Evidence map›Paper›PMID 34577794›Full record

ArticleMedicina (Kaunas, Lithuania)2021

Herpes Infections in Suspected Cases of Yellow Fever in the Democratic Republic of the Congo.

Sheila Makiala-Mandanda, Jessica L Abbate, Elisabeth Pukuta-Simbu, Steve Ahuka-Mundeke, Jean-Jacques Muyembe-Tamfum, Eric M Leroy, Pierre Becquart

Open access · goldAbstract read
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
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

7 authors at 4 institutions in 3 countries.

Sheila Makiala-MandandaCentre International de Recherches Médicales de Franceville (CIRMF), BP 769 Franceville, Gabon.
Jessica L AbbateUnité Mixte de Recherche MIVEGEC, Institut de Recherche pour le Développement, UMR IRD/CNRS/Université de Montpellier, 34394 Montpellier, France.
Elisabeth Pukuta-SimbuInstitut National de Recherche Biomédicale (INRB), BP 1197 Kinshasa, Democratic Republic of the Congo.
Steve Ahuka-MundekeDépartement de Microbiologie, Cliniques Universitaires de Kinshasa (CUK), BP 127 Kinshasa, Democratic Republic of the Congo.
Jean-Jacques Muyembe-TamfumDépartement de Microbiologie, Cliniques Universitaires de Kinshasa (CUK), BP 127 Kinshasa, Democratic Republic of the Congo.
Eric M LeroyUnité Mixte de Recherche MIVEGEC, Institut de Recherche pour le Développement, UMR IRD/CNRS/Université de Montpellier, 34394 Montpellier, France.
Pierre BecquartUnité Mixte de Recherche MIVEGEC, Institut de Recherche pour le Développement, UMR IRD/CNRS/Université de Montpellier, 34394 Montpellier, France.
Centre National de la Recherche Scientifique · FRNational Institute of Biomedical Research · CDUniversity of Kinshasa · CDInstitut de Recherche pour le Développement · FR

Funding

Centre International de Recherches Médicales de Franceville N/AInstitut National de Recherche Biomédicale N/A
6 · The paper itself

Abstract

In the battle to quickly identify potential yellow fever arbovirus outbreaks in the Democratic Republic of the Congo, active syndromic surveillance of acute febrile jaundice patients across the country is a powerful tool. However, patients who test negative for yellow fever virus infection are too often left without a diagnosis. By retroactively screening samples for other potential viral infections, we can both try to find sources of patient disease and gain information on how commonly they may occur and co-occur. Several human arboviruses have previously been identified, but there remain many other viral families that could be responsible for acute febrile jaundice. Here, we assessed the prevalence of human herpes viruses (HHVs) in these acute febrile jaundice disease samples. Total viral DNA was extracted from serum of 451 patients with acute febrile jaundice. We used real-time quantitative PCR to test all specimens for cytomegalovirus (CMV), herpes simplex virus (HSV), human herpes virus type 6 (HHV-6) and varicella-zoster virus (VZV). We found 21.3% had active HHV replication (13.1%, 2.4%, 6.2% and 2.4% were positive for CMV, HSV, HHV-6 and VZV, respectively), and that nearly half (45.8%) of these infections were characterized by co-infection either among HHVs or between HHVs and other viral infection, sometimes associated with acute febrile jaundice previously identified. Our results show that the role of HHV primary infection or reactivation in contributing to acute febrile jaundice disease identified through the yellow fever surveillance program should be routinely considered in diagnosing these patients.

Indexed as

Herpesviridae InfectionsYellow FeverCytomegalovirusDemocratic Republic of the CongoDNA, ViralHerpesvirus 3, HumanHumansDNA, ViralDemocratic Republic of the Congoherpesyellow fever

Identifiers

PMID34577794
PMCPMC8468251
OpenAlexW3169619591

What OpenQuestion holds

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LicenceCC BY
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.