Evidence map›Paper›PMID 37591995›Full record

ArticleNature microbiology2023

Sensitive poliovirus detection using nested PCR and nanopore sequencing: a prospective validation study.

Alexander G Shaw, Tresor Kabeya Mampuela, Emmanuel Lokilo Lofiko, Catherine Pratt, Catherine Troman, Erika Bujaki, Áine O'Toole, Joyce Odeke Akello, Adrienne Amuri Aziza, Eddy Kinganda Lusamaki and 15 more

Open access · hybridAbstract read
In one paragraph

Article in Nature microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 6% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
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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

25 authors at 9 institutions in 5 countries.

Alexander G Shaw *MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK. a.shaw@imperial.ac.uk.ORCID 0000-0002-3166-872X
Tresor Kabeya Mampuela *Service de Microbiologie, Departement de Biologie Médicale, Cliniques Universitaires de Kinshasa (CUK), Université de Kinshasa (UNIKIN), Kinshasa, Democratic Republic of the Congo.
Emmanuel Lokilo Lofiko *Institut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Catherine Pratt *College of Public Health, University of Nebraska Medical Center, Omaha, NE, USA.ORCID 0000-0001-6132-2570
Catherine TromanMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Erika BujakiDepartment of Vaccines, National Institute for Biological Standards and Control (NIBSC), Medicines and Healthcare products Regulatory Agency, Potters Bar, UK.
Áine O'TooleInstitute of Ecology and Evolution, University of Edinburgh, Ashworth Laboratories, Edinburgh, UK.ORCID 0000-0001-8083-474X
Joyce Odeke AkelloMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.ORCID 0000-0002-0483-426X
Adrienne Amuri AzizaInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.ORCID 0000-0002-5516-0779
Eddy Kinganda LusamakiService de Microbiologie, Departement de Biologie Médicale, Cliniques Universitaires de Kinshasa (CUK), Université de Kinshasa (UNIKIN), Kinshasa, Democratic Republic of the Congo.ORCID 0000-0001-9795-0165
Jean Claude MakangaraService de Microbiologie, Departement de Biologie Médicale, Cliniques Universitaires de Kinshasa (CUK), Université de Kinshasa (UNIKIN), Kinshasa, Democratic Republic of the Congo.ORCID 0000-0002-1791-2247
Marceline AkongaInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Yvonne LayInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Bibiche NsundaInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Bailey WhiteCollege of Public Health, University of Nebraska Medical Center, Omaha, NE, USA.
David JorgensenMRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.
Elizabeth PukutaInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Yogolelo RizikiInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of the Congo.
Kathleen E RankinBill and Melinda Gates Foundation, Seattle, WA, USA.
Andrew RambautInstitute of Ecology and Evolution, University of Edinburgh, Ashworth Laboratories, Edinburgh, UK.ORCID 0000-0003-4337-3707
Steve Ahuka-MundekeService de Microbiologie, Departement de Biologie Médicale, Cliniques Universitaires de Kinshasa (CUK), Université de Kinshasa (UNIKIN), Kinshasa, Democratic Republic of the Congo.
Jean-Jacques MuyembeService de Microbiologie, Departement de Biologie Médicale, Cliniques Universitaires de Kinshasa (CUK), Université de Kinshasa (UNIKIN), Kinshasa, Democratic Republic of the Congo.
Javier MartinDepartment of Vaccines, National Institute for Biological Standards and Control (NIBSC), Medicines and Healthcare products Regulatory Agency, Potters Bar, UK.
Nicholas C Grassly *MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK.ORCID 0000-0001-6067-4507
Placide Mbala-Kingebeni *Service de Microbiologie, Departement de Biologie Médicale, Cliniques Universitaires de Kinshasa (CUK), Université de Kinshasa (UNIKIN), Kinshasa, Democratic Republic of the Congo.
National Institute of Biomedical Research · CDUniversity of Kinshasa · CDImperial College London · GBNational Institute for Biological Standards and Control · GBUniversity of Edinburgh · GBUniversity of Nebraska Medical Center · USGates Foundation · USInserm · FRNIHR Imperial Biomedical Research Centre · GB

Funding

Medical Research Council MR/R015600/1Wellcome TrustWellcome Trust 206298/Z/17/Z
6 · The paper itself

Abstract

Timely detection of outbreaks is needed for poliovirus eradication, but gold standard detection in the Democratic Republic of the Congo takes 30 days (median). Direct molecular detection and nanopore sequencing (DDNS) of poliovirus in stool samples is a promising fast method. Here we report prospective testing of stool samples from suspected polio cases, and their contacts, in the Democratic Republic of the Congo between 10 August 2021 and 4 February 2022. DDNS detected polioviruses in 62/2,339 (2.7%) of samples, while gold standard combination of cell culture, quantitative PCR and Sanger sequencing detected polioviruses in 51/2,339 (2.2%) of the same samples. DDNS provided case confirmation in 7 days (median) in routine surveillance conditions. DDNS enabled confirmation of three serotype 2 circulating vaccine-derived poliovirus outbreaks 23 days (mean) earlier (range 6-30 days) than the gold standard method. The mean sequence similarity between sequences obtained by the two methods was 99.98%. Our data confirm the feasibility of implementing DDNS in a national poliovirus laboratory.

Indexed as

Nanopore SequencingPoliovirusDansyl CompoundsPolymerase Chain ReactionDansyl Compoundsdimethylaminonaphthalene-5-sulfonaminoethylmethylamine

Identifiers

PMID37591995
PMCPMC10465353
OpenAlexW4385948888

What OpenQuestion holds

Textmetadata
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.