Viral Diversity in Benthic Abyssal Ecosystems: Ecological and Methodological Considerations

Author:

Rosani Umberto1ORCID,Corinaldesi Cinzia2,Luongo Gabriella3,Sollitto Marco45,Dal Monego Simeone6,Licastro Danilo6,Bongiorni Lucia7,Venier Paola1ORCID,Pallavicini Alberto4ORCID,Dell’Anno Antonio3

Affiliation:

1. Department of Biology, University of Padova, Via U. Bassi 58/b, 35121 Padova, Italy

2. Department of Materials, Environmental Sciences and Urban Planning, Polytechnic University of Marche, Via Brecce Bianche, 60131 Ancona, Italy

3. Department of Life and Environmental Sciences, Polytechnic University of Marche, Via Brecce Bianche, 60131 Ancona, Italy

4. Department of Life Sciences, University of Trieste, Via Licio Giorgeri 5, 34127 Trieste, Italy

5. Faculty of Mathematics, Natural Sciences and Information Technologies, University of Primorska, 6000 Koper, Slovenia

6. Laboratorio di Genomica ed Epigenomica, AREA Scienze Park, Padriciano 99, 34149 Trieste, Italy

7. Consiglio Nazionale delle Ricerche, Istituto di Scienze Marine, Tesa 104–Arsenale, Castello 2737/F, 30122 Venezia, Italy

Abstract

Viruses are the most abundant ‘biological entities’ in the world’s oceans. However, technical and methodological constraints limit our understanding of their diversity, particularly in benthic abyssal ecosystems (>4000 m depth). To verify advantages and limitations of analyzing virome DNA subjected either to random amplification or unamplified, we applied shotgun sequencing-by-synthesis to two sample pairs obtained from benthic abyssal sites located in the North-eastern Atlantic Ocean at ca. 4700 m depth. One amplified DNA sample was also subjected to single-molecule long-read sequencing for comparative purposes. Overall, we identified 24,828 viral Operational Taxonomic Units (vOTUs), belonging to 22 viral families. Viral reads were more abundant in the amplified DNA samples (38.5–49.9%) compared to the unamplified ones (4.4–5.8%), with the latter showing a greater viral diversity and 11–16% of dsDNA viruses almost undetectable in the amplified samples. From a procedural point of view, the viromes obtained by direct sequencing (without amplification step) provided a broader overview of both ss and dsDNA viral diversity. Nevertheless, our results suggest that the contextual use of random amplification of the same sample and long-read technology can improve the assessment of viral assemblages by reducing off-target reads.

Funder

Italian PRIN 2017

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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