A Universal Next-Generation Sequencing Protocol To Generate Noninfectious Barcoded cDNA Libraries from High-Containment RNA Viruses

Author:

Moser Lindsey A.1,Ramirez-Carvajal Lisbeth23,Puri Vinita4,Pauszek Steven J.2,Matthews Krystal5,Dilley Kari A.4,Mullan Clancy6,McGraw Jennifer6,Khayat Michael6,Beeri Karen7,Yee Anthony4,Dugan Vivien4,Heise Mark T.6,Frieman Matthew B.5,Rodriguez Luis L.2,Bernard Kristen A.1,Wentworth David E.4,Stockwell Timothy B.4,Shabman Reed S.4

Affiliation:

1. Department of Pathobiological Sciences, University of Wisconsin—Madison, Madison, Wisconsin, USA

2. Plum Island Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Greenport, New York, USA

3. Plum Island Animal Disease Center-Oak Ridge Institute for Science and Education (ORISE) Research Participation Program, Oak Ridge, Tennessee, USA

4. Virology Group, J. Craig Venter Institute, Rockville, Maryland, USA

5. Department of Microbiology and Immunology, University of Maryland at Baltimore, Baltimore, Maryland, USA

6. Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA

7. Sequencing Group, J. Craig Venter Institute, La Jolla, California, USA

Abstract

This report establishes and validates a standard operating procedure (SOP) for select agents (SAs) and other biosafety level 3 and/or 4 (BSL-3/4) RNA viruses to rapidly generate noninfectious, barcoded cDNA amenable for next-generation sequencing (NGS). This eliminates the burden of testing all processed samples derived from high-consequence pathogens prior to transfer from high-containment laboratories to lower-containment facilities for sequencing. Our established protocol can be scaled up for high-throughput sequencing of hundreds of samples simultaneously, which can dramatically reduce the cost and effort required for NGS library construction. NGS data from this SOP can provide complete genome coverage from viral stocks and can also detect virus-specific reads from limited starting material. Our data suggest that the procedure can be implemented and easily validated by institutional biosafety committees across research laboratories.

Funder

U.S. Department of Homeland Security

Publisher

American Society for Microbiology

Subject

Computer Science Applications,Genetics,Molecular Biology,Modelling and Simulation,Ecology, Evolution, Behavior and Systematics,Biochemistry,Physiology,Microbiology

Reference45 articles.

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4. Federal Select Agent Program . 2014. Guidance on the regulation of select agent and toxin nucleic acids. Division of Select Agents and Toxins Centers for Disease Control and Prevention Atlanta GA and Agriculture Select Agent Services Animal and Plant Health Inspection Service US Department of Agriculture Riverdale MD. http://www.selectagents.gov/guidance-regulation.html

5. Host Factors in Positive-Strand RNA Virus Genome Replication

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