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Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts

Hepatitis C virus (HCV) is enveloped RNA virus, encoding for a polyprotein that is processed by cellular proteases. The virus is responsible for liver cirrhosis, allograft rejection, and human hepatocellular carcinoma. Based on studies including compositional analysis, odds ratio analysis, parity an...

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Главные авторы: Rzhepakovsky, I. V., Ржепаковский, И. В.
Формат: Статья
Язык:English
Опубликовано: 2023
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Online-ссылка:https://dspace.ncfu.ru/handle/20.500.12258/23498
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spelling ir-20.500.12258-234982025-02-11T09:15:27Z Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts Rzhepakovsky, I. V. Ржепаковский, И. В. Allograft rejection Liver transplantation Codon usage Liver cirrhosis Hepatitis C virus (HCV) Hepatocellular carcinoma Similarity index Relative codon deoptimization index Hepatitis C virus (HCV) is enveloped RNA virus, encoding for a polyprotein that is processed by cellular proteases. The virus is responsible for liver cirrhosis, allograft rejection, and human hepatocellular carcinoma. Based on studies including compositional analysis, odds ratio analysis, parity analysis, skew analysis, relative synonymous codon usage, codon bias, and protein properties, it was evident that codon usage bias in HCV is dependent upon the nucleotide composition. Codon context analysis revealed CTC-CTG as a preferred codon pair. While CGA and CGT codons were rare, none of the codons were rare in HCV-like viruses envisaged in the present study. Many of the preferred codon pairs were valine amino acid-initiated, which possibly infers viral infectivity; hence the role of selection forces appears to act on the HCV genome, which was further validated by neutrality analysis where selection accounted for 87.28%, while mutation accounted for 12.72% force shaping codon usage. Furthermore, codon usage was correlated with the length of the genome. HCV viruses prefer valine-initiated codon pairs, while HCV-like viruses prefer alanine-initiated codon pairs. The HCV host range is very narrow and is confined to only humans and chimpanzees. Based on indices including codon usage correlation analysis, similarity index, and relative codon deoptimization index, it is evident in the study that the chimpanzee is the primary host of the virus. The present study helped elucidate the preferred host for HCV. The information presented in the study paved the way for generating an attenuated vaccine candidate through viral recoding, with finely tuned nucleotide composition and a perfect balance of preferred and rare codons. 2023-05-24T14:02:23Z 2023-05-24T14:02:23Z 2023 Статья Khandia, R., Khan, A.A., Karuvantevida, N., Gurjar, P., Rzhepakovsky, I.V., Legaz, I. Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts // Pathogens. - 2023. - 12(2), art. no. 325. - DOI: 10.3390/pathogens12020325 http://hdl.handle.net/20.500.12258/23498 en Pathogens application/pdf application/pdf
institution СКФУ
collection Репозиторий
language English
topic Allograft rejection
Liver transplantation
Codon usage
Liver cirrhosis
Hepatitis C virus (HCV)
Hepatocellular carcinoma
Similarity index
Relative codon deoptimization index
spellingShingle Allograft rejection
Liver transplantation
Codon usage
Liver cirrhosis
Hepatitis C virus (HCV)
Hepatocellular carcinoma
Similarity index
Relative codon deoptimization index
Rzhepakovsky, I. V.
Ржепаковский, И. В.
Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts
description Hepatitis C virus (HCV) is enveloped RNA virus, encoding for a polyprotein that is processed by cellular proteases. The virus is responsible for liver cirrhosis, allograft rejection, and human hepatocellular carcinoma. Based on studies including compositional analysis, odds ratio analysis, parity analysis, skew analysis, relative synonymous codon usage, codon bias, and protein properties, it was evident that codon usage bias in HCV is dependent upon the nucleotide composition. Codon context analysis revealed CTC-CTG as a preferred codon pair. While CGA and CGT codons were rare, none of the codons were rare in HCV-like viruses envisaged in the present study. Many of the preferred codon pairs were valine amino acid-initiated, which possibly infers viral infectivity; hence the role of selection forces appears to act on the HCV genome, which was further validated by neutrality analysis where selection accounted for 87.28%, while mutation accounted for 12.72% force shaping codon usage. Furthermore, codon usage was correlated with the length of the genome. HCV viruses prefer valine-initiated codon pairs, while HCV-like viruses prefer alanine-initiated codon pairs. The HCV host range is very narrow and is confined to only humans and chimpanzees. Based on indices including codon usage correlation analysis, similarity index, and relative codon deoptimization index, it is evident in the study that the chimpanzee is the primary host of the virus. The present study helped elucidate the preferred host for HCV. The information presented in the study paved the way for generating an attenuated vaccine candidate through viral recoding, with finely tuned nucleotide composition and a perfect balance of preferred and rare codons.
format Статья
author Rzhepakovsky, I. V.
Ржепаковский, И. В.
author_facet Rzhepakovsky, I. V.
Ржепаковский, И. В.
author_sort Rzhepakovsky, I. V.
title Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts
title_short Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts
title_full Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts
title_fullStr Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts
title_full_unstemmed Insights into Synonymous Codon Usage Bias in Hepatitis C Virus and Its Adaptation to Hosts
title_sort insights into synonymous codon usage bias in hepatitis c virus and its adaptation to hosts
publishDate 2023
url https://dspace.ncfu.ru/handle/20.500.12258/23498
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