PubMed HealthSearch

Biomedical subjects

Leyi Wang

Publications and source records attributed to Leyi Wang.

2 recordsLinked to original sources

Detection and genomic characterization of cryptosporidium parvum virus 1 (CSpV1): A potential biomarker for Cryptosporidium parvum detection in bovine calves.

Cryptosporidium parvum is a ubiquitous enteric parasite that infects a diverse range of vertebrate species. The detection of C. parvum can be confounded when oocysts are intermittently shed below an assay's limit of detection, yielding a false-negative result. We therefore investigated the utility of Cryptosporidium parvum virus 1 (CSpV1), a putative symbiont of Cryptosporidium parvum, as a surrogate target for detecting the parasite in bovine calves. Using real-time polymerase chain reaction (qPCR), we tested 422 samples for Cryptosporidium spp., C. parvum-associated targets, and CSpV1. Among the 189 samples positive for at least one target, CSpV1 was detected in 24 (12.70%) samples without concurrent detection of Cryptosporidium. Additionally, we analyzed CSpV1 genomic sequences to ascertain its value as an epidemiological biomarker. Evaluation of dsRNA1 amino acid sequences identified country-associated patterns, suggesting potential utility for geographic distribution analyses. These findings suggest that CSpV1 may serve as a biological signature of C. parvum and support further investigation into its usefulness as an adjunct molecular target.

Biomarker

Chronic heart failure and GPX3 promoter methylation: A clinical-epigenetic analysis.

BACKGROUND: Selenoprotein GPX3 is linked to Chronic Heart Failure (CHF), but its promoter methylation patterns in CHF remain unclear. OBJECTIVE: To explore CpG methylation in the GPX3 promoter region and its association with clinical parameters in CHF. METHODS: Twenty CHF patients and twenty healthy controls were included. Methylation levels of CpG sites within the GPX3_FA28 promoter region were quantified. Group differences were assessed using appropriate statistical tests. Restricted cubic spline (RCS) models were applied to explore dose-response associations between differentially methylated CpG sites and clinical indicators across multiple physiological systems. RESULTS: Significant locus-specific methylation alterations were identified in CHF patients. CpG_5 showed hypermethylation (P = 0.017), while CpG_9 (P = 0.045) and CpG_19 (P = 0.008) were hypomethylated compared with controls. Patients with NYHA class I/II exhibited higher methylation at CpG_1 (P = 0.028) and CpG_2 (P = 0.040). CpG_5 methylation displayed nonlinear associations (P < 0.05) with total bilirubin (inverted U-shape), carbon dioxide (triphasic), total cholesterol (U-shape), and plateletcrit (wave-like). CpG_9 correlated with activated partial thromboplastin time and hematopoietic markers, while CpG_19 was linked to eosinophil percentage and erythrocyte parameters. CONCLUSIONS: GPX3 promoter methylation displays apparent locus specificity in CHF. Different CpG sites may contribute to CHF pathophysiology through distinct epigenetic mechanisms. These findings highlight the potential of GPX3 methylation as a stratified biomarker in CHF.

Humans