• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

青枯雷尔氏菌宿主适应菌株的植物体内比较转录组学

In planta comparative transcriptomics of host-adapted strains of Ralstonia solanacearum.

作者信息

Ailloud Florent, Lowe Tiffany M, Robène Isabelle, Cruveiller Stéphane, Allen Caitilyn, Prior Philippe

机构信息

UMR Peuplements Végétaux et Bioagresseurs en Milieu Tropical, Centre de coopération International en Recherche Agronomique pour le Développement, Saint-Pierre, France; Laboratoire de la Santé des Végétaux, Agence Nationale Sécurité Sanitaire Alimentaire Nationale, Saint-Pierre, France.

Department of Plant Pathology, University of Wisconsin-Madison , Madison, WI , United States.

出版信息

PeerJ. 2016 Jan 5;4:e1549. doi: 10.7717/peerj.1549. eCollection 2016.

DOI:10.7717/peerj.1549
PMID:26788428
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4715432/
Abstract

Background. Ralstonia solanacearum is an economically important plant pathogen with an unusually large host range. The Moko (banana) and NPB (not pathogenic to banana) strain groups are closely related but are adapted to distinct hosts. Previous comparative genomics studies uncovered very few differences that could account for the host range difference between these pathotypes. To better understand the basis of this host specificity, we used RNAseq to profile the transcriptomes of an R. solanacearum Moko strain and an NPB strain under in vitro and in planta conditions. Results. RNAs were sequenced from bacteria grown in rich and minimal media, and from bacteria extracted from mid-stage infected tomato, banana and melon plants. We computed differential expression between each pair of conditions to identify constitutive and host-specific gene expression differences between Moko and NPB. We found that type III secreted effectors were globally up-regulated upon plant cell contact in the NPB strain compared with the Moko strain. Genes encoding siderophore biosynthesis and nitrogen assimilation genes were highly up-regulated in the NPB strain during melon pathogenesis, while denitrification genes were up-regulated in the Moko strain during banana pathogenesis. The relatively lower expression of oxidases and the denitrification pathway during banana pathogenesis suggests that R. solanacearum experiences higher oxygen levels in banana pseudostems than in tomato or melon xylem. Conclusions. This study provides the first report of differential gene expression associated with host range variation. Despite minimal genomic divergence, the pathogenesis of Moko and NPB strains is characterized by striking differences in expression of virulence- and metabolism-related genes.

摘要

背景。青枯雷尔氏菌是一种具有重要经济意义的植物病原菌,其寄主范围异常广泛。莫科(香蕉)菌株组和NPB(对香蕉无致病性)菌株组关系密切,但适应不同的寄主。先前的比较基因组学研究发现,能够解释这些致病型寄主范围差异的差异非常少。为了更好地理解这种寄主特异性的基础,我们使用RNA测序技术对青枯雷尔氏菌莫科菌株和NPB菌株在体外和植物体内条件下的转录组进行了分析。结果。对在丰富培养基和基本培养基中生长的细菌,以及从感染中期的番茄、香蕉和甜瓜植株中提取的细菌进行了RNA测序。我们计算了每对条件之间的差异表达,以确定莫科菌株和NPB菌株之间组成型和寄主特异性的基因表达差异。我们发现,与莫科菌株相比,NPB菌株在与植物细胞接触后,III型分泌效应子整体上调。在甜瓜致病过程中,编码铁载体生物合成的基因和氮同化基因在NPB菌株中高度上调,而在香蕉致病过程中,反硝化基因在莫科菌株中上调。香蕉致病过程中氧化酶和反硝化途径的相对较低表达表明,青枯雷尔氏菌在香蕉假茎中经历的氧气水平高于番茄或甜瓜木质部。结论。本研究首次报道了与寄主范围变异相关的差异基因表达。尽管基因组差异很小,但莫科菌株和NPB菌株的致病机制在毒力和代谢相关基因的表达上存在显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db85/4715432/08fd3602c71d/peerj-04-1549-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db85/4715432/d13dc414da8e/peerj-04-1549-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db85/4715432/95c6d8252b80/peerj-04-1549-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db85/4715432/08fd3602c71d/peerj-04-1549-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db85/4715432/d13dc414da8e/peerj-04-1549-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db85/4715432/95c6d8252b80/peerj-04-1549-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db85/4715432/08fd3602c71d/peerj-04-1549-g003.jpg

相似文献

1
In planta comparative transcriptomics of host-adapted strains of Ralstonia solanacearum.青枯雷尔氏菌宿主适应菌株的植物体内比较转录组学
PeerJ. 2016 Jan 5;4:e1549. doi: 10.7717/peerj.1549. eCollection 2016.
2
Comparative genomic analysis of Ralstonia solanacearum reveals candidate genes for host specificity.青枯雷尔氏菌的比较基因组分析揭示了宿主特异性的候选基因。
BMC Genomics. 2015 Apr 8;16(1):270. doi: 10.1186/s12864-015-1474-8.
3
First Report of Ralstonia solanacearum Race 2 Biovar 1 Causing Moko Disease of Banana in Malaysia.青枯雷尔氏菌2号小种生物变种1引起马来西亚香蕉莫科病的首次报道
Plant Dis. 2014 Feb;98(2):275. doi: 10.1094/PDIS-03-13-0321-PDN.
4
Moko Disease-Causing Strains of Ralstonia solanacearum from Brazil Extend Known Diversity in Paraphyletic Phylotype II.来自巴西的引起莫科病的青枯雷尔氏菌菌株扩展了已知的并系II型系统发育型的多样性。
Phytopathology. 2014 Nov;104(11):1175-82. doi: 10.1094/PHYTO-12-13-0334-R.
5
Characterization and Association of Rips Repertoire to Host Range of Novel Strains by In Silico Approaches.通过计算机模拟方法对新型菌株的Rips基因库进行表征及其与宿主范围的关联研究
Microorganisms. 2023 Apr 6;11(4):954. doi: 10.3390/microorganisms11040954.
6
Validation of PCR Diagnostic Assays for Detection and Identification of All Sequevars Causing Moko Disease in Banana.用于检测和鉴定引起香蕉巴拿马病的所有序列的 PCR 诊断检测方法的验证。
Phytopathology. 2024 Nov;114(11):2375-2384. doi: 10.1094/PHYTO-06-24-0190-R. Epub 2024 Nov 23.
7
Degradation of the Plant Defense Signal Salicylic Acid Protects Ralstonia solanacearum from Toxicity and Enhances Virulence on Tobacco.植物防御信号水杨酸的降解可保护青枯雷尔氏菌免受毒性影响并增强其对烟草的毒力。
mBio. 2016 Jun 21;7(3):e00656-16. doi: 10.1128/mBio.00656-16.
8
A duplex PCR assay for the detection of Ralstonia solanacearum phylotype II strains in Musa spp.一种用于检测香蕉属植物中茄科劳尔氏菌II型菌株的双重PCR检测方法
PLoS One. 2015 Mar 26;10(3):e0122182. doi: 10.1371/journal.pone.0122182. eCollection 2015.
9
Comparative genomics and phylogenomics of the Ralstonia solanacearum Moko ecotype and its symptomatological variants.青枯雷尔氏菌莫科生态型及其症状变体的比较基因组学和系统发育基因组学
Genet Mol Biol. 2022 Dec 2;45(4):e20220038. doi: 10.1590/1678-4685-GMB-2022-0038. eCollection 2022.
10
Prediction of Host-Specific Genes by Pan-Genome Analyses of the Korean Species Complex.通过对韩国物种复合体的泛基因组分析预测宿主特异性基因。
Front Microbiol. 2019 Mar 15;10:506. doi: 10.3389/fmicb.2019.00506. eCollection 2019.

引用本文的文献

1
Characterization and Association of Rips Repertoire to Host Range of Novel Strains by In Silico Approaches.通过计算机模拟方法对新型菌株的Rips基因库进行表征及其与宿主范围的关联研究
Microorganisms. 2023 Apr 6;11(4):954. doi: 10.3390/microorganisms11040954.
2
Comprehensive Analysis Reveals the Genetic and Pathogenic Diversity of Species Complex and Benefits Its Taxonomic Classification.综合分析揭示了物种复合体的遗传和致病多样性,并有利于其分类学分类。
Front Microbiol. 2022 May 6;13:854792. doi: 10.3389/fmicb.2022.854792. eCollection 2022.
3
Dynamic expression of Ralstonia solanacearum virulence factors and metabolism-controlling genes during plant infection.

本文引用的文献

1
Comparative genomic analysis of Ralstonia solanacearum reveals candidate genes for host specificity.青枯雷尔氏菌的比较基因组分析揭示了宿主特异性的候选基因。
BMC Genomics. 2015 Apr 8;16(1):270. doi: 10.1186/s12864-015-1474-8.
2
Ralstonia solanacearum uses inorganic nitrogen metabolism for virulence, ATP production, and detoxification in the oxygen-limited host xylem environment.青枯雷尔氏菌在氧气受限的寄主木质部环境中利用无机氮代谢来实现致病、产生ATP以及解毒。
mBio. 2015 Mar 17;6(2):e02471. doi: 10.1128/mBio.02471-14.
3
Performance of genetic programming optimised Bowtie2 on genome comparison and analytic testing (GCAT) benchmarks.
青枯雷尔氏菌致病因子和代谢控制基因在植物感染过程中的动态表达
BMC Genomics. 2021 Mar 9;22(1):170. doi: 10.1186/s12864-021-07457-w.
4
Taxonomy and Phylogenetic Research on Ralstonia solanacearum Species Complex: A Complex Pathogen with Extraordinary Economic Consequences.青枯雷尔氏菌复合种的分类学和系统发育研究:一种具有重大经济影响的复杂病原体
Pathogens. 2020 Oct 25;9(11):886. doi: 10.3390/pathogens9110886.
5
Complete Genome Sequence of the Plant Pathogen Ralstonia solanacearum Strain CIAT-078, Isolated in Colombia, Obtained Using Oxford Nanopore Technology.利用牛津纳米孔技术获得的、从哥伦比亚分离出的植物病原菌青枯雷尔氏菌CIAT-078的全基因组序列
Microbiol Resour Announc. 2020 May 28;9(22):e00448-20. doi: 10.1128/MRA.00448-20.
6
Transposable elements contribute to the genome plasticity of species complex.转座元件有助于物种复合体的基因组可塑性。
Microb Genom. 2020 May;6(5). doi: 10.1099/mgen.0.000374. Epub 2020 May 7.
7
Calcium transcriptionally regulates movement, recombination and other functions of Xylella fastidiosa under constant flow inside microfluidic chambers.钙在微流控室内恒流条件下转录调控韧皮部难养菌的运动、重组和其他功能。
Microb Biotechnol. 2020 Mar;13(2):548-561. doi: 10.1111/1751-7915.13512. Epub 2019 Nov 14.
8
Prediction of Host-Specific Genes by Pan-Genome Analyses of the Korean Species Complex.通过对韩国物种复合体的泛基因组分析预测宿主特异性基因。
Front Microbiol. 2019 Mar 15;10:506. doi: 10.3389/fmicb.2019.00506. eCollection 2019.
9
Contribution of a lectin, LecM, to the quorum sensing signalling pathway of Ralstonia solanacearum strain OE1-1.LecM 凝集素对罗尔斯通氏菌 OE1-1 群体感应信号通路的贡献。
Mol Plant Pathol. 2019 Mar;20(3):334-345. doi: 10.1111/mpp.12757. Epub 2018 Nov 6.
10
Identification of Cyclic Dipeptides from Escherichia coli as New Antimicrobial Agents against Ralstonia Solanacearum.从大肠杆菌中鉴定环二肽作为抗青枯雷尔氏菌的新型抗菌剂。
Molecules. 2018 Jan 19;23(1):214. doi: 10.3390/molecules23010214.
遗传编程优化的Bowtie2在基因组比较与分析测试(GCAT)基准测试中的性能。
BioData Min. 2015 Jan 8;8(1):1. doi: 10.1186/s13040-014-0034-0. eCollection 2015.
4
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.使用DESeq2对RNA测序数据的倍数变化和离散度进行适度估计。
Genome Biol. 2014;15(12):550. doi: 10.1186/s13059-014-0550-8.
5
BEDTools: The Swiss-Army Tool for Genome Feature Analysis.BEDTools:用于基因组特征分析的瑞士军刀工具。
Curr Protoc Bioinformatics. 2014 Sep 8;47:11.12.1-34. doi: 10.1002/0471250953.bi1112s47.
6
Trimmomatic: a flexible trimmer for Illumina sequence data.Trimmomatic:一款适用于 Illumina 测序数据的灵活修剪工具。
Bioinformatics. 2014 Aug 1;30(15):2114-20. doi: 10.1093/bioinformatics/btu170. Epub 2014 Apr 1.
7
Evaluation of read count based RNAseq analysis methods.基于读段计数的 RNAseq 分析方法评估。
BMC Genomics. 2013;14 Suppl 8(Suppl 8):S2. doi: 10.1186/1471-2164-14-S8-S2. Epub 2013 Dec 9.
8
Nitrate assimilation contributes to Ralstonia solanacearum root attachment, stem colonization, and virulence.硝酸盐同化作用有助于青枯菌附着根部、定殖茎部并增强其毒性。
J Bacteriol. 2014 Mar;196(5):949-60. doi: 10.1128/JB.01378-13. Epub 2013 Dec 20.
9
Novel plant inputs influencing Ralstonia solanacearum during infection.影响青枯菌侵染过程的新型植物投入品。
Front Microbiol. 2013 Nov 20;4:349. doi: 10.3389/fmicb.2013.00349. eCollection 2013.
10
Count-based differential expression analysis of RNA sequencing data using R and Bioconductor.基于计数的 RNA 测序数据分析使用 R 和 Bioconductor。
Nat Protoc. 2013 Sep;8(9):1765-86. doi: 10.1038/nprot.2013.099. Epub 2013 Aug 22.