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Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo
Lymphocytic choriomeningitis virus (LCMV) is a prototypic arenavirus. The function of untranslated regions (UTRs) of the LCMV genome has not been well studied except for the extreme 19 nucleotide residues of both the 5′ and 3′ termini. There are internal UTRs composed of 58 and 41 nucleotide residue...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474432/ https://www.ncbi.nlm.nih.gov/pubmed/32824338 http://dx.doi.org/10.3390/v12080896 |
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author | Taniguchi, Satoshi Yoshikawa, Tomoki Shimojima, Masayuki Fukushi, Shuetsu Kurosu, Takeshi Tani, Hideki Fukuma, Aiko Kato, Fumihiro Nakayama, Eri Maeki, Takahiro Tajima, Shigeru Lim, Chang-Kweng Ebihara, Hideki Kyuwa, Shigeru Morikawa, Shigeru Saijo, Masayuki |
author_facet | Taniguchi, Satoshi Yoshikawa, Tomoki Shimojima, Masayuki Fukushi, Shuetsu Kurosu, Takeshi Tani, Hideki Fukuma, Aiko Kato, Fumihiro Nakayama, Eri Maeki, Takahiro Tajima, Shigeru Lim, Chang-Kweng Ebihara, Hideki Kyuwa, Shigeru Morikawa, Shigeru Saijo, Masayuki |
author_sort | Taniguchi, Satoshi |
collection | PubMed |
description | Lymphocytic choriomeningitis virus (LCMV) is a prototypic arenavirus. The function of untranslated regions (UTRs) of the LCMV genome has not been well studied except for the extreme 19 nucleotide residues of both the 5′ and 3′ termini. There are internal UTRs composed of 58 and 41 nucleotide residues in the 5′ and 3′ UTRs, respectively, in the LCMV S segment. Their functional roles have yet to be elucidated. In this study, reverse genetics and minigenome systems were established for LCMV strain WE and the function of these regions were analyzed. It was revealed that nucleotides 20–40 and 20–38 located downstream of the 19 nucleotides in the 5′ and 3′ termini, respectively, were involved in viral genome replication and transcription. Furthermore, it was revealed that the other internal UTRs (nucleotides 41–77 and 39–60 in the 5′ and 3′ termini, respectively) in the S segment were involved in virulence in vivo, even though these regions did not affect viral growth capacity in Vero cells. The introduction of LCMV with mutations in these regions attenuates the virus and may enable the production of LCMV vaccine candidates. |
format | Online Article Text |
id | pubmed-7474432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74744322020-09-17 Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo Taniguchi, Satoshi Yoshikawa, Tomoki Shimojima, Masayuki Fukushi, Shuetsu Kurosu, Takeshi Tani, Hideki Fukuma, Aiko Kato, Fumihiro Nakayama, Eri Maeki, Takahiro Tajima, Shigeru Lim, Chang-Kweng Ebihara, Hideki Kyuwa, Shigeru Morikawa, Shigeru Saijo, Masayuki Viruses Article Lymphocytic choriomeningitis virus (LCMV) is a prototypic arenavirus. The function of untranslated regions (UTRs) of the LCMV genome has not been well studied except for the extreme 19 nucleotide residues of both the 5′ and 3′ termini. There are internal UTRs composed of 58 and 41 nucleotide residues in the 5′ and 3′ UTRs, respectively, in the LCMV S segment. Their functional roles have yet to be elucidated. In this study, reverse genetics and minigenome systems were established for LCMV strain WE and the function of these regions were analyzed. It was revealed that nucleotides 20–40 and 20–38 located downstream of the 19 nucleotides in the 5′ and 3′ termini, respectively, were involved in viral genome replication and transcription. Furthermore, it was revealed that the other internal UTRs (nucleotides 41–77 and 39–60 in the 5′ and 3′ termini, respectively) in the S segment were involved in virulence in vivo, even though these regions did not affect viral growth capacity in Vero cells. The introduction of LCMV with mutations in these regions attenuates the virus and may enable the production of LCMV vaccine candidates. MDPI 2020-08-16 /pmc/articles/PMC7474432/ /pubmed/32824338 http://dx.doi.org/10.3390/v12080896 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Taniguchi, Satoshi Yoshikawa, Tomoki Shimojima, Masayuki Fukushi, Shuetsu Kurosu, Takeshi Tani, Hideki Fukuma, Aiko Kato, Fumihiro Nakayama, Eri Maeki, Takahiro Tajima, Shigeru Lim, Chang-Kweng Ebihara, Hideki Kyuwa, Shigeru Morikawa, Shigeru Saijo, Masayuki Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo |
title | Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo |
title_full | Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo |
title_fullStr | Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo |
title_full_unstemmed | Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo |
title_short | Analysis of the Function of the Lymphocytic Choriomeningitis Virus S Segment Untranslated Region on Growth Capacity In Vitro and on Virulence In Vivo |
title_sort | analysis of the function of the lymphocytic choriomeningitis virus s segment untranslated region on growth capacity in vitro and on virulence in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7474432/ https://www.ncbi.nlm.nih.gov/pubmed/32824338 http://dx.doi.org/10.3390/v12080896 |
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