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SARS-CoV-2 genomic surveillance in Rwanda: Introductions and local transmission of the B.1.617.2 (Delta) variant of concern
Yvan Butera; Samuel L. Hong; Muhammed Semakula; Nena Bollen; Verity Hill; Aine O'Toole; Barney I. Potter; Dieudonne Mutangana; Reuben Sindayiheba; Robert Rutayisire; Maria Artesi; Vincent Bours; Nadine Rujeni; Simon Dellicour; Keith Durkin; Leon Mutesa; Guy Baele.
Affiliation
  • Yvan Butera; Center for Human Genetics, College of Medicine and Health Sciences, University of Rwanda, Kigali, Rwanda; Rwanda National Joint Task Force COVID-19, Rwanda Biom
  • Samuel L. Hong; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium
  • Muhammed Semakula; Center for Excellence in Data Science, University of Rwanda, Kigali, Rwanda; Centre for Statistics, Hasselt Biostatistics and Statistical Bioinformatics Center,
  • Nena Bollen; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium
  • Verity Hill; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, Scotland
  • Aine O'Toole; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, Scotland
  • Barney I. Potter; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium
  • Dieudonne Mutangana; Rwanda National Joint Task Force COVID-19, Rwanda Biomedical Centre, Ministry of Health, Kigali, Rwanda; School of Science, College of Science and Technology,
  • Reuben Sindayiheba; National Reference Laboratory, Rwanda Biomedical Center, Kigali, Rwanda
  • Robert Rutayisire; Rwanda National Joint Task Force COVID-19, Rwanda Biomedical Centre, Ministry of Health, Kigali, Rwanda; National Reference Laboratory, Rwanda Biomedical Center
  • Maria Artesi; Laboratory of Human Genetics, GIGA Research Institute, Liege, Belgium
  • Vincent Bours; Laboratory of Human Genetics, GIGA Research Institute, Liege, Belgium; Department of Human Genetics, University Hospital of Liege, Liege, Belgium
  • Nadine Rujeni; Rwanda National Joint Task Force COVID-19, Rwanda Biomedical Centre, Ministry of Health, Kigali, Rwanda; School of Health Sciences, College of Medicine and Heal
  • Simon Dellicour; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium; Spatial Epidemiology Laboratory, University Libre de Bru
  • Keith Durkin; Laboratory of Human Genetics, GIGA Research Institute, Liege, Belgium
  • Leon Mutesa; Center for Human Genetics, College of Medicine and Health Sciences, University of Rwanda, Kigali, Rwanda; Rwanda National Joint Task Force COVID-19, Rwanda Biom
  • Guy Baele; Department of Microbiology, Immunology and Transplantation, Rega Institute, KU Leuven, Leuven, Belgium
Preprint in English | medRxiv | ID: ppmedrxiv-22275802
ABSTRACT
The emergence of the SARS-CoV-2 Delta variant of concern (lineage B.1.617.2) in late 2020 resulted in a new wave of infections in many countries across the world, where it often became the dominant lineage in a relatively short amount of time. We here report on a novel genomic surveillance effort in Rwanda in the time period from June to September 2021, leading to 201 SARS-CoV-2 genomes being generated, the majority of which were identified as the Delta variant of concern. We show that in Rwanda, the Delta variant almost completely replaced the previously dominant A.23.1 and B.1.351 (Beta) lineages in a matter of weeks, and led to a tripling of the total number of COVID-19 infections and COVID-19-related fatalities over the course of only three months. We estimate that Delta in Rwanda had an average growth rate advantage of 0.034 (95% CI 0.025-0.045) per day over A.23.1, and of 0.022 (95% CI 0.012-0.032) over B.1.351. Phylogenetic analysis reveals the presence of at least seven local Delta transmission clusters, with two of these clusters occurring close to the border with the Democratic Republic of the Congo, and another cluster close to the border with Tanzania. A smaller Delta cluster of infections also appeared close to the border with Uganda, illustrating the importance of monitoring cross-border traffic to limit the spread between Rwanda and its neighboring countries. We discuss our findings against a background of increased vaccination efforts in Rwanda, and also discuss a number of breakthrough infections identified during our study. Concluding, our study has added an important collection of data to the available genomes for the Eastern Africa region, with the number of Delta infections close to the border with neighboring countries highlighting the need to further strengthen genomic surveillance in the region to obtain a better understanding of the impact of border crossings on lowering the epidemic curve in Rwanda.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Prognostic study / Rct Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Prognostic study / Rct Language: English Year: 2022 Document type: Preprint
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