Bois noir (BN) associated with ‘Candidatus Phytoplasma solani’ (Stolbur) is regularly found in Austrian vine growing regions. Investigations between 2003 and 2008 indicated sporadic presence of the confirmed disease vector Hyalesthes obsoletus and frequent infections of bindweed and grapevine. Infections of nettles were rare. In contrast present investigations revealed a mass occurrence of H. obsoletus almost exclusively on stinging nettle. The high population densities of H. obsoletus on Urtica dioica were accompanied by frequent occurrence of ‘Ca. P. solani’ in nettles and planthoppers. Sequence analysis of the molecular markers secY, stamp, tuf and vmp1 of stolbur revealed a single genotype named CPsM4_At1 in stinging nettles and more than 64 and 90 % abundance in grapevine and H. obsoletus, respectively. Interestingly, this genotype showed tuf b type restriction pattern previously attributed to bindweed associated ‘Ca. P. solani’ strains, but a different sequence assigned as tuf b2 compared to reference tuf b strains. All other marker genes of CPsM4_At1 clustered with tuf a and nettle derived genotypes verifying distinct nettle phytoplasma genotypes. Transmission experiments with H. obsoletus and Anaceratagallia ribauti resulted in successful transmission of five different strains including the major genotype to Catharanthus roseus and in transmission of the major genotype to U. dioica. Altogether, five nettle and nine bindweed associated genotypes were described. Bindweed types were verified in 34 % of grapevine samples, in few positive Reptalus panzeri, rarely in bindweeds and occasionally in Catharanthus roseus infected by H. obsoletus or A. ribauti. ‘Candidatus Phytoplasma convolvuli’ (bindweed yellows) was ascertained in nettle and bindweed samples.
Quantitative PCR (qPCR) and community fingerprinting methods, such as the Terminal Restriction Fragment Length Polymorphism (T-RFLP) analysis,are well-suited techniques for the examination of microbial community structures. The use of phylum and class-specific primers can provide enhanced sensitivity and phylogenetic resolution as compared with domain-specific primers. To date, several phylum- and class-specific primers targeting the 16S ribosomal RNA gene have been published. However, many of these primers exhibit low discriminatory power against non-target bacteria in PCR. In this study, we evaluated the precision of certain published primers in silico and via specific PCR. We designed new qPCR and T-RFLP primer pairs (for the classes Alphaproteobacteria and Betaproteobacteria, and the phyla Bacteroidetes, Firmicutes and Actinobacteria) by combining the sequence information from a public dataset (SILVA SSU Ref 102 NR) with manual primer design. We evaluated the primer pairs via PCR using isolates of the above-mentioned groups and via screening of clone libraries from environmental soil samples and human faecal samples. As observed through theoretical and practical evaluation, the primers developed in this study showed a higher level of precision than previously published primers, thus allowing a deeper insight into microbial community dynamics.
Spore‐forming, plant growth‐promoting bacteria (PGPR) offer extraordinary opportunities for increasing plant productivity in climate change scenarios. Plant–water relationships, root development and photosynthetic performances are all key aspects of plant physiology determining yield, and the ability of PGPR to influence these in a coordinated manner is crucial for their success. In this study, we dissected the mode of action of a commercial Bacillus paralicheniformis FMCH001 in promoting soybean (Glycine max, seed variety: Sculptor) establishment in well‐watered and drought conditions. We found that FMCH001 colonizes the roots, improved root growth and allowed plants to absorb more nutrients from the soil. FMCH001 inoculation had no effect on abscisic acid in leaf or xylem sap, while significantly improved photosynthesis rate, stomatal conductance and transpiration rate at 28 days after planting when drought stress exposed for 7 days, with depressed leaf water potential and osmotic potential. Moreover, the bacterium increased water use efficiency and the inoculated soybean plants exposed to drought used 22.94% less water as compared to control, despite producing comparable biomass. We propose that the ability of the bacterium to promote root growth and also modulate plant water relations are key mechanisms that allow FMCH001 to promote growth and survival in dicotyledon plants.
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