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Molecular Genotyping of HBV by using Nested PCR-RFLP among Hepatitis B Patients in Daerah Istimewa Yogyakarta Province and Surrounding Area

Indonesian Journal of Biotechnology · Vol. 13 No. 2 (2008)

DOI
10.22146/ijbiotech.7801
ISSN
2089-2241, 0853-8654
Terbit
2008-12-05
Penerbit
Universitas Gadjah Mada
Bahasa
eng

Abstrak

Hepatitis B virus (HBV) can be classified into 8 genotypes, genotype A to H. Genotype of HBV is important for clinical and etiological investigations. Research for HBV genotyping, HBV transmission study using nested PCR and HBV genotyping based on RFLP using restriction enzymes have been reported. However, both of those methods have been not applied for HBV genotyping study among hepatitis B patients in endemic area, like Indonesia yet. Molecular genotyping of HBV will describe epidemiology, pathogenesis and clinical implication of HBV. Combination of nested PCR and RFLP (nested PCR-RFLP) method to determine HBV genotype in Indonesia is still less information. The objectives of study were to develop a system for HBV genotyping by nested PCR combined with RFLP (nested PCR-RFLP) method based on nucleotide sequence of surface protein encoding gene (S gene) in HBV genome and to confirm HBV genotypes which predominantly found among hepatitis B patients in Daerah Istimewa Yogyakarta Province and surrounding area. Total of 149 sera from chronic hepatitis B patients from Daerah Istimewa Yogyakarta and surrounding areas were collected for in this work. Viral DNA were extracted from sera of hepatitis B patients and used as template for first round nested PCR amplification using outer primers set. Amplicons of first round PCR were used as template for second round amplification using inner primers set. Then, amplicons of second round nested PCR were restriction digested by Sty I and Bsr I enzymes. For HBV genotyping then the restriction products were analyzed by RFLP based on restriction pattern. Results showed that the first round nested PCR amplification generated DNA fragments of whole S gene in length 1.233 bp, and in second round nested PCR amplification using inner primer set generated DNA fragments 585 bp in length. Genotype analysis for all samples using nested PCR-RFLP methods by restriction digested of Sty I and Bsr I enzymes found only 2 HBV genotypes among hepatitis B patients, namely genotype B and C. Quantification data showed that most of hepatitis B patients found infected by HBV genotype B (92,8%), genotype C (3,6%) and unidentified genotype (3,6%). Nested PCR-RFLP methods for HBV genotyping is simple and inexpensive for clinical diagnostic in large scale.

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  • Universitas Gadjah Mada
  • National Institute of Technology and Evaluation
  • Justus-Liebig-Universität Gießen
  • Jenderal Soedirman University
  • Universitas Teuku Umar
  • Universitas Islam Negeri Ar-Raniry
  • The University of Tokyo
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Rekan penulisOrganisasiArtikel bersama
Michael KannJustus-Liebig-Universität Gießen7
Tri WibawaUniversitas Gadjah Mada5
Hevi WihadmadyatamiUniversitas Gadjah Mada4
Warih Pulung NugrahaniAfiliasi tidak diketahui3
Krisna Noli AndrianUniversitas Gadjah Mada3
Jaka WidadaUniversitas Gadjah Mada2
Diana SavitriUniversitas Gadjah Mada2
Irhamna PutriAfiliasi tidak diketahui2
Medania PurwaningrumUniversitas Gadjah Mada2
Hera NirwatiUniversitas Gadjah Mada2
Sp.A SutaryoUniversitas Gadjah Mada2
Diani MentariJenderal Soedirman University1
Rinawati RinawatiUniversitas Teuku Umar1
E. SuharyantoUniversitas Gadjah Mada1
Muhammad AdnanUniversitas Islam Negeri Ar-Raniry1
Matin NuhamunadaUniversitas Gadjah Mada1
Lisna HidayatiUniversitas Gadjah Mada1
Abdul Rahman SiregarUniversitas Gadjah Mada1
Shinta HartantoUniversitas Gadjah Mada1
Sofia MubarikaUniversitas Gadjah Mada1
Camelia HerdiniUniversitas Gadjah Mada1
Bambang HariwiyantoUniversitas Gadjah Mada1
Akira HosoyamaNational Institute of Technology and Evaluation1
Atsushi YamazoeNational Institute of Technology and Evaluation1
Hideaki NojiriThe University of Tokyo1
M. MurwantokoAfiliasi tidak diketahui1
Ch. Retna HandayaniAfiliasi tidak diketahui1
Rarastoeti PratiwiUniversitas Gadjah Mada1
T. TrijokoUniversitas Gadjah Mada1
Aushia Tanzih Al HaqUniversitas Gadjah Mada1
Ida TjahajatiUniversitas Gadjah Mada1
Muh. Disna FaizalUniversitas Gadjah Mada1
Subagus WahyuonoUniversitas Gadjah Mada1
Tri Rini NuringtyasUniversitas Gadjah Mada1
Dian Ayuning TyasUniversitas Gadjah Mada1

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Sumber metadata: OAI-PMH (metadata jurnal) https://jurnal.ugm.ac.id/ijbiotech/oai, pertama di-harvest 8 Nov 2026, terakhir terlihat 8 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en-US">Molecular Genotyping of HBV by using Nested PCR-RFLP among Hepatitis B Patients in Daerah Istimewa Yogyakarta Province and Surrounding Area</dc:title>
	<dc:creator>Haryanto, Aris</dc:creator>
	<dc:creator>Mulyani, Nenny Sri</dc:creator>
	<dc:creator>Widowati, Titis</dc:creator>
	<dc:creator>Wijayanti, Nastiti</dc:creator>
	<dc:creator>Hadi, Purnomo</dc:creator>
	<dc:description xml:lang="en-US">Hepatitis B virus (HBV) can be classified into 8 genotypes, genotype A to H. Genotype of HBV is important for clinical and etiological investigations. Research for HBV genotyping, HBV transmission study using nested PCR and HBV genotyping based on RFLP using restriction enzymes have been reported. However, both of those methods have been not applied for HBV genotyping study among hepatitis B patients in endemic area, like Indonesia yet. Molecular genotyping of HBV will describe epidemiology, pathogenesis and clinical implication of HBV. Combination of nested PCR and RFLP (nested PCR-RFLP) method to determine HBV genotype in Indonesia is still less information. The objectives of study were to develop a system for HBV genotyping by nested PCR combined with RFLP (nested PCR-RFLP) method based on nucleotide sequence of surface protein encoding&lt;/div&gt;&lt;div&gt;gene (S gene) in HBV genome and to confirm HBV genotypes which predominantly found among hepatitis B patients in Daerah Istimewa Yogyakarta Province and surrounding area. Total of 149 sera from chronic hepatitis B patients from Daerah Istimewa Yogyakarta and surrounding areas were collected for in this work. Viral DNA were extracted from sera of hepatitis B patients and used as template for first round nested PCR amplification using outer primers set. Amplicons of first round PCR were used as template for second round amplification using inner primers set. Then, amplicons of second round nested PCR were restriction digested by Sty I and Bsr I enzymes. For HBV genotyping then the restriction products were analyzed by RFLP based on restriction pattern. Results showed that the first round nested PCR amplification generated DNA fragments of whole S gene in length 1.233 bp, and in second round nested PCR amplification using inner primer set generated DNA fragments 585 bp in length. Genotype analysis for all samples using nested PCR-RFLP methods by restriction digested of Sty I and Bsr I enzymes found only 2 HBV genotypes among hepatitis B patients, namely genotype B and C. Quantification&lt;/div&gt;&lt;div&gt;data showed that most of hepatitis B patients found infected by HBV genotype B (92,8%), genotype C (3,6%) and unidentified genotype (3,6%). Nested PCR-RFLP methods for HBV genotyping is simple and inexpensive for clinical diagnostic in large scale.</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Gadjah Mada</dc:publisher>
	<dc:date>2008-12-05</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en-US">Original Research Articles</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.ugm.ac.id/ijbiotech/article/view/7801</dc:identifier>
	<dc:identifier>10.22146/ijbiotech.7801</dc:identifier>
	<dc:source xml:lang="en-US">Indonesian Journal of Biotechnology; Vol 13, No 2 (2008)</dc:source>
	<dc:source>2089-2241</dc:source>
	<dc:source>0853-8654</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.ugm.ac.id/ijbiotech/article/view/7801/6042</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2015 Indonesian Journal of Biotechnology</dc:rights>
</oai_dc:dc>