bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.03.11.642625

Global Phylogenomic Analysis and Genome Homology Reveals New rare Phylogenetic groups, "Synonymous" Species, and the Need to Simplify Nomenclature and Pathogens Identification in the Bacillus cereus Group

Abstract

Bacteria in the Bacillus cereus Group sensu lato (Bc Group sl) may have serious detrimental effects on the health and safety of numerous foods. Over the past decade, phylogenetic studies have shifted toward the delineation of an increasing number of closely related species. For an improved understanding, this study attempts to fill existing gaps in the data to build a complete, robust and useful phylogenetic structure that contains all 29 currently described species. The obtained phylogenetic structure features all of the known major phylogenetic groups (designated I to VII) and their subgroups, but also highlights the existence of seven new rare groups or sub-groups. The positioning of the 29 species revealed that some are synonymous, which casts doubt on the accuracy of their genomic delimitation. Four species matched with the previously described sub-groups III-5, III-9 and III-12, which are specifically known for their virulence potential. B. thuringiensis strains were dispersed throughout the majors groups II to VI, demonstrating that this species is not a genomic species restricted to group IV but should be instead considered a variety largely spread into the Bc Group sl. A similar pattern was observed for B. mycoides in 10 phylogenetic groups/species. These results highlight the need for a simplified nomenclature of the Bc Group sl, which should be developed through a collaboration between relevant stakeholders. In the meantime, an updated version of the panC database is proposed, named CereusID, that integrates data from the present work and enables the identification of all phylogenetic entities within Bc Group sl: https://toolcereusid.shinyapps.io/cereusid/.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

guinebretiere, m.-h., Couvert, O., LE MARC, Y., POSTOLLEC, F.. 2025-03-14. Global Phylogenomic Analysis and Genome Homology Reveals New rare Phylogenetic groups, "Synonymous" Species, and the Need to Simplify Nomenclature and Pathogens Identification in the Bacillus cereus Group. https://doi.org/10.1101/2025.03.11.642625

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Structural variation in repeat elements is widespread in normal human tissues and in tumorigenesis

Somatic mosaicism contributes to genomic variation, yet postzygotic structural variants remain under-characterized. We performed long- and short-read WGS from multiple individuals (n=47 normal tissues; n=168 samples) and identified mosaic structural variants in all individuals and germ layers, impacting a median 285.2 kb/genome. Nearly half of breakpoints were independently validated, with tissue distributions reflecting both early and late developmental origins. Most mosaic variants were repeat-mediated and 8.3% overlapped functional elements, an enrichment compared to germline variants. To extend these analyses in samples where long-read sequencing is infeasible, we measured repeat alterations from short-read sequencing, recapitulating mosaic tissue-specific differences. We characterized tumor- and tissue- specific variation in repeats across 15 cancer types and found tumor-related repeat variation to be similar in scale to that of normal mosaic variation. Tracking repeat changes in cell-free DNA provided a noninvasive approach for tumor monitoring. Our analyses revealed widespread repeat-driven structural variation in health and disease.

genomics↗

RNA isoform-resolved multiplexed sequencing with bioorthogonal barcoding

RNA isoform dysregulation drives disease pathogenesis and is the target of FDA-approved splice-switching therapeutics. However, multiplexed sequencing methods discard splice junction information because only 3' termini are barcoded and counted. Here, we repurpose acylation and click chemistries to conjugate bioorthogonal barcodes (bobcodes) directly onto multiple internal positions along cellular RNAs. Bobcoded RNAs from multiple samples are pooled for multiplexed cDNA synthesis, during which reverse transcriptase switches from each RNA template onto its tethered bobcode with greater than 99% accuracy in species mixing experiments. Bobcode attachment intervals set cDNA insert sizes without a library fragmentation step, and priming with poly(dT) or random hexamers selects between 3'-end counting and full-length isoform capture. A bioorthogonal barcode-sequencing (BOB-seq v0.1) drug screen identifies transcriptome-wide on- and off-target RNA splicing effects and outperforms existing multiplexing RNA sequencing methods in workflow simplicity, sample-to-sample variability, and barcoding accuracy. Bobcodes add isoform resolution to scalable multiplexed RNA sequencing.

genomics↗

Structural polymorphism and population-variable coding capacity of HERV-K(HML-2) in human pangenomes

Approximately 8% of the human genome is derived from ancient retroviral infections. The most recently integrated of these endogenous retroviruses is the HERV-K(HML-2) clade, whose expression has been associated with cancer, amyotrophic lateral sclerosis, and embryogenesis. Studies of HERV expression, particularly HML-2, have relied predominantly on short-read sequencing. However, the high similarity among HML-2 proviruses prevents many short reads from being assigned uniquely to individual loci. We therefore compared haplotype-resolved long-read genome assemblies from 292 donors to resolve variation in proviral structure and coding capacity. Several loci previously thought to be fixed were structurally polymorphic. Tandem arrays occurred at 13 loci and contained up to six proviral copies in a single array. At 8q11.23, we identified a previously undescribed full-length provirus in one haplotype. All 583 other haplotypes carried a solo-LTR. We found that standard reference genomes failed to represent the coding capacity retained in many individuals, whose proviruses contained intact open reading frames despite disruptive mutations in the reference sequences. Short-read genotypes left 32.5% of the tested donor-variant pairs unresolved at sites associated with viral reading frames. These findings show why HML-2 expression must be interpreted in the context of the structural and coding alleles each individual carries.

genomics↗