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Biology subjects

Moss, A. G.

Publications and source records attributed to Moss, A. G..

3 recordsLinked to original sources

Comparative genomics and microbiome profiling reveal a conserved Vibrio rich mucus microbiota of the Florida false coral (Ricordea florida)

Mucus is a critical interface between marine invertebrates and their environment and plays key roles in host defense. Despite its ecological importance, little is known about the microbial communities associated with mucus-producing corallimorpharians. Here, we used a multi-omics approach to characterize the mucus microbiome and immune repertoire of the Florida false coral, Ricordea florida. Culture-dependent and culture-independent analyses revealed that R. florida mucus harbors a bacterial community distinct from surrounding seawater and consistently dominated by Vibrio species. Whole-genome sequencing of 13 cultured Vibrio isolates representing nine distinct lineages revealed substantial taxonomic diversity, including several highly divergent strains that may represent undescribed species. Comparative genomic analyses identified enrichment of genes associated with carbohydrate acquisition, glycoside hydrolysis, and host colonization, including multiple components of the Tad/Flp adhesion system, suggesting adaptation to the mucus microenvironment. To investigate host factors that may shape microbial associations, we assembled and annotated a host transcriptome from healthy and immune-challenged polyps. This analysis identified a diverse innate immune repertoire, including Toll-like receptors, NOD-like receptors, lectins, scavenger receptors, complement-associated proteins, antiviral defense pathways, and membrane attack complex/perforin domain-containing effectors. Together, these findings demonstrate that R. florida supports a conserved, Vibrio-rich mucus microbiome and possesses a complex innate immune system capable of mediating host-microbe interactions at the mucosal surface. This study provides a foundation for understanding microbial colonization, immune defense, and holobiont function in an understudied cnidarian lineage.

microbiology↗

Independent innexin radiation shaped signaling in ctenophores.

Innexins facilitate cell-cell communication by forming gap junctions or non-junctional hemichannels, which play important roles in metabolic, chemical, ionic, and electrical coupling. The lack of knowledge regarding the evolution and role of these channels in ctenophores (comb jellies), the likely sister group to the rest of animals, represents a substantial gap in our understanding of the evolution of intercellular communication in animals. Here we identify and phylogenetically characterize the complete set of innexins of four ctenophores: Mnemiopsis leidyi, Hormiphora californensis, Pleurobrachia bachei, and Beroe ovata. Our phylogenetic analyses suggest that ctenophore innexins diversified independently from those of other animals and were established early in the emergence of ctenophores. We identified a four-innexin genomic cluster, which was present in the last common ancestor of these four species and has been largely maintained in these lineages. Evidence from correlated spatial and temporal gene expression of the M. leidyi innexin cluster suggest that this cluster has been maintained due to constraints related to gene regulation. We describe basic electrophysiological properties of putative ctenophore hemichannels from muscle cells using intracellular recording techniques, showing substantial overlap with the properties of bilaterian innexin channels. Together, our results suggest that the last common ancestor of animals had gap junctional channels also capable of forming functional innexin hemichannels, and that innexin genes have independently evolved in major lineages throughout Metazoa.

evolutionary biology↗

Comparative genomic analysis and characterization of Staphylococcus sp. AOAB, isolated from a notoriously invasive Mnemiopsis leidyi gut revealed multiple antibiotic resistance determinants

Here, we describe the isolation and characterization of a coagulase-negative, vancomycin and oxacillin-susceptible novel bacterium of the genus Staphylococcus. Staphylococcus sp. strain AOAB was isolated from the stomodeum (gut) of the Mnemiopsis leidyi from Mobile Bay, Alabama USA. A polyphasic taxonomic approach comprised of phenotypic, chemotaxonomic and genotypic characteristics was used for analysis. The dominant respiratory quinone detected was MK-7 (100%). Major cellular fatty acids were anteiso-C15:0 (40.52%), anteiso-C17:0 (13.04 %), C-18:0 (11.53%) and C-20:0 (10.45%). The polar lipid profile consisted of glycolipid, phospholipid, phosphatidylglycerol and diphosphatidylglycerol. Although strain AOAB had a 16SrRNA gene sequence similarity of 99% with S. warneri SG1, S. pasteuri, S. devriesei KS-SP_60, S. lugdunensis HKU09-01, S. epidermidis RP62A, S. haemolyticus JCSC1435 and S. hominis DM 122, it was be distinguished from those species based on Multi-Locus Sequence Analysis (MLSA) using 6 marker genes (16S rRNA, hsp60, rpoB, dnaJ, sodA and tuf). MLSA revealed strain AOAB to be closely related to S. warneri SG1 and S. pasteuri SP1 but distinct from two hitherto known species. These results were confirmed by Average Nucleotide Identity (closest ANI of 84.93% and 84.58% identity against S. warneri SG1 and S. pasteuri SP1 respectively). In-silico DNA-DNA hybridization was <70% (33.1 % and 32.8% against S. warneri SG1 and S. pasteuri SP1 respectively), which further confirmed that the strain was a potential novel Staphylococcus species.

genomics↗