Prediction of reproductive performance of ewes based on the early production data, ewe birth rank, dam age, and dam birth rank.

This research aimed to analyze whether ewes' total reproductive performance up to the fourth year of life (RP4) can be predicted based on the data available at an early stage of a ewe's productive life. The RP4 of 133 Romanov ewes was measured in terms of the total number of lambs born per ewe (TNLE) and total birth weight of lambs per ewe (TBLE). Multiple regression was used to analyze whether early reproductive performance indicators (first litter size - FLS, age at first lambing - AFL, first lambing interval - FLI), ewe birth rank, dam age, and dam birth rank can be used as the predictors of RP4. Predicted R 2 and 95 % prediction intervals were used as indicators of the precision of prediction. Average TNLE and TBLE at the end of fourth year of ewe life were 11.84 lambs and 37.96 kg, respectively. FLS and FLI significantly ( P < 0.05 ) influenced TNLE and TBLE, while AFL was not a significant ( P > 0.05 ) variable. Ewes with shorter FLI had significantly ( P < 0.05 ) higher TNLE (10.94 lambs) and TBLE (36.17 kg) than ewes with long FLI (TNLE  =  9.12 lambs and TBLE  =  28.05 kg). R 2 predicted for TNLE and TBLE was 7.54 % and 11.49 %, respectively. The ewe's birth rank and the dam's birth rank significantly ( P < 0.05 ) influenced TNLE and TBLE. Ewes born as singletons and ewes from singleton-born dams had significantly ( P < 0.05 ) lower TNLE and TBLE than ewes born as triplets and ewes from triplet-born dams. R 2 predicted for TNLE was 16.76 %, and 25.69 % for TBLE. FLS and FLI are better predictors of RP4 than AFL. The birth rank of ewe and dam also proved significant predictors of RP4. For both sets of predictors (early reproductive indicators and birth rank data), low values of R 2 predicted indicate that precise prediction of RP4 cannot be made.

Differences in fungal contamination of broiler litter between summer and winter fattening periods.

This study aimed to compare fungal contamination of poultry litter between warm and cold seasons. It was carried out in commercial production conditions over two five-week fattening periods: one in the summer (July-August) and one in the winter (December-January). Broilers were reared on a litter composed of chopped straw and sawdust. Litter fungal concentration and composition were investigated weekly, along with litter temperature, moisture, and pH. Litter concentration of total fungi increased over both fattening periods, with no differences in median concentrations between them. Season also had no effect on yeast, Aspergillus section Nigri, and Cladosporium, Fusarium, and Rhizopus spp. concentrations, while the Aspergillus section Flavi and Aspergillus spp. combined showed higher concentrations in the summer, and Mucor and Penicillium spp. in the winter. Total fungal concentration highly correlated with litter temperature, moisture, and pH, regardless of the season. Our findings can be useful in the assessment and control of potential harmful effect of fungi on the health of poultry and poultry farm workers.

Effect of RNF4-SacII gene polymorphism on reproductive traits of Landrace × Large White crossbred sows.

The aim of the present study was to investigate whether and to what extent the RNF4-SacII gene polymorphism influences reproduction performances in hyperprolific sow lines. The study involved 101 Landrace x Large White crossbred sows, with 461 records collected on the following reproductive traits: Total Number of piglets Born per litter (TNB), Number of piglets Born Alive per litter (NBA), Number of StillBorn piglets per litter (NSB), piglet Pre-Weaning Mortality (PWM) and Number of piglets at Weaning per litter (NW). The least square method with the GLM procedure in SAS with eight effects was used to pursue the data analysis. Study results revealed that TT homozygotes and TC heterozygotes had a significantly higher (p < .05) NW than CC homozygotes for the life-span performance in all parities and first parity analysed. In the fourth parity analysed, TNB and NBA in TC genotype were significantly higher (p < .05) as compared with TT genotype. Based on the life-span performance, significant effect (p < .05) was recorded for order of parity on TNB, NBA and NW, for farrowing season on TNB and NSB, and for lactation length on PWM. In the second parity, significant effect (p < .05) was recorded for sire of boar on NSB and for gestation length on TNB. Only in the fourth parity, significant effect (p < .05) of RNF4 gene was observed on NBA. There was significant additive effect (p < .05) of the RNF4 gene polymorphism identified on NW in all parities analysed, and significant additive and dominance effects (p < .05) on NSB in the third parity analysed. In conclusion, additional research on related production pig genotypes is necessary to elucidate the effect of RNF4 gene mutation on reproductive traits.

Abundance of IFN-α and IFN-γ gene transcripts and absence of IL-2 transcripts in the blood of chickens vaccinated with live or inactivated NDV.

As immune responses to live and inactivated vaccines might differ, temporal responses of broiler chickens to vaccination were examined on the basis of the abundance in the circulating blood of gene transcripts of IFN-α, IFN-γ and IL-2, critical cytokines for immune responses. Blood samples were collected 6, 12 and 24 hours, and 7 and 14 days following vaccination with either live or inactivated Newcastle disease virus, La Sota strain, at 14 days of age, and the abundance of transcripts for each cytokine was assayed by real-time RT-PCR. Physiological saline and vaccine emulsion without viral antigen were administered to control groups for live and inactivated vaccine groups, respectively. The abundance of IFN-γ transcripts was elevated during the early times following vaccination and had reached baseline by the seventh day but the abundance of IFN-α transcripts remained elevated. Transcripts for neither IFN gene were detected in the control birds. The abundance of transcripts for each IFN was not different between the two vaccinated groups at any time. Transcripts for IL-2 were detected only in spleens from chicken embryos that had been inoculated with the live virus. The results show that cells stimulated to produce IFN-α and IFN-γ enter the circulating blood but those stimulated to produce IL-2 do not, or in very low number, and the IFN responses to both vaccines are the same.