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Author Notes:

Correspondence: Alejandra Rojas (alerojaspy@gmail.com), Jesse Waggoner (jesse.waggoner@emoryhealthcare.org)

Author Contributions Alejandra Rojas and Jesse Waggoner conceived and designed the experiments, performed the experiments, analyzed the data, contributed reagents/materials/analysis tools, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.

Fátima Cardozo performed the experiments, analyzed the data, contributed reagents/materials/analysis tools, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.

César Cantero, Sanny López and Cynthia Bernal performed the experiments, analyzed the data, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.

Victoria Stittleburg performed the experiments, analyzed the data, authored or reviewed drafts of the paper, approved the final draft.

Francisco Eugenio Gimenez Acosta analyzed the data, authored or reviewed drafts of the paper, approved the final draft.

Laura Mendoza, Benjamin A. Pinsky, Ivalena Arévalo de Guillén and Malvina Páez analyzed the data, contributed reagents/materials/analysis tools, prepared figures and/or tables, authored or reviewed drafts of the paper, approved the final draft.

We thank the members of the study team based at the Instituto de Investigaciones en Ciencias de la Salud, Universidad Nacional de Asunción, and Hospital Villa Elisa in Paraguay for their dedication and excellent work, and we are grateful to the study participants and their families.

The authors would like to thank Diagnostic Bioprobes who kindly provided the ZIKVG.CE kits used in this study as well as Muktha Natrajan and Varun Phadke for their thoughtful comments during the preparation of this manuscript.

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

The authors declare there are no competing interests.

Subject:

Research Funding:

Research was supported by National Institutes of Health grant K08 AI110528 (Jesse Waggoner)

In addition, the development of this collaboration was supported by funding from the Consejo Nacional de Ciencia y Tecnología (CONACYT) in Paraguay (Alejandra Rojas: PVCT16-66 and Jesse Waggoner: PVCT17-65).

Keywords:

  • Science & Technology
  • Multidisciplinary Sciences
  • Science & Technology - Other Topics
  • Dengue virus
  • NS1
  • RT-PCR
  • Diagnosis
  • Hospitalization
  • Anti-NS1 antibody
  • Viral load
  • SEROTYPE-SPECIFIC DIFFERENCES
  • REVERSE TRANSCRIPTION-PCR
  • EARLY CLINICAL-FEATURES
  • LABORATORY FEATURES
  • NS1 ANTIGEN
  • NONSTRUCTURAL PROTEIN-1
  • FEBRILE ILLNESSES
  • VIRUS-INFECTION
  • SINGLE-REACTION
  • DISEASE

Characterization of dengue cases among patients with an acute illness, Central Department, Paraguay

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Journal Title:

PeerJ

Volume:

Volume 7, Number 10

Publisher:

, Pages e7852-e7852

Type of Work:

Article | Final Publisher PDF

Abstract:

Background. In 2018, Paraguay experienced a large dengue virus (DENV) outbreak. The primary objective of this study was to characterize dengue cases in the Central Department, where the majority of cases occur, and identify factors associated with DENV infection. Methods. Patients were enrolled from January-May 2018 if they presented with a suspected arboviral illness. Acute-phase specimens (≤8 days after symptom onset) were tested using rRT-PCR, a rapid diagnostic test for DENV nonstructural protein 1 (NS1) and anti-DENV IgM and IgG, and ELISA for IgG against NS1 from Zika virus (ZIKV). Results. A total of 231 patients were enrolled (95.2% adults) at two sites: emergency care and an outpatient clinical site. Patients included 119 (51.5%) dengue cases confirmed by rRT-PCR (n = 115, 96.6%) and/or the detection of NS1 and anti-DENV IgM (n = 4, 3.4%). DENV-1 was the predominant serotype (109/115, 94.8%). Epidemiologically, dengue cases and non-dengue cases were similar, though dengue cases were less likely to reside in a house/apartment or report a previous dengue case. Clinical and laboratory findings associated with dengue included red eyes, absence of sore throat, leucopenia and thrombocytopenia. At an emergency care site, 26% of dengue cases (26/100) required hospitalization. In univariate analysis, hospitalization was associated with increased viral load, anti-DENV IgG, and thrombocytopenia. Among dengue cases that tested positive for IgG against ZIKV NS1, the odds of DENV NS1 detection in the acute phase were decreased 10-fold (OR 0.1, 0.0–0.3). Conclusions. Findings from a predominantly adult population demonstrate clinical and laboratory factors associated with DENV infections and the potential severity of dengue in this group. The combination of viral load and specific IgG antibodies warrant further study as a prognostic to identify patients at risk for severe disease.

Copyright information:

Copyright 2019 Rojas et al.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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