The Perils of Pathogen Discovery: Origin of a Novel Parvovirus-Like Hybrid Genome Traced to Nucleic Acid Extraction Spin Columns

Author:

Naccache Samia N.12,Greninger Alexander L.12,Lee Deanna12,Coffey Lark L.3,Phan Tung3,Rein-Weston Annie12,Aronsohn Andrew4,Hackett John5,Delwart Eric L.13,Chiu Charles Y.126

Affiliation:

1. Department of Laboratory Medicine, University of California, San Francisco, California, USA

2. UCSF-Abbott Viral Diagnostics and Discovery Center, San Francisco, California, USA

3. Blood Systems Research Institute, San Francisco, California, USA

4. Center for Liver Disease, University of Chicago Medical Center, Chicago, Illinois, USA

5. Abbott Diagnostics, Abbott Park, Illinois, USA

6. Department of Medicine, Division of Infectious Diseases, University of California, San Francisco, California, USA

Abstract

ABSTRACT Next-generation sequencing was used for discovery and de novo assembly of a novel, highly divergent DNA virus at the interface between the Parvoviridae and Circoviridae . The virus, provisionally named parvovirus-like hybrid virus (PHV), is nearly identical by sequence to another DNA virus, NIH-CQV, previously detected in Chinese patients with seronegative (non-A-E) hepatitis. Although we initially detected PHV in a wide range of clinical samples, with all strains sharing ∼99% nucleotide and amino acid identity with each other and with NIH-CQV, the exact origin of the virus was eventually traced to contaminated silica-binding spin columns used for nucleic acid extraction. Definitive confirmation of the origin of PHV, and presumably NIH-CQV, was obtained by in-depth analyses of water eluted through contaminated spin columns. Analysis of environmental metagenome libraries detected PHV sequences in coastal marine waters of North America, suggesting that a potential association between PHV and diatoms (algae) that generate the silica matrix used in the spin columns may have resulted in inadvertent viral contamination during manufacture. The confirmation of PHV/NIH-CQV as laboratory reagent contaminants and not bona fide infectious agents of humans underscores the rigorous approach needed to establish the validity of new viral genomes discovered by next-generation sequencing.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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