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Ma, K.-W.

Publications and source records attributed to Ma, K.-W..

3 recordsLinked to original sources

Misregulation of the jasmonate signaling pathway leads to altered plant microbiota interaction and plant stress responses

The model plant Arabidopsis thaliana hosts diverse microbial communities collectively known as the microbiota. The plant microbiota is generally taxonomically structured. Some of the members can promote plant fitness including growth and stress tolerance. However, microbial imbalance can also result in deleterious effects, a phenomenon known as dysbiosis that was first coined in the gut microbiome field. To unveil the regulatory mechanism to maintain plant homeostatic interaction with microbiota, we performed screening using defined synthetic bacterial communities. We identified an Arabidopsis mutant with altered microbial profiles, an overall increase of microbial load and microbiota-dependent growth defects. Transcriptomic and chemical complementation analyses confirmed that the aforementioned microbiota-dependent phenotypes are contributed by an upregulation of the jasmonate signaling pathway. Upregulation of the jasmonate pathway further promotes microbial growth, possibly forming a positive feedback loop. Even though activation of the jasmonate signaling pathway is known to enhance plant stress tolerance, hyperactivation of the pathway alters plant tolerance or resistance against multiple stressors. Plant association with the microbiota together with proper regulation of the jasmonate signaling pathway are thus essential to maintain plant response to environmental stressors.

plant biology↗

Simultaneous tracking of near-isogenic bacterial strains in synthetic Arabidopsis microbiota by chromosomally-integrated barcodes

DNA amplicon-based microbiota profiling currently relies on polymorphisms in microbial marker genes to estimate species diversity and abundance. However, this technique cannot resolve genetic differences among microbial individuals of the same species. We report here the development of modular bacterial tags (MoBacTags) encoding DNA barcodes. These tags facilitate tracking of near-isogenic bacterial commensals in synthetic communities (SynComs), which allow assessment of the contributions of individual bacterial genes to root microbiota establishment in Arabidopsis thaliana. Chromosomally-integrated DNA barcodes are co-amplified with endogenous marker genes of the community by integrating corresponding primer binding sites into the barcode. We generated MoBacTag-labeled strains of wild-type Pseudomonas capeferrum WCS358 and of pqqF and cyoB mutants with known defects in gluconic acid-mediated host immunosuppression and validated reduced root colonization of both mutants in a 15-member synthetic microbiota. We detected a reduced SynCom load on roots in the presence of the WCS358:pqqF mutant, but not WCS358:cyoB, revealing distinct pqqF and cyoB activities in a community context. Using MoBacTags, we also show that WCS358 pqqF mutant-specific colonization and community establishment is not trans-complemented by wild-type WCS358. Given that gluconic acid production in P. capeferrum is indirectly abolished in the pqqF mutant by disruption of pyrroloquinoline quinone (PQQ) biosynthesis, we propose that drastic changes in the root-associated community result from depletion of the cofactor PQQ, which might serve as a common good during root microbiota establishment. Our proof-of-principle experiments illustrate how MoBacTags can be applied to assess scaling of individual bacterial genetic determinants in the plant microbiota.

microbiology↗

Spatially Restricted Immune Responses Allow for Root Meristematic Activity During Bacterial Colonisation

Plants circumscribe microbe-associated molecular pattern (MAMP)-triggered immune responses to weak points of the roots. This spatially restricted immunity was suggested to avoid constitutive responses to rhizosphere microbiota. To demonstrate its relevance, we combined cell-type specific expression of the plant flagellin receptor (FLS2) with fluorescent defence markers and mapped immune competency at cellular resolution. Our analysis distinguishes cell-autonomous and non-cell autonomous responses and reveals lignification to be tissue-independent, contrasting cell-type specific suberisation. Importantly, our analysis divides the non-responsive meristem into a central zone refractory to FLS2 expression, and a cortex that becomes highly sensitised by FLS2 expression, causing meristem collapse upon MAMP exposure. Meristematic epidermal expression generates super-competent lines that detect native bacterial flagellin and bypass the absence of response to commensals, providing a powerful tool for studying root immunity. Our precise manipulations and read-outs demonstrate incompatibility of meristematic activity and defence and the importance of cell-resolved studies of plant immunity.

plant biology↗