These data establish that this phage constitutes a novel species within a newly proposed genus inside the family Darmviridae, expanding the known geographic distribution of crAss-like phages, highlight translational versatility among Segatella-infecting viruses, and emphasize the importance of expanding virome cohorts to underrepresented regions.
Abstract
Bacteriophages of the order Crassvirales are currently believed to be the most prevalent dsDNA phages in the human gut virome, yet their global biogeography and genomic diversity remain poorly characterized due to an overrepresentation of industrialized Western studies in public repositories. In this study, we integrated computational metagenomics and molecular approaches to identify and validate the first complete Crassvirales genome from an Egyptian population. De novo assembly and viral profiling yielded a 101,034 bp circular genome (contig k141_108779) predicted to infect the non-industrialized gut symbiont Segatella copri. The genome displays the notable feature of amber stop codon reassignments (NCBI Genetic Code 15), where canonical (TAG) stop codons encode glutamine (Q). This alternative code increases coding density to 91%. Population-level PCR surveillance and Sanger dideoxynucleotide sequencing across 252 individual Egyptian fecal samples, pooled in 10 composites, confirmed the active circulation and local sequence heterogeneity of this lineage within the community. Phylogenomic and intergenomic similarity analysis demonstrated that the isolate shares less than 50% total average nucleotide identity with all recognized type strains. These data establish that this phage constitutes a novel species within a newly proposed genus inside the family Darmviridae. Our findings expand the known geographic distribution of crAss-like phages, highlight translational versatility among Segatella-infecting viruses, and emphasize the importance of expanding virome cohorts to underrepresented regions.
The selective isolation and whole genome sequencing (WGS) of Bifidobacterium crudilactis from a pure culture of dairy origin from India offers valuable insights for further exploration of its promising probiotic potential and functional characteristics.
Sneha Kedia, P. S. Rani, Mahanga Nyambero et al.· Gut Pathogens· 0 citations
This study provides genome- and spatially resolved views of dominant SCB in holothurians and offers evolutionary insights into host-interface diversification in the deep-sea holothurian body wall.
Margolisiella madlensis
, previously known as bay scallop Marosporida (BSM), is an apicomplexan parasite implicated in recurrent summer mortality of the bay scallop
Argopecten irradians
in the Northeastern United States. It is a member of the class Marosporida, a major apicomplexan lineage that has so far lacked nuclear genomic resources. Here we report the draft nuclear genome of
M. madlensis
23004-MA1, assembled from PacBio HiFi and Illumina sequencing data. The assembly comprises 41.0 Mb in 6,697 scaffolds. Interspersed repeats accounted for 40.3% of the assembly, while repetitive and low-complexity sequences together accounted for 45.8%. To our knowledge, this is the first nuclear genome available for the class Marosporida. Therefore, this genome provides an essential reference for comparative studies of apicomplexan evolution and establishes a basis for future work on parasite biology, molecular detection, and host-parasite interactions in marine invertebrates.
PHORAGER (Prophage Hunting, vOtu Retrieval, Annotation and Genomic ExploRation), a scalable Nextflow pipeline for the standardised identification and quality assessment of prophages from bacterial genomes, validated using 30,824 publicly available ESKAPE pathogen genomes.
Xena Dyball, Alise J. Ponsero, James A. D. Docherty et al.· bioRxiv· 0 citations
Vibrio parahaemolyticus is a leading cause of seafood-associated gastroenteritis worldwide. Traditional serotyping based on 13 O and 71 K antigens fails to classify many isolates, designated as K-untypable (KUT), whose genetic basis and evolutionary dynamics remain unclear. In this study, we conducted whole-genome sequencing of 47 O4:KUT strains from 40 clinical and 7 retail aquatic products (snail, river shrimp, Macrobrachium rosenbergii, etc.) to decipher the genomic diversity and structural variation in their O/K antigen loci. Phylogenomic analysis revealed a polyphyletic population structure spanning multiple sequence types, with O/K antigen loci classified into 13 distinct structural types comprising 149 biosynthetic genes. These clusters exhibited mosaic architectures and varied functional profiles. Notably, pervasive phylogenetic incongruence and robust recombination signals identified horizontal gene transfer as the primary mechanism driving O/K antigen loci diversification. Our findings reveal the evolutionary mechanisms of the foodborne O4:KUT serotype prevalent in local seafood and clinical samples from Huzhou, China, and provide a preliminary gene-signature framework that may inform the future development of molecular serotyping assays.
Peng Zhang, L. Ji, Wei Yan et al.· Microorganisms· 0 citations