Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2

Early diagnosis of dengue virus (DENV) infection is affirmative for patient management and control of the disease. Detection of nonstructural-1 (NS1) antigen has been proven to provide early detection of DENV infection. Commercial NS1 antigen assays are available in Indonesia with variable sensitivi...

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Main Authors: BETI ERNAWATI DEWI, FITHRIYAH FITHRIYAH, ANDRIANSJAH RUKMANA, PAISAL PAISAL, DEKA LARASATI, TJAHJANI MIRAWATI SUDIRO
Format: Article
Language:English
Published: Indonesian Society for Microbiology 2012-04-01
Series:Microbiology Indonesia
Subjects:
Online Access:https://jurnal.permi.or.id/index.php/mionline/article/view/135
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spelling doaj-03d5a7d93d174c1a86f712e16b0c2c6c2021-08-20T12:58:41ZengIndonesian Society for MicrobiologyMicrobiology Indonesia1978-34772087-85752012-04-016110.5454/mi.6.1.3Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2BETI ERNAWATI DEWIFITHRIYAH FITHRIYAHANDRIANSJAH RUKMANAPAISAL PAISALDEKA LARASATITJAHJANI MIRAWATI SUDIROEarly diagnosis of dengue virus (DENV) infection is affirmative for patient management and control of the disease. Detection of nonstructural-1 (NS1) antigen has been proven to provide early detection of DENV infection. Commercial NS1 antigen assays are available in Indonesia with variable sensitivity. In an attempt to develop an NS1-based diagnostic test, we successfully cloned NS1 gene of DENV2 to a glutathione Stransferase- based vector pGEX6P-1 in Escherichia coli system. The recombinant protein (pG2NS12) was expressed in E. coli BL21. After induction with isopropyl-β-D-thiogalactoside 0.1 mM for 4 h at 25 °C a recombinant protein GST-NS1 with molecular size of approximately 75 kDa was  obtained. The fusion protein was insoluble and found in the pellet fraction of the cell lysate. Addition of lysozyme (10 mg mL-1) and DNase-I (7.2 mg mL-1) in the lysis buffer was necessary to collect proteins from the pellet fraction. The proteins in the cell pellet were fractionated through Sephadex-G100 column, and GST-NS1 was further purified with Glutathione-Sepharose 4B beads. To obtain pure recombinant NS1 protein to be used in the immunization of mice, the fusion protein was cut with PreScission Protease® by addition of 0.075% Triton-X 100 was necessary to cut the fusion protein. We found that antibodies that recognized the recombinant NS1 protein and DENV2 virus were produced in mice immunized with purified NS1 protein. Therefore, our recombinant NS1 could be used to produce antibody that is potentially useful for developing diagnostic assay to determine the presence of dengue virus NS1 antigen in patient sera.https://jurnal.permi.or.id/index.php/mionline/article/view/135cloningdengue virusexpressionnon structural protein NS-1
collection DOAJ
language English
format Article
sources DOAJ
author BETI ERNAWATI DEWI
FITHRIYAH FITHRIYAH
ANDRIANSJAH RUKMANA
PAISAL PAISAL
DEKA LARASATI
TJAHJANI MIRAWATI SUDIRO
spellingShingle BETI ERNAWATI DEWI
FITHRIYAH FITHRIYAH
ANDRIANSJAH RUKMANA
PAISAL PAISAL
DEKA LARASATI
TJAHJANI MIRAWATI SUDIRO
Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2
Microbiology Indonesia
cloning
dengue virus
expression
non structural protein NS-1
author_facet BETI ERNAWATI DEWI
FITHRIYAH FITHRIYAH
ANDRIANSJAH RUKMANA
PAISAL PAISAL
DEKA LARASATI
TJAHJANI MIRAWATI SUDIRO
author_sort BETI ERNAWATI DEWI
title Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2
title_short Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2
title_full Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2
title_fullStr Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2
title_full_unstemmed Cloning and Expression of Nonstructural Protein NS1 of Dengue Virus Serotype 2
title_sort cloning and expression of nonstructural protein ns1 of dengue virus serotype 2
publisher Indonesian Society for Microbiology
series Microbiology Indonesia
issn 1978-3477
2087-8575
publishDate 2012-04-01
description Early diagnosis of dengue virus (DENV) infection is affirmative for patient management and control of the disease. Detection of nonstructural-1 (NS1) antigen has been proven to provide early detection of DENV infection. Commercial NS1 antigen assays are available in Indonesia with variable sensitivity. In an attempt to develop an NS1-based diagnostic test, we successfully cloned NS1 gene of DENV2 to a glutathione Stransferase- based vector pGEX6P-1 in Escherichia coli system. The recombinant protein (pG2NS12) was expressed in E. coli BL21. After induction with isopropyl-β-D-thiogalactoside 0.1 mM for 4 h at 25 °C a recombinant protein GST-NS1 with molecular size of approximately 75 kDa was  obtained. The fusion protein was insoluble and found in the pellet fraction of the cell lysate. Addition of lysozyme (10 mg mL-1) and DNase-I (7.2 mg mL-1) in the lysis buffer was necessary to collect proteins from the pellet fraction. The proteins in the cell pellet were fractionated through Sephadex-G100 column, and GST-NS1 was further purified with Glutathione-Sepharose 4B beads. To obtain pure recombinant NS1 protein to be used in the immunization of mice, the fusion protein was cut with PreScission Protease® by addition of 0.075% Triton-X 100 was necessary to cut the fusion protein. We found that antibodies that recognized the recombinant NS1 protein and DENV2 virus were produced in mice immunized with purified NS1 protein. Therefore, our recombinant NS1 could be used to produce antibody that is potentially useful for developing diagnostic assay to determine the presence of dengue virus NS1 antigen in patient sera.
topic cloning
dengue virus
expression
non structural protein NS-1
url https://jurnal.permi.or.id/index.php/mionline/article/view/135
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