Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 Isolate

The availability of specific and rapid detection methods is essential for monitoring the health status of farmed species, particularly in viral disease as in this case early diagnosis is a critical factor in containing disease outbreaks. Jembrana Disease Virus (JDV) is a lentivirus that causes an ac...

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Main Authors: Asmarani Kusumawati, Rarastoeti Pratiwi, Pudji Astuti, Penny Humaidah Hamid
Format: Article
Language:English
Published: Universitas Gadjah Mada, Yogyakarta 2015-11-01
Series:Indonesian Journal of Biotechnology
Online Access:http://journal.ugm.ac.id/ijbiotech/article/view/7819
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spelling doaj-7f2d29aeb0004436b85e6e3a0c7da5e92020-11-24T23:28:52ZengUniversitas Gadjah Mada, YogyakartaIndonesian Journal of Biotechnology0853-86542089-22412015-11-011516535Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 IsolateAsmarani KusumawatiRarastoeti PratiwiPudji AstutiPenny Humaidah HamidThe availability of specific and rapid detection methods is essential for monitoring the health status of farmed species, particularly in viral disease as in this case early diagnosis is a critical factor in containing disease outbreaks. Jembrana Disease Virus (JDV) is a lentivirus that causes an acute, severe disease syndrome in infected Bali cattle in Indonesia, resulting in heavy economic losses because of the high mortalities. The virus-host interaction and the modes of transmission are still unknown. The goal of the research was to design<br />a probe candidate of Jembrana Disease Virus based on envelope-transmembrane (env-tm) gene to optimize Jembrana disease detection method. The DNA fragment derived from env-tm of JDV was used, cloned in pGEX-TM and expressed in E.coli DH 5&alpha;. Sequence analysis was conducted with BLAST programs from NCBI. Sequence analyses of the fragments of env-tm clone, indicated that it has a very closed genetic relation with 97,68% homology identity. Probe was designed based on the conserved region of env-tm using Geneious resulted in JT2 252 bp long. BLAST analyses showed that probes had high specifity to other strains of JDV in Indonesia.<br /><br />Key words : probe, env-tm, JDV, specifity, sensitivity.http://journal.ugm.ac.id/ijbiotech/article/view/7819
collection DOAJ
language English
format Article
sources DOAJ
author Asmarani Kusumawati
Rarastoeti Pratiwi
Pudji Astuti
Penny Humaidah Hamid
spellingShingle Asmarani Kusumawati
Rarastoeti Pratiwi
Pudji Astuti
Penny Humaidah Hamid
Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 Isolate
Indonesian Journal of Biotechnology
author_facet Asmarani Kusumawati
Rarastoeti Pratiwi
Pudji Astuti
Penny Humaidah Hamid
author_sort Asmarani Kusumawati
title Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 Isolate
title_short Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 Isolate
title_full Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 Isolate
title_fullStr Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 Isolate
title_full_unstemmed Characterization of envelope-transmembrane Gene of Jembrana Disease Virus Tabanan 1995 Isolate
title_sort characterization of envelope-transmembrane gene of jembrana disease virus tabanan 1995 isolate
publisher Universitas Gadjah Mada, Yogyakarta
series Indonesian Journal of Biotechnology
issn 0853-8654
2089-2241
publishDate 2015-11-01
description The availability of specific and rapid detection methods is essential for monitoring the health status of farmed species, particularly in viral disease as in this case early diagnosis is a critical factor in containing disease outbreaks. Jembrana Disease Virus (JDV) is a lentivirus that causes an acute, severe disease syndrome in infected Bali cattle in Indonesia, resulting in heavy economic losses because of the high mortalities. The virus-host interaction and the modes of transmission are still unknown. The goal of the research was to design<br />a probe candidate of Jembrana Disease Virus based on envelope-transmembrane (env-tm) gene to optimize Jembrana disease detection method. The DNA fragment derived from env-tm of JDV was used, cloned in pGEX-TM and expressed in E.coli DH 5&alpha;. Sequence analysis was conducted with BLAST programs from NCBI. Sequence analyses of the fragments of env-tm clone, indicated that it has a very closed genetic relation with 97,68% homology identity. Probe was designed based on the conserved region of env-tm using Geneious resulted in JT2 252 bp long. BLAST analyses showed that probes had high specifity to other strains of JDV in Indonesia.<br /><br />Key words : probe, env-tm, JDV, specifity, sensitivity.
url http://journal.ugm.ac.id/ijbiotech/article/view/7819
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AT pudjiastuti characterizationofenvelopetransmembranegeneofjembranadiseasevirustabanan1995isolate
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