Serological Evidence of Widespread Zika Transmission across the Philippines.
Adolescent
Adult
Antibodies, Viral
/ blood
Child
Cross Reactions
Dengue
/ epidemiology
Dengue Virus
/ immunology
Female
Humans
Immunoglobulin G
/ blood
Immunoglobulin M
/ blood
Male
Philippines
/ epidemiology
Seroepidemiologic Studies
Young Adult
Zika Virus
/ immunology
Zika Virus Infection
/ epidemiology
Philippines
Zika
dengue
diagnostics
force of infection
serology
Journal
Viruses
ISSN: 1999-4915
Titre abrégé: Viruses
Pays: Switzerland
ID NLM: 101509722
Informations de publication
Date de publication:
23 07 2021
23 07 2021
Historique:
received:
29
06
2021
revised:
15
07
2021
accepted:
20
07
2021
entrez:
28
8
2021
pubmed:
29
8
2021
medline:
4
2
2022
Statut:
epublish
Résumé
Zika virus (ZIKV) exposure across flavivirus-endemic countries, including the Philippines, remains largely unknown despite sporadic case reporting and environmental suitability for transmission. Using laboratory surveillance data from 2016, 997 serum samples were randomly selected from suspected dengue (DENV) case reports across the Philippines and assayed for serological markers of short-term (IgM) and long-term (IgG) ZIKV exposure. Using mixture models, we re-evaluated ZIKV IgM/G seroprevalence thresholds and used catalytic models to quantify the force of infection (attack rate, AR) from age-accumulated ZIKV exposure. While we observed extensive ZIKV/DENV IgG cross-reactivity, not all individuals with active DENV presented with elevated ZIKV IgG, and a proportion of dengue-negative cases (DENV IgG-) were ZIKV IgG-positive (14.3%, 9/63). We identified evidence of long-term, yet not short-term, ZIKV exposure across Philippine regions (ZIKV IgG+: 31.5%, 314/997) which was geographically uncorrelated with DENV exposure. In contrast to the DENV AR (12.7% (95%CI: 9.1-17.4%)), the ZIKV AR was lower (5.7% (95%CI: 3-11%)) across the country. Our results provide evidence of widespread ZIKV exposure across the Philippines and suggest the need for studies to identify ZIKV infection risk factors over time to better prepare for potential future outbreaks.
Identifiants
pubmed: 34452307
pii: v13081441
doi: 10.3390/v13081441
pmc: PMC8402696
pii:
doi:
Substances chimiques
Antibodies, Viral
0
Immunoglobulin G
0
Immunoglobulin M
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Wellcome Trust
ID : 206250/Z/17/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/V031112/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 206471/Z/17/Z
Pays : United Kingdom
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