Transmission dynamics of SARS-CoV-2 within-host diversity in two major hospital outbreaks in South Africa

Author:

San James E1ORCID,Ngcapu Sinaye23,Kanzi Aquillah M1,Tegally Houriiyah1,Fonseca Vagner1ORCID,Giandhari Jennifer1,Wilkinson Eduan1,Nelson Chase W45ORCID,Smidt Werner16,Kiran Anmol M78,Chimukangara Benjamin1,Pillay Sureshnee1,Singh Lavanya1,Fish Maryam1,Gazy Inbal1,Martin Darren P9,Khanyile Khulekani1,Lessells Richard1,de Oliveira Tulio110

Affiliation:

1. KwaZulu-Natal Research Innovation and Sequencing Platform (KRISP), School of Laboratory Medicine & Medical Sciences, University of KwaZulu- Natal, Durban, South Africa

2. Centre for the AIDS Programme of Research in South Africa (CAPRISA), Durban, South Africa

3. Department of Medical Microbiology, University of KwaZulu-Natal, Durban, South Africa

4. Biodiversity Research Center, Academia Sinica, Taipei, Taiwan

5. Institute for Comparative Genomics, American Museum of Natural History, New York, NY, USA

6. Africa Health Research Institute (AHRI), Durban, South Africa

7. Malawi-Liverpool-Wellcome Trust, Queen Elizabeth Central Hospital, College of Medicine, Blantyre, Malawi

8. Centre for Inflammation Research, Queens Research Institute, University of Edinburgh, Edinburgh, UK

9. Institute of Infectious Diseases and Molecular Medicine, Division of Computational Biology, Department of Integrative Biomedical Sciences, University of Cape Town, South Africa

10. Department of Global Health, University of Washington, Seattle, WA, USA

Abstract

Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes acute, highly transmissible respiratory infection in humans and a wide range of animal species. Its rapid global spread has resulted in a major public health emergency, necessitating commensurately rapid research to improve control strategies. In particular, the ability to effectively retrace transmission chains in outbreaks remains a major challenge, partly due to our limited understanding of the virus’ underlying evolutionary dynamics within and between hosts. We used high-throughput sequencing whole-genome data coupled with bottleneck analysis to retrace the pathways of viral transmission in two nosocomial outbreaks that were previously characterised by epidemiological and phylogenetic methods. Additionally, we assessed the mutational landscape, selection pressures, and diversity at the within-host level for both outbreaks. Our findings show evidence of within-host selection and transmission of variants between samples. Both bottleneck and diversity analyses highlight within-host and consensus-level variants shared by putative source-recipient pairs in both outbreaks, suggesting that certain within-host variants in these outbreaks may have been transmitted upon infection rather than arising de novo independently within multiple hosts. Overall, our findings demonstrate the utility of combining within-host diversity and bottleneck estimations for elucidating transmission events in SARS-CoV-2 outbreaks, provide insight into the maintenance of viral genetic diversity, provide a list of candidate targets of positive selection for further investigation, and demonstrate that within-host variants can be transferred between patients. Together these results will help in developing strategies to understand the nature of transmission events and curtail the spread of SARS-CoV-2.

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

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