Browsing by Author "Sanni, Timothy M"
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Item Open Access Application of principal component and discriminant analyses to morpho-structural indices of indigenous and exotic chickens raised under intensive management system(Department of Animal Science, Nasarawa State University, Keffi., 2012-04-23) Yakubu, Abdulmojeed; Ajayi, O.O; Adeleke, M.A; Sanni, Timothy M; Peters, S.O; Imumorin, I.G; Ozoje, M.O; Ikeobi, C.O.N; Adebambo, O.AThe 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 normalfeathered (NF), frizzle-feathered (FF), naked-neck (NN) and Anak Titan (AT) genotypes. Phenotypic correlation among body weight and most biometric traits ranged from 0.227ā 0.876, ā0.7ā0.901, 0.034ā0.968 and ā0.207ā0.849 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 fromthis study may be considered useful in breed improvement programmes for selection, characterization, conservation and better management of Nigerian indigenous chickenItem Open Access DIFFERENTIAL RESPONSES OF NIGERIAN NATIVE SHEEP BREEDS TO ASSAULTS OF SUBACUTE Trypanosoma vivax INFECTION IN THE TROPICS: POLYMERASE CHAIN REACTION-BASED ASSAY EVIDENCES(Department of Animal Science, Nasarawa State University, Keffi., 2018-04-03) Yakubu, Abdulmojeed; Ikeobi, C.O.N; Onasanya, Gbolabo O; Sanni, Timothy M; Ozoje, M.O; Amusan, S.A; Decampos, J.S; Ofori, J.A; Ibrahim, A.AMolecular-based assay is reported to efficiently detect higher levels of subacute infection of the African Animal Trypanosomosis (AAT). Based on our previous research data, this study reports the detection of subacute Trypanosoma vivax (T. vivax) infection, sequel to polymerase chain reaction (PCR)-based assay diagnosis in four extant Nigerian sheep breeds namely, Balami, Yankassa, Uda and West African Dwarf (WAD) sampled from four geographical locations in Nigeria, the detected T.vivax infection was associated with thermo-tolerance traits of our animals. The study approach involved the use of the PCR-based assay to amplify a DNA fragment size of 400 bp within the genome of the pathogenic parasite in 161 sheep of both sexes. Our findings showed that T. vivax pathogen caused significant assault (P<0.05) on infected Nigerian native sheep compared with non-infected counterparts as depicted by the elevated thermo-tolerance traits. The WAD breed was found to have improved thermo-tolerance performance especially in body temperature when exposed to the assault of T. vivax infection compared with the Uda, Balami and Yankassa sheep breeds (P<0.05). The sheep breed showed very significant effect (P<0.01) on thermo-tolerance traits. Balami sheep was the most thermalvulnerable breed while WAD was least affected by the assault of thermal stress. Pathogenic T. vivax is culpable in the alteration of body thermo-tolerance of local sheep populations in Nigeria with the attendant health implications. Current research noted that WAD breed performed better under stressful assaults of T. vivax infection.Item Open Access GENE FLOW BETWEEN NIGERIAN SHEEP BREEDS AS REVEALED BY MICRO SATELLITE DNA MARKERS(Department of Animal Science, Nasarawa State University, Keffi., 2020-02-11) Yakubu, Abdulmojeeb; Agaviezor, B.0; Peters, S.O; Ajayi, F.O; Gunn, Hollingsheed H; Adefenwa, M.A; Adebambo, O.A; Ozoje, M.O; Ikeobi, C.O.N; Wheto, M.; Ajayi, O.O; Amusan, S.A; Ekundayo, J.O; Sanni, Timothy M; Okpeku, M.; Onasanya, Gbolabo O; Donato, Marcos De; Ilori, M.B; Kizilkaya, Kadir; Imumorin, I.GThe presence and level of gene flow between the four major Nigerian sheep breeds (West African Dwarf (WAD), Yankasa, Balami and Uda) was assessed using microsatellite DNA markers. DNA was extracted from 50~1of whole blood using the ZymoBeadā¢ Genomic DNA Kit The DNA was amplified by PCR in a MyCyclerā¢ Thermal Cycler (Biorad, Hercules, CA) using 15microsatellite markers selected. DNA fragment analysis of microsatellite markers was carried out using the Applied BioSystems 3730xl DNA Analyzer (Applied Biosystems, Carlsbad, CA, USA). The level of gene flow or population structure was assessed by STRUCTURE software and barplots generated by DISTRUCT. At K=2, two clusters was constituted from breeds descending from Balami and Yankasa, both of which are from Northern region in Nigeria. At K=3 and K=4, one more cluster emerged and further analyses did not reveal any additional strong high level substructure, so separating the entire the entire datasets into 3 major clusters was chosen as the final configuration. There are however, several cases of adm ixtures in the genome of some of the individuals that constitute the cluster. Yankasa and Salami breed had more cases of admixtures followed by Udawhile the WAD was the least breed with cases of admixturesItem Open Access Genetic Diversity in Exon 2 of the Major Histocompatibility Complex Class II DQB1 Locus in Nigerian Goats(Department of Animal Science, Nasarawa State University, Keffi., 2013-04-12) Yakubu, Abdulmojeed; Salako, Adebowale E.; Donato, Marcos De; Takeet, Michael I.; Peters, S.O; Adefenwa, Mufliat A; Okpeku, Moses; Wheto, Mathew; Agaviezor, Brilliant O.; Sanni, Timothy M; Ajayi, Oyeyemi O.; Onasanya, Gbolabo O; Ekundayo, Oludotun J; Ilori, Babatunde M; Amusan, Samuel A; Imumorin, I.GThe DQB1 locus is located in the major histocompatibility complex (MHC) class II region and involved in immune response. We identified 20 polymorphic sites in a 228 bp fragment of exon 2, one of the most critical regions of the MHC DQB1 gene, in 60 Nigerian goats. Four sites are located in the peptide binding region, and 10 amino acid substitutions are peculiar to Nigerian goats, compared with published sequences. A significantly higher ratio of nonsynonymous/synonymous substitutions (dN/dS) suggests that allelic sequence evolution is driven by balancing selection (P\0.01). In silico functional analysis using PANTHER predicted that substitution P56R, with a subPSEC score of -4.00629 (Pdeleterious = 0.73229), is harmful to protein function. The phylogenetic tree from consensus sequences placed the two northern breeds closer to each other than either was to the southern goats. This first report of sequence diversity at the DQB1 locus for any African goat breed may be useful in the search for disease-resistant genotypesItem Open Access Molecular Diagnosis of Subclinical African Trypanosoma vivax Infection and Association with Physiological Indices and Serum Metabolites in Extensively Managed Goats in the Tropics(Department of Animal Science, Nasarawa State University, Keffi., 2013-06-27) Sanni, Timothy M; Onasanya, Gbolabo O; Adefenwa, Mufliat A; Yakubu, Abdulmojeed; Ikeobi, C.O.N; Adebambo, O.A; Talabi, Adewale O.; Ozoje, M.O; Wheto, M.; Takeet, Michael I.; Peters, S.O; Donato, Marcos De; Thomas, Bolaji N.; Imumorin, I.GTrypanosomosis remains a major challenge to livestock production in much of tropical Sub-Saharan Africa, while diagnosis and treatment still depend on inefficient parasitological techniques. Endemic infections depend on animal reservoirs with subclinical parasitemia. We report molecular diagnosis of subclinical Trypanosoma vivax (T. vivax) infection using polymerase chain reaction (PCR) for the first time in Nigerian goats and associate parasite presence with gross physiological traits and serum metabolites in extensively managed Nigerian goats. PCR was used to amplify a 400 bp DNA fragment of the parasite genome in 205 goats across three geographical zones of the country. Results showed a high subclinical infection rate (SCIR) of 71.7% in the total goats examined. Overall SCIRs of 71%, 75.9% and 55.6% were recorded in West African Dwarf, Red Sokoto and Sahel goats respectively, while geographical SCIRs were 71.2% (Southwest), 75% (Northwest) and 70% (Northeast). T. vivax presence had significant (P < 0.05) effect on respiratory rate and is associated with higher creatinine levels in sera. Logistic regression analyses with Hosmer-Lemeshow goodness- of-fit showed that respiratory rate is the most important predictive trait for the presence of T. vivax infection (P < 0.05). Goats appear to be a viable reservoir for T. vivax infection of other livestock. Molecular diagnosis of subclinical trypanosomosis using PCR could be useful for large scale epidemiological studies, early diagnosis of subclinical infection and treatment of the disease in extensively managed tropical goats.Item Open Access Molecular-based detection of sub-clinical African Trypanosoma vivax infection and its association with some selected serum biochemical references and blood electrolytes in four traditionally bred Nigerian native Sheep.(Department of Animal Science, Nasarawa State University, Keffi., 2018-09-12) Yakubu, Abdulmojeed; Onasanya, Gbolabo O; Sanni, Timothy M; Amusan, A. S; Decampos, J.S; Talabi, Adewale O.; Ozoje, M.O; Balogun, Joshua Babalola; Wheto, M.; Ikeobi, C.O.NTrypanosomosis remains a major challenge to livestock production in much of tropical Sub- Saharan Africa, while diagnosis and treatment still depends on inefficient parasitological techniques. Endemic infections of trypanosomosis depend on animal reservoirs with sub-clinical parasitemia. We report molecular diagnosis of sub-clinical Trypanosoma vivax (T. vivax) infection using polymerase chain reaction (PCR) for the first time in Nigerian sheep and associate parasite presence with gross physiological traits and biochemical references in extensively managed tropical sheep. PCR was used to amplify a 400 bp DNA fragment of the parasite genome in 161 sheep of both sexes across four geographical zones of Nigeria. Results showed a high sub-clinical infection rate (SCIR) of 73.9% in the total sheep investigated. Overall, SCIRs of 85.4%, 75%, 62.5% and 72.5% were recorded in Balami, West African Dwarf, Uda and Yankassa sheep, respectively; while geographical SCIRs were 73.5 % (South-West), 71.7 % (North-West), 73.5 % (North-East) and 88.0 % (North-Central). SCIRs of 73.5 % were found in ewes and 76.3 % in rams. T. vivax infection presence had a significant (p<0.05) effect on blood urea nitrogen (BUN), Alanine transaminase or Alanine aminotransferase (AST) and alkaline phosphatase (ALP) where infected sheep had a higher ALP levels of 242.24 +21.72 IU/dl than non-infected sheep (189.86 +10.77 IU/dl). Also T. vivax infected sheep had higher AST (185.92+13.90 IU/L) than non-infected counterparts (167.31+15.58 IU/L). Tropical sheep appear to be a fertile reservoir for T. vivax infection of other livestock. Molecular diagnosis of sub-clinical trypanosomosis using PCR-based assay is suitable for large scale epidemiological studies of trypanosomosis, early diagnosis of sub-clinical infection and treatment of the disease in extensively managed tropical sheepItem Open Access Morphological and microsatellite DNA diversity of Nigerian indigenous sheep(Department of Animal Science, Nasarawa State University, Keffi., 2012-04-22) Agaviezor, B.O; Peters, S,O; Adefenwa, Mufliat A; Yakubu, Abdulmojeed; Adebambo, O.A; Ozoje, M.O; Ikeobi, C.O.N; Wheto, M.; Ajayi, O.O; Amusan, S.A; Ekundayo, Oludotun J; Sanni, Timothy M; Okpeku, M; Onasanya, Gbolabo O; Donato, Marcos De; Ilori, Babatunde M; Kizilkaya, Kadir; Imumorin, I.GBackground: Sheep is important in the socio-economic lives of people around the world. It is estimated that more than half of our once common livestock breeds are now endangered. Since genetic characterization of Nigerian sheep is still lacking, we analyzed ten morphological traits on 402 animals and 15 microsatellite DNA markers in 384 animals of the 4 Nigerian sheep breeds to better understand genetic diversity for breeding management and germplasm conservation. Results: Morphological traits of Uda and Balami were significantly (P < 0.05) higher than Yankasa, which were both higher than West African Dwarf (WAD) sheep. Stepwise discriminant analysis showed tail length, rump height, chest girth, ear length and chest depth as the most discriminating variables for classification. Mahalanobis distances show the least differentiation between Uda and Balami and the largest between WAD and Balami sheep. While 93.3% of WAD sheep were correctly assigned to their source genetic group, 63.9% of Yankasa, 61.2% of Balami and 45.2% of Uda were classified correctly by nearest neighbour discriminant analysis. The overall high Polymorphism Information Content (PIC) of all microsatellite markers ranged from 0.751 to 0.927 supporting their use in genetic characterization. Expected heterozygosity was high for all loci (0.783 to 0.93). Mean heterozygote deficiency across all populations (0.171 to 0.534) possibly indicate significant inbreeding (P < 0.05). Mean values for FST, FIT and FIS statistics across all loci were 0.088, 0.394 and 0.336 respectively. Yankasa and Balami are the most closely related breeds (DA = 0.184) while WAD and Balami are the farthest apart breeds (DA = 0.665), which is coincident with distance based on morphological analysis and population structure assessed by STRUCTURE. Conclusions: These results suggest that within-breed genetic variation in Nigerian sheep is higher than between-breeds and may be a valuable tool for genetic improvement and conservation. The higher genetic variability in Yankasa suggests the presence of unique ancestral alleles reflecting the presence of certain functional genes which may result in better adaptability in more agro-ecological zones of Nigeria. These genetic characteristics are potentially useful in planning improvement and conservation strategies in Nigerian indigenous sheepItem Open Access SINGLE NUCLEOTIDE POLYMORPHISM-BASE CHARACTERIZATION OF HSP 90A1A GENE IN SOME NIGERIAN CATTLE BREEDS.(Department of Animal Science, Nasarawa State University, Keffi., 2019-10-21) Onasanya, Gbolabo O; Thiruvenkadan, A.K; Sreekumar, C.; Tirumurugaan, G.K; Msalya, G.M; Sanni, Timothy M; Decampos, J.S; Amusan, A. S; Olowofeso, Oladeji; Fafiolu, A.O; Okpeku, M.; Yakubu, Abdulmojeed; Ikeobi, C.O.NHeat shock protein (HSP) 90 gene is a member of HSPs that act as molecular chaperons whenever animals come under thermal assault, they fulfill essential roles of providing cellular protection, immune response, protein synthesis, protein folding and unfolding, protection proteins from cellular stress, inhibitory apoptosis and adaptation during thermal assault. A total of ninety (90) adult bulls from across four extant breeds of Nigerian Zebu cattle comprising of White Fulani (25), Sokoto Gudali (21), Red Bororo (21) and Ambala (23) sampled from northern parts of Nigeria. Genomic DNA was extracted from 90 animal skin tissue samples and was subjected to polymerase chain analyses followed by sequencing of the PCR products for detection SNPs of HSP 90 gene in four Nigerian breeds of cattle. Single Nucleotide polymorphisms (SNPs) within the nucleotide sequences of four Nigerian bovine HSP90 gene of were visualised detected and bio-edited by chromatogram analyses using SeqMan Ngen Tool (DNASTARĀ®, Inc., Madison, Wisconsin, U.S.A). We pioneered a preliminary single nucleotide polymorphism study of HSP 90 gene for the first time in Nigerian zebu cattle. Sequence data detected 6 SNP loci within the coding region of exon 1 of HSP 90 gene which includes: 2 Indels (White Fulani: Del384C i.e. insertion of C at 384th base position and Red Bororo: Del355G i.e. insertion of G at 355th base position), 1 transversion (Sokoto Gudali: C112A) and 3 transitions (White Fulani: G390A, Red Bororo: T55C and C190T).We therefore, hypothesize that the detected SNPs should further be associated thermo-tolerance traits to unravel their possible effect on thermal-tolerance performance, adaptability and susceptibility of different Nigerian cattle breeds to environmental stress load and thermal assaults of tropical conditionsItem Open Access Single nucleotide polymorphisms at heat shock protein 90 gene and their association with thermo-tolerance potential in selected indigenous Nigerian cattle(Department of Animal Science, Nasarawa State University, Keffi., 2020-06-28) Yakubu, Abdulmojeed; Onasanya, Gbolabo O; Msalya, G.M; Thiruvenkadan, A.K; Sreekumar, Chirukandoth; Tirumurugaan, Gopalan K.; Okpeku, M.; Sanni, Timothy M; Decampos, J.S; Amusan, S.A; Olowofeso, Oladeji; Fafiolu, A.O; Ikeobi, C.O.NHeat shock protein (HSP) 90 gene provides protection and adaptation to thermal assault and certain polymorphisms have been associated to heat tolerance in humans and animals. Single nucleotide polymorphisms (SNPs) of HSP 90 gene were used to evaluate the scientific basis of heat tolerance in four zebu breeds of Nigeria. The DNA was extracted from skin tissue of 90 adult bulls representing White Fulani (WF), Sokoto Gudali (SG), Red Bororo (RB), and Ambala (AM). The SNPs were determined in DNAs using PCR, sequencing, and visualization and bio-editing by chromatogram in SeqMan Ngen tool. Subsequently, respective genotypes were constructed and genotypic and allelic frequencies were computed. Also, body parameters related to heat stress (HS) including body temperature (BT), rectal temperature (RT), and respiratory rates (RR) were taken for each animal before biological sampling and heat tolerance coefficient (HTC) was calculated. We detected four SNPs distinct/specific for each breed as follows: change from thymine (T) to guanine (G) at position 116 (T116G) in RB, G to cytosine (C) at 220 (G220C) in SG, G to adenine (A) at two positions, 346 (G346A) and 390 (G390A) in AM and WF, respectively. Heterozygous SNPs showed significantly lower values (P < 0.0001) for BT, RT, RR, and HTC than homozygous genotypes at all positions.We hypothesize that animals with heterozygous SNPs in exon 3 of HSP 90 may be tolerant to HS. These SNPs can be used as bio-markers for screening large populations of cattle for tolerance to hot tropical conditions in Nigeria and other sub-humid places.