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Armijos-Jaramillo, V.

Publications and source records attributed to Armijos-Jaramillo, V..

4 recordsLinked to original sources

A machine learning framework for interpreting phylogenetic tree patterns in interkingdom horizontal gene transfer

Horizontal gene transfer (HGT), the movement of genetic material between unrelated organisms, is widely recognized as an important driver of genome evolution in bacteria. In eukaryotes, however, the evolutionary impact of HGT remains debated. The identification of interkingdom HGT (iHGT) is especially challenging due to the lack of gold standard methods. Traditionally, iHGT identification has relied on manual inspection of phylogenetic trees, a process that is subjective, difficult to reproduce, and not scalable to large datasets. In this study, we present a computational framework that formalizes phylogenetic tree interpretation into a supervised machine-learning problem. We define five recurrent phylogenetic patterns--iHGT, NoHGT, Limited donor evidence, Multiple major clades (Multiple MC), and Patchy phylogeny--capturing clear and ambiguous evolutionary scenarios. To operationalize these patterns, we developed a feature-extraction pipeline that quantifies taxonomic composition and phylogenetic topology using seven biological descriptors derived from gene trees. These features were used to train and evaluate multiple machine-learning models, among which a Random Forest (RF) classifier achieved the best performance (AUC-ROC = 0.98; accuracy = 0.89). Model interpretability analyses revealed that topological distance to additional clades and lineage diversity are the most informative predictors, reflecting key signals used in expert-driven phylogenetic interpretation. The RF model was further validated using 1,000 simulated phylogenies and 1,438 real iHGT candidates, achieving low misclassification rates (7.8% and 10.43%, respectively). Benchmarking against AVP (Alienness vs. Predictor), a comparable tool for iHGT detection, demonstrated improved performance across all evaluation metrics, highlighting the advantages of incorporating global phylogenetic structure into the classification process. This study provides a reproducible and scalable framework for phylogenetic pattern classification that captures complex evolutionary signals while maintaining biological interpretability. Beyond improving iHGT detection, the approach offers a more nuanced representation of evolutionary scenarios by explicitly accounting for inconclusive cases, supporting more robust inference in comparative genomics. Authors summaryHorizontal gene transfer is the movement of genes between unrelated organisms rather than through normal inheritance from parent to offspring. While this process is known to play a major role in bacterial evolution, its importance in complex organisms such as fungi, plants, and animals remains debated. One reason for this uncertainty is that identifying these events often depends on manually interpreting phylogenetic trees, a process that can be subjective, difficult to reproduce, and impractical for analyzing the rapidly growing amount of genomic data. In this study, we developed a computational framework that transforms phylogenetic tree interpretation into a machine-learning problem. Instead of simply classifying genes as transferred or non-transferred, our approach recognizes several distinct evolutionary scenarios, including cases where the evidence is ambiguous or inconclusive. To achieve this, we extracted biologically meaningful features from phylogenetic trees describing evolutionary relationships and taxonomic diversity, and used them to train machine-learning models capable of recognizing recurrent phylogenetic patterns. Our framework successfully classified complex evolutionary scenarios and outperformed an existing automated method for interkingdom horizontal gene transfer detection. More broadly, this work demonstrates how expert-driven evolutionary reasoning can be translated into scalable and reproducible computational approaches. As genomic datasets continue to expand, such methods may help improve evolutionary inference and support more rigorous comparative genomics analyses.

bioinformatics↗

SARS-CoV-2, an evolutionary perspective of interaction with human ACE2 reveals undiscovered amino acids necessary for complex stability

The emergence of SARS-CoV-2 has resulted in more than 200,000 infections and nearly 9,000 deaths globally so far. This novel virus is thought to have originated from an animal reservoir, and acquired the ability to infect human cells using the SARS-CoV cell receptor hACE2. In the wake of a global pandemic it is essential to improve our understanding of the evolutionary dynamics surrounding the origin and spread of a novel infectious disease. One way theory predicts selection pressures should shape viral evolution is to enhance binding with host cells. We first assessed evolutionary dynamics in select betacoronavirus spike protein genes to predict where these genomic regions are under directional or purifying selection between divergent viral lineages at various scales of relatedness. With this analysis, we determine a region inside the receptor-binding domain with putative sites under positive selection interspersed among highly conserved sites, which are implicated in structural stability of the viral spike protein and its union with human receptor hACE2. Next, to gain further insights into factors associated with coronaviruses recognition of the human host receptor, we performed modeling studies of five different coronaviruses and their potential binding to hACE2. Modeling results indicate that interfering with the salt bridges at hot spot 353 could be an effective strategy for inhibiting binding, and hence for the prevention of coronavirus infections. We also propose that a glycine residue at the receptor binding domain of the spike glycoprotein can have a critical role in permitting bat variants of the coronaviruses to infect human cells.

microbiology↗

ShadowCaster: compositional methods under the shadow of phylogenetic models for the detection of horizontal gene transfer events in prokaryotes.

Horizontal gene transfer (HGT) plays an important role in the evolution of many organisms, especially in prokaryotes where commonly occurs. Microbial communities can improve survival due to the evolutionary innovations induced by HGT events. Thus, several computational approaches have arisen to identify such events in recipient genomes. However, this has been proven to be a complex task due to the generation of a great number of false positives and the prediction disagreement among the existing methods. Phylogenetic reconstruction methods turned out to be the most reliable but they are not extensible to all genes/species and are computationally demanding when dealing with large datasets. On the other hand, the so-called surrogate methods that use heuristic solutions either based on nucleotide composition patterns or phyletic distribution of BLAST hits can be applied easily to genomic scale, however, they fail in identifying common HGT events. Here, we present ShadowCaster, a hybrid approach that sequentially combines compositional features under the shadow of phylogenetic models independent of tree reconstruction to improve the detection of HTG events in prokaryotes. ShadowCaster predicted successfully close and distant HTG events in both artificial and bacterial genomes. It detected HGT related to heavy metal resistance in the genome of Rhodanobacter denitrificans with higher accuracy than the most popular state-of-the-art computational approaches. ShadowCasters predictions showed the highest agreement among those obtained with other assayed methods. ShadowCaster is released as an open-source software under the GPLv3 license. Source code is hosted at https://github.com/dani2s/ShadowCaster and documentation at https://shadowcaster.readthedocs.io/en/latest/.

bioinformatics↗

CompScore: boosting structure-based virtual screening performance by incorporating docking scoring functions components into consensus scoring

Consensus scoring has become a commonly used strategy within structure-based virtual screening (VS) workflows with improved performance compared to those based in a single scoring function. However, no research has been devoted to analyze the worth of docking scoring functions components in consensus scoring. We implemented and tested a method that incorporates docking scoring functions components into the setting of high performance VS workflows. This method uses genetic algorithms for finding the combination of scoring components that maximizes the VS enrichment for any target. Our methodology was validated using a dataset that contains ligands and decoys for 102 targets that has been widely used in VS validation studies. Results show that our approach outperforms other methods for all targets. It also boosts the initial enrichment performance of the traditional use of whole scoring functions in consensus scoring by an average of 45%. CompScore is freely available at: http://bioquimio.udla.edu.ec/compscore/

bioinformatics↗