RNA Sequencing Analysis of the Broad-Host-Range Strain Sinorhizobium fredii NGR234 Identifies a Large Set of Genes Linked to Quorum Sensing-Dependent Regulation in the Background of a traI and ngrI Deletion Mutant

被引:25
作者
Krysciak, Dagmar [1 ]
Grote, Jessica [1 ]
Orbegoso, Mariita Rodriguez [1 ]
Utpatel, Christian [1 ]
Foerstner, Konrad U. [2 ]
Li, Lei [2 ,3 ]
Schmeisser, Christel [1 ]
Krishnan, Hari B. [4 ]
Streit, Wolfgang R. [1 ]
机构
[1] Univ Hamburg, Biozentrum Klein Flottbek, Abt Mikrobiol & Biotechnol, Hamburg, Germany
[2] Univ Wurzburg, Core Unit Syst Med, D-97070 Wurzburg, Germany
[3] Univ Wurzburg, Inst Mol Infekt Biol, D-97070 Wurzburg, Germany
[4] Univ Missouri, Plant Genet Res Unit, USDA ARS, Columbia, MO USA
关键词
NITROGEN-FIXING SYMBIONT; RHIZOBIUM-MELILOTI; TI PLASMID; BRADYRHIZOBIUM-JAPONICUM; PROTEIN SECRETION; STATIONARY-PHASE; MOLECULAR-BASIS; ANTISENSE RNA; EXPRESSION; BIOTIN;
D O I
10.1128/AEM.01835-14
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The alphaproteobacterium Sinorhizobium fredii NGR234 has an exceptionally wide host range, as it forms nitrogen-fixing nodules with more legumes than any other known microsymbiont. Within its 6.9-Mbp genome, it encodes two N-acyl-homoserine-lactone synthase genes (i.e., traI and ngrI) involved in the biosynthesis of two distinct autoinducer I-type molecules. Here, we report on the construction of an NGR234-Delta traI and an NGR234-Delta ngrI mutant and their genome-wide transcriptome analysis. A high-resolution RNA sequencing (RNA-seq) analysis of early-stationary-phase cultures in the NGR234-Delta traI background suggested that up to 316 genes were differentially expressed in the NGR234-Delta traI mutant versus the parent strain. Similarly, in the background of NGR234-Delta ngrI 466 differentially regulated genes were identified. Accordingly, a common set of 186 genes was regulated by the TraI/R and NgrI/R regulon. Coregulated genes included 42 flagellar biosynthesis genes and 22 genes linked to exopolysaccharide (EPS) biosynthesis. Among the genes and open reading frames (ORFs) that were differentially regulated in NGR234-Delta traI were those linked to replication of the pNGR234a symbiotic plasmid and cytochrome c oxidases. Biotin and pyrroloquinoline quinone biosynthesis genes were differentially expressed in the NGR234-Delta ngrI mutant as well as the entire cluster of 21 genes linked to assembly of the NGR234 type III secretion system (T3SS-II). Further, we also discovered that genes responsible for rhizopine catabolism in NGR234 were strongly repressed in the presence of high levels of N-acyl-homoserine-lactones. Together with nodulation assays, the RNA-seq-based findings suggested that quorum sensing (QS)-dependent gene regulation appears to be of higher relevance during nonsymbiotic growth rather than for life within root nodules.
引用
收藏
页码:5655 / 5671
页数:17
相关论文
共 99 条
[21]   Symbiotic use of pathogenic strategies: rhizobial protein secretion systems [J].
Deakin, William J. ;
Broughton, William J. .
NATURE REVIEWS MICROBIOLOGY, 2009, 7 (04) :312-320
[22]   The Pseudomonas aeruginosa Transcriptome in Planktonic Cultures and Static Biofilms Using RNA Sequencing [J].
Doetsch, Andreas ;
Eckweiler, Denitsa ;
Schniederjans, Monika ;
Zimmermann, Ariane ;
Jensen, Vanessa ;
Scharfe, Maren ;
Geffers, Robert ;
Haeussler, Susanne .
PLOS ONE, 2012, 7 (02)
[23]   High-Resolution Transcriptome Maps Reveal Strain-Specific Regulatory Features of Multiple Campylobacter jejuni Isolates [J].
Dugar, Gaurav ;
Herbig, Alexander ;
Foerstner, Konrad U. ;
Heidrich, Nadja ;
Reinhardt, Richard ;
Nieselt, Kay ;
Sharma, Cynthia M. .
PLOS GENETICS, 2013, 9 (05)
[24]   Pyruvate carboxylase from Rhizobium etli: Mutant characterization, nucleotide sequence, and physiological role [J].
Dunn, MF ;
Encarnacion, S ;
Araiza, G ;
Vargas, MC ;
Davalos, A ;
Peralta, H ;
Mora, Y ;
Mora, J .
JOURNAL OF BACTERIOLOGY, 1996, 178 (20) :5960-5970
[25]   Anaplerotic Function of Phosphoenolpyruvate Carboxylase in Bradyrhizobium japonicum USDA110 [J].
Dunn, Michael F. .
CURRENT MICROBIOLOGY, 2011, 62 (06) :1782-1788
[26]   Gene Expression Omnibus: NCBI gene expression and hybridization array data repository [J].
Edgar, R ;
Domrachev, M ;
Lash, AE .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :207-210
[27]   SIMILARITY BETWEEN THE RHIZOBIUM-MELILOTI FLIP GENE AND PATHOGENICITY-ASSOCIATED GENES FROM ANIMAL AND PLANT-PATHOGENS [J].
FINAN, TM ;
GOUGH, C ;
TRUCHET, G .
GENE, 1995, 152 (01) :65-67
[28]   Molecular basis of symbiosis between Rhizobium and legumes [J].
Freiberg, C ;
Fellay, R ;
Bairoch, A ;
Broughton, WJ ;
Rosenthal, A ;
Perret, X .
NATURE, 1997, 387 (6631) :394-401
[29]   Investigations of Rhizobium biofilm formation [J].
Fujishige, NA ;
Kapadia, NN ;
De Hoff, PL ;
Hirsch, AM .
FEMS MICROBIOLOGY ECOLOGY, 2006, 56 (02) :195-206
[30]   Localization of OccR-activated and TraR-activated promoters that express two ABC-type permeases and the traR gene of Ti plasmid pTiR10 [J].
Fuqua, C ;
Winans, SC .
MOLECULAR MICROBIOLOGY, 1996, 20 (06) :1199-1210