Epidemiological and microbiological investigation of a large increase in vibriosis, northern Europe, 2018

Author:

Amato Ettore12ORCID,Riess Maximilian13ORCID,Thomas-Lopez Daniel14ORCID,Linkevicius Marius15ORCID,Pitkänen Tarja67ORCID,Wołkowicz Tomasz8,Rjabinina Jelena9,Jernberg Cecilia3,Hjertqvist Marika10,MacDonald Emily2,Antony-Samy Jeevan Karloss2,Dalsgaard Bjerre Karsten11,Salmenlinna Saara5,Fuursted Kurt4,Hansen Anette10,Naseer Umaer2

Affiliation:

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

2. Department of Infection Control and Preparedness, Norwegian Institute of Public Health, Oslo, Norway

3. Department of Microbiology, Public Health Agency of Sweden, Department of Microbiology, Stockholm, Sweden

4. Department of Bacteria, Parasites and Fungi, Division of Infectious Disease Preparedness, Statens Serum Institut, Copenhagen, Denmark

5. Finnish Institute for Health and Welfare, Department of Health Security, Helsinki, Finland

6. University of Helsinki, Helsinki, Finland

7. Finnish Institute for Health and Welfare, Department of Health Security, Kuopio, Finland

8. National Institute of Public Health, Warsaw, Poland

9. Health Board, Department of CD Surveillance and Control, Tallinn, Estonia

10. Public Health Agency of Sweden, Department of Communicable Disease Control and Health Protection, Stockholm, Sweden

11. Data Integration and Analysis, Division of Infectious Disease Preparedness, Statens Serum Institut, Copenhagen, Denmark

Abstract

Background Vibriosis cases in Northern European countries and countries bordering the Baltic Sea increased during heatwaves in 2014 and 2018. Aim We describe the epidemiology of vibriosis and the genetic diversity of Vibrio spp. isolates from Norway, Sweden, Denmark, Finland, Poland and Estonia in 2018, a year with an exceptionally warm summer. Methods In a retrospective study, we analysed demographics, geographical distribution, seasonality, causative species and severity of non-travel-related vibriosis cases in 2018. Data sources included surveillance systems, national laboratory notification databases and/or nationwide surveys to public health microbiology laboratories. Moreover, we performed whole genome sequencing and multilocus sequence typing of available isolates from 2014 to 2018 to map their genetic diversity. Results In 2018, we identified 445 non-travel-related vibriosis cases in the study countries, considerably more than the median of 126 cases between 2014 and 2017 (range: 87–272). The main reported mode of transmission was exposure to seawater. We observed a species-specific geographical disparity of vibriosis cases across the Nordic-Baltic region. Severe vibriosis was associated with infections caused by Vibrio vulnificus (adjOR: 17.2; 95% CI: 3.3–90.5) or Vibrio parahaemolyticus (adjOR: 2.1; 95% CI: 1.0–4.5), age ≥ 65 years (65–79 years: adjOR: 3.9; 95% CI: 1.7–8.7; ≥ 80 years: adjOR: 15.5; 95% CI: 4.4–54.3) or acquiring infections during summer (adjOR: 5.1; 95% CI: 2.4–10.9). Although phylogenetic analysis revealed diversity between Vibrio spp. isolates, two V. vulnificus clusters were identified. Conclusion Shared sentinel surveillance for vibriosis during summer may be valuable to monitor this emerging public health issue.

Publisher

European Centre for Disease Control and Prevention (ECDC)

Subject

Virology,Public Health, Environmental and Occupational Health,Epidemiology

Reference35 articles.

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