Characterization of Dengue Virus 4 Cases in Paraguay, 2019–2020

Author:

Rojas Alejandra1,Shen John2,Cardozo Fátima13,Bernal Cynthia1ORCID,Caballero Oliver1,Ping Sara4,Key Autum5,Haider Ali4,de Guillén Yvalena1,Langjahr Patricia6ORCID,Acosta Maria Eugenia1ORCID,Aria Laura1,Mendoza Laura1,Páez Malvina1,Von-Horoch Marta7,Luraschi Patricia7,Cabral Sandra7,Sánchez María Cecilia3,Torres Aurelia3,Pinsky Benjamin A.89ORCID,Piantadosi Anne45,Waggoner Jesse J.24ORCID

Affiliation:

1. Instituto de Investigaciones en Ciencias de la Salud, Universidad Nacional de Asunción, San Lorenzo 111241, Paraguay

2. Rollins School of Public Health, Emory University, Atlanta, GA 30322, USA

3. Departamento de Laboratorio de Análisis Clínicos, Hospital Central—Instituto de Previsión Social, Asunción 001531, Paraguay

4. Department of Medicine, Division of Infectious Diseases, Emory University, 1760 Haygood Drive NE, Room E-169, Bay E-1, Atlanta, GA 30322, USA

5. Department of Pathology, Emory University, Atlanta, GA 30322, USA

6. Facultad de Ciencias Químicas, Universidad Nacional de Asunción, Campus Universitario, San Lorenzo 111421, Paraguay

7. Departamento de Epidemiología, Hospital Central—Instituto de Previsión Social, Asunción 001531, Paraguay

8. Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305, USA

9. Department of Medicine, Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA

Abstract

In 2019–2020, dengue virus (DENV) type 4 emerged to cause the largest DENV outbreak in Paraguay’s history. This study sought to characterize dengue relative to other acute illness cases and use phylogenetic analysis to understand the outbreak’s origin. Individuals with an acute illness (≤7 days) were enrolled and tested for DENV nonstructural protein 1 (NS1) and viral RNA by real-time RT-PCR. Near-complete genome sequences were obtained from 62 DENV-4 positive samples. From January 2019 to March 2020, 799 participants were enrolled: 253 dengue (14 severe dengue, 5.5%) and 546 other acute illness cases. DENV-4 was detected in 238 dengue cases (94.1%). NS1 detection by rapid test was 52.5% sensitive (53/101) and 96.5% specific (387/401) for dengue compared to rRT-PCR. DENV-4 sequences were grouped into two clades within genotype II. No clustering was observed based on dengue severity, location, or date. Sequences obtained here were most closely related to 2018 DENV-4 sequences from Paraguay, followed by a 2013 sequence from southern Brazil. DENV-4 can result in large outbreaks, including severe cases, and is poorly detected with available rapid diagnostics. Outbreak strains seem to have been circulating in Paraguay and Brazil prior to 2018, highlighting the importance of sustained DENV genomic surveillance.

Funder

Doris Duke Charitable Foundation

National Institute of Allergy and Infectious Diseases

Consejo Nacional de Ciencia y Tecnología

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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