Novel genetic variants of Hepatitis B Virus in fulminant hepatitis

Fulminant hepatitis (FH) is a life-threatening liver disease characterised by intense immune attack and massive liver cell death. The common precore stop codon mutation of hepatitis B virus (HBV), A1896, is frequently associated with FH, but lacks specificity. This study attempts to uncover all poss...

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Main Authors: Chook, Jack Bee *, Ngeow, Yun Fong, Tee, Kok Keng, Peh, Suat Cheng *, Mohamed, Rosmawati
Format: Article
Language:English
Published: Hindawi 2017
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Online Access:http://eprints.sunway.edu.my/871/1/Chook%20JB%202017%20Novel%20Genetic%20variants%20of%20fulminant%20HBV%20J%20Pathog.pdf
http://eprints.sunway.edu.my/871/
http://doi.org/10.1155/2017/1231204
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spelling my.sunway.eprints.8712019-04-30T08:24:20Z http://eprints.sunway.edu.my/871/ Novel genetic variants of Hepatitis B Virus in fulminant hepatitis Chook, Jack Bee * Ngeow, Yun Fong Tee, Kok Keng Peh, Suat Cheng * Mohamed, Rosmawati R Medicine (General) Fulminant hepatitis (FH) is a life-threatening liver disease characterised by intense immune attack and massive liver cell death. The common precore stop codon mutation of hepatitis B virus (HBV), A1896, is frequently associated with FH, but lacks specificity. This study attempts to uncover all possible viral nucleotides that are specifically associated with FH through a compiled sequence analysis of FH and non-FH cases from acute infection. We retrieved 67 FH and 280 acute non-FH cases of hepatitis B from GenBank and applied support vector machine (SVM) model to seek candidate nucleotides highly predictive of FH. Six best candidates with top predictive accuracy, 92.5%, were used to build a SVM model; they are C2129 (85.3%), T720 (83.0%), Y2131 (82.4%), T2013 (82.1%),K2048 (82.1%), and A2512 (82.1%). This model gave a high specificity (99.3%), positive predictive value (95.6%), and negative predictive value (92.1%), but only moderate sensitivity (64.2%).We successfully built a SVM model comprising six variants that are highly predictive and specific for FH: four in the core region and one each in the polymerase and the surface regions. These variants indicate that intracellular virion/core retention could play an important role in the progression to FH. Hindawi 2017-12-19 Article PeerReviewed text en http://eprints.sunway.edu.my/871/1/Chook%20JB%202017%20Novel%20Genetic%20variants%20of%20fulminant%20HBV%20J%20Pathog.pdf Chook, Jack Bee * and Ngeow, Yun Fong and Tee, Kok Keng and Peh, Suat Cheng * and Mohamed, Rosmawati (2017) Novel genetic variants of Hepatitis B Virus in fulminant hepatitis. Journal of Pathogens, 2017. pp. 1-6. ISSN 2090-3057 http://doi.org/10.1155/2017/1231204 doi:10.1155/2017/1231204
institution Sunway University
building Sunway Campus Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Sunway University
content_source Sunway Institutional Repository
url_provider http://eprints.sunway.edu.my/
language English
topic R Medicine (General)
spellingShingle R Medicine (General)
Chook, Jack Bee *
Ngeow, Yun Fong
Tee, Kok Keng
Peh, Suat Cheng *
Mohamed, Rosmawati
Novel genetic variants of Hepatitis B Virus in fulminant hepatitis
description Fulminant hepatitis (FH) is a life-threatening liver disease characterised by intense immune attack and massive liver cell death. The common precore stop codon mutation of hepatitis B virus (HBV), A1896, is frequently associated with FH, but lacks specificity. This study attempts to uncover all possible viral nucleotides that are specifically associated with FH through a compiled sequence analysis of FH and non-FH cases from acute infection. We retrieved 67 FH and 280 acute non-FH cases of hepatitis B from GenBank and applied support vector machine (SVM) model to seek candidate nucleotides highly predictive of FH. Six best candidates with top predictive accuracy, 92.5%, were used to build a SVM model; they are C2129 (85.3%), T720 (83.0%), Y2131 (82.4%), T2013 (82.1%),K2048 (82.1%), and A2512 (82.1%). This model gave a high specificity (99.3%), positive predictive value (95.6%), and negative predictive value (92.1%), but only moderate sensitivity (64.2%).We successfully built a SVM model comprising six variants that are highly predictive and specific for FH: four in the core region and one each in the polymerase and the surface regions. These variants indicate that intracellular virion/core retention could play an important role in the progression to FH.
format Article
author Chook, Jack Bee *
Ngeow, Yun Fong
Tee, Kok Keng
Peh, Suat Cheng *
Mohamed, Rosmawati
author_facet Chook, Jack Bee *
Ngeow, Yun Fong
Tee, Kok Keng
Peh, Suat Cheng *
Mohamed, Rosmawati
author_sort Chook, Jack Bee *
title Novel genetic variants of Hepatitis B Virus in fulminant hepatitis
title_short Novel genetic variants of Hepatitis B Virus in fulminant hepatitis
title_full Novel genetic variants of Hepatitis B Virus in fulminant hepatitis
title_fullStr Novel genetic variants of Hepatitis B Virus in fulminant hepatitis
title_full_unstemmed Novel genetic variants of Hepatitis B Virus in fulminant hepatitis
title_sort novel genetic variants of hepatitis b virus in fulminant hepatitis
publisher Hindawi
publishDate 2017
url http://eprints.sunway.edu.my/871/1/Chook%20JB%202017%20Novel%20Genetic%20variants%20of%20fulminant%20HBV%20J%20Pathog.pdf
http://eprints.sunway.edu.my/871/
http://doi.org/10.1155/2017/1231204
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