JCM Figure table search 04
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
JCM.01519-07v1
46/4/1268    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pas, S. D.
Right arrow Articles by Niesters, H. G. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pas, S. D.
Right arrow Articles by Niesters, H. G. M.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, April 2008, p. 1268-1273, Vol. 46, No. 4
0095-1137/08/$08.00+0     doi:10.1128/JCM.01519-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Comparison of Reverse Hybridization, Microarray, and Sequence Analysis for Genotyping Hepatitis B Virus{triangledown}

Suzan D. Pas,1* Nathalie Tran,2 Robert A. de Man,3 C. Burghoorn-Maas,1 Guy Vernet,2 and Hubert G. M. Niesters1,{dagger}

Department of Virology,1 Gastroenterology, Erasmus MC University Medical Centre Rotterdam, The Netherlands,3 bioMérieux, Lyon, France2

Received 30 July 2007/ Returned for modification 12 October 2007/ Accepted 7 February 2008

Hepatitis B virus (HBV) genotyping has become important in epidemiological and clinical diagnoses, given the relationship between the viral genotype and the progression of disease or the appearance of antiviral resistance. Since genotyping by sequence and phylogenetic analyses is not convenient in the clinical setting, we evaluated InnoLipa HBV genotyping (Innogenetics, Belgium) and an HBV DNA-Chip (bioMerieux, France) prototype assay and compared their sequencing of the gold standard S gene, using a cohort of 275 individual patient samples. All but two samples, belonging to distant and individual subgroups within a single genotype, were detected by InnoLipa HBV assay. Four samples with dual infections belonging to genotypes A and G were identified only by InnoLipa HBV assay. Using an HBV DNA-Chip assay, one sample could not be amplified due to a low viral load. Four samples were identified as genotype C and two as genotype D by sequencing but were classified as genotype A (two samples) and D (two samples) and as A (one sample) and G (one sample) by the DNA-Chip assay. In conclusion, the InnoLipa HBV genotyping strip assay detected dual infections and was an easy and quick tool for genotyping, with a sensitivity of 99.3% and a specificity of 100% compared to sequence analysis. HBV DNA-Chip assay showed a sensitivity and specificity of 97.5 and 97.8%, respectively.


* Corresponding author. Mailing address: Erasmus MC, Department of Virology, L355, 's Gravendijkwal 230, 3015 CE, Rotterdam, The Netherlands. Phone: 31 10 704.4404. Fax: 31 10 704.3441. E-mail: s.pas{at}erasmusmc.nl

{triangledown} Published ahead of print on 20 February 2008.

{dagger} Current address: University Medical Centre Groningen, Department of Medical Microbiology, Section of Clinical Virology, Room 2.040, Hanzeplein 1, 9713 GZ Groningen, The Netherlands. Phone: 31-50 361 5060. Fax: 31-50 363 3528. E-mail: H.G.M.Niesters{at}mmb.umcg.nl.


Journal of Clinical Microbiology, April 2008, p. 1268-1273, Vol. 46, No. 4
0095-1137/08/$08.00+0     doi:10.1128/JCM.01519-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Antimicrob. Agents Chemother. Clin. Microbiol. Rev.
Clin. Vaccine Immunol. ALL ASM JOURNALS

Copyright © 2008 by the American Society for Microbiology. All rights reserved.