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Selem, N.

Publications and source records attributed to Selem, N..

2 recordsLinked to original sources

A global synthesis of yeast in microbiomes

Yeasts are widespread members of microbial communities across terrestrial, aquatic, and host-associated environments, yet they remain underrepresented in microbiome studies due to low abundance and methodological biases. By combining a literature review with a meta-analysis of [~]44,000 fungal metabarcoding samples from the GlobalFungi database, we show that yeasts occur in over 90% of samples, confirming their global ubiquity. Basidiomycetous lineages--especially Agaricomycotina--were most frequently detected, whereas Saccharomycotina were more restricted to anthropogenic and aquatic settings. Although yeasts typically comprised only [~]0.1% of fungal reads, their distributions were non-random and reflected distinct habitat preferences across environments. In [~]3% of samples, yeasts exceeded 25% of reads, with genera such as Aureobasidium, Hanseniaspora, and Saccharomyces episodically dominating nutrient-rich or human-influenced environments. Cosmopolitan genera including Vishniacozyma, Solicoccozyma, and Rhodotorula were broadly distributed but remain underreported in microbiome surveys. Shotgun metagenomic data further confirmed yeast presence across diverse microbiomes, though with consistently low coverage, reflecting the "curse of low abundance." Despite their rarity, yeasts likely play disproportionate roles in nutrient cycling, plant growth, and host interactions. We recommend inclusive multi-kingdom approaches--improved primers, long-read sequencing, and quantitative tools--to better integrate yeasts in microbiomes.

microbiology↗

Expanding Gene Families Helps Generate The Metabolic Robustness Required For Antibiotic Biosynthesis

Introductory paragraphExpanding the genetic repertoire of an organism by gene duplication or horizontal gene transfer (HGT) can aid adaptation. Streptomyces species are prolific producers of bioactive specialised metabolites with adaptive functions in nature and some have found utility in human medicine such as antibiotics. Whilst the biosynthesis of these specialised metabolites is directed by dedicated biosynthetic gene clusters (BGCs), little attention has been focussed on how these organisms have evolved robustness into their genomes to facilitate the metabolic plasticity required to provide chemical precursors for biosynthesis. Here we show that specific expansions of gene families in central carbon metabolism have evolved and become fixed in Streptomyces bacteria to enable plasticity and robustness that maintain cell functionality whilst costly specialised metabolites are produced. These expanded gene families, in addition to being a metabolic adaptation, make excellent targets for metabolic engineering of industrial specialised metabolite producing bacteria.

microbiology↗