Comparison of metagenomic and targeted methods for sequencing human pathogenic viruses from wastewater

Author:

Child Harry T.1ORCID,Airey George2,Maloney Daniel M.3,Parker Abby4,Wild Jonathan4,McGinley Suzie4,Evens Nicholas5,Porter Jonathan5,Templeton Kate4,Paterson Steve2,van Aerle Ronny67ORCID,Wade Matthew J.7,Jeffries Aaron R.1,Bassano Irene8

Affiliation:

1. Biosciences, Faculty of Health and Life Sciences, University of Exeter, Exeter, United Kingdom

2. Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom

3. Institute of Ecology and Evolution, University of Edinburgh, Edinburgh, United Kingdom

4. Viral Genotyping Reference Laboratory Edinburgh, NHS Lothian, Royal Infirmary of Edinburgh, Edinburgh, United Kingdom

5. Environment Agency, National Monitoring, Starcross, Exeter, United Kingdom

6. International Centre of Excellence for Aquatic Animal Health, Cefas, Weymouth, United Kingdom

7. Centre for Sustainable Aquaculture Futures, University of Exeter, Exeter, United Kingdom

8. Analytics & Data Science Directorate, UK Health Security Agency, London, United Kingdom

Abstract

ABSTRACT Wastewater-based epidemiology is a powerful tool for monitoring the emergence and spread of viral pathogens at the population scale. Typical polymerase chain reaction (PCR)-based methods of quantitative and genomic monitoring of viruses in wastewater provide high sensitivity and specificity. However, these methods are limited to the surveillance of target viruses in a single assay and require prior knowledge of the target genome(s). Metagenomic sequencing methods may represent a target-agnostic approach to viral wastewater monitoring, allowing for the detection of a broad range of target viruses, including potentially novel and emerging pathogens. In this study, targeted and untargeted metagenomic sequencing methods were compared with tiled-PCR sequencing for the detection and genotyping of viral pathogens in wastewater samples. Deep shotgun metagenomic sequencing was unable to generate sufficient genome coverage of human pathogenic viruses for robust genomic epidemiology, with samples dominated by bacteria. Hybrid-capture enrichment of shotgun libraries for respiratory viruses led to significant increases in genome coverage for a range of targets. Tiled-PCR sequencing led to further improvements in genome coverage compared to hybrid capture for severe acute respiratory syndrome coronavirus 2, enterovirus D68, norovirus GII, and human adenovirus F41 in wastewater samples. In conclusion, untargeted shotgun sequencing was unsuitable for genomic monitoring of the low virus concentrations in wastewater samples analyzed in this study. Hybrid-capture enrichment represented a viable method for simultaneous genomic epidemiology of a range of viral pathogens, while tiled-PCR sequencing provided the optimal genome coverage for individual viruses with the minimum sequencing depth. IMPORTANCE Most public health initiatives that monitor viruses in wastewater have utilized quantitative polymerase chain reaction (PCR) and whole genome PCR sequencing, mirroring techniques used for viral epidemiology in individuals. These techniques require prior knowledge of the target viral genome and are limited to monitoring individual or small groups of viruses. Metagenomic sequencing may offer an alternative strategy for monitoring a broad spectrum of viruses in wastewater, including novel and emerging pathogens. In this study, while amplicon sequencing gave high viral genome coverage, untargeted shotgun sequencing of total nucleic acid samples was unable to detect human pathogenic viruses with enough sensitivity for use in genomic epidemiology. Enrichment of shotgun libraries for respiratory viruses using hybrid-capture technology provided genotypic information on a range of viruses simultaneously, indicating strong potential for wastewater surveillance. This type of targeted metagenomics could be used for monitoring diverse targets, such as pathogens or antimicrobial resistance genes, in environmental samples.

Funder

Department of Health and Social Care, UK

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

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