O. Oyelakin, A. Aki̇nyemi̇, J. Ekelemu, A. Oloyede, B. Abiona
{"title":"Molecular Characterization and Haemolysis of Bacteria Associated with Tilapia zilli from Ijaka-Oke Location on Yewa River","authors":"O. Oyelakin, A. Aki̇nyemi̇, J. Ekelemu, A. Oloyede, B. Abiona","doi":"10.9734/AJEA/2016/19984","DOIUrl":null,"url":null,"abstract":"Fishes are a source of animal protein, rich in minerals, amino acids, and essential fatty acids. \nFishes can be confronted with microbial contamination in their natural habitat and their \ntransformation products can be a source of microbial infections and food poisoning. In the natural \nhabitat, microorganisms are usually found on the entire outer surface (skin and gills) and in the \nintestines of fishes. Genetic diversity study of the bacteria isolates was done using RAPD \ntechnique. Bacteria were isolated from the gills, gut and skin of Tilapia zilli from Ijaka-Oke location \non Yewa River. Morphometric characteristics of the 20 Tilapia zilli sampled was done. DNA were \nextracted from 20 bacteria isolates using CTAB method, PCR amplification of the 20 isolated DNA \nwas carried out using five RAPD primers. Haemolysis of the 20 bacteria was also carried out using \n7% of sheep blood in Nutrient Agar and it was used to culture a pure colony of the isolates and \nincubated at 37°C for 18 hours. The mean total length of the fishes was 30.00±9.00 (cm), weight 220±4.3 (g), head length 7.4±2.00 (cm) and standard length 21.30±4.50 (cm). The water quality \nparameters were also recorded with the water temperature at 22.90C, the pH of the water was 6.1 \nand Dissolved Oxygen 6.89 mg/l. Fifty – two (52) polymorphic markers were generated from the 5 \nRAPD markers. There were also 15 monomorphic markers from the primers. A total number of 67 \nmarkers were generated. The haemolysis showed that none of the bacteria displayed complete \nhaemolysis.","PeriodicalId":7714,"journal":{"name":"American Journal of Experimental Agriculture","volume":"30 1","pages":"1-7"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Experimental Agriculture","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/AJEA/2016/19984","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Fishes are a source of animal protein, rich in minerals, amino acids, and essential fatty acids.
Fishes can be confronted with microbial contamination in their natural habitat and their
transformation products can be a source of microbial infections and food poisoning. In the natural
habitat, microorganisms are usually found on the entire outer surface (skin and gills) and in the
intestines of fishes. Genetic diversity study of the bacteria isolates was done using RAPD
technique. Bacteria were isolated from the gills, gut and skin of Tilapia zilli from Ijaka-Oke location
on Yewa River. Morphometric characteristics of the 20 Tilapia zilli sampled was done. DNA were
extracted from 20 bacteria isolates using CTAB method, PCR amplification of the 20 isolated DNA
was carried out using five RAPD primers. Haemolysis of the 20 bacteria was also carried out using
7% of sheep blood in Nutrient Agar and it was used to culture a pure colony of the isolates and
incubated at 37°C for 18 hours. The mean total length of the fishes was 30.00±9.00 (cm), weight 220±4.3 (g), head length 7.4±2.00 (cm) and standard length 21.30±4.50 (cm). The water quality
parameters were also recorded with the water temperature at 22.90C, the pH of the water was 6.1
and Dissolved Oxygen 6.89 mg/l. Fifty – two (52) polymorphic markers were generated from the 5
RAPD markers. There were also 15 monomorphic markers from the primers. A total number of 67
markers were generated. The haemolysis showed that none of the bacteria displayed complete
haemolysis.