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ye, x.

Publications and source records attributed to ye, x..

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16S rRNA Survey Reveals the Potential of Oral Microbiota in Distinguishing Patients with Chronic Heart Failure from Healthy Controls

BackgroundOral microbiota can reflect physiological functions and pathological conditions in human body. Patients with chronic heart failure (CHF) exhibit distinct oral health status compared to healthy controls (HCs), which is attributed to the differences in dominant microbial communities present in the oral cavity. Up to date, there are few studies examined the association between CHF and dominant oral microbiota. To fill in this research gap, this study aimed to investigate the differences of oral microbiota between CHF patients and HCs, to identify valuable novel biomarkers for CHF. MethodsChronic heart failure patients and healthy volunteers were recruited. Oral microbiota samples were then collected using oral swabs, and 16S rRNA sequencing was employed to analyze the microbiota. Statistical analysis was conducted to identify key bacteria at multiple taxonomic levels in the oral microbiota samples from both the CHF patient and healthy control groups, with a focus on core genera to identify potential biomarkers and evaluate their diagnostic efficacy. ResultsThere were 60 CHF patients and 30 HCs were recruited, with 42 CHF patients with New York Heart Association (NYHA) functional class II-IV and 28 HCs were included in the final analysis. The alpha diversity was higher in HCs, while beta diversity was higher in CHF patients. The CHF patients showed significant differences from HCs at five gene (phylum, class, order, family and genus) levels by analyzing the relative richness of microbiota at different taxomal levels. Altogether 14 microbes could distinguish CHF patients from HCs, i.e., Abiotrophia, Butyrivibrio, Lactobacillus, Capnocytophaga and Neisseria which are more abundant in CHF patients, and Actinomyces, Anaerovorax, Eubacterium, Kingella, Mogibacterium, Peptococcus, Peptostreptococcus, Solobacterium and TM7_genus_incertae_sedis which are more abundant in HCs. Furthermore, the AUC of their combined diagnosis was 83.7% (95% confidential interval 74.1%-93.3%), which have high reliability for the diagnostic significance. In accordance to Spearmans correlation, Eubacterium, Solobacterium and Rhizobium were core genera and the abundance of Eubacterium and Solobacterium exhibited downward trends as NYHA class increases. ConclusionThis study revealed the dysbiosis of the oral microbiota in CHF patients and identified potential biomarkers for CHF diagnosis and management. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=113 SRC="FIGDIR/small/669863v1_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@d60f6eorg.highwire.dtl.DTLVardef@18f17ceorg.highwire.dtl.DTLVardef@163f0daorg.highwire.dtl.DTLVardef@599bcd_HPS_FORMAT_FIGEXP M_FIG C_FIG

microbiology↗

Vitamin D regulates olfactory function via dual transcriptional and mTOR-dependent translational control of synaptic proteins

Vitamin D (VitD) deficiency, affecting over 1 billion people worldwide, is associated with neurological dysfunction, but its cell-type-specific neural mechanisms remain unclear. Using a dietary mouse model, we show that VitD bidirectionally regulates olfactory acuity: deficiency impairs odor discrimination, while supplementation enhances sensitivity. Single-nucleus and spatial transcriptomics pinpoint selective vitamin D receptor (VDR) expression in olfactory bulb (OB) tufted cells, where it drives synaptic protein expression. Genetic VDR knockdown replicates deficiency-associated olfactory deficits, establishing VDR as essential for synaptic and translational regulation. Notably, we identify mTOR-mediated protein synthesis as a critical convergence point--pharmacological mTOR inhibition (rapamycin) rescues synaptic protein deficits and behavioral impairments in VitD-deficient mice. These findings delineate a noncanonical VDR-mTOR-translational axis--complementing conventional transcriptional regulation--through which VitD serves as a nutrient-sensitive neuromodulator that integrates dietary status with synaptic functions and sensory processing. Our study expands the physiological role of VitD beyond traditional endocrine signaling and reveals mechanistic insights that may inform novel therapeutic strategies for neurological and psychiatric conditions associated with VitD deficiency.

neuroscience↗