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January 18, 2026Journal of General Virology1 citationsOpen Access

A replication-competent deltavirus from the marsupial fat-tailed dunnart Sminthopsis crassicaudata

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ZDZoé DenisVCValérie CourgnaudMPMarcos de la Peña

Key Points

  • The study aims to isolate and analyze a complete deltavirus genome from the fat-tailed dunnart and assess its replication capabilities.
  • Reanalyzed public metatranscriptomes from the Australian fat-tailed dunnart.
  • Assembled the complete marsupial deltavirus genome.
  • Tested replication in human, simian, rodent, and Tasmanian devil cells.
  • Conducted phylogenetic analysis of the delta antigen.
  • Isolated a 1,680-nt deltavirus genome with a rod-like structure.
  • Demonstrated successful replication in multiple host cell types, with varying kinetics.
  • Identified conserved ribozymes and unique dimeric cDNA replicon features.

Abstract

Deltaviruses are circular, negative-sense RNA agents that replicate autonomously but depend on heterologous envelope glycoproteins for spread. Only partial sequences of deltaviruses had been reported from marsupials. By reanalysing public metatranscriptomes from the Australian fat-tailed dunnart ( Sminthopsis crassicaudata ), we assemble the first complete marsupial deltavirus genome and test its replication in human and animal cells. The fat-tailed dunnart deltavirus (FtDDeV) is a 1,680-nt circular RNA that folds into a canonical unbranched rod-like structure and encodes a 195-aa delta antigen (FtDDAg). Genomic and antigenomic HDV-like ribozymes are present and conserve catalytic core motifs. Phylogenetic analyses cluster FtDDAg with the Tasmanian devil sequence, and both are quite close to RDAg from the neotropical rodent species Proechimys semispinosus . A dimeric FtDDeV cDNA replicon supports time-dependent DAg accumulation in human, simian, rodent and Tasmanian devil cells, with faster kinetics in rodents and marsupial cells. FtDDAg accumulation patterns in host nuclei show characteristic viral hubs, observed with other deltaviruses. No obvious coinfecting helper viruses were detected in FtDDeV-positive libraries. Our study extends the confirmed host range of deltaviruses to marsupials and provides a replication-competent clone to investigate helper usage, host restriction and deltavirus evolution.

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Cite This Study

Denis et al. (2026) studied this question.

synapsesocial.com/papers/696c774feb60fb80d1395890https://doi.org/10.1099/jgv.0.002203
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