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Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus
Rice stripe virus-infected females of the small brown planthopper (SBPH, Laodelphax striatellus) usually lay fewer eggs with a longer hatch period, low hatchability, malformation and retarded or defective development compared with healthy females. To explore the molecular mechanism of those phenomen...
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/PMC4899684/ https://www.ncbi.nlm.nih.gov/pubmed/27277140 http://dx.doi.org/10.1038/srep27216 |
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author | Liu, Beibei Qin, Faliang Liu, Wenwen Wang, Xifeng |
author_facet | Liu, Beibei Qin, Faliang Liu, Wenwen Wang, Xifeng |
author_sort | Liu, Beibei |
collection | PubMed |
description | Rice stripe virus-infected females of the small brown planthopper (SBPH, Laodelphax striatellus) usually lay fewer eggs with a longer hatch period, low hatchability, malformation and retarded or defective development compared with healthy females. To explore the molecular mechanism of those phenomena, we analyzed the differential proteomics profiling of the ova between viruliferous and healthy female insects using an isobaric tag for relative and absolute quantitation (iTRAQ) approach. We obtained 147 differentially accumulated proteins: 98 (66.7%) proteins increased, but 49 (33.3%) decreased in the ova of the viruliferous females. RT-qPCR was used to verify the 12 differential expressed proteins from iTRAQ, finding that trends in the transcriptional change for the 12 genes were consistent with those at the proteomic level. Differentially expressed proteins that were associated with meiosis (serine/threonine-protein phosphatase 2B and cyclin B3) and mitosis (cyclin B3 and dynein heavy chain) in viruliferous ova may contribute to low hatchability and defective or retarded development. Alterations in the abundance of proteins involved in the respiratory chain and nutrition metabolism may affect embryonic development. Our study begins to explain macroscopical developmental phenomena and explore the mechanisms by which Rice stripe virus impacts the development of SBPH. |
format | Online Article Text |
id | pubmed-4899684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48996842016-06-13 Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus Liu, Beibei Qin, Faliang Liu, Wenwen Wang, Xifeng Sci Rep Article Rice stripe virus-infected females of the small brown planthopper (SBPH, Laodelphax striatellus) usually lay fewer eggs with a longer hatch period, low hatchability, malformation and retarded or defective development compared with healthy females. To explore the molecular mechanism of those phenomena, we analyzed the differential proteomics profiling of the ova between viruliferous and healthy female insects using an isobaric tag for relative and absolute quantitation (iTRAQ) approach. We obtained 147 differentially accumulated proteins: 98 (66.7%) proteins increased, but 49 (33.3%) decreased in the ova of the viruliferous females. RT-qPCR was used to verify the 12 differential expressed proteins from iTRAQ, finding that trends in the transcriptional change for the 12 genes were consistent with those at the proteomic level. Differentially expressed proteins that were associated with meiosis (serine/threonine-protein phosphatase 2B and cyclin B3) and mitosis (cyclin B3 and dynein heavy chain) in viruliferous ova may contribute to low hatchability and defective or retarded development. Alterations in the abundance of proteins involved in the respiratory chain and nutrition metabolism may affect embryonic development. Our study begins to explain macroscopical developmental phenomena and explore the mechanisms by which Rice stripe virus impacts the development of SBPH. Nature Publishing Group 2016-06-09 /pmc/articles/PMC4899684/ /pubmed/27277140 http://dx.doi.org/10.1038/srep27216 Text en Copyright © 2016, Macmillan Publishers Limited 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 Liu, Beibei Qin, Faliang Liu, Wenwen Wang, Xifeng Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus |
title | Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus |
title_full | Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus |
title_fullStr | Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus |
title_full_unstemmed | Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus |
title_short | Differential proteomics profiling of the ova between healthy and Rice stripe virus-infected female insects of Laodelphax striatellus |
title_sort | differential proteomics profiling of the ova between healthy and rice stripe virus-infected female insects of laodelphax striatellus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4899684/ https://www.ncbi.nlm.nih.gov/pubmed/27277140 http://dx.doi.org/10.1038/srep27216 |
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