Circulation, viral diversity and genomic rearrangement in mpox virus in the Netherlands during the 2022 outbreak and beyond

Author:

Schuele Leonard1ORCID,Boter Marjan1,Nieuwenhuijse David F.1,Götz Hannelore12,Fanoy Ewout3,de Vries Henry345,Vieyra Bruno2,Bavalia Roisin3,Hoornenborg Elske35,Molenkamp Richard1,Jonges Marcel6,van den Ouden Anton7,Simões Margarida89,van den Lubben Mariken3,Koopmans Marion1,Welkers Matthijs R. A.36ORCID,Oude Munnink Bas B.1ORCID

Affiliation:

1. Department of Viroscience Erasmus MC University Medical Center Rotterdam Netherlands

2. Department of Public Health (Infectious Disease Control and Center Sexual Health) Public Health Service Rotterdam‐Rijnmond Rotterdam Netherlands

3. Department of Infectious Diseases Public Health Service Amsterdam Amsterdam Netherlands

4. Department of Dermatology, Amsterdam UMC Location University of Amsterdam Amsterdam Netherlands

5. Amsterdam Institute for Infection and Immunology Infectious Diseases Amsterdam Netherlands

6. Department of Medical Microbiology and Infection Prevention, Amsterdam UMC location AMC University of Amsterdam Amsterdam Netherlands

7. Molecular Biology Systems BV Goes Netherlands

8. Centre for Infectious Disease Control (CIb) National Institute for Public Health and the Environment (RIVM) Bilthoven Netherlands

9. European Program for Public Health Microbiology Training (EUPHEM) European Centre for Disease Prevention and Control, (ECDC) Stockholm Sweden

Abstract

AbstractMpox is an emerging zoonotic disease which has now spread to over 113 countries as of August 2023, with over 89,500 confirmed human cases. The Netherlands had one of the highest incidence rates in Europe during the peak of the outbreak. In this study, we generated 158 near‐complete mpox virus (MPXV) genomes (12.4% of nationwide cases) that were collected throughout the Netherlands from the start of the outbreak in May 2022 to August 2023 to track viral evolution and investigate outbreak dynamics. We detected 14 different viral lineages, suggesting multiple introductions followed by rapid initial spread within the country. The estimated evolutionary rate was relatively high compared to previously described in orthopoxvirus literature, with an estimated 11.58 mutations per year. Genomic rearrangement events occurred at a rate of 0.63% and featured a large deletion event. In addition, based on phylogenetics, we identified multiple potential transmission clusters which could be supported by direct source‐ and contact tracing data. This led to the identification of at least two main transmission locations at the beginning of the outbreak. We conclude that whole genome sequencing of MPXV is essential to enhance our understanding of outbreak dynamics and evolution of a relatively understudied and emerging zoonotic pathogen.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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