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A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana
We selected and sequenced the entire genomes of three strains of Chinese sacbrood virus (CSBV): LNQY-2008 (isolated in Qingyuan, Liaoning Province), SXYL-2015 (isolated in Yulin, Shanxi Province), and JLCBS-2014 (isolated in Changbaishan, Jilin Province), by VP1 amino acid (aa) analysis. These strai...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112594/ https://www.ncbi.nlm.nih.gov/pubmed/27853294 http://dx.doi.org/10.1038/srep37424 |
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author | Hu, Ying Fei, Dongliang Jiang, Lili Wei, Dong Li, Fangbing Diao, Qingyun Ma, Mingxiao |
author_facet | Hu, Ying Fei, Dongliang Jiang, Lili Wei, Dong Li, Fangbing Diao, Qingyun Ma, Mingxiao |
author_sort | Hu, Ying |
collection | PubMed |
description | We selected and sequenced the entire genomes of three strains of Chinese sacbrood virus (CSBV): LNQY-2008 (isolated in Qingyuan, Liaoning Province), SXYL-2015 (isolated in Yulin, Shanxi Province), and JLCBS-2014 (isolated in Changbaishan, Jilin Province), by VP1 amino acid (aa) analysis. These strains are endemic in China and infect Apis cerana. Nucleotide sequences, deduced amino acid sequences, genetic backgrounds, and other molecular biological characteristics were analysed. We also examined sensitivity of these virus strains to temperature, pH, and organic solvents, as well as to other physicochemical properties. On the basis of these observations, we compared pathogenicity and tested cross-immunogenicity and protective immunity, using antisera raised against each of the three strains. Our results showed that compared with SXYL-2015, LNQY-2008 has a 10-aa deletion and 3-aa deletion (positions 282–291 and 299–301, respectively), whereas JLCBS-2014 has a 17-aa deletion (positions 284–300). However, the three strains showed no obvious differences in physicochemical properties or pathogenicity. Moreover, there was immune cross-reactivity among the antisera raised against the different strains, implying good protective effects of such antisera. The present study should significantly advance the understanding of the pathogenesis of Chinese sacbrood disease, and offers insights into comprehensive prevention and treatment of, as well as possible protection from, the disease by means of an antiserum. |
format | Online Article Text |
id | pubmed-5112594 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51125942016-11-25 A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana Hu, Ying Fei, Dongliang Jiang, Lili Wei, Dong Li, Fangbing Diao, Qingyun Ma, Mingxiao Sci Rep Article We selected and sequenced the entire genomes of three strains of Chinese sacbrood virus (CSBV): LNQY-2008 (isolated in Qingyuan, Liaoning Province), SXYL-2015 (isolated in Yulin, Shanxi Province), and JLCBS-2014 (isolated in Changbaishan, Jilin Province), by VP1 amino acid (aa) analysis. These strains are endemic in China and infect Apis cerana. Nucleotide sequences, deduced amino acid sequences, genetic backgrounds, and other molecular biological characteristics were analysed. We also examined sensitivity of these virus strains to temperature, pH, and organic solvents, as well as to other physicochemical properties. On the basis of these observations, we compared pathogenicity and tested cross-immunogenicity and protective immunity, using antisera raised against each of the three strains. Our results showed that compared with SXYL-2015, LNQY-2008 has a 10-aa deletion and 3-aa deletion (positions 282–291 and 299–301, respectively), whereas JLCBS-2014 has a 17-aa deletion (positions 284–300). However, the three strains showed no obvious differences in physicochemical properties or pathogenicity. Moreover, there was immune cross-reactivity among the antisera raised against the different strains, implying good protective effects of such antisera. The present study should significantly advance the understanding of the pathogenesis of Chinese sacbrood disease, and offers insights into comprehensive prevention and treatment of, as well as possible protection from, the disease by means of an antiserum. Nature Publishing Group 2016-11-17 /pmc/articles/PMC5112594/ /pubmed/27853294 http://dx.doi.org/10.1038/srep37424 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Hu, Ying Fei, Dongliang Jiang, Lili Wei, Dong Li, Fangbing Diao, Qingyun Ma, Mingxiao A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana |
title | A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana |
title_full | A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana |
title_fullStr | A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana |
title_full_unstemmed | A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana |
title_short | A comparison of biological characteristics of three strains of Chinese sacbrood virus in Apis cerana |
title_sort | comparison of biological characteristics of three strains of chinese sacbrood virus in apis cerana |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112594/ https://www.ncbi.nlm.nih.gov/pubmed/27853294 http://dx.doi.org/10.1038/srep37424 |
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