| 1st International Conference on Fisheries and Marine Science | |
| Determination of the aerolysin gene in Aeromonas hydrophila using the polymerase chain reaction (pcr) technique | |
| Christy, G.^1 ; Kusdawarti, R.^2 ; Handijatno, D.^2 | |
| Program Study of Aquaculture, Faculty of Fisheries and Marine, Universitas Airlangga, Surabaya, Indonesia^1 | |
| Department of Fish Health Management and Aquaculture, Faculty of Fisheries and Marine, Universitas Airlangga, Surabaya, Indonesia^2 | |
| 关键词: Aeromonas hydrophila; Biochemical tests; Blood agars; Cytotoxins; Fish disease; Mortality rate; Polymerase chain reaction techniques; Virulence factors; | |
| Others : https://iopscience.iop.org/article/10.1088/1755-1315/236/1/012097/pdf DOI : 10.1088/1755-1315/236/1/012097 |
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| 来源: IOP | |
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【 摘 要 】
Aeromonas hydrophila is a bacterium that often causes outbreaks of fish diseases with high mortality rates. A. hydrophila has several virulence factors such as cytotoxin, protease, s-layers, and aerolysin. Aerolysin is an important virulence factor, as it is a marker of a strain of Aeromonas that can be virulent or not. This study aims to prove whether or not there is an aerolysin gene in the A.hydrophila isolates or not. The study was carried out using a PCR test on the A.hydrophila isolates from the Fish Disease and Environtmental Examination, Serang Banten (SRIsolate) and on the ATCC of A. hydrophila (ATCC Isolate) as a positive control. Biochemical tests and hemolysis in Blood Agar were carried out before the PCR test was carried out. The primer sequence used in the PCR process was "5'-'cctatggcctgagcgagaag'- '3» for the forward and "5'-'ccagttccagtcccaccact'-'3» for the reverse. The results show that the SR isolates have an aerolysin gene. These results show the formation of a band with a length of 430 bp that matches the amplicon target on the SR isolates.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| Determination of the aerolysin gene in Aeromonas hydrophila using the polymerase chain reaction (pcr) technique | 539KB |
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