Evidence map›Paper›PMID 27315120›Full record

ArticlePloS one2016

Epidemiology and Molecular Characterization of Human Respiratory Syncytial Virus in Senegal after Four Consecutive Years of Surveillance, 2012-2015.

Amary Fall, Ndongo Dia, El Hadj Abdel Kader Cisse, Davy E Kiori, Fatoumata Diene Sarr, Sara Sy, Debora Goudiaby, Vincent Richard, Mbayame Ndiaye Niang

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
–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

41 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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.

Amary FallInstitut Pasteur de Dakar, Unité de Virologie Médicale, Dakar, Sénégal.
Ndongo DiaInstitut Pasteur de Dakar, Unité de Virologie Médicale, Dakar, Sénégal.
El Hadj Abdel Kader CisseInstitut Pasteur de Dakar, Unité de Virologie Médicale, Dakar, Sénégal.
Davy E KioriInstitut Pasteur de Dakar, Unité de Virologie Médicale, Dakar, Sénégal.
Fatoumata Diene SarrInstitut Pasteur de Dakar, Unité d'Epidémiologie des maladies infectieuses, Dakar, Sénégal.
Sara SyInstitut Pasteur de Dakar, Unité de Virologie Médicale, Dakar, Sénégal.
Debora GoudiabyInstitut Pasteur de Dakar, Unité de Virologie Médicale, Dakar, Sénégal.
Vincent RichardInstitut Pasteur de Dakar, Unité d'Epidémiologie des maladies infectieuses, Dakar, Sénégal.
Mbayame Ndiaye NiangInstitut Pasteur de Dakar, Unité de Virologie Médicale, Dakar, Sénégal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe burden of respiratory syncytial virus (RSV) infection remains poorly defined in Africa. To address this, we carried out a descriptive and retrospective pilot study, with a focus on the epidemiology of RSV in Senegal after 4 years of surveillance. METHODOLOGY AND

resultsFrom January 2012 to October 2015 swabs were collected from consenting ILI outpatients. Viral detection was performed using RV16 kit enabling direct subtyping of RSV-A and B. For the molecular characterization of HRSV, the second hypervariable region of the Glycoprotein (G) gene was targeted for sequencing. We enrolled 5338 patients with 2803 children younger than five years of age (52.5%). 610 (11.4%) were positive for RSV infection: 276 (45.2%) were group A infections, 334 (54.8%) were group B infections and 21 (3.4%) were A/B co-infections. RSV detection rate is significantly higher (P < 0.0001) in children below 5 years. We noted that the annual distribution of RSV varied substantially by season and for the predominant subtype. Globally, results show a clear circulation pattern in the second half of each year; between June and September and possibly extended into November. The majority of RSV-A strains from Senegal clustered with strains that were previously assigned NA1 and novel ON1 genotype sequences. RSV-B sequences from Senegal clustered with the BA9 genotype. At the amino acid level, RSV-A strains from Senegal show proximity with the genotype ON1 characterized by a 72 nt insertion in G, resulting in 24 extra amino acids of which 23 are duplications of aa 261-283.

conclusionGlobally our results show a clear circulation pattern of RSV in the second half of each year, between June and September and possibly extending into November, with children under 5 being more susceptible. Molecular studies identified the novel strains ON1 and BA9 as the major genotypes circulating in Senegal between 2012 and 2015.

Indexed as

PhylogenyAdolescentAdultAmino Acid SequenceChildChild, PreschoolFemaleGenotypeHumansInfantInfant, NewbornMaleMiddle AgedPilot ProjectsRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus Infections

Identifiers

PMID27315120
PMCPMC4912143

What OpenQuestion holds

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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.