Respiratory viral co-infections among SARS-CoV-2 cases confirmed by virome capture sequencing

Author:

Kim Ki Wook1ORCID,Deveson Ira W.2,Pang Chi Nam I.3,Yeang Malinna4,Naing Zin4,Adikari Thiruni5,Hammond Jillian M.2,Stevanovski Igor2,Beukers Alicia G.6,Verich Andrey5,Yin Simon7,McFarlane David7,Wilkins Marc R.3,Stelzer-Braid Sacha8,Bull Rowena A.5,Craig Maria E.9,Hal Sebastiaan J. van6,Rawlinson William D.4

Affiliation:

1. School of Women’s and Children’s Health, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia

2. Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Sydney, Australia

3. School of Biotechnology and Biomolecular Sciences, Faculty of Science, University of New South Wales, Sydney, NSW, Australia

4. Virology Research Laboratory, Serology and Virology Division (SAViD), NSW Health Pathology, Prince of Wales Hospital, Sydney, NSW, Australia

5. The Kirby Institute for Infection and Immunity, University of New South Wales, Sydney, NSW, Australia

6. NSW Health Pathology, Department of Infectious Diseases and Microbiology, Royal Prince Alfred Hospital, Sydney, NSW, Australia

7. Research Technology Services, Research Infrastructure Division, University of New South Wales, Sydney, NSW, Australia

8. School of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, NSW, Australia

9. Institute of Endocrinology and Diabetes, The Children's Hospital at Westmead, Sydney, NSW, Australia

Abstract

Abstract Accumulating evidence supports the high prevalence of co-infections among Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) patients, and their potential to worsen the clinical outcome of COVID-19. However, there are few data on Southern Hemisphere populations, and most studies to date have investigated a narrow spectrum of viruses using targeted qRT-PCR. Here we assessed respiratory viral co-infections among SARS-CoV-2 patients in Australia, through respiratory virome characterization. Nasopharyngeal swabs of 92 SARS-CoV-2-positive cases were sequenced using pan-viral hybrid-capture and the Twist Respiratory Virus Panel. In total, 8% of cases were co-infected, with rhinovirus (6%) or influenzavirus (2%). Twist capture also achieved near-complete sequencing (>90% coverage, >10-fold depth) of the SARS-CoV-2 genome in 95% of specimens with Ct<30. Our results highlight the importance of assessing all pathogens in symptomatic patients, and the dual-functionality of Twist hybrid-capture, for SARS-CoV-2 whole-genome sequencing without amplicon generation and the simultaneous identification of viral co-infections with ease.

Publisher

Research Square Platform LLC

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