:1n9 ↑, C22:6n3 ↓, total saturation ↓, total monounsaturaion ↑). In conclusion, FBs exposures neither impaired growth nor induced substantial lipid peroxidation, but hepatotoxicity was proven with histopathological alterations at the applied exposure period and doses. FA results imply an enzymatic disturbance in FA metabolism, agreeing with earlier findings in rats.

The effects of combined short-term (3 days) exposure to Fusarium mycotoxins at both the EU recommended limit (T-2/HT-2 toxin: 0.25 mg/kg; DON/3-AcDON/15-AcDON: 5 mg/kg; FB₁: 20 mg/kg) and twice the dose (T-2/HT-2 toxin: 0.5 mg/kg, DON/3-AcDON/15-AcDON: 10 mg/kg, and FB₁: 40 mg/kg feed) on the kidneys of laying hens were examined. Our study aimed to investigate how these mycotoxins interacted with membrane lipid fatty acid (FA) composition and lipid peroxidation processes. It was observed that the levels of conjugated dienes and trienes were higher than the control in the low-mix group on day 3, and malondialdehyde concentration was higher on days 2 and 3. The proportion of phospholipid (PL) FAs showed that saturated and monounsaturated FAs increased. Still, both n3 and n6 polyunsaturated FAs decreased significantly on day 2 of exposure in the high-mix group. Among the n3 FAs, the level of docosahexaenoic (C22:6 n3) and among n6 FAs, arachidonic (C20:4 n6) acids decreased mainly on day 2 in the high-mix group. The results suggest that the combined exposure to Fusarium mycotoxins induced lipid peroxidation in the kidneys of laying hens, which resulted in marked changes in the PL FA profile. Histological examination revealed time- and dose-dependent increases as consequences of mycotoxin exposure.

In ovo administration of DL-methionine and post-hatch Hydrogel® supplements were tested to examine the impact of early feeding on performance and immune-related traits in a commercial broiler stock. One thousand one hundred and twenty Ross 308 eggs were incubated and assigned to seven treatment groups: intact (no in ovo administration) and immediate feed access (C1), in ovo saline treatment and immediate feed access (C2), intact and delayed feeding (ID), in ovo saline treatment and delayed feeding (IoS), in ovo DL-Methionine treatment and delayed feeding (IoM), intact and delayed access to feed, but immediate access to commercial Hydrogel® without (Hyd) or with 5mg/kg (HydM) DL-methionine post-hatch. The results showed, that the in-ovo methionine may have positive effects on the weight gain of the birds (p < 0.001) compared to the commercial Hydrogel® however, it cannot compete with the immediate feeding. The number of heterophils decreased significantly (p < 0.001) by day 21 in ID and IoS compared to the immediately fed control (C1). The number of lymphocytes, monocytes, and eosinophils, increased in treatments supplemented with methionine (p < 0.05) (IoM,HydM) indicating enhanced immune protection. There were no differences in the total antioxidant capacity (FRAP) and malonaldehyde concentration (MDA) (p = 0.07) in the examined groups. The Cytochrome P450 H1 (CYP2H1) gene was downregulated in all treatment groups (on days 21 and 35) indicating a slower metabolism, particularly in the ID group compared to C1 and C2 (p < 0.001). The HydM treatment could upregulate the IL2 expression as the immediate feeding, while only IoM treatment resulted in significant downregulation by day 35 (p < 0.001). IL6 was upregulated in all treatment groups (p < 0.001) except for HydM, where the gene expression did not differ from the housekeeping gene. Early administration of dietary methionine has a positive effect on performance and the immune system, however, none of the early feeding methods can compete with immediate feed access. The possible positive effects of early nutrition and its epigenetic impact should be examined in further studies.

Delayed feed access post-hatch negatively impacts growth and intestinal development in broilers. Threonine (Thr) is known to support epithelial tissue development. This study evaluated the effects of early feeding strategies, including in ovo Thr administration and hydrogel provision, on broiler performance, gut and liver histomorphology, and leukocyte profiles. Control birds were fed immediately post-hatch, while others experienced a 48 h feed delay. One group received in ovo Thr on day 17 of incubation, while others were given Hydrogel^® with or without Thr during the first 48 h post-hatch. Immediate feed birds showed the best performance (p < 0.05), while early Thr supplementation (in ovo or hydrogel) partially mitigated the negative effects of delayed feed access. On day 21, birds treated with in ovo Thr had 4% higher body weight (BW) than untreated birds (p < 0.05). Birds given hydrogel post-hatch showed no significant BW differences compared to other groups (p > 0.05), but 48 h delayed, non-supplemented birds had 34.3% lower BW than immediate-fed birds (p < 0.05). Compensation was linked to improved gut architecture, though no significant effects were observed on leukocyte profiles or liver histology. In ovo Thr feeding is recommended to mitigate the adverse effects of a two-day delay in feed access for broiler chickens.

Varroa destructor is one of the most destructive enemies of the honey bee, Apis mellifera all around the world. Several control methods are known to control V. destructor, but the efficacy of several alternative control methods remains unexplored. Irradiation can be one of these unknown solutions but before practical application, the effectiveness, and the physiological effects of ionizing radiation on the host and the parasite are waiting to be tested. Therefore, the objective of our study was to investigate the effects of different doses (15, 50, 100, and 150 Gy) of high-energy X-ray irradiation through mortality rates and hemocyte composition changes in A. mellifera workers and record the mortality rates of the parasite. The mortality rate was recorded during short-term (12, 24, and 48 h) and long-term periods (3, 6, 12, 18, and 24d). The sensitivity of the host and the parasite in case of the higher doses of radiation tested (50, 100, and 150 Gy) been demonstrated by total mortality of the host and 90 % of its parasite has been observed on the 18th day after the irradiation. V. destructor showed higher sensitivity (1.52-times higher than the adult honey bee workers) at the lowest dose (15 Gy). A. mellifera hemocytes were influenced significantly by radiation dosage and the elapsed time after treatment. The higher radiation doses increased plasmatocyte numbers in parallel with the decrease in prohemocyte numbers. On the contrary, the numbers of granulocytes and oencoytes increased in the treated samples, but the putative effects of the different dosages on the recorded number of these hemocyte types could not be statistically proven. In summary, based on the outcome of our study X-ray irradiation can be deemed an effective tool for controlling phoretic V. destructor. However, further research is needed to understand the physiological response of the affected organisms.