Cyclic di-GMP (c-di-GMP) is a ubiquitous bacterial second messenger molecule that is an important virulence regulator in the plant pathogen Intracellular levels of c-di-GMP are modulated by diguanylate cyclase (DGC) enzymes that synthesize c-di-GMP and by phosphodiesterase (PDE) enzymes that degrade c-di-GMP. The regulatory role of the PDE enzymes in has not been determined. Using a combination of single, double, and triple deletion mutants, we determined the effects of each of the four putative PDE-encoding genes (, , , and ) in on cellular processes related to virulence. Our results indicate that and are the two phosphodiesterases most active in virulence regulation in Ea1189. The deletion of resulted in a measurably significant increase in the intracellular pool of c-di-GMP, and the highest intracellular concentrations of c-di-GMP were observed in the Ea1189 Δ and Ea1189 Δ mutants. The regulation of virulence traits due to the deletion of the genes showed two patterns. A stronger regulatory effect was observed on amylovoran production and biofilm formation, where both Ea1189 Δ and Ea1189 Δ mutants exhibited significant increases in these two phenotypes In contrast, the deletion of two or more genes was required to affect motility and virulence phenotypes. Our results indicate a functional redundancy among the genes in for certain traits and indicate that the intracellular degradation of c-di-GMP is mainly regulated by and , but they also suggest a role for in regulating motility and virulence. Precise control of the expression of virulence genes is essential for successful infection of apple hosts by the fire blight pathogen, The presence and buildup of a signaling molecule called cyclic di-GMP enables the expression and function of some virulence determinants in , such as amylovoran production and biofilm formation. However, other determinants, such as those for motility and the type III secretion system, are expressed and functional when cyclic di-GMP is absent. Here, we report studies of enzymes called phosphodiesterases, which function in the degradation of cyclic di-GMP. We show the importance of these enzymes in virulence gene regulation and the ability of to cause plant disease.
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http://dx.doi.org/10.1128/AEM.02233-18 | DOI Listing |
BMC Infect Dis
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Shenzhen Third People's Hospital, National Clinical Research Centre for Infectious Disease, The Second Affiliated Hospital of Southern University of Science and Technology, Shenzhen, China.
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The State Key Laboratory Breeding Base of Basic Science of Stomatology & Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Medical Research Institute, Wuhan University, Wuhan, China.
In contrast to mammalian cells, bacterial cells lack mRNA polyadenylated tails, presenting a hurdle in isolating mRNA amidst the prevalent rRNA during single-cell RNA-seq. This study introduces a novel method, ribosomal RNA-derived cDNA depletion (RiboD), seamlessly integrated into the PETRI-seq technique, yielding RiboD-PETRI. This innovative approach offers a cost-effective, equipment-free, and high-throughput solution for bacterial single-cell RNA sequencing (scRNA-seq).
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Centre in Artificial Intelligence Driven Drug Discovery, Faculty of Applied Sciences, Macao Polytechnic University, Macao, China.
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View Article and Find Full Text PDFPLoS Biol
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University of Würzburg, Faculty of Medicine, Institute of Molecular Infection Biology, Würzburg, Germany.
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