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Lehenberger, P.

Publications and source records attributed to Lehenberger, P..

2 recordsLinked to original sources

Deterministic colonization arises early during the transition of soil bacteria to the phyllosphere and is shaped by plant-microbe interactions.

BackgroundUpon seed germination, soil bacteria are activated to transition to the plant and eventually colonize mature tissues like leaves. These bacteria are poised to significantly influence plant health, but we know little about their colonization routes. We studied the mechanisms of the transition of soil bacteria to germinating plants and leaves by experimentally manipulating inoculation times and using in-planta isolation to understand bacteria that can make the complex soil-to-leaf transition. Using a trackable, labeled Pseudomonas viridiflava (Pv3D9) amended to soil, we tested how plant-microbe-microbe interactions shape assembly mechanisms in natural soil communites. ResultsWe found that the stages of the transition of bacteria from soil to leaves before true leaf emergence were important in establishing uniquely diverse leaf bacteriomes. A wide diversity of leaf-associated taxa can individually make this transition, but most are still shaped by stochastic processes. Interestingly, deterministic processes drove some important taxa only when they transitioned from soil to leaves, but not when they were inoculated later. The opportunistic pathogen Pv3D9 promoted plant growth in a natural soil, likely by activating plant immunity. These effects in turn strongly affected the soil-to-leaf transition of almost strictly taxa that colonized deterministically, demonstrating the important role of plant-microbe-microbe interactions in controlling deterministic processes. ConclusionsDiverse, well-adapted bacterial taxa make the soil-to-leaf transition during natural colonization resulting in characteristic diversity in healthy leaf microbiomes. The domination of stochastic mechanisms during this colonization indicates that many taxa must strongly compete to establish their niche. During this complex transition, however, specific important taxa emerge that are driven by deterministic processes, suggesting they occupy unique niches. The malleability of these processes suggests that they may be controlled, for example by targeted soil manipulations. This finding is significant given the important roles of these bacteria in plant health and offers directions forward for engineering beneficial plant microbiomes.

microbiology↗

Mod5 mediates a molecular trade-off between optimal gene expression and antifungal resistance.

Increasing antifungal drug resistance is a major concern associated with human fungal pathogens like Aspergillus fumigatus. Genetic mutation and epimutation mechanisms clearly drive resistance, yet the epitranscriptome remains relatively untested. Here, deletion of the A. fumigatus tRNA-modifying isopentenyl transferase ortholog, Mod5, led to altered stress response and unexpected resistance against the antifungal drug 5-fluorocytosine (5-FC). After confirming the canonical isopentenylation activity of Mod5 by LC-MS/MS and Nano-tRNAseq, we performed simultaneous profiling of transcriptomes and proteomes to reveal a comparable overall response to 5-FC stress; however, a premature activation of cross-pathway control (CPC) genes in the knockout was further increased after antifungal treatment. We identified several orthologues of the A. nidulans Major Facilitator Superfamily (MFS) transporter nmeA as specific CPC-client genes in A. fumigatus. Overexpression of Mod5-target tRNATyrG{Psi}A in the {Delta}mod5 strain rescued select phenotypes but failed to reverse 5-FC resistance, whereas deletion of nmeA largely, but incompletely, reverted the resistance phenotype, implying additional relevant exporters. In conclusion, 5-FC resistance in the absence of Mod5 and i6A likely originates from multifaceted transcriptional and translational changes that skew the fungus towards premature CPC-dependent activation of antifungal toxic-intermediate exporter nmeA, offering a potential mechanism reliant on RNA modification to facilitate transient antifungal resistance.

microbiology↗