Limited genomic reconstruction of SARS-CoV-2 transmission history within local epidemiological clusters

Author:

Gallego-García Pilar1,Varela Nair12,Estévez-Gómez Nuria12,De Chiara Loretta12,Fernández-Silva Iria3,Valverde Diana123,Sapoval NicolaeORCID,Treangen Todd J4ORCID,Regueiro Benito256,Cabrera-Alvargonzález Jorge Julio25,del Campo Víctor27,Pérez Sonia25ORCID,Posada David123ORCID

Affiliation:

1. CINBIO, Universidade de Vigo, Vigo 36310, Spain

2. Galicia Sur Health Research Institute (IIS Galicia Sur), SERGAS-UVIGO

3. Department of Biochemistry, Genetics, and Immunology, Universidade de Vigo, Vigo 36310, Spain

4. Department of Computer Science, Rice University, Houston, TX 77005, USA

5. Department of Microbiology, Complexo Hospitalario Universitario de Vigo (CHUVI), Sergas, Vigo 36213, Spain

6. Microbiology and Parasitology Department, Medicine and Odontology, Universidade de Santiago, Santiago de Compostela 15782, Spain

7. Department of Preventive Medicine, Complexo Hospitalario Universitario de Vigo (CHUVI), Sergas, Vigo 36213, Spain

Abstract

AbstractA detailed understanding of how and when severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) transmission occurs is crucial for designing effective prevention measures. Other than contact tracing, genome sequencing provides information to help infer who infected whom. However, the effectiveness of the genomic approach in this context depends on both (high enough) mutation and (low enough) transmission rates. Today, the level of resolution that we can obtain when describing SARS-CoV-2 outbreaks using just genomic information alone remains unclear. In order to answer this question, we sequenced forty-nine SARS-CoV-2 patient samples from ten local clusters in NW Spain for which partial epidemiological information was available and inferred transmission history using genomic variants. Importantly, we obtained high-quality genomic data, sequencing each sample twice and using unique barcodes to exclude cross-sample contamination. Phylogenetic and cluster analyses showed that consensus genomes were generally sufficient to discriminate among independent transmission clusters. However, levels of intrahost variation were low, which prevented in most cases the unambiguous identification of direct transmission events. After filtering out recurrent variants across clusters, the genomic data were generally compatible with the epidemiological information but did not support specific transmission events over possible alternatives. We estimated the effective transmission bottleneck size to be one to two viral particles for sample pairs whose donor–recipient relationship was likely. Our analyses suggest that intrahost genomic variation in SARS-CoV-2 might be generally limited and that homoplasy and recurrent errors complicate identifying shared intrahost variants. Reliable reconstruction of direct SARS-CoV-2 transmission based solely on genomic data seems hindered by a slow mutation rate, potential convergent events, and technical artifacts. Detailed contact tracing seems essential in most cases to study SARS-CoV-2 transmission at high resolution.

Funder

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia

ACIS, SERGAS, Consellería de Sanidade, Xunta de Galicia

C3.ai Digital Transformation Institute

FONDO SUPERA COVID19, Banco Santander-CSIC-CRUE

Publisher

Oxford University Press (OUP)

Subject

Virology,Microbiology

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