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Ricaurte, D.

Publications and source records attributed to Ricaurte, D..

2 recordsLinked to original sources

Signals of microbial growth learned from single amplicon samples

Irregularities in metagenomic whole-genome shotgun (WGS) read coverage can arise in quickly replicating microbial populations. These irregularities, summarized as peak-to-trough ratios (PTRs), are correlated with growth rates. This study seeks to explore the presence of similar coverage irregularities in 16S amplicon datasets, where multicopy diverged 16S genes provide an opportunity to explore coverage at different positions on the bacterial chromosome. To this end, we propose a model of Operational Taxonomic Unit (OTU) observations under replication and sequence similarity, from which we derive a method for simultaneous copy number correction and dynamics estimation by gradient descent. We conduct a series of benchmarks on synthetic data, determining a set of heuristics for when such methods may be applied, and compare our method with WGS-based methods on a real dataset. We find no correlation between coPTR estimates and our method, suggesting further modifications to our method may be required.

bioinformatics↗

Spatiotemporal dynamics during niche remodeling by super-colonizing microbiota in the mammalian gut

While fecal microbiota transplantation (FMT) has been shown to be effective in reversing gut dysbiosis, we lack an understanding for the fundamental processes underlying microbial engraftment in the mammalian gut. Here, we explored a murine gut colonization model leveraging natural inter-individual variations in gut microbiomes to elucidate the spatiotemporal dynamics of FMT. We identified a natural super-donor consortium that universally engrafts into diverse recipients and resists reciprocal colonization. Temporal profiling of the gut microbiome showed an ordered succession of rapid engraftment by early colonizers within 72 hours followed by a slower emergence of late colonizers over 15-30 days. Moreover, engraftment was localized to distinct compartments of the gastrointestinal tract in a species-specific manner. Spatial metagenomic characterization suggested engraftment was mediated by simultaneous transfer of spatially co-localizing species from the super-donor consortia. These results offer a mechanism of super-donor colonization by which nutritional niches are expanded in a spatiotemporally- dependent manner.

microbiology↗