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This study was conducted to evaluate the variation in antibody from Newcastle disease (ND) vaccinated breeder birds and their progenies. The chicks were evaluated for maternally derived antibody (MDA) against ND virus and also the MDA transfer rate for each genotype. The local parent stocks were Frizzle-feathered, Normal-feathered, and Naked neck while an exotic parent stock (Anak Titan) was used for the purpose of comparison. Sera samples were collected from chicks generated at day 3 post-hatch, and sera were also collected from the parent stocks. The sera samples were stored at -20 °C until analysed. Enzyme linked immuno-sorbent assay (ELISA) test was used for the detection and quantification of antibodies to ND in the parent stocks and the chicks using IDEXX Newcastle Disease ELISA test kit. The least squares means of antibody titers for parent stocks were 413.333 ± 68.853, 426.333 ± 121.949, 481.667 ± 145.454, and 1148.333 ± 532.843 for Frizzle-feathered, Normal-feathered, Naked Neck, and Anak Titan, and the calculated MDA transfer rate was 96.4, 93.8, 88.7, and 34.7 % for Frizzle-feathered, Normal-feathered, Naked neck, and Anak Titan, respectively. The mean antibody titers for chicks were 398.6 ± 43.871, 400.0 ± 53.952, 427.0 ± 89.353, and 398.8 ± 57.593 for Frizzle-feathered, Normal-feathered, Naked neck, and Anak Titan, respectively. The antibody titers from parent stocks were higher than those observed in chicks for all the genotypes. The values obtained in this study indicated that parent stocks with their progenies were below protective level. The local parent stocks had higher transfer rate when compared to their exotic counterpart. Hence, there is an indication from this finding that the local chickens had a better transfer rate in relation to Anak Titan which is an exotic breed. Therefore, there is the presence of genetic variability for antibody transfer in the Nigerian local chickens and can be incorporated in designing a breeding program for better adaptive potential.

This study was carried out to assess the prevalence of mange in sheep and goats in five local government areas (LGAs) of Ogun State in South Western Nigeria. A total of 4,973 sheep and 7,902 goats of West African Dwarf breeds were sampled of which only 4 (0.08%) of sheep and 42 (0.53%) of goats were confirmed positive for mange infestation. In all the LGAs sampled, Odeda LGA had the highest concentration of sheep (39%) and goats (51%) while Abeokuta South had the least percentage of sheep (1%) and goats (1%). All the mange-infested cases in sheep were recorded in just one LGA (Ewekoro) which constituted 0.24% of the population within the location. For goats, three out of five LGAs namely: Obafemi Owode, Ewekoro and Abeokuta North had prevalence of 1.46%, 0.53% and 0.72% respectively. There was no significant (P > 0.05) difference between non-infested and infested animals in terms of packed cell volume (31.79 ± 0.87% vs. 31.41 ± 1.13%), haemoglobin (10.51 ± 0.21 g/100 ml vs. 10.28 ± 0.37 g/100 ml) and red blood cells (8.71 ± 0.29 × 1012/l vs. 9.40 ± 0.37 × 1012/l). The infested group however showed significantly (P

The objectives of this study were to investigate the relationships between body weight and morpho-structural indices to predict body weight from their orthogonal body shape characters using principal component analysis and to morphologically classify the chicken genotypes using multivariate discriminant analysis. Data used were from 273 randomly selected 12-weeks-old indigenous chickens of normal-feathered (NF), frizzle-feathered (FF), naked-neck (NN) and Anak Titan (AT) genotypes. Phenotypic correlation among body weight and most biometric traits ranged from 0.227-0.876, -0.7-0.901, 0.034-0.968 and -0.207-0.849 for NF, NN and AT chickens, respectively. Factor analysis with varimax rotation of interrelated traits revealed three principal components which accounted for 83.1%, 74.4%, 78.8% and 76.5% of the total variance in NF, FF, NN and AT chickens in the order listed. Breast girth, keel length, thigh length, shank length and wing length were found to be the most discriminating variables to separate the chicken genotypes. The longest distance (72.54) occurred between AT and NF genotypes while the shortest distance (4.27) was recorded for FF and NN genotypes. Classification results showed that 85.2% of AT genotype was correctly classified into their source population. However, 22.7% of NF was misclassified as NN, while 33.3% of NN was misclassified as NF chickens. These results suggest that there is high rate of gene flow between these two indigenous chicken genotypes. Information obtained from this study may be considered useful in breed improvement programmes for selection, characterization, conservation and better management of Nigerian indigenous chickens.

A total of 970 eggs were collected from matings involving three genotypes of Nigerian local chickens (Normal-feathered, Frizzle-feathered and Naked neck) and one exotic broiler breeder strain (Anak Titan) to evaluate the effect of crossbreeding on fertility, hatchability and embryonic mortality. Mating was achieved through artificial insemination. Sire genotype significantly (P

Six-hundred-and-seven-day-old chicks were generated from Nigerian local chickens consisting of three genotypes (Normal-feathered; Frizzled-feathered; Naked neck) and an exotic broiler breeder (Anak Titan) to evaluate growth performance for possible meat-type chicken development. Growth parameters measured were body weight, breast girth and keel length on weekly basis for 20 weeks. Effects of sire, dam and chick genotypes were significant (P0.001) on growth traits. At week 20, chickens sired by the Anak Titan weighed 1,614.82 g followed by Normal-feathered local chickens with body weight of 1,211.32 g. Progenies of Anak Titan and Naked neck dams weighed 1,761.96 and 1,292.80 g at week 20, respectively. Among purebreds, Anak Titan weighed 35.05 g at day-old and had heaviest body weight of 2,360.29 g at 20 weeks compared to the three local strains. The average body weights for the crossbred, Normal-feathered × Anak Titan at day-old and week 20 were 36.39 and 1,577.63 g, respectively. This was followed by Anak Titan × Naked neck with 33.32 g at day-old and 1,514.14 g at week 20. Sex had significant effect (P0.05) at weeks 16 and 20 with the males having higher mean values than their female counterparts. This study revealed that crosses involving Anak Titan sire × Naked neck dam had highest growth performance, and there was no strain differences among the growth performance of purebred Nigerian local chickens.

The agouti-signaling protein (ASIP) plays a major role in mammalian pigmentation as an antagonist to melanocortin-1 receptor gene to stimulate pheomelanin synthesis, a major pigment conferring mammalian coat color. We sequenced a 352 bp fragment of ASIP gene spanning part of exon 2 and part of intron 2 in 215 animals representing six goat breeds from Nigeria and the United States: West African Dwarf, predominantly black; Red Sokoto, mostly red; and Sahel, mostly white from Nigeria; black and white Alpine, brown and white Spanish and white Saanen from the US. Twenty haplotypes from nine mutations representing three intronic, one silent and five missense (p.S19R, p.N35K, p.L36V, p.M42L and p.L45W) mutations were identified in Nigerian goats. Approximately 89 % of Nigerian goats carry haplotype 1 (TGCCATCCG) which seems to be the wild type configuration of mutations in this region of the gene. Although we found no association between these polymorphisms in the ASIP gene and coat color in Nigerian goats, in-silico functional analysis predicts putative deleterious functional impact of the p.L45W mutation on the basic amino-terminal domain of ASIP. In the American goats, two intronic mutations, g.293G>A and g.327C>A, were identified in the Alpine breed, although the g.293G>A mutation is common to American and Nigerian goat populations. All Sannen and Sahel goats in this study belong to haplotypes 1 of both populations which seem to be the wild-type composite ASIP haplotype. Overall, there was no clear association of this portion of the ASIP gene interrogated in this study with coat color variation. Therefore, additional genomic analyses of promoter sequence, the entire coding and non-coding regions of the ASIP gene will be required to obtain a definite conclusion.