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. 2018 May 15;9(3):e00185-18.
doi: 10.1128/mBio.00185-18.

Microscopic and Molecular Evidence of the First Elasmobranch Adomavirus, the Cause of Skin Disease in a Giant Guitarfish, Rhynchobatus djiddensis

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Microscopic and Molecular Evidence of the First Elasmobranch Adomavirus, the Cause of Skin Disease in a Giant Guitarfish, Rhynchobatus djiddensis

Jennifer A Dill et al. mBio. .

Abstract

Only eight families of double-stranded DNA (dsDNA) viruses are known to infect vertebrate animals. During an investigation of papillomatous skin disease in an elasmobranch species, the giant guitarfish (Rhynchobatus djiddensis), a novel virus, distinct from all known viral families in regard to particle size, morphology, genome organization, and helicase phylogeny was discovered. Large inclusion bodies containing 75-nm icosahedral viral particles were present within epithelial cell nuclei in the proliferative skin lesions. Deep metagenomic sequencing revealed a 22-kb circular dsDNA viral genome, tentatively named guitarfish "adomavirus" (GAdoV), with only distant homology to two other fish viruses, Japanese eel endothelial cell-infecting virus (JEECV) and a recently reported marbled eel virus. Phylogenetic analysis of the helicase domain places the guitarfish virus in a novel clade that is equidistant between members of the Papillomaviridae and Polyomaviridae families. Specific PCR, quantitative PCR, and in situ hybridization were used to detect, quantify, and confirm that GAdoV DNA was localized to affected epithelial cell nuclei. Changes in the viral titer, as well as the presence of a hybridization signal, coincided with the progression and then final resolution of gross and microscopic lesions. The results indicate that GAdoV is the causative agent of the proliferative skin lesions.IMPORTANCE Cartilaginous fish, including the sharks and rays, evolved from ancestral fish species at least 400 million years ago. Even though they are the descendants of one of the most ancient vertebrate lineages, reports of viral diseases in these species are rare and poorly documented. Deep sequencing revealed a highly divergent virus, tentatively named guitarfish adomavirus, that is distantly related to known papillomaviruses and polyomaviruses. Out of the eight predicted viral genes, only the helicase could be identified as viral by sequence homology searches (BLAST), exemplifying the difficulties of discovering novel viruses within seas of unidentifiable "dark matter" associated with deep sequencing data. The novel adomavirus represents the first viral genome shown to cause clinical disease in a cartilaginous fish species, the giant guitarfish. Our findings demonstrate that emerging fish viruses are fertile ground to expand our understanding of viral evolution in vertebrates.

Keywords: adomavirus; cartilaginous fish; giant guitarfish; metagenomics; pathology; skin disease; virus discovery.

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Figures

FIG 1
FIG 1
Progression and regression of adomavirus-induced skin lesions in a giant guitarfish over an 18-week period. (A) Quantification of virus using an adomavirus-specific qPCR. (B) Transmission electron microscopic image of an epithelial cell nucleus with a large array of nonencapsulated, 75-nm, icosahedral, viral particles during active infection in September. (C to H) The images in panels C to H compare lesion changes and FISH results. (C) Gross image of guitarfish with active lesions in September. The ventral skin has multiple reddened, raised areas of epithelial proliferation. (D) Histologically, the diseased skin had numerous epithelial cell nuclei enlarged by amphophilic viral inclusions that marginated nuclear chromatin. (E) Using FISH, strongly positive fluorescent signals were localized to affected epithelial cell nuclei with an adomavirus probe. (F) Gross image of the guitarfish demonstrating normal skin 18 weeks later in February. (G and H) Epithelial cells and their nuclei were microscopically normal, with no viral inclusions (G), and no hybridization signal was detected using FISH (H).
FIG 2
FIG 2
Host range, phylogeny, and genomic characteristics of guitarfish adomavirus. (A) Spatial range, host phylogeny, and evolution time scale of the giant guitarfish host species from which adomaviruses have been characterized. The host phylogeny was reconstructed according to a previous comprehensive study (24). The fish host clade detected with adomavirus infection is labeled red. For clarity, extensive diversification of Clupeocephala and Carangimorpharia during the last 250 million years is condensed. (B) Genome size and organization of guitarfish adomavirus in comparison to sea bass papillomavirus and guitarfish polyomavirus. The viral genome from marbled eel and Japanese eel (KU221231 and NC_015123) are tentatively renamed “adomavirus” in reference to the classification analysis by Welch et al. (submitted). All adomavirus genomes, as shown in panel C, are larger than 15 kb. (C) Bayesian inference phylogeny of the helicase domain. The three adomaviruses from guitarfish, Japanese eel, and marble eel are shown in orange. Fish papillomaviruses (PV) and polyomaviruses (PyV) are shown with green branches. Even though the Japanese eel and marbled eel viruses contain a helicase that is homologous to polyomavirus LT, further comparative genomics (Welch et al., submitted) indicated that the eel helicase phylogeny is the result of chimerization, and the two eel viruses are de facto adoma-like viruses as recognized by their genome size, organization, and virion structure. PV, papillomavirus; PyV, polyomavirus. (D) Pairwise protein identity comparisons between representative adomaviruses, polyomavirus, and papillomavirus.

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References

    1. Gilbert C, Feschotte C. 2010. Genomic fossils calibrate the long-term evolution of hepadnaviruses. PLoS Biol 8:e1000495. doi:10.1371/journal.pbio.1000495. - DOI - PMC - PubMed
    1. Ng TF, Kondov NO, Deng X, Van Eenennaam A, Neibergs HL, Delwart E. 2015. A metagenomics and case-control study to identify viruses associated with bovine respiratory disease. J Virol 89:5340–5349. doi:10.1128/JVI.00064-15. - DOI - PMC - PubMed
    1. Ng TF, Marine R, Wang C, Simmonds P, Kapusinszky B, Bodhidatta L, Oderinde BS, Wommack KE, Delwart E. 2012. High variety of known and new RNA and DNA viruses of diverse origins in untreated sewage. J Virol 86:12161–12175. doi:10.1128/JVI.00869-12. - DOI - PMC - PubMed
    1. Ng TF, Chen LF, Zhou Y, Shapiro B, Stiller M, Heintzman PD, Varsani A, Kondov NO, Wong W, Deng X, Andrews TD, Moorman BJ, Meulendyk T, MacKay G, Gilbertson RL, Delwart E. 2014. Preservation of viral genomes in 700-y-old caribou feces from a subarctic ice patch. Proc Natl Acad Sci U S A 111:16842–16847. doi:10.1073/pnas.1410429111. - DOI - PMC - PubMed
    1. Lauber C, Seitz S, Mattei S, Suh A, Beck J, Herstein J, Börold J, Salzburger W, Kaderali L, Briggs JAG, Bartenschlager R. 2017. Deciphering the origin and evolution of hepatitis B viruses by means of a family of non-enveloped fish viruses. Cell Host Microbe 22:387–399.e6. doi:10.1016/j.chom.2017.07.019. - DOI - PMC - PubMed