Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticus

The objective of this study was to analyse the size of DNA fragment from both resistant and susceptible groupers (Epinephelus fuscoguttatus) after infection by Vibrio alginolyticus. This study was conducted by two steps, firstly, determination of Lethal Concentration (LC50) of Vibrio alginolyticus t...

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Main Author: St Hidayah Triana
Format: Article
Language:English
Published: Fakultas MIPA Universitas Jember 2010-01-01
Series:Jurnal Ilmu Dasar
Subjects:
Online Access:https://jurnal.unej.ac.id/index.php/JID/article/view/101
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spelling doaj-0e8f2cb2b9bf4ecd9bfad577213e5b202020-11-25T02:02:21ZengFakultas MIPA Universitas JemberJurnal Ilmu Dasar1411-57352442-56132010-01-01111816101Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticusSt Hidayah Triana0FPIK UMI MakassarThe objective of this study was to analyse the size of DNA fragment from both resistant and susceptible groupers (Epinephelus fuscoguttatus) after infection by Vibrio alginolyticus. This study was conducted by two steps, firstly, determination of Lethal Concentration (LC50) of Vibrio alginolyticus to obtain fish which resistant and susceptible against Vibrio alginolyticus infection. Secondly, analysis of DNA fragment from both resistant and susceptible fish against Vibrio alginolyticus infection by PCR-RAPD method. In order to analyse the fragment of DNA from the fish, DNA was extracted and the concentration was counted using Kit. Sixteen primers were used, which six primers (RAPD 1-6) were from RAPD Kit, other primers were OPA-14, -A, -B, -C, and -D, YNZ 22, UBC-122, -158, -456, and -457. The results demonstrated that the concentration of bacteria that caused 50 % of fish mortality (LC50)was 7.4 × 105 CFU/L. Based on this concentration, the number of fish which were resistant and susceptible against Vibrio alginolyticus infection were obtained. For the DNA fragment analysis, the concentration of DNA after extraction ranges from 448 μg/ml to 3320 μg/ml with the purity ranges from 86-95 %. From 16 primers used for PCR-RAPD, only 6 primers showed DNA fragments in the gel electrophoresis. Those primers are OPA-14, YNZ 22, UBC-122, -158, -456, and -457. The number of DNA fragments was higher in the group of resistant fish (average 6.4 fragments) than in the group of susceptible fish (average 4.9 fragments). Fifty seven percent (57%) from resistant fish showed specific DNA fragments with size 2.0 kb, indicate that these fragment sizes have a potential role to be used as a marker for obtaining the resistant fish against bacterial infection.https://jurnal.unej.ac.id/index.php/JID/article/view/101analysis of dna fragmentepinephelus fuscoguttatusvibrio alginolyticuspcr rapd
collection DOAJ
language English
format Article
sources DOAJ
author St Hidayah Triana
spellingShingle St Hidayah Triana
Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticus
Jurnal Ilmu Dasar
analysis of dna fragment
epinephelus fuscoguttatus
vibrio alginolyticus
pcr rapd
author_facet St Hidayah Triana
author_sort St Hidayah Triana
title Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticus
title_short Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticus
title_full Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticus
title_fullStr Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticus
title_full_unstemmed Analysis of DNA Fragment Obtained from Groupers (Epinephelus fuscoguttatus) Challenged by Vibrio alginolyticus
title_sort analysis of dna fragment obtained from groupers (epinephelus fuscoguttatus) challenged by vibrio alginolyticus
publisher Fakultas MIPA Universitas Jember
series Jurnal Ilmu Dasar
issn 1411-5735
2442-5613
publishDate 2010-01-01
description The objective of this study was to analyse the size of DNA fragment from both resistant and susceptible groupers (Epinephelus fuscoguttatus) after infection by Vibrio alginolyticus. This study was conducted by two steps, firstly, determination of Lethal Concentration (LC50) of Vibrio alginolyticus to obtain fish which resistant and susceptible against Vibrio alginolyticus infection. Secondly, analysis of DNA fragment from both resistant and susceptible fish against Vibrio alginolyticus infection by PCR-RAPD method. In order to analyse the fragment of DNA from the fish, DNA was extracted and the concentration was counted using Kit. Sixteen primers were used, which six primers (RAPD 1-6) were from RAPD Kit, other primers were OPA-14, -A, -B, -C, and -D, YNZ 22, UBC-122, -158, -456, and -457. The results demonstrated that the concentration of bacteria that caused 50 % of fish mortality (LC50)was 7.4 × 105 CFU/L. Based on this concentration, the number of fish which were resistant and susceptible against Vibrio alginolyticus infection were obtained. For the DNA fragment analysis, the concentration of DNA after extraction ranges from 448 μg/ml to 3320 μg/ml with the purity ranges from 86-95 %. From 16 primers used for PCR-RAPD, only 6 primers showed DNA fragments in the gel electrophoresis. Those primers are OPA-14, YNZ 22, UBC-122, -158, -456, and -457. The number of DNA fragments was higher in the group of resistant fish (average 6.4 fragments) than in the group of susceptible fish (average 4.9 fragments). Fifty seven percent (57%) from resistant fish showed specific DNA fragments with size 2.0 kb, indicate that these fragment sizes have a potential role to be used as a marker for obtaining the resistant fish against bacterial infection.
topic analysis of dna fragment
epinephelus fuscoguttatus
vibrio alginolyticus
pcr rapd
url https://jurnal.unej.ac.id/index.php/JID/article/view/101
work_keys_str_mv AT sthidayahtriana analysisofdnafragmentobtainedfromgroupersepinephelusfuscoguttatuschallengedbyvibrioalginolyticus
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