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Biology subjects

Jayakumar, D.

Publications and source records attributed to Jayakumar, D..

4 recordsLinked to original sources

Genomic Evolution of SARS-CoV-2 Delta Variants Pre- and Post-Omicron Emergence using Alignment-free Machine Learning models

The SARS-CoV-2 Delta variant (B.1.617.2), initially classified as a variant of concern due to its enhanced transmissibility and vaccine-escape mutations, underwent further genomic changes following the emergence of the Omicron variant (B.1.1.529). This study investigates the genomic differences in Delta variant spike gene sequences collected before and after the emergence of Omicron. A total of 190 sequences were analyzed using an alignment-free approach incorporating k-mer-based feature extraction and machine learning models, including convolutional neural networks (CNN), K-means clustering, and random forest classification. The random forest model achieved 93% accuracy, with significant F1 scores, effectively distinguishing the two Delta variant groups. Comparative analysis revealed 157 persistent mutations and four vanished mutations in the post-Omicron group. Cluster analysis showed notable shifts, indicating stable yet evolving genomic patterns over time. The study demonstrates the advantage of alignment-free methods in detecting subtle sequence variations that alignment-based approaches may overlook. These findings enhance our understanding of SARS-CoV-2 evolution and provide a framework for identifying key genomic signatures relevant to public health. The methodology and insights gained offer potential applications in variant surveillance, vaccine design, and viral evolutionary studies, supporting preparedness for future SARS-CoV-2 variant emergence.

genomics↗

Temporal changes in miR-23a-5p levels in subclinical atherosclerosis: A Potential biomarker.

A high-cholesterol diet (HCD) is a well-established contributor to oxidative stress, inflammation, and atherogenesis, yet the temporal progression of these pathological changes and the regulatory role of circulating microRNAs (miRNAs) remain incompletely understood. In this study, we investigated the effects of prolonged HCD exposure to rats on lipid metabolism, oxidative stress, inflammation, endothelial dysfunction, and miRNA expression in a rat model. Male Wistar rats were fed either a standard diet or HCD for 30, 60, 90, or 120 days. Biochemical analyses revealed a progressive dyslipidemic profile characterized by elevated total cholesterol, triglycerides, LDL, VLDL, and atherogenic index, alongside a significant reduction in HDL. Lipid peroxidation levels increased markedly with HCD duration, while antioxidant markers PON1 and ApoA1 were significantly reduced and oxLDL levels were elevated. Inflammatory cytokines (CRP, TNF-, IL-6, IL-8) and VCAM-1 were significantly increased, indicating systemic inflammation and endothelial activation. Notably, miR-23a-5p and miR-15b-5p were elevated in the serum of HCD-fed rats, with miR-23a-5p peaking at day 120. Correlation analyses revealed that miR-23a-5p expression positively correlated with oxLDL and inversely with ApoA1 and PON1 levels, suggesting its involvement in oxidative and lipoprotein dysregulation. These findings demonstrate that prolonged HCD induces a coordinated cascade of oxidative, inflammatory, and lipoprotein alterations, with miR-23a-5p emerging as promising biomarkers and potential regulators of redox and lipid homeostasis in atherogenesis.

molecular biology↗

Ironing out the role of Nrf2 in cardiac iron metabolism during myocardial infarction

Background and PurposeIron plays a crucial role in maintaining cardiac health. However, existing research has focused on understanding how cardiac cells regulates intercellular iron levels through their own cell-autonomous cardiac hepcidin/ferroportin axis. In Addition, several studies have explored the mechanisms linking cardiac dysfunction with iron imbalance. Recent insights also emphasize the importance of Nrf2, a key transcriptional regulator that not only counteracts iron-mediated oxidative stress, but also governs several genes involved in iron metabolism. Consequently, the Nrf2/hepcidin/ferroportin axis is emerging as a central hub connecting cardiac iron metabolism with redox alterations. However, the precise mechanisms linking these components remain elusive. This study aims to elucidate how disruptions in the Nrf2/hepcidin/ferroportin axis contribute to the altered iron metabolism in Myocardial infarction (MI). Experimental ApproachMI was induced in adult Wistar rats by subcutaneous administration of isoproterenol (ISO; 85 mg/kg body weight) for two days. H9c2 cardiomyoblasts were differentiated into cardiomyocytes using all-trans-retinoic acid (ATRA, 2.5M for 5-days) and subjected to hypoxic stress using CoCl2 (100M). In vitro pharmacological suppression of Nrf2 was performed using brusatol (50nM). Key ResultsMorphological examination revealed maladaptive remodeling, and histopathological analysis demonstrated disoriented myofibrils with intense neutrophil infiltration and necrotic impressions in MI-affected animals. Furthermore, elevated levels of labile redox-active iron and inflammatory markers were observed in serum of ISO induced animals. qPCR & Western blot analysis indicated an increase in HIF-1 and hepcidin levels, and downregulation of FTH levels in MI-induced animals, with no significant changes observed in FPN-1. The transcriptional activity of Nrf2 is enhanced in the MI-heart. Moreover, increased levels of NCOA4, beclin-1, and LC3-II/LC3-I, along with decreased p62, suggest enhanced ferritinophagy in MI-induced hearts. Nrf2 was pharmacologically suppressed in differentiated H9c2 cardiomyocytes to explore its potential role in MI pathophysiology. Remarkably, this inhibition rescued CoCl2-induced hypoxic stress, as evidenced by the decreased ferritinophagy and apoptotic cell death. Conclusion and ImplicationsAugmented Nrf2-transcriptional activity disrupts iron metabolism through the hepcidin/ferroportin axis, leading to iron sequestration and promoting ferritinophagy within cardiomyocytes, thereby exacerbating MI.

biochemistry↗

Scopoletin Augments DJ1/Nrf2 Signalling and Prevents Protein Aggregation in Parkinson’s disease

Given the role of oxidative stress in PD pathogenesis and off-target side effects of currently available drugs, several natural phytochemicals seems to be promising in the management of PD. Here, we tested the hypothesis that scopoletin, an active principle obtained from Morinda citrifolia (MC), efficiently quenches oxidative stress through DJ-1/Nrf2 signalling and ameliorates rotenone-induced PD. Despite reducing the oxidative stress, administration of MC extract (MCE) has lessened the protein aggregation as evident from decreased levels of nitrotyrosine and -Synuclein. In vitro studies revealed that scopoletin lessened rotenone-induced apoptosis in SH-SY5Y cells through preventing oxidative injury. Particularly, scopoletin markedly up-regulated DJ-1, which then promoted the nuclear translocation of Nrf2 and transactivation of antioxidant genes. Furthermore, we found that scopoletin prevent the nuclear exportation of Nrf2 by reducing the levels of Keap1 and thereby enhancing the neuronal defence system. Overall, our findings suggest that scopoletin acts through DJ-1 mediated Nrf2 signalling to protect the brain from rotenone-induced oxidative stress and PD. Thus, we postulate that scopoletin could be a potential drug to treat PD.

biochemistry↗