Rapid Detection of the Aeromonas sp. group using Conventional PCR at the Aquaculture Technology Development Center, Cangkringan, Sleman, Special Region of Yogyakarta

Authors

  • Mohammad Nurhafid Aquaculture Study Program, Faculty of Fisheries and Marine Sciences, Jenderal Soedirman University St.Dr.Soeparno, Karangwangkal, Purwokerto 53122, Central Java, Indonesia. Author https://orcid.org/0000-0002-7648-6751
  • Astuti Department Of Fish Pest and Disease Laboratory, Aquculture Technology Development Center, Cangkringan, Sleman, Yogyakarta Special Region, 55583 Indonesia Author
  • Reza Muhammad Riady Aquaculture Study Program, Faculty of Fisheries and Marine Sciences, Jenderal Soedirman University St.Dr.Soeparno, Karangwangkal, Purwokerto 53122, Central Java, Indonesia. Author https://orcid.org/0000-0001-9140-8738
  • Ufianah Aquaculture Study Program, Faculty of Fisheries and Marine Sciences, Jenderal Soedirman University St.Dr.Soeparno, Karangwangkal, Purwokerto 53122, Central Java, Indonesia. Author
  • Eko Pardiyanto Artha Genetikalab Indonesia, Banguntapan, Bantul, Yogyakarta Special Region, 55198 Indonesia Author
  • Faldo Ody Ruanda Artha Genetikalab Indonesia, Banguntapan, Bantul, Yogyakarta Special Region, 55198 Indonesia Author

DOI:

https://doi.org/10.62521/c8cxaf15

Keywords:

Aeromonas sp. Pathogen bacteria, Fish disease, Aquaculture

Abstract

The catfish is a freshwater cultivated fish that can be found all over Indonesia. However, the problems that occur in general are usually attacks by pathogens from the Aeromonas sp group. This research aims to optimize the rapid detection of the Aeromonas sp group using PCR at the Aquaculture Technology Development Center, Cangkringan, Sleman, special region of Yogyakarta. The research was conducted by survey with purposive sampling. Isolation was carried out using two growth media, namely Tryptone Soy Agar (TSA) and Glutamate Starch Phenile (GSP). Colonies that had characteristics of the Aeromonas sp group were subjected to PCR amplification using specific primers for the Aeromonas sp group. The results of the amplification resulted in DNA that matched the target, namely 953bp, which showed that the sample belonged to the Aeromonas sp group. Based on this technique, the level of accuracy in detecting pathogens is higher than conventional methods.

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References

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Published

2024-05-02

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How to Cite

Rapid Detection of the Aeromonas sp. group using Conventional PCR at the Aquaculture Technology Development Center, Cangkringan, Sleman, Special Region of Yogyakarta. (2024). Journal Of Artha Biological Engineering, 1(1), 51-59. https://doi.org/10.62521/c8cxaf15

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