Abstract
Bacteria must sense alterations in their environment and respond with changes in function and/or structure in order to cope. Extracytoplasmic function sigma factors (ECF σs) modulate transcription in response to cellular and environmental signals. The symbiotic nitrogen-fixing alphaproteobacterium Sinorhizobium meliloti carries genes for 11 ECF-like σs (RpoE1 to -E10 and FecI). We hypothesized that some of these play a role in mediating the interaction between the bacterium and its plant symbiotic partner. The bacterium senses changes in its immediate environment as it establishes contact with the plant root, initiates invasion of the plant as the root nodule is formed, traverses several root cell layers, and enters plant cortical cells via endocytosis. We used genetics, transcriptomics, and functionality to characterize the entire S. meliloti cohort of ECF σs. We discovered new targets for individual σs, confirmed others by overexpressing individual ECF σs, and identified or confirmed putative promoter motifs for nine of them. We constructed precise deletions of each ECF σ gene and its demonstrated or putative anti-σ gene and also a strain in which all 11 ECF σ and anti-σ genes were deleted. This all-ECF σ deletion strain showed no major defects in free-living growth, in Biolog Phenotype MicroArray assays, or in response to multiple stresses. None of the ECF σs were required for symbiosis on the host plants Medicago sativa and Medicago truncatula: the strain deleted for all ECF σ and anti-σ genes was symbiotically normal.IMPORTANCE Fixed (reduced) soil nitrogen plays a critical role in soil fertility and successful food growth. Much soil fertility relies on symbiotic nitrogen fixation: the bacterial partner infects the host plant roots and reduces atmospheric dinitrogen in exchange for host metabolic fuel, a process that involves complex interactions between the partners mediated by changes in gene expression in each partner. Here we test the roles of a family of 11 extracytoplasmic function (ECF) gene regulatory proteins (sigma factors [σs]) that interact with RNA polymerase to determine if they play a significant role in establishing a nitrogen-fixing symbiosis or in responding to various stresses, including cell envelope stress. We discovered that symbiotic nitrogen fixation occurs even when all 11 of these regulatory genes are deleted, that most ECF sigma factors control accessory functions, and that none of the ECF sigma factors are required to survive envelope stress.
Highlights
Bacteria must sense alterations in their environment and respond with changes in function and/or structure in order to cope
Sinorhizobium meliloti strain Rm1021 possesses 11 extracytoplasmic stress function (ECF) factors. families are differentiated by the presence of four conserved structural domains (1 to 4) [9]
Rhizobia are known for the large size, complexity, and plasticity of their genomes [64]; it is unsurprising that many S. meliloti Extracytoplasmic function sigma factors (ECF s) would be retained to carry out narrow functions for adaptation to specific environmental conditions and that closely related Sinorhizobium species would differ in composition, regulation, and genomic contexts of ECF s
Summary
Bacteria must sense alterations in their environment and respond with changes in function and/or structure in order to cope. We test the roles of a family of 11 extracytoplasmic function (ECF) gene regulatory proteins (sigma factors [s]) that interact with RNA polymerase to determine if they play a significant role in establishing a nitrogen-fixing symbiosis or in responding to various stresses, including cell envelope stress. Plant flavonoids stimulate the bacterial transcription factor NodD to induce expression of the bacterial nodulation (nod) genes [7, 8], which encode enzymes that synthesize Nod factor, which provokes formation of root nodules [1] Another key transcriptional regulator is the FixL-FixJ two-component system, which induces the expression of the nitrogen fixation apparatus (nif and fix genes) in bacteroids in response to low levels of free oxygen in infected plant cells [4]. At least 94 distinct groups have been defined within the ECF family, indicative of their broad diversity [16, 17]
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