Evidence map›Paper›PMID 41593468›Full record

ArticleParasites & vectors2026

Detection of dengue virus serotype 2 in local Aedes aegypti populations, Madeira Island, Portugal, 2025.

Líbia Zé-Zé, Vítor Borges, Bruna Raquel Gouveia, Victoria Mary Cox, Manuel Silva, João Dourado Santos, José Alves, Wes Hinsley, Inês Campos Freitas, Daniel Sobral and 6 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Líbia Zé-Zé *Department of Infectious Diseases, Centre for Vectors and Infectious Diseases Research (CEVDI), National Institute of Health Doutor Ricardo Jorge (INSA), Águas de Moura, Portugal. libia.zeze@insa.min-saude.pt.
Vítor Borges *Genomics and Bioinformatics Unit, Department of Infectious Diseases, National Institute of Health Doutor Ricardo Jorge (INSA), Lisbon, Portugal.
Bruna Raquel GouveiaRegional Directorate of Health, Funchal, Madeira, Portugal.
Victoria Mary CoxMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Manuel SilvaDepartment of Infectious Diseases, Centre for Vectors and Infectious Diseases Research (CEVDI), National Institute of Health Doutor Ricardo Jorge (INSA), Águas de Moura, Portugal.
João Dourado SantosGenomics and Bioinformatics Unit, Department of Infectious Diseases, National Institute of Health Doutor Ricardo Jorge (INSA), Lisbon, Portugal.
José AlvesServiço de Saúde da RAM (SESARAM), Hospital Dr. Nélio Mendonça, Funchal, Madeira, Portugal.
Wes HinsleyMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Inês Campos FreitasDepartment of Infectious Diseases, Centre for Vectors and Infectious Diseases Research (CEVDI), National Institute of Health Doutor Ricardo Jorge (INSA), Águas de Moura, Portugal.
Daniel SobralGenomics and Bioinformatics Unit, Department of Infectious Diseases, National Institute of Health Doutor Ricardo Jorge (INSA), Lisbon, Portugal.
Rita FernandesDepartment of Infectious Diseases, Centre for Vectors and Infectious Diseases Research (CEVDI), National Institute of Health Doutor Ricardo Jorge (INSA), Águas de Moura, Portugal.
Fátima AmaroDepartment of Infectious Diseases, Centre for Vectors and Infectious Diseases Research (CEVDI), National Institute of Health Doutor Ricardo Jorge (INSA), Águas de Moura, Portugal.
João Paulo GomesGenomics and Bioinformatics Unit, Department of Infectious Diseases, National Institute of Health Doutor Ricardo Jorge (INSA), Lisbon, Portugal.
Hugo Costa OsórioDepartment of Infectious Diseases, Centre for Vectors and Infectious Diseases Research (CEVDI), National Institute of Health Doutor Ricardo Jorge (INSA), Águas de Moura, Portugal.
Nuno Rodrigues Faria *MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Maria João Alves *Department of Infectious Diseases, Centre for Vectors and Infectious Diseases Research (CEVDI), National Institute of Health Doutor Ricardo Jorge (INSA), Águas de Moura, Portugal.

Funding

European Commission DURABLE "Research Network against Epidemics" -EC/ EU4Health Programme 101102733European Commission "Sustainable use and integration of enhanced infrastructure into routine genome-based surveillance and outbreak investigation activities in Portugal" - GENEO 101113460Fundação para a Ciência e a Tecnologia 10.54499/LA/P/0083/2020, 10.54499/UIDP/50009/2020, and 10.54499/UIDB/50009/2020Fundação para a Ciência e a Tecnologia LA/P/0059/2020, FCT/MCTES UIB/00211/2020 - DOI 10.54499/UIDB/00211, FCT/MCTES UIP/00211/2020 - DOI 10.54499/UIDP/00211Wellcome Trust Dengue and Zika Immunology and Genomics Multi-Country Network (DeZi Network) 316633/Z/24/Z
6 · The paper itself

Abstract

backgroundSince 2010, dengue virus (DENV) has caused sporadic outbreaks across Europe, namely in Croatia, Spain, France, Italy and the Portuguese island of Madeira. Aedes aegypti mosquito is established in the Autonomous Region of Madeira, and along the eastern Black Sea coast of Cyprus. In Madeira Island, an outbreak of DENV serotype 1 occurred between 2012 and 2013, resulting in 1080 confirmed cases. Despite ongoing entomological surveillance, no further local transmission was detected in the following decade.

methodsIn January 2025, following two suspected dengue cases on Madeira Island, increased entomological surveillance efforts were implemented to confirm a local event transmission of DENV. A network of mosquito traps was complemented by targeted surveillance using 17 BG-PRO traps positioned in the vicinity of suspected human cases. Daily collections of adult A. aegypti, collected from 10 January to 31 March 2025, were screened by reverse transcription polymerase chain reaction (RT-PCR) for Aedes-borne viruses in the reference laboratory. Viral sequencing was performed using target enrichment and bioinformatics with INSaFLU-TELEVIR. The climate-driven suitability for dengue transmission by A. aegypti was also investigated. Serological and molecular tests were conducted on samples from suspected human cases.

resultsOut of 80 analysed A. aegypti pools (N = 393 mosquitoes), 1 pool, with 9 mosquitoes collected near the home of suspected human cases, tested positive for DENV. The dengue whole genome sequence from this sample was determined and classified as DENV-2 lineage 2II_F.1.1.3. The same virus was retrospectively confirmed in one of the clinical cases. Analysis of mosquito abundance and climate data confirmed the occurrence of this local transmission event during a period of low mosquito abundance and low climatic suitability.

conclusionsHere, we report an in-depth analysis of a local dengue transmission event that occurred in Funchal, the capital of Madeira Island, in January 2025, with whole-genome evidence of DENV-2II_F.1.1.3 in field-caught A. aegypti mosquitoes. Retrospective analysis confirmed the presence of the same virus in one of the two clinical cases, establishing a direct link between human and mosquito infections, and highlighting the risk of off-season arboviral introductions.

Indexed as

AedesDengueDengue VirusMosquito VectorsAnimalsFemaleHumansPhylogenyPortugalSerogroupAedes aegyptiDengue virusMadeira IslandSurveillance

Identifiers

PMID41593468
PMCPMC12917965

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.