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Taneja, J.

Publications and source records attributed to Taneja, J..

2 recordsLinked to original sources

Decoding Host-Pathogen Interactions in Staphylococcus aureus: Insights into Allelic Variation and Antimicrobial Resistance Prediction Using Artificial Intelligence and Machine Learning based approaches

This novel study leveraged advanced machine learning techniques to elucidate the molecular mechanisms of antimicrobial resistance (AMR) in 300Staphylococcus aureus isolates across six critical antibiotics. Employing a diverse array of deep learning and ensemble models, we conducted an in-depth analysis of genetic markers and allelic variations to characterize resistance determinants. Our investigation revealed that the XGBoost ensemble model demonstrated the most exceptional performance, achieving a remarkable 95% test accuracy, 100% training accuracy, and an unprecedented ROC AUC of 0.9855. Comparative analysis of multiple machine learning approaches, including Long Short-Term Memory (LSTM), Convolutional Neural Network (CNN), Multi-Layer Perceptron (MLP), Decision Tree, and Stochastic Gradient Descent (SGD) models, provided detailed insights into resistance prediction. The SHAP (SHapley Additive exPlanations) analysis unveiled critical genetic markers, with "cat_allele_Cluster_1015_Allele_8" emerging as the most influential feature driving resistance predictions. Notably, the models exhibited varying performance across different antibiotics, with consistently high accuracy and F1-scores for ciprofloxacin, clindamycin, gentamicin, and sulfamethoxazole/trimethoprim. Our findings not only demonstrate the potential of advanced machine learning techniques in predicting antimicrobial resistance but also provide crucial insights into the molecular mechanisms underlying S. aureus drug resistance. By identifying key genetic determinants and their relative importance, this study offers a sophisticated approach to understanding resistance patterns, potentially guiding future diagnostic strategies, targeted therapies, and antimicrobial stewardship practices in clinical settings.

bioinformatics↗

SPRAY-INDUCED GENE SILENCING IDENTIFIES PATHOGEN PROCESSES CONTRIBUTING TO POWDERY MILDEW PROLIFERATION

Spray-induced gene silencing (SIGS) is an emerging tool for crop pest protection. It utilizes exogenously applied double stranded RNA to specifically reduce pest target gene expression using endogenous RNA interference machinery. Powdery mildews, widespread obligate biotrophic fungi infect agricultural crops including wheat, barley, cucurbits, grapevine, and ornamentals such as roses. In this study, SIGS methods were developed and optimized for powdery mildews using the known azole-fungicide target CYP51 and the Golovinomyces orontii-Arabidopsis thaliana pathosystem. Additional screening resulted in the identification of conserved gene targets and processes important to powdery mildew proliferation: apoptosis-antagonizing transcription factor in essential cellular metabolism and stress response; lipase a, lipase 1, and acetyl-CoA oxidase in lipid catabolism; 9-cis-epoxycarotenoid dioxygenase, xanthoxin dehydrogenase, and a putative abscisic acid G-protein coupled receptor predicted to function in manipulation of the plant hormone abscisic acid; and the secreted effector EC2. Powdery mildew is the dominant disease impacting grapes and extensive powdery mildew resistance to applied fungicides has been reported. Therefore, we developed SIGS for the Erysiphe necator-Vitis vinifera system and tested six successful targets identified using the G. orontii-A. thaliana system. For all targets tested, a similar reduction in powdery mildew disease was observed between systems. This indicates screening of broadly conserved targets in the G. orontii-A. thaliana pathosystem identifies targets and processes for the successful control of other powdery mildews. The flexibility, specificity, reduced environmental and health risks, and rapid transition from the bench to the field make SIGS an exciting prospect for commercial powdery mildew control.

microbiology↗