Evidence map›Paper›PMID 41071829›Full record

ArticlePLoS neglected tropical diseases2025

Detection of dengue, malaria, and additional causes of acute febrile illness: The need for expanded testing, Bayelsa State, Nigeria.

Dayo Olufemi Akanbi, Bio Belu Abaye, Francisco Averhoff, Michael G Berg, Gregory S Orf, Kabiru M Lawan, Geoff A Beckett, Ayotunde Bolatito Omotoso, Maximillian Mata, Gavin A Cloherty and 10 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. 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

20 authors.

Dayo Olufemi AkanbiNigeria Field Epidemiology and Laboratory Training Program, Abuja, Nigeria.ORCID 0009-0009-9496-5391
Bio Belu AbayeNigeria Field Epidemiology and Laboratory Training Program, Abuja, Nigeria.
Francisco AverhoffAbbott Diagnostics, Abbott Park, Illinois, United States of America.
Michael G BergAbbott Diagnostics, Abbott Park, Illinois, United States of America.
Gregory S OrfAbbott Diagnostics, Abbott Park, Illinois, United States of America.
Kabiru M LawanDepartment of Veterinary Public Health and Preventive Medicine, Ahmadu Bello University, Zaria, Nigeria.
Geoff A BeckettIndependent Researcher, Decatur, Georgia, United States of America.
Ayotunde Bolatito OmotosoDepartment of Behavioural Sciences, University of Ilorin, Ilorin, Nigeria.
Maximillian MataAbbott Diagnostics, Abbott Park, Illinois, United States of America.
Gavin A ClohertyAbbott Diagnostics, Abbott Park, Illinois, United States of America.
Lucious ChabukaCentre for Epidemic Response and Innovation (CERI), School of Data Science and Computational Thinking, Stellenbosch University, Stellenbosch, South Africa.
Tulio de OliveiraCentre for Epidemic Response and Innovation (CERI), School of Data Science and Computational Thinking, Stellenbosch University, Stellenbosch, South Africa.
Kenneth W Mac-FisiEpidemiology Unit, Bayelsa State Ministry of Health, Yenagoa, State Secretariat, Yenagoa, Bayelsa State, Nigeria.
Azibadighi WalterEpidemiology Unit, Bayelsa State Ministry of Health, Yenagoa, State Secretariat, Yenagoa, Bayelsa State, Nigeria.
Inara Isaac MarkEpidemiology Unit, Bayelsa State Ministry of Health, Yenagoa, State Secretariat, Yenagoa, Bayelsa State, Nigeria.
George EdekiDepartment of Statistics, University of Ibadan, Ibadan, Oyo State, Nigeria.
Abdoulaye SinayokoWorld Health Organization, Abuja, FCT, Nigeria.
Muazzam NasrullahInjury Control Research Center, West Virginia University, Morgantown, West Virginia, United States of America.
Binafeigha Ihekerenma JustinaDiete-Koki Memorial Hospital Opolo, Yenagoa, Bayelsa State, Nigeria.
Muhammad Shakir BalogunNigeria Field Epidemiology and Laboratory Training Program, Abuja, Nigeria.

Funding

World Health Organization 001
6 · The paper itself

Abstract

Dengue virus (DENV) infection has not been previously reported from Bayelsa State, Nigeria. We aimed to determine the prevalence of dengue virus (DENV) infection, malaria, and coinfection, and other pathogens among febrile patients in the capital city, Yenagoa.We conducted a cross-sectional study among persons aged ≥1 year who presented with acute febrile illnesses (AFI) at four hospitals in Bayelsa State during 20 May - 15 June 2022. Blood samples from 443 participants were tested for DENV seromarkers (NS1, IgM, IgG), using serology and RT-PCR, and malaria was diagnosed by thick smear microscopy. Sociodemographic and risk factor data were collected using electronic questionnaires administered via smart phones/tablets and analyzed using univariate and multivariate methods. Metagenomic libraries were prepared and enriched by viral target capture and sequenced by NGS. The seroprevalence of acute DENV infection was 14.5% (n = 64) while the prevalence of malaria was 42.4% (n = 188); 6.5% (n = 29) of participants were coinfected with acute DENV infection and malaria. An additional 17.6% (n = 78) of participants had markers for past DENV infection. Rural/suburban residence and age ≥ 31 years were significantly correlated with having any dengue seromarker. Residence in a larger household (≥5 persons), and borehole water-use were predictors for malaria fever. RT-PCR results revealed multiple DENV serotypes, with serotype 3 dominant. Sequencing of unknown AFI cases revealed numerous viral causes such as adenovirus, EBV, and hepatitis A, as well as additional dengue and malarial infections missed by conventional testing. Of interest were Coxsackievirus A5 (hand, foot and mouth disease; HFMD) which has been diversifying locally for years in Nigeria and an mPox clade IIb (lineage A.2.3) strain that emerged in Nigeria during the 2022 global outbreak. The results of this study provide the first documentation of human DENV infection in Bayelsa State, Nigeria and suggests that dengue is an emerging and important cause of febrile illness in this area. Our findings support the need for routine testing to identify DENV among patients who present with acute febrile disease. Metagenomic NGS results highlight the benefits of unbiased surveillance to identify circulating and emerging pathogens.

Indexed as

CoinfectionDengueFeverMalariaAdolescentAdultAgedAntibodies, ViralChildChild, PreschoolCross-Sectional StudiesDengue VirusFemaleHumansInfantMaleAntibodies, Viral

Identifiers

PMID41071829
PMCPMC12533896

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.