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Identification of Staphylococcus species isolated from preputium of Aceh cattle based on 16S rRNA gene sequences analysis.


ABSTRACT: Aim:This research aimed to identify Staphylococcus species isolated from preputial swabs of healthy Aceh cattle, based on 16S ribosomal RNA gene analysis. Materials and Methods:The bacterium was isolated from preputial swabs of healthy Aceh cattle. The total DNA from the isolated bacteria was extracted using the Genomic DNA Mini Kit followed by polymerase chain reaction (PCR) amplification of the 16S rRNA gene. The product of PCR amplification was then sequenced and aligned to the known sequences in the GenBank database by multiple alignments and was also analyzed by bioinformatics software to construct a phylogenetic tree. Results:The results revealed that the bacterial isolate 3A had genetically closed relation to Staphylococcus pasteuri with <97% maximum identity. Data derived from the phylogenetic tree revealed that the bacterial isolate 3A was also related to Staphylococcus warneri, yet, it shows a different evolutionary distance with the ancestors (S. pasteuri). Conclusion:The results of this research suggested that the bacterium 3A, isolated from preputial swabs of healthy Aceh cattle, is a Staphylococcus species.

SUBMITTER: Hambal M 

PROVIDER: S-EPMC6868254 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Identification of <i>Staphylococcus</i> species isolated from preputium of Aceh cattle based on 16S rRNA gene sequences analysis.

Hambal Muhammad M   Admi Masda M   Safika Safika S   Sari Wahyu Eka WE   Ferasyi Teuku Reza TR   Dasrul Dasrul D   Balqis Ummu U   Darmawi Darmawi D  

Veterinary world 20191008 10


<h4>Aim</h4>This research aimed to identify <i>Staphylococcus</i> species isolated from preputial swabs of healthy Aceh cattle, based on 16S ribosomal RNA gene analysis.<h4>Materials and methods</h4>The bacterium was isolated from preputial swabs of healthy Aceh cattle. The total DNA from the isolated bacteria was extracted using the Genomic DNA Mini Kit followed by polymerase chain reaction (PCR) amplification of the 16S rRNA gene. The product of PCR amplification was then sequenced and aligned  ...[more]

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