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Biology subjects

Pinski, A.

Publications and source records attributed to Pinski, A..

2 recordsLinked to original sources

Genome editing of key domestication genes overcomes self-incompatibility and bitter taste in cultivated buckwheat

Buckwheat (Fagopyrum spp.) is a climate-resilient pseudocereal, yet its global adoption is constrained by the distylous self-incompatibility of common buckwheat (F. esculentum) and grain bitterness of Tartary buckwheat (F. tataricum). While the S-locus early flowering 3 (FeS-ELF3) gene has been identified as a key regulator of self-compatibility, a stable genetic transformation of F. esculentum has not yet been developed. In this study, we developed an Agrobacterium-mediated transformation protocol of F. esculentum (27% transformation efficiency) and applied it to the agronomically relevant Panda cultivar. Inactivation of the FeS-ELF3 gene using the CRISPR/Cas9 system yielded self-compatible lines with long-homostylous flowers. fes-elf3 mutants showed a distinct architectural shift: mutant plants were shorter and had shorter inflorescences than wild-type plants. Notably, these traits did not compromise yield, as the mutants produced a similar number of seeds per plant in the greenhouse. In F. tataricum, we targeted the rutin-degrading enzyme (FtRDE2), which was suspected to be a driver of grain bitterness by hydrolysing rutin into the bitter quercetin. Metabolic profiling of seeds of two ftrde2 mutant lines revealed significantly lower quercetin levels in both. Analysis of enzyme extracts confirmed the loss of rutinosidase activity; the mutant samples maintained stable rutin concentrations without the characteristic increase in quercetin observed in the control. Furthermore, organoleptic sensory evaluation of flour demonstrated that respondents identified the control as significantly more bitter than the flour from the ftrde2 mutants. These precise edits show proof-of-concept of overcoming domestication barriers: self-incompatibility and palatability, establishing a framework for rapid improvement of buckwheat.

plant biology↗

Acute SARS-CoV-2 infection is associated with an expansion of bacteria pathogens in the nose including Pseudomonas aeruginosa

Much of the research conducted on SARS-CoV-2 and COVID-19 has focused on the systemic host response, especially that generated by severely ill patients. Very few studies have investigated the impact of acute SARS-CoV-2 within the nasopharynx, the site of initial infection and viral replication. In this study we profiled changes in the nasal microbial communities as well as in host transcriptional profile during acute SARS-CoV-2 infection using 16S amplicon sequencing and RNA sequencing. These analyses were coupled to viral genome sequencing. Our microbiome analysis revealed that the nasal microbiome of COVID patients was unique and was marked by an expansion of bacterial pathogens. Some of these microbes (i.e. Acinetobacter) were shared with COVID negative health care providers from the same medical center but absent in COVID negative outpatients seeking care at the same institutions suggesting acquisition of nosocomial respiratory pathogens. Specifically, we report a distinct increase in the prevalence and abundance of the pathogen Pseudomonas aeruginosa in COVID patients that correlated with viral RNA load. These data suggest that the inflammatory environment caused by SARS-CoV-2 infection and potentially exposure to the hospital environment leads to an expansion of bacterial pathogens in the nasal cavity that could contribute to increased incidence of secondary bacterial infections. Additionally, we observed a robust host transcriptional response in the nasal epithelia of COVID patients, indicative of an antiviral innate immune repones and neuronal damage. Finally, analysis of viral genomes did not reveal an association between viral loads and viral sequences.

microbiology↗