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Biology subjects

Gadhamshetty, V.

Publications and source records attributed to Gadhamshetty, V..

4 recordsLinked to original sources

Predictors Recover Most of the Metagenomic Signal for Antibiotic Resistance Gene Occurrence: A Cross-City Test of Geographic Transferability in Urban Wastewater

Antibiotic resistance genes (ARGs) travel from cities into rivers and coastal waters through wastewater treatment plants. Monitoring them normally requires metagenomic sequencing, which is sufficiently costly that most utilities can sample only occasionally. Weather and location data are freely available on a daily basis for virtually any location worldwide, making them attractive predictors for identifying where limited sequencing resources should be prioritized. However, whether such models generalize to previously unseen cities remains largely untested, as most published studies train and evaluate models within the same catchments, thereby assessing interpolation rather than geographic transferability. To address this gap, we paired 235 wastewater metagenomes collected from five European cities with 23 abiotic predictors spanning geospatial, meteorological, hydrological, radiative, and temporal domains. Model performance was evaluated using leave-one-group-out (LOGO) cross-validation, in which all samples from one city were withheld for testing while the remaining cities were used for training. CatBoost achieved a median LOGO ROC-AUC of 0.929 and a median F1-score of 0.750. Using freely available environmental reanalysis predictors (meteorological, hydrological, radiative, geospatial, and temporal) - without any metagenomic sequencing - CatBoost achieved a mean ROC-AUC of 0.722, recovering 78% of the predictive performance of the full omics-integrated model. Removing latitude and longitude reduced ROC-AUC by only 0.003, whereas replacing random cross-validation with city-wise validation reduced ROC-AUC by 0.052. Predictive performance varied across ARG classes, ranging from a ROC-AUC of 0.981 for {beta}-lactam resistance genes to 0.762 for glycopeptide resistance genes. These findings demonstrate that freely available environmental reanalysis predictors - spanning meteorological, hydrological, radiative, geospatial, and temporal domains - recover 78% of the predictive signal for antibiotic resistance gene occurrence in urban wastewater, allowing scarce sequencing capacity to be directed to the catchments where it changes a decision.

microbiology↗

The genome assembly and detection of biosynthetic gene clusters among four novel microbial isolates from deep subsurface rock biofilms

Tunnels in deep underground mines provide a unique interface between the surface and deep subsurface habitats. There, microbes from the surface may enter the deep tunnels as surface air is drawn into the deep mine tunnels to provide ventilation. This extreme hosting environment provides a condition for microbes to develop novel capabilities, such as the production of natural products of biotechnology or medicinal importance. This study characterized the genomes of four novel isolates from deep subsurface biofilms of the previously abandoned gold mine, which was used as a model for the underground study. Here the microbiome samples were obtained from thin, whitish, glistening biofilm samples naturally formed on the rock walls (1478 meters deep at SURF). These samples are herein referred to as "cave silver" biofilms. The samples provide 10 GB of high-quality whole genome sequences that were assembled into contigs/scaffolds and structurally and functionally annotated against various databases. Subsequently, the genomes were analyzed for biosynthetic gene clusters (BGCs) encoding secondary metabolites of biotechnology and medical importance using the antiSMASH and the NaPDoS web servers, respectively. In brief, the assemblies produced four drafted genomes of different lengths and annotated features for each strains genome, including gene clusters involved in the quorum sensing (QS) pathway. Several BGC-encoded secondary metabolites of natural products or compounds such as polyketides (PKS, PKS III, ketosynthase domain-KS), non-ribosomal peptides (condensation domain, NRPS), and terpenoids (terpenes I, polyenes type II), were identified. Furthermore, many overexpressed enzymes, most of which are shared among the strains and some unique to individual bacteria strains, were identified, revealing possible shared and individualized strain activities in the biofilms during the sample collection. CRISPR peptides were also detected in three of the four bacteria strains. In this study, we examine the genomes of microbes colonizing extreme subsurface environments and how these conditions promote the development of microbial systems that are potentially capable of producing medicinally natural products and secondary metabolites that may be used to enhance advancements in biotechnology products. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=134 SRC="FIGDIR/small/675994v1_ufig1.gif" ALT="Figure 1"> View larger version (32K): org.highwire.dtl.DTLVardef@17a82f0org.highwire.dtl.DTLVardef@2a73f0org.highwire.dtl.DTLVardef@121c3e9org.highwire.dtl.DTLVardef@1c51f9b_HPS_FORMAT_FIGEXP M_FIG C_FIG ImportanceDeep subsurface environments host unique microbial communities with specialized adaptations. By characterizing genomes from "cave silver" biofilms, this study reveals biosynthetic gene clusters and pathways for secondary metabolite production, including polyketides, peptides, and terpenoids. These findings highlight the potential of extreme-environment microbes as a novel source of biotechnologically and medically valuable natural products.

genomics↗

CREID- A ChemoReceptor-Effector Interaction Database

The ChemoReceptor-Effector Interaction Database (CREID) is a collection of bacterial chemoreceptor and effector protein and interaction data to understand the process that chemoreceptors and effectors play in various environments. Our website includes terms associated with chemosensory pathways to educate users and those involved in collaborative research to help them understand this complex biological network. It includes 2,440 proteins involved in chemoreceptor and effector systems from 7 different bacterial families with 1,996 chemoeffector interactions. It is available at https://react-creid.bicbioeng.org. Key HighlightsO_LICREID links bacterial chemoreceptors with their associated effectors. C_LIO_LIResearchers interested in what attracts or repels bacteria can use CREID as a comprehensive source for information. C_LIO_LIBiosensor developers can leverage CREID to discover better interactions for their applications. C_LIO_LICREID reveals knowledge gaps in chemoreceptor-effector interactions for both model and non-model organisms. C_LI

bioengineering↗

Classification of bacterial nanowire proteins using Machine Learning and Feature Engineering model

Nanowires (NW) have been extensively studied for Shewanella spp. and Geobacter spp. and are mostly produced by Type IV pili or multiheme c-type cytochrome. Electron transfer via NW is the most studied mechanism in microbially induced corrosion, with recent interest in application in bioelectronics and biosensor. In this study, a machine learning (ML) based tool was developed to classify NW proteins. A manually curated 999 protein collection was developed as an NW protein dataset. Gene ontology analysis of the dataset revealed microbial NW is part of membranal proteins with metal ion binding motifs and plays a central role in electron transfer activity. Random Forest (RF), support vector machine (SVM), and extreme gradient boost (XGBoost) models were implemented in the prediction model and were observed to identify target proteins based on functional, structural, and physicochemical properties with 89.33%, 95.6%, and 99.99% accuracy. Dipetide amino acid composition, transition, and distribution protein features of NW are key important features aiding in the models high performance.

systems biology↗