bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.11.24.690235

Scuticociliate Detection and Microbiome Composition in Museum Collections of Diadema Antillarum

Abstract

BackgroundThe mass mortality of the long-spined sea urchin Diadema antillarum has caused widespread ecological changes across Caribbean reefs, with recent studies identifying the etiological agent as pathogenic ciliate designated as a D. antillarum Scuticociliatosis Philaster-clade (DaScPc). The origin and ecological trajectory of DaScPc remain unresolved, raising critical questions about whether it represents a novel introduction or a resident commensal symbiont that transitioned into pathogenicity. MethodsTo address this, we tested 50 individual preserved museum specimens of D. antillarum collected between 1960 and 2020, with targeted PCR amplification of ciliate 18S, 28S, and 5.8S/ITS rRNA genes for spine, body wall, and coelomic fluid samples (n=100). Following up on recent work that identified bacterial biomarkers of DaSc, we also characterized the microbial communities associated with these museum specimens using 16S rRNA amplicon sequencing. Results. Our results reveal the presence of identical DaScPc 18S rRNA sequences in 21% of tested samples, 28S rRNA PCR yielded sequences at 96-98 % nt identity in only 2% of the tested samples, and we got no amplification from the 5.8S/ITS region. While these findings suggest possible long-term persistence or repeated emergence of this ciliate, the lack of 28S rRNA matches and lack of detection of ITS2 demonstrates that DaScPc 18S rRNA gene detections may be false positives for the ciliate over a highly conserved rRNA region. The microbial composition of the samples didnt yield any of the previously identified disease-associated bacterial biomarkers and showed large shifts in the overall microbial community based on collection period and the facility where the samples are housed. This study demonstrates that museum-preserved echinoderm tissues retain ecologically informative microbial DNA and establishes a molecular framework for disentangling pathogen provenance and its caveats. It also highlights the value and limitations of natural history collections in reconstructing marine disease ecology.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Vilanova-Cuevas, B., Hewson, I.. 2025-11-24. Scuticociliate Detection and Microbiome Composition in Museum Collections of Diadema Antillarum. https://doi.org/10.1101/2025.11.24.690235

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

KEEP EXPLORING

Related preprints

A population-scale landscape of the subgingival microbiome reveals divergent routes to periodontal dysbiosis

Periodontitis is an archetypical mucosal inflammatory disease in which microbiome dysbiosis at the tooth-epithelial interface interacts with host genetic and behavioral risk factors to drive immune-mediated tissue destruction. Although subgingival microbiome compositional shifts are thought to parallel disease severity, microbiome variation at the population-level and its relationship to periodontal clinical phenotypes and disease-modifying factors remain poorly defined. Here, we use unsupervised manifold learning to map the compositional landscape of the subgingival microbiome in 1,355 adults spanning periodontal health to severe periodontitis. We identified eight latent microbiome states organized along a branching continuum from eubiosis to dysbiosis. An intermediate microbial configuration marked ecological destabilization and bifurcation into two distinct periodontitis-associated dysbiotic trajectories, distinguished by links to gingival inflammation and smoking. Although the microbiome trajectories broadly tracked periodontal destruction, a minority of individuals showed discordant microbiome-clinical phenotypes, with some individuals with periodontitis retaining otherwise eubiotic microbiomes enriched for low-abundance pathobionts, while some cases of health or mild disease had highly dysbiotic communities, suggesting distinct host susceptibility. Together, these findings define a population-scale ecological landscape of the subgingival microbiome, reveal divergent trajectories to periodontal dysbiosis, and highlight heterogeneity in the relationship between microbial community structure and clinical disease expression.

microbiology↗

The iron-binding siderophore enterobactin is required for the response of multi-drug resistant Klebsiella pneumoniae to zinc limitation

To persist during infection Klebsiella pneumoniae must overcome nutrient iron and zinc limitation imposed by the host immune system through a process called nutritional immunity. Secreted small molecule siderophores are a major virulence determinant of Klebsiella pneumoniae pathogenesis and are presumed to overcome nutritional immunity by binding iron for bacterial acquisition. In this work, we set out to identify how a multi-drug resistant K. pneumoniae grows in zinc limited environments. Using unbiased transcriptomics, proteomics, and an arrayed transposon screen, we identified that synthesis and uptake of the siderophore enterobactin is required to allow for growth in low zinc conditions. Iron-specific chelators did not replicate this phenotype and addition of supplemental iron through heme in growth media could not complement severe growth defects of enterobactin mutant K. pneumoniae experiencing zinc limitation. Finally, zinc starvation induced enterobactin production independent of the canonical zinc uptake regulator (Zur) transcription factor suggesting an unidentified regulatory mechanism by which Gram-negative pathogens may respond to zinc stress. Together, these studies expand the role of enterobactin beyond iron regulation and highlight a previously unreported link between iron and zinc homeostasis in Klebsiella pneumoniae.

microbiology↗

A microbiota-derived protease links phage susceptibility to host epithelial responses

Bacteriophages are major ecological drivers of gut microbial ecology, yet whether bacterial mechanisms that determine phage susceptibility have consequences for the mammalian host remains poorly understood. Here, we identify dipeptidyl peptidase 11 (Dpp11a), the predominant active serine protease of the prevalent gut commensal Phocaeicola vulgatus, as an unexpected bacterial defence factor. Dpp11a protects against environmental proteases and confers resistance to bacteriophage infection. Metatranscriptomic analyses further reveal increased expression of both dpp11a and P. vulgatus-associated phage transcripts in ulcerative colitis stool samples, indicating that both components of this interaction are transcriptionally active in disease-associated human microbiomes. Using the microfluidic gut-on-a-chip co-culture model HuMiX, we show that the absence of Dpp11 is accompanied by altered epithelial tight-junction remodelling during phage-bacterial infection. Together, our findings reveal that the consequences of bacterial phage defence can extend beyond phage-bacterium interactions to the mammalian epithelium.

microbiology↗