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Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome
Rotaviruses (RVs) can evolve through the process of reassortment, whereby the 11 double-stranded RNA genome segments are exchanged among strains during co-infection. However, reassortment is limited in cases where the genes or encoded proteins of co-infecting strains are functionally incompatible. I...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571167/ https://www.ncbi.nlm.nih.gov/pubmed/28839154 http://dx.doi.org/10.1038/s41598-017-08068-w |
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author | Mingo, Rebecca Zhang, Shu Long, Courtney P. LaConte, Leslie E. W. McDonald, Sarah M. |
author_facet | Mingo, Rebecca Zhang, Shu Long, Courtney P. LaConte, Leslie E. W. McDonald, Sarah M. |
author_sort | Mingo, Rebecca |
collection | PubMed |
description | Rotaviruses (RVs) can evolve through the process of reassortment, whereby the 11 double-stranded RNA genome segments are exchanged among strains during co-infection. However, reassortment is limited in cases where the genes or encoded proteins of co-infecting strains are functionally incompatible. In this study, we employed a helper virus-based reverse genetics system to identify NSP2 gene regions that correlate with restricted reassortment into simian RV strain SA11. We show that SA11 reassortants with NSP2 genes from human RV strains Wa or DS-1 were efficiently rescued and exhibit no detectable replication defects. However, we could not rescue an SA11 reassortant with a human RV strain AU-1 NSP2 gene, which differs from that of SA11 by 186 nucleotides (36 amino acids). To map restriction determinants, we engineered viruses to contain chimeric NSP2 genes in which specific regions of AU-1 sequence were substituted with SA11 sequence. We show that a region spanning AU-1 NSP2 gene nucleotides 784–820 is critical for the observed restriction; yet additional determinants reside in other gene regions. In silico and in vitro analyses were used to predict how the 784–820 region may impact NSP2 gene/protein function, thereby informing an understanding of the reassortment restriction mechanism. |
format | Online Article Text |
id | pubmed-5571167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55711672017-09-01 Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome Mingo, Rebecca Zhang, Shu Long, Courtney P. LaConte, Leslie E. W. McDonald, Sarah M. Sci Rep Article Rotaviruses (RVs) can evolve through the process of reassortment, whereby the 11 double-stranded RNA genome segments are exchanged among strains during co-infection. However, reassortment is limited in cases where the genes or encoded proteins of co-infecting strains are functionally incompatible. In this study, we employed a helper virus-based reverse genetics system to identify NSP2 gene regions that correlate with restricted reassortment into simian RV strain SA11. We show that SA11 reassortants with NSP2 genes from human RV strains Wa or DS-1 were efficiently rescued and exhibit no detectable replication defects. However, we could not rescue an SA11 reassortant with a human RV strain AU-1 NSP2 gene, which differs from that of SA11 by 186 nucleotides (36 amino acids). To map restriction determinants, we engineered viruses to contain chimeric NSP2 genes in which specific regions of AU-1 sequence were substituted with SA11 sequence. We show that a region spanning AU-1 NSP2 gene nucleotides 784–820 is critical for the observed restriction; yet additional determinants reside in other gene regions. In silico and in vitro analyses were used to predict how the 784–820 region may impact NSP2 gene/protein function, thereby informing an understanding of the reassortment restriction mechanism. Nature Publishing Group UK 2017-08-24 /pmc/articles/PMC5571167/ /pubmed/28839154 http://dx.doi.org/10.1038/s41598-017-08068-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mingo, Rebecca Zhang, Shu Long, Courtney P. LaConte, Leslie E. W. McDonald, Sarah M. Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome |
title | Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome |
title_full | Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome |
title_fullStr | Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome |
title_full_unstemmed | Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome |
title_short | Genetic determinants restricting the reassortment of heterologous NSP2 genes into the simian rotavirus SA11 genome |
title_sort | genetic determinants restricting the reassortment of heterologous nsp2 genes into the simian rotavirus sa11 genome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5571167/ https://www.ncbi.nlm.nih.gov/pubmed/28839154 http://dx.doi.org/10.1038/s41598-017-08068-w |
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