Hyperendemic dengue transmission and identification of a locally evolved DENV-3 lineage, Papua New Guinea 2007-2010

PLoS Negl Trop Dis. 2018 Mar 1;12(3):e0006254. doi: 10.1371/journal.pntd.0006254. eCollection 2018 Mar.

Abstract

Background: Dengue is endemic in the Western Pacific and Oceania and the region reports more than 200,000 cases annually. Outbreaks of dengue and severe dengue occur regularly and movement of virus throughout the region has been reported. Disease surveillance systems, however, in many areas are not fully established and dengue incidence is underreported. Dengue epidemiology is likely least understood in Papua New Guinea (PNG), where the prototype DENV-2 strain New Guinea C was first isolated by Sabin in 1944 but where routine surveillance is not undertaken and little incidence and prevalence data is available.

Methodology/principal findings: Serum samples from individuals with recent acute febrile illness or with non-febrile conditions collected between 2007-2010 were tested for anti-DENV neutralizing antibody. Responses were predominantly multitypic and seroprevalence increased with age, a pattern indicative of endemic dengue. DENV-1, DENV-2 and DENV-3 genomes were detected by RT-PCR within a nine-month period and in several instances, two serotypes were identified in individuals sampled within a period of 10 days. Phylogenetic analysis of whole genome sequences identified a DENV-3 Genotype 1 lineage which had evolved on the northern coast of PNG which was likely exported to the western Pacific five years later, in addition to a DENV-2 Cosmopolitan Genotype lineage which had previously circulated in the region.

Conclusions/significance: We show that dengue is hyperendemic in PNG and identify an endemic, locally evolved lineage of DENV-3 that was associated with an outbreak of severe dengue in Pacific countries in subsequent years, although severe disease was not identified in PNG. Additional studies need to be undertaken to understand dengue epidemiology and burden of disease in PNG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Antibodies, Neutralizing / blood
  • Antibodies, Viral / blood
  • Child
  • Child, Preschool
  • Cost of Illness
  • Dengue / blood
  • Dengue / epidemiology*
  • Dengue / transmission*
  • Dengue / virology
  • Dengue Virus / genetics*
  • Dengue Virus / immunology
  • Disease Outbreaks
  • Endemic Diseases*
  • Female
  • Genotype
  • Humans
  • Infant
  • Male
  • Middle Aged
  • Papua New Guinea / epidemiology
  • Phylogeny
  • RNA, Viral / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Seroepidemiologic Studies
  • Serogroup
  • Severe Dengue / epidemiology*
  • Severe Dengue / virology
  • Whole Genome Sequencing
  • Young Adult

Substances

  • Antibodies, Neutralizing
  • Antibodies, Viral
  • RNA, Viral

Grants and funding

This study was supported by funds awarded to AI from the University of Western Australia. DLS was supported by an AusAID Scholarship awarded to him by the Australian Government Department of Foreign Affairs and Trade (DFAT). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.