Evidence map›Paper›PMID 36962260›Full record

ArticlePLOS global public health2022

March 2019 dengue fever outbreak at the Kenyan south coast involving dengue virus serotype 3, genotypes III and V.

Eric M Muthanje, Gathii Kimita, Josphat Nyataya, Winrose Njue, Cyrus Mulili, Julius Mugweru, Beth Mutai, Sarah N Kituyi, John Waitumbi

Open access · goldFull text read
In one paragraph

Article in PLOS global public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
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

17 citing papers in PubMed, 23 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Eric M MuthanjeDepartment of Biological Sciences, University of Embu, Embu, Kenya.ORCID https://orcid.org/0000-0001-6769-6274
Gathii KimitaUnited States Army Medical Research Directorate-Africa, Basic Science Laboratory, Kisumu, Kenya.ORCID https://orcid.org/0000-0003-4555-4480
Josphat NyatayaUnited States Army Medical Research Directorate-Africa, Basic Science Laboratory, Kisumu, Kenya.ORCID https://orcid.org/0000-0003-1333-327X
Winrose NjueUnited States Army Medical Research Directorate-Africa, Basic Science Laboratory, Kisumu, Kenya.ORCID https://orcid.org/0000-0002-0612-9740
Cyrus MuliliUnited States Army Medical Research Directorate-Africa, Basic Science Laboratory, Kisumu, Kenya.
Julius MugweruDepartment of Biological Sciences, University of Embu, Embu, Kenya.ORCID https://orcid.org/0000-0002-8799-660X
Beth MutaiUnited States Army Medical Research Directorate-Africa, Basic Science Laboratory, Kisumu, Kenya.
Sarah N KituyiDepartment of Biological Sciences, University of Embu, Embu, Kenya.ORCID https://orcid.org/0000-0003-3890-7794
John WaitumbiUnited States Army Medical Research Directorate-Africa, Basic Science Laboratory, Kisumu, Kenya.ORCID https://orcid.org/0000-0003-2540-4397
United States Army Medical Research Directorate - Africa · KEUniversity of Embu · KE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The first description of a disease resembling dengue fever (DF) was in the 15th century slave trade era by Spanish sailors visiting the Tanzania coast. The disease, then associated with evil spirits is now known to be caused by four serotypes of dengue virus (DENV1-4) that are transmitted by Aedes mosquitoes. Kenya has experienced multiple outbreaks, mostly associated with DENV-2. In this study, plasma samples obtained from 37 febrile patients during a DF outbreak at Kenya's south coast in March 2019 were screened for DENV. Total RNA was extracted and screened for the alpha- and flavi-viruses by real-time polymerase chain reaction (qPCR). DENV-3 was the only virus detected. Shotgun metagenomics and targeted sequencing were used to obtain DENV whole genomes and the complete envelope genes (E gene) respectively. Sequences were used to infer phylogenies and time-scaled genealogies. Following Maximum likelihood and Bayesian phylogenetic analysis, two DENV-3 genotypes (III, n = 15 and V, n = 2) were found. We determined that the two genotypes had been in circulation since 2015, and that both had been introduced independently. Genotype III's origin was estimated to have been from Pakistan. Although the origin of genotype V could not be ascertained due to rarity of these sequences globally, it was most related to a 2006 Brazilian isolate. Unlike genotype III that has been described in East and West Africa multiple times, this was the second description of genotype V in Kenya. Of note, there was marked amino acid variances in the E gene between study samples and the Thailand DENV-3 strain used in the approved Dengvaxia vaccine. It remains to be seen whether these variances negatively impact the efficacy of the Dengvaxia or future vaccines.

Identifiers

PMID36962260
PMCPMC10021577
OpenAlexW4220850143

What OpenQuestion holds

Textfull text, public
LicenceCC0
measurements read32
reference markers read2
identifiers read7
Read underepoch 390

Registered trials

None linked

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.