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Omics · dataset · 2026

From taxa to transcripts: investigating the snail holobiont in the context of helminth infection

Listed in ZivaHub and Deakin Research Online and DMU Figshare — shown once because both records carry DOI 10.17034/32805470.v1

Helminth parasites have complex life cycles that often require intermediate invertebrate hosts, such as freshwater snails.

Description

While much is known about the immunology and pathology of helminth infections, the role of the host-associated microbiome in these interactions remains underexplored. This thesis investigates the dynamic interplay between schistosome parasites, their snail hosts, and the host snail microbiota, with a focus on Biomphalaria glabrata as the intermediate host of Schistosoma mansoni.

Drawing from recent studies and experimental insights, this work examines how helminth infection alters snail microbiome composition and function, and conversely, how the snail microbiome may influence parasite success.<br><br>Chapters explore the ecological and evolutionary importance of parasitic life cycles, the immune responses of snails to schistosome infection, and the snail microbiota’s potential role in either resisting or facilitating parasite establishment.

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Multi-omic methods, including metagenomics, transcriptomics, and metabolomics, are assessed as tools for dissecting host–microbiome–parasite interactions at a systems level. Evidence suggests that schistosome infection drives microbial dysbiosis in snails, which may reflect or influence intermediate host physiology and immune activation. Additionally, hypotheses are proposed regarding parasite-driven microbiome manipulation and microbiota-mediated resistance.<br><br>By integrating ecological, immunological, and molecular perspectives, this thesis provides a framework for understanding the snail holobiont during helminth infection.

These insights hold potential for novel strategies in schistosomiasis control, including snail microbiome-based interventions targeting the intermediate host. <br><br><i>Thesis is embargoed until 31 July 2027.</i><br>

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Catalogue records · 1

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Inferred from text
Evolutionary biology 72%
Provenance · 3 source records, 15 field assertions
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ZivaHuboai:figshare.com:article/328054705 d agoJSON v1
Deakin Research Onlineoai:figshare.com:article/328054705 d agoJSON v1
DMU Figshareoai:figshare.com:article/328054705 d agoJSON v1
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