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Takayasu, L.

Publications and source records attributed to Takayasu, L..

6 recordsLinked to original sources

High Resolution Spatial Mapping of Microbiome-Host Interactions via in situ Polyadenylation and Spatial RNA Sequencing

Inter-microbial and host-microbial interactions are thought to be critical for the functioning of the gut microbiome, but few tools are available to measure these interactions. Here, we report a method for unbiased spatial sampling of microbiome-host interactions in the gut at one micron resolution. This method combines enzymatic in situ polyadenylation of both bacterial and host RNA with spatial RNA-sequencing. Application of this method in a mouse model of intestinal neoplasia revealed the biogeography of the mouse gut microbiome as function of location in the intestine, frequent strong inter-microbial interactions at short length scales, shaping of local microbiome niches by the host, and tumor-associated changes in the architecture of the host-microbiome interface. This method is compatible with broadly available commercial platforms for spatial RNA-sequencing, and can therefore be readily adopted to broadly study the role of short-range, bidirectional host-microbe interactions in microbiome health and disease.

genomics↗

Microscale Spatial Dysbiosis in Oral biofilms Associated with Disease

Microbiome dysbiosis has largely been defined using compositional analysis of metagenomic sequencing data; however, differences in the spatial arrangement of bacteria between healthy and diseased microbiomes remain largely unexplored. In this study, we measured the spatial arrangement of bacteria in dental implant biofilms from patients with healthy implants, peri-implant mucositis, or peri-implantitis, an oral microbiome-associated inflammatory disease. We discovered that peri-implant biofilms from patients with mild forms of the disease were characterized by large single-genus patches of bacteria, while biofilms from healthy sites were more complex, mixed structures. Based on these findings, we propose a model of peri-implant dysbiosis where changes in biofilm spatial architecture allow the colonization of new community members. This model indicates that spatial structure could be used as a potential biomarker for community stability and has implications in diagnosis and treatment of peri-implant diseases. These results enhance our understanding of peri-implant disease pathogenesis and may be broadly relevant for spatially structured microbiomes.

microbiology↗

Comprehensive non-black box classification of highly correlated ecological time series pairs containing many zeros: the case of gut microbiome of mice

We developed a new data analysis method, named Coexistence-Exclusion-Synchronization- Antisynchronization (CESA), to reveal statistically significant correlations from a set of integer compositional abundance time series of Operational Taxonomic Unit (OTU) data of mouse gut microbiota. First, time series are transformed to 0 (absence) and 1 (presence), and statistical tests are applied to extract significant coexistence and mutual exclusion relationships. Subsequently, for all pairs, the difference time series are transformed to +1 (up), 0 (even), and -1 (down), and synchronized and antisynchronized pairs are classified based on statistical tests after carefully removing the effect of spurious correlation caused by changes in compositional shares. We performed a comprehensive classification of all pairs based on the p-values in terms of coexistence and synchronization, including time series data with many zeros, which are difficult to analyze using conventional methods. We found that almost all OTUs (419 out of 420) have significant correlations with at least one OTU in one of the four characteristics: coexisting, exclusive, synchronizing, or antisynchronizing. Considering OTU pairs, about 25% of all possible pairs (22,356 out of 87,990) show a high correlation with the p-values less than 10-5, which is less than the inverse of the total number of pairs. Interaction among phyla are summarized as a network diagram. Author summaryThe gut microbiota ecosystem is often thought to be stable. However, when observed over a long period, there are turnovers in the microbiota, each OTU time series is highly non-stationary, and even species with high overall abundance are often observed to have zero values in some periods. In this study, we developed a comprehensive data analysis method for extracting significant correlations between any pair of OTUs, including OTUs whose observed values contain many zeros or exhibit clear non-stationarity, for which processing methods have not yet been established. We focused on pairwise correlations in terms of coexistence, exclusivity, synchrony, and antisynchrony of increase/decrease, and all combinations of pairs were checked by statistical tests based on the p-values. In order to remove spurious correlations in compositional time series, a new method was introduced to correct the sample sizes for the remaining OTUs, hypothetically assuming a situation in which one OTU was not present. Low abundance OTUs are often overlooked in traditional analyses. However, it becomes evident that all OTUs, including those with low abundance, interact strongly with each other. Additionally, our findings suggest that coexistence and synchrony can be summarized as cooperative relationships, while exclusion and antisynchrony can be summarized as antagonistic relationships. Cooperative interactions are more likely to occur between pairs of OTUs in the same phyla, and antagonistic interactions are more likely to appear between OTUs in different phyla. The time series data analysis method developed in this paper includes no black-box, making it broadly applicable to compositional time series data with integer values.

microbiology↗

Dietary fiber induces a fat preference associated with the gut microbiota

Eating behavior is essential to human health. However, whether future eating behavior is subjected to the conditioning of precedent dietary composition is unknown. This study aimed to investigate the effect of dietary fiber consumption on subsequent nutrient-specific food preferences between palatable high-fat and high-sugar diets and explore its correlation with the gut microbiota. C57BL/6NJcl male mice were subjected to a 2-week dietary intervention and fed either a control (n = 6) or inulin (n = 6) diet. Afterwards, all mice were subjected to a 3-day eating behavioral test to self-select a high-fat or a high-sugar diet. The test diet feed intakes were recorded, and the mices fecal samples were analyzed to evaluate the gut microbiota composition. The inulin mice exhibited a preference for a high-fat diet over a high-sugar diet, associated with distinct gut microbiota compositions profiles between the inulin and control mice. The gut microbiota Bacteroides acidifaciens (99.68%), Bacteroides caecemuris (99.37%), and Bacteroides xylanolyticus (92.28%) positively correlated with a preference for fat. Further studies involving fecal microbiota transplantation and eating behavior-related neurotransmitter analyses may clarify the role of gut microbiota on food preferences. Food preferences induced by dietary intervention are a novel observation, and the gut microbiome may be significantly associated with this preference.

microbiology↗

Gastrointestinal transit mathematical model in mice treated with antibiotics

High-resolution fecal pharmacokinetics are crucial for optimizing therapeutic design and evaluating gastrointestinal motility. However, empirical studies with detailed time series data remain limited. This study aims to characterize fecal pharmacokinetics through high-frequency sampling and parallelized fecal concentration quantification, establishing a simple pharmacokinetics model with physiologically interpretable parameters. We quantified vancomycin concentrations in fecal samples collected at a minimum interval of 4 hours from C57BL/6J mice following a single oral administration of either a low (1 mg/mL) or high (20 mg/mL) dose. Fecal concentrations gradually increased and exhibited an exponential decay, leading to the development of a compartmental model with an absorption phase. This simple model accurately fit the experimental data and provided physiological explanations for intra- and inter-individual pharmacokinetics variability. The results suggest that inter-individual differences in pharmacokinetics are attributable to fecal elimination capacity, which may be influenced by drug dosage via changes in gastrointestinal motility. Since the model predicts antibiotic concentrations within the gastrointestinal tract, it can be applied to fundamental studies investigating the effects of antibiotics on the gut microbiome and gastrointestinal motility.

physiology↗

Lifelong temporal dynamics of the gut microbiome associated with longevity in mice

The temporal changes of the gut microbiome are thought to be critical for understanding its interactions with host aging, but lifelong dynamics within the same individual remain largely unknown. Here we firstly report the high temporal resolution dynamics of gut microbiomes in mice sharing the same genetic background and environment from their birth to natural death, spanning >1,000 days. The 16S rRNA sequencing analysis revealed 9 patterns of OTU temporal dynamics and 38 common "life-core" bacterial species/operational taxonomic units (OTUs) in [≥]80% of all samples across the lifespan of individual mice. The life-core OTUs are largely represented by the phylum Bacteroidota, whereas the transient bacterial group predominantly includes the phylum Firmicutes (Bacillota). Despite the shared genetic background and dietary habits, the gut microbiome structure significantly diversified with age and among individuals. A positive correlation existed between longevity and the microbiome -diversity in middle age (200-500 days) followed by a negative correlation in old age (>700 days), likely influenced by the increase in diversity during the last days of life. The abundance of several "life-core" species also exhibited non-static correlation trends with lifespan. Overall, this research characterized the gut microbiomes based on its persistence over hosts lifetime and suggested a non-static host-microbiome relationship within individual mice.

microbiology↗