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Bahar, O.

Publications and source records attributed to Bahar, O..

3 recordsLinked to original sources

Annual dynamics and distribution of Xylella fastidiosa in infected almond trees

This research focused on studying the dynamics of the bacterial pathogen Xylella fastidiosa in almond trees at different developmental stages and in various tree parts. The objective was to understand the annual distribution and concentration of X. fastidiosa within almond trees. Different tree parts, including leaf petioles, annual and perennial shoots, fruit parts, flowers, and roots, from ten X. fastidiosa-infected almond trees were sampled over two years. The distribution and concentration of X. fastidiosa were determined using qPCR and serial dilution plating. Throughout the study, X. fastidiosa was never found in the fruit, flowers, and roots of almond trees, but it was present in leaves and annual and perennial shoots. We show that the inability of X. fastidiosa to colonize roots is likely due to incompatibility with the GF677 rootstock. The presence of X. fastidiosa in shoots remained consistent throughout the year, while in leaf petioles it varied across developmental stages, with lower detection during early and late stages of the season. Similarly, viable X. fastidiosa cells could be isolated from shoots at all developmental stages, while in leaf petioles no successful isolations were achieved during the vegetative and nut growth stage. Examining the development of almond leaf scorch symptoms over time in trees with preliminary infections revealed that once symptoms have appeared on a single branch, other asymptomatic limbs were likely already colonized by the bacterium, hence, selective pruning of symptomatic branches is unlikely to cure the tree. Overall, this study enhances our understanding of X. fastidiosa dynamics in almonds and may have practical applications for its detection and control in almond orchards.

plant biology↗

Bacterial Outer Membrane Vesicles Induce a Transcriptional Shift in Arabidopsis Towards Immune System Activation Leading to Suppression of Pathogen Growth in Planta

Gram negative bacteria form spherical blebs on their cell periphery, which later dissociate and released into the surrounding environment. Previous studies have shown that these nano scale structures, derived primarily from the bacterial outer membrane and are termed outer membrane vesicles (OMVs), induce typical immune outputs in both mammals and plants. On the other hand, these same structures have been shown to promote infection and disease. To better understand the broad transcriptional change plants undergo following exposure to OMVs, we treated Arabidopsis thaliana (Arabidopsis) seedlings with OMVs purified from the Gram-negative plant pathogenic bacterium Xanthomonas campestris pv. campestris and performed RNA-seq analysis on OMV- and mock-treated samples at 2, 6 and 24 h post challenge. We found that the most pronounced transcriptional shift occurred in the first two time points, as was reflected by both the number of differentially expressed genes (DEGs) and the average fold change. Gene ontology enrichment analysis revealed that OMVs induce a major transcriptional shift in Arabidopsis towards immune system activation, upregulating a multitude of immune-related pathways including a variety of immune receptors and transcriptional factors. Comparing Arabidopsis response to OMVs and to single purified elicitors, revealed that while OMVs induce a similar suite of genes and pathways as single elicitors, some differential pathways activated by OMVs were detected including response to drug and apoptosis, which may indicate exposure to toxic compounds via OMV. To examine whether the observed transcriptional shift in Arabidopsis leads to an effective immune response, plants were pretreated with OMVs and then inoculated with a bacterial pathogen. OMV-mediated priming led to a significant reduction in bacterial titer in inoculated leaves two days following inoculation. Mutations in the elongation factor receptor (EFR), flagellin receptor (FLS2), or the brassinosteroid-insensitive 1-associated kinase (BAK1) receptor, did not significantly affect OMV-priming. All together these results show that OMV induce a broad transcriptional shift in Arabidopsis leading to upregulation of multiple immune pathways, and that this transcriptional change is reflected in the ability to better resist bacterial infection.

plant biology↗

Sulfated RaxX, which represents an unclassified group of ribosomally synthesized post-translationally modified peptides, binds a host immune receptor

The rice immune receptor XA21 is activated by the sulfated microbial peptide RaxX (required for activation of XA21-mediated immunity X) produced by Xanthomonas oryzae pv. oryzae (Xoo). Mutational studies and targeted proteomics revealed that RaxX is processed and secreted by the protease/transporter RaxB, whose function can be partially fulfilled by a noncognate peptidase-containing transporter B (PctB). RaxX is cleaved at a Gly-Gly motif, yielding a mature peptide that retains the necessary elements for RaxX function as an immunogen and host peptide hormone mimic. These results indicate that RaxX is a founding member of a previously unclassified and understudied group of tyrosine sulfated RiPPs (ribosomally synthesized, post-translationally modified peptides). We further demonstrate that sulfated RaxX directly binds XA21 with high affinity. This work reveals a complete, previously uncharacterized biological process: bacterial RiPP biosynthesis, secretion, binding to a eukaryotic receptor and triggering of a robust host immune response.

microbiology↗