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Ortner, D.

Publications and source records attributed to Ortner, D..

2 recordsLinked to original sources

Plant sexual and asexual contributions to the seed microbiome

The seed microbiome plays a key role in the assembly of the plant microbiome, which has major impacts on plant functioning. Nonetheless, little is known about the origin of the seed microbiome. We investigated the relative contributions of two hypothesized transmission routes: sexual inheritance (via reproductive organs) and asexual inheritance (via the plant vascular system). To do that, we sampled shoot endophytes both before bloom and at seed maturity stages, apple flower ovaries and pollen sacs, and mature seeds from field-grown apple trees (Malus domestica BO_SCPLOWORKHC_SCPLOW. cv Gala Galaxy Selecta). We showed that bacterial richness, diversity and composition differ among tissue types, with shoots before bloom harboring a higher diversity than ovary and pollen. Source tracking revealed that both sexual (30.3%) and asexual (23.8%) pathways contributed to seed microbiome assembly, with shoots at seed maturity being the dominant source. Notably, a large proportion (49.5%) of the seed microbiome originated from unknown sources. Lastly, the transmission pathways significantly differed among bacterial genera, with Pseudomonas primarily linked to shoots, Rhizobacter to pollen and Burkholderia to the ovary. Insights into seed microbiome origin offers new opportunities to enhance seed health and crop productivity through microbiome-assisted breeding.

ecology↗

Epidermal activation of Hedgehog signaling establishes an immunosuppressive microenvironment in basal cell carcinoma by modulating skin immunity

Genetic activation of Hedgehog (HH)/GLI signaling causes basal cell carcinoma (BCC), a very frequent non-melanoma skin cancer. Small molecule targeting of the essential HH effector Smoothened (SMO) proved an efficient medical therapy of BCC, although lack of durable responses and frequent development of drug resistance pose major challenges to anti-HH treatments. In light of the recent breakthroughs in cancer immunotherapy, we analyzed in detail the possible immunosuppressive mechanisms in HH/GLI-induced BCC. Using a genetic mouse model of BCC, we identified profound differences in the infiltration of BCC lesions with cells of the adaptive and innate immune system. Epidermal activation of HH/GLI led to an accumulation of immunosuppressive regulatory T cells, and to an increased expression of immune checkpoint molecules including PD-1/PD-L1. Anti-PD1 monotherapy, however, did not reduce tumor growth, presumably due to the lack of immunogenic mutations in common BCC mouse models, as shown by whole-exome sequencing. BCC lesions also displayed a marked infiltration with neutrophils, the depletion of which unexpectedly promoted BCC growth. The results provide a comprehensive survey of the immune status of murine BCC and provide a basis for the design of efficacious rational combination treatments. This study also underlines the need for predictive immunogenic mouse models of BCC to evaluate in vivo the efficacy of immunotherapeutic strategies.

cancer biology↗