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比较多组学系统分析揭示了糖酵解/糖异生信号通路在鱼类来源的 GBS YM001 毒力减弱中发挥重要作用。

Comparative multi-omics systems analysis reveal the glycolysis / gluconeogenesis signal pathway play an important role in virulence attenuation in fish-derived GBS YM001.

机构信息

Guangxi Academy of Fishery Sciences, Nanning,China,P.R. China.

出版信息

PLoS One. 2019 Aug 26;14(8):e0221634. doi: 10.1371/journal.pone.0221634. eCollection 2019.

DOI:10.1371/journal.pone.0221634
PMID:31449567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6709914/
Abstract

Streptococcus agalactiae(GBS) is a seriously threat to the farmed tilapia, and oral vaccination was considered to be the most desirable means which requires deep understanding of virulence mechanism of the fish-derived GBS. Our previous genome study of the fish-derived attenuated strain YM001 showed that there were two large deletions in YM001 compared to its parental virulent strain HN016. In this study, a combined transcriptomic and proteomic analysis was performed on YM001 and HN016 strains, and the important genes were verified by RT-qPCR in bacteria strains and infected-tilapia tissues. Overall, we have shown that a total of 958 genes and 331 proteins were significantly differential expressed between YM001 and HN016. By functional annotation of these DEGs and DEPs, genes that were enriched in pentose phosphate pathway(pgm, ptsG, pgi pfkA, fbaA and FBP3) and pyruvate metabolism pathway(pdhA, pdhB, pdhC and pdhD) were identifed as important candidate genes for leads low growth ability in attenuated strain, which may be an important reasons leading virulence attenuation in the end. The expression levels the candidate genes in pentose phosphate pathway and pyruvate metabolism pathway were significant differential expressed in tilapia' brain and spleen when infected with YM001 and HN016. Our study indicated that the pentose phosphate pathway and pyruvate metabolism pathway that affecting the growth of the strain may be one of the important reasons for the virulence attenuation in HN016.

摘要

无乳链球菌(GBS)是对养殖罗非鱼的严重威胁,口服疫苗被认为是最理想的方法,这需要深入了解鱼类来源的 GBS 的毒力机制。我们之前对鱼类来源的减毒菌株 YM001 的基因组研究表明,与亲本毒力菌株 HN016 相比,YM001 中有两个大的缺失。在这项研究中,对 YM001 和 HN016 菌株进行了联合转录组和蛋白质组分析,并通过细菌菌株和感染罗非鱼组织中的 RT-qPCR 验证了重要基因。总的来说,我们已经表明,YM001 和 HN016 之间共有 958 个基因和 331 个蛋白显著差异表达。通过对这些 DEGs 和 DEPs 的功能注释,发现富集在戊糖磷酸途径(pgm、ptsG、pgi pfkA、fbaA 和 FBP3)和丙酮酸代谢途径(pdhA、pdhB、pdhC 和 pdhD)中的基因是减毒菌株生长能力降低的重要候选基因,这可能是导致毒力减弱的重要原因。在感染 YM001 和 HN016 时,候选基因在戊糖磷酸途径和丙酮酸代谢途径中的表达水平在罗非鱼的大脑和脾脏中存在显著差异。我们的研究表明,影响菌株生长的戊糖磷酸途径和丙酮酸代谢途径可能是 HN016 毒力减弱的重要原因之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/aa2763ac8cad/pone.0221634.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/4d204347b66f/pone.0221634.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/4c301f7cb565/pone.0221634.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/b60d7e4ac946/pone.0221634.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/be88b0c21de8/pone.0221634.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/ea6ca0c0560c/pone.0221634.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/aa2763ac8cad/pone.0221634.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/4d204347b66f/pone.0221634.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/4c301f7cb565/pone.0221634.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/b60d7e4ac946/pone.0221634.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/be88b0c21de8/pone.0221634.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/ea6ca0c0560c/pone.0221634.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/6709914/aa2763ac8cad/pone.0221634.g006.jpg

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