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The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine
Spiroplasma eriocheiris, a pathogen that causes mass mortality of Chinese mitten crab Eriocheir sinensis, is a wall less bacteria and belongs to the Mollicutes. This study was designed to investigate the effects of colchicine on S. eriocheiris growth, cell morphology, and proteins expression. We fou...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988712/ https://www.ncbi.nlm.nih.gov/pubmed/29872058 http://dx.doi.org/10.1038/s41598-018-26614-y |
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author | Liu, Peng Du, Jie Zhang, Jia Wang, Jian Gu, Wei Wang, Wen Meng, Qingguo |
author_facet | Liu, Peng Du, Jie Zhang, Jia Wang, Jian Gu, Wei Wang, Wen Meng, Qingguo |
author_sort | Liu, Peng |
collection | PubMed |
description | Spiroplasma eriocheiris, a pathogen that causes mass mortality of Chinese mitten crab Eriocheir sinensis, is a wall less bacteria and belongs to the Mollicutes. This study was designed to investigate the effects of colchicine on S. eriocheiris growth, cell morphology, and proteins expression. We found that in the presence of colchicine, the spiroplasma cells lost their helicity, and the length of the cells in the experimental group was longer than that of the control. With varying concentrations of the colchicine treatment, the total time to achieve a stationary phase of the spiroplasma was increased, and the cell population was decreased. The virulence ability of S. eriocheiris to E. sinensis was effectively reduced in the presence of colchicine. To expound the toxical mechanism of colchicine on S. eriocheiris, 208 differentially expressed proteins of S. eriocheiris were reliably quantified by iTRAQ analysis, including 77 up-regulated proteins and 131 down-regulated proteins. Especially, FtsY, putative Spiralin, and NADH oxidase were down-regulated. F(0)F(1) ATP synthase subunit delta, ParB, DNABs, and NAD(FAD)-dependent dehydrogenase were up-regulated. A qRT-PCR was conducted to detect 7 expressed genes from the iTRAQ results during the incubation. The qRT-PCR results were consistent with the iTRAQ results. All of our results indicate that colchicine have a strong impact on the cell morphology and cellular metabolism of S. eriocheiris. |
format | Online Article Text |
id | pubmed-5988712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59887122018-06-20 The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine Liu, Peng Du, Jie Zhang, Jia Wang, Jian Gu, Wei Wang, Wen Meng, Qingguo Sci Rep Article Spiroplasma eriocheiris, a pathogen that causes mass mortality of Chinese mitten crab Eriocheir sinensis, is a wall less bacteria and belongs to the Mollicutes. This study was designed to investigate the effects of colchicine on S. eriocheiris growth, cell morphology, and proteins expression. We found that in the presence of colchicine, the spiroplasma cells lost their helicity, and the length of the cells in the experimental group was longer than that of the control. With varying concentrations of the colchicine treatment, the total time to achieve a stationary phase of the spiroplasma was increased, and the cell population was decreased. The virulence ability of S. eriocheiris to E. sinensis was effectively reduced in the presence of colchicine. To expound the toxical mechanism of colchicine on S. eriocheiris, 208 differentially expressed proteins of S. eriocheiris were reliably quantified by iTRAQ analysis, including 77 up-regulated proteins and 131 down-regulated proteins. Especially, FtsY, putative Spiralin, and NADH oxidase were down-regulated. F(0)F(1) ATP synthase subunit delta, ParB, DNABs, and NAD(FAD)-dependent dehydrogenase were up-regulated. A qRT-PCR was conducted to detect 7 expressed genes from the iTRAQ results during the incubation. The qRT-PCR results were consistent with the iTRAQ results. All of our results indicate that colchicine have a strong impact on the cell morphology and cellular metabolism of S. eriocheiris. Nature Publishing Group UK 2018-06-05 /pmc/articles/PMC5988712/ /pubmed/29872058 http://dx.doi.org/10.1038/s41598-018-26614-y Text en © The Author(s) 2018 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 Liu, Peng Du, Jie Zhang, Jia Wang, Jian Gu, Wei Wang, Wen Meng, Qingguo The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine |
title | The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine |
title_full | The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine |
title_fullStr | The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine |
title_full_unstemmed | The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine |
title_short | The structural and proteomic analysis of Spiroplasma eriocheiris in response to colchicine |
title_sort | structural and proteomic analysis of spiroplasma eriocheiris in response to colchicine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988712/ https://www.ncbi.nlm.nih.gov/pubmed/29872058 http://dx.doi.org/10.1038/s41598-018-26614-y |
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