Targeted whole-genome recovery of single viral species in a complex environmental sample

Author:

Chen Liyin1,Chen Anqi1,Zhang Xinge Diana1ORCID,Saenz Robles Maria Teresa2ORCID,Han Hee-Sun34ORCID,Xiao Yi1,Xiao Gao1ORCID,Pipas James M.2,Weitz David A.15ORCID

Affiliation:

1. John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138

2. Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260

3. Department of Chemistry, University of Illinois Urbana-Champaign, Urbana, IL 61801

4. Carl R. Woese Institute for Genomic Biology, University of Illinois Urbana-Champaign, Urbana, IL 61801

5. Department of Physics, Harvard University, Cambridge, MA 02138

Abstract

Characterizing unknown viruses is essential for understanding viral ecology and preparing against viral outbreaks. Recovering complete genome sequences from environmental samples remains computationally challenging using metagenomics, especially for low-abundance species with uneven coverage. We present an experimental method for reliably recovering complete viral genomes from complex environmental samples. Individual genomes are encapsulated into droplets and amplified using multiple displacement amplification. A unique gene detection assay, which employs an RNA-based probe and an exonuclease, selectively identifies droplets containing the target viral genome. Labeled droplets are sorted using a microfluidic sorter, and genomes are extracted for sequencing. We demonstrate this method’s efficacy by spiking two known viral genomes, Simian virus 40 (SV40, 5,243 bp) and Human Adenovirus 5 (HAd5, 35,938 bp), into a sewage sample with a final abundance in the droplets of around 0.1% and 0.015%, respectively. We achieve 100% recovery of the complete sequence of the spiked-in SV40 genome with uniform coverage distribution. For the larger HAd5 genome, we cover approximately 99.4% of its sequence. Notably, genome recovery is achieved with as few as one sorted droplet, which enables the recovery of any desired genomes in complex environmental samples, regardless of their abundance. This method enables single-genome whole-genome amplification and targeting characterizations of rare viral species and will facilitate our ability to access the mutational profile in single-virus genomes and contribute to an improved understanding of viral ecology.

Funder

US National institute for health

Publisher

Proceedings of the National Academy of Sciences

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