bioRxiv Science⌕ Search

Biology subjects

Mogro, E. G.

Publications and source records attributed to Mogro, E. G..

5 recordsLinked to original sources

Scan Cluster: A versatile database-independent prediction tool for multi-genome identification of homologous gene clusters.

The exploration of colocalized gene sets, such as Biosynthetic Gene Clusters (BGCs) and symbiotic islands, is fundamental in modern genome mining. However, many existing prediction tools rely heavily on curated databases or predefined rules, inherently biasing detection toward known clusters. To address these limitations, we introduce Scan Cluster, a robust and flexible Python-based bioinformatic tool designed to identify user-defined, conserved gene clusters across diverse genomes without database-driven constraints. Scan Cluster leverages BLAST or HMMER to detect homologous proteins and evaluates their colocalization, accommodating complex evolutionary events such as orientation inversions, the insertion of alien genes, gene deletions, and the integration of insertion sequences. Beyond identification, the software performs progressive multiple cluster alignments and generates distance trees to assess cluster similarity, producing outputs ready for visualization in iTOL and Clinker. We validated Scan Cluster against standard tools like antiSMASH and DeepBGC, demonstrating high accuracy in delineating complete cluster boundaries. Its utility was further confirmed through the analysis of the nos and complex nod-nif-fix symbiotic gene clusters in rhizobia strains, successfully tracking genetic decay and grouping diverse architectures. Scan Cluster provides an accessible, low-resource framework to explore the evolutionary and functional dynamics of novel genetic clusters.

bioinformatics↗

Identification and functional analysis of recent IS transposition events in rhizobia

Rhizobia are alpha- and betaproteobacteria that, through the establishment of symbiotic interactions with leguminous plants, are able to fix atmospheric nitrogen as ammonium. The successful establishment of a symbiotic interaction is highly dependent on the availability of nitrogen sources in the soil, and on the specific rhizobia strain. Insertion sequences (ISs) are simple transposable genetic elements that can move to different locations within the host genome and are known to play an important evolutionary role, contributing to genome plasticity by acting as recombination hot-spots, and disrupting coding and regulatory sequences. Disruption of coding sequences may have occurred either in a common ancestor of the species or more recently. By means of ISComapare, we identified Differentially Located ISs (DLIS) in nearly related rhizobial strains of the genera Bradyrhizobium, Mesorhizobium, Rhizobium and Sinorhizobium. Our results revealed that recent IS transposition events dont seem to be playing a major role in adaptation. Nevertheless, DLIS could have a role enabling the activation and inactivation of certain genes that could dynamically affect the competition and survival of rhizobia in the rhizosphere.

microbiology↗

Identification of Ensifer meliloti genes required for survival during peat-based bioinoculant maturation by STM-seq

Rhizobial inoculants are sold either as rhizobia within a liquid matrix; or as rhizobia adhered to granules composed of peat prill or finely ground peat moss. During the production of peat-based inoculants, immediately after mixing the rhizobia culture with partially dry sterile peat, the inoculant is stored for a period of 4-5 weeks, inducing a series of changes that results in an increased capability of the rhizobia to survive in the seeds. The number of viable rhizobia on preinoculated seeds at the point of sale, however, is often a limiting factor, as is the inefficiency of the inoculant bacteria to compete with the local rhizobia for the host colonization. In the present work, we used STM-seq for the genomewide screening of Ensifer meliloti mutants affected in the survival during the maturation of peat-based inoculant formulations. Through this approach, we identified hundreds of genes that proved to be relevant to this process. These results also provide a base knowledge that could be used to more completely understand the survival mechanisms used by rhizobia during the maturation of peat-based inoculants, as well as for the design of new inoculant formulations. HighlightsRhizobial inoculants provide an ecological means of nitrogen fertilization compatible with the implementation of sustainable agricultural practices. Their successful usage, however, suffers from two main limitations: the low number of viable rhizobia on preinoculated seeds at the point of sale, and the inefficiency to compete with the local rhizobia for host colonization. Here, we used a high-throughput mutant-screening technology, STM-seq, to uncover which rhizobial genes are involved in the rhizobial survival during the preparation and storage of peat-based inoculant formulations. Our findings provide useful information about the stresses faced by rhizobia during peat-inoculant maturation and storage, which could assist both for the selection of better rhizobial strains, and for the improvement of the inoculant formulations. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=109 SRC="FIGDIR/small/508585v2_ufig1.gif" ALT="Figure 1"> View larger version (36K): org.highwire.dtl.DTLVardef@1433abdorg.highwire.dtl.DTLVardef@c54ff7org.highwire.dtl.DTLVardef@4fb2borg.highwire.dtl.DTLVardef@105e0c8_HPS_FORMAT_FIGEXP M_FIG C_FIG

microbiology↗

Analysis of SARS-CoV-2 synonymous codon usage evolution throughout the COVID-19 pandemic.

SARS-CoV-2, the seventh coronavirus known to infect humans, can cause severe life-threatening respiratory pathologies. To better understand SARS-CoV-2 evolution, genome-wide analyses have been made, including the general characterization of its codons usage profile. Here we present a bioinformatic analysis of the evo-lution of SARS-CoV-2 codon usage over time using complete genomes collected since December 2019. Our results show that SARS-CoV-2 codon usage pattern is antagonistic to, and it is getting farther away from that of the human host. Further, a selection of deoptimized codons over time, which was accompanied by a decrease in both the codon adaptation index and the effective number of codons, was observed. All together, these findings suggest that SARS-CoV-2 could be evolving, at least from the perspective of the synonymous codon usage, to become less pathogenic. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=92 SRC="FIGDIR/small/472912v1_ufig1.gif" ALT="Figure 1"> View larger version (29K): org.highwire.dtl.DTLVardef@d9d710org.highwire.dtl.DTLVardef@1b66a3corg.highwire.dtl.DTLVardef@f89a6eorg.highwire.dtl.DTLVardef@162d443_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioinformatics↗

Easy identification of insertion sequence mobilization events in related bacterial strains with ISCompare.

MotivationBacterial genomes are composed by a core and an accessory genome. The first composed of housekeeping and essential genes, while the second is composed, in its majority, of mobile genetic elements, including transposable elements (TEs). Insertion sequences (ISs), the smallest TEs, have an important role in genome evolution, and contribute to bacterial genome plasticity and adaptability. ISs can spread in a genome, presenting different locations in nearly related strains, and producing phenotypic variations. Few tools are available which can identify differentially located ISs (DLIS) on assembled genomes. ResultsWe developed ISCompare to profile IS mobilization events in related bacterial strains using complete or draft genome assemblies. ISCompare was validated using artificial genomes with simulated random IS insertions and real sequences, achieving the same or better results than other available tools, with the advantage that ISCompare can analyse multiple ISs at the same time and outputs a list of candidate DLIS. We think that ISCompare provides an easy and straightforward approach to look for differentially located ISs on bacterial genomes. Availability and implementationISCompare was implemented in python3 and its source code is freely available for download at https://github.com/maurijlozano/ISCompare. Supplementary informationSupplementary data are available at https://github.com/maurijlozano/ISCompare.

bioinformatics↗