PcsR2 Is a LuxR-Type Regulator That Is Upregulated on Wheat Roots and Is Unique to .

Front Microbiol

Molecular and Environmental Plant Sciences Program, Texas A&M University, College Station, TX, United States.

Published: November 2020

LuxR solos are common in plant-associated bacteria and increasingly recognized for playing important roles in plant-microbe interkingdom signaling. Unlike the LuxR-type transcriptional regulators of prototype LuxR/LuxI quorum sensing systems, solos do not have a LuxI-type autoinducer synthase gene associated with them. LuxR solos in plant-pathogenic bacteria are important for virulence and in plant endosymbionts contribute to symbiosis. In the present study, we characterized an atypical LuxR solo, PcsR2, in the biological control species 30-84 that is highly conserved among sequenced s strains. Unlike most LuxR solos in the plant-associated bacteria characterized to date, is not associated with a proline iminopeptidase gene and the protein has an atypical N-terminal binding domain. We created a deletion mutant and used quantitative RT-PCR to show that the expression of and genes in the operon immediately downstream was upregulated ∼10-fold when the wild type strain was grown on wheat roots compared to planktonic culture. PcsR2 was involved in upregulation. Using a GFP transcriptional reporter, we found that expression of responded specifically to root-derived substrates as compared to leaf-derived substrates but not to endogenous AHLs. Compared to the wild type, the mutant was impaired in the ability to utilize root carbon and nitrogen sources in wheat root macerate and to colonize wheat roots. Phenazine production and most biofilm traits previously shown to be correlated with phenazine production also were diminished in the mutant. Gene expression of several of the proteins in the phenazine regulatory network including PhzR, Pip (phenazine inducing protein) and RpeA/RpeB were reduced in the mutant, and overexpression of these genes restored phenazine production in the mutant to wild-type levels, indicating PcsR2 affects the activity of the these regulatory genes upstream of RpeA/RpeB via an undetermined mechanism. Our results indicate PcsR2 upregulates the expression of the adjacent operon in response to unknown wheat root-derived signals and belongs to a novel subfamily of LuxR-type transcriptional regulators found in sequenced strains.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7683790PMC
http://dx.doi.org/10.3389/fmicb.2020.560124DOI Listing

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