Evidence map›Paper›PMID 30135221›Full record

ArticlemSphere2018

Investigation of the Plasma Virome from Cases of Unexplained Febrile Illness in Tanzania from 2013 to 2014: a Comparative Analysis between Unbiased and VirCapSeq-VERT High-Throughput Sequencing Approaches.

Simon H Williams, Samuel Cordey, Nishit Bhuva, Florian Laubscher, Mary-Anne Hartley, Noémie Boillat-Blanco, Zainab Mbarack, Josephine Samaka, Tarsis Mlaganile, Komal Jain and 3 more

Erratum issuedAbstract readComparative Study
In one paragraph

Article in mSphere, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

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

  1. Pooled it
  2. Pooled it
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Agnostic Sequencing for Detection of Viral Pathogens.Clinical microbiology reviews · 2023
    Review
  11. Review
  12. Blood virosphere in febrile Tanzanian children.Emerging microbes & infections · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Viral Metagenomics of Blood Donors and Blood-Derived Products Using Next-Generation Sequencing.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2019
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Simon H Williams *Center for Infection & Immunity, Columbia University, New York, New York, USA.
Samuel Cordey *Laboratory of Virology, University Hospitals of Geneva, Geneva, Switzerland.
Nishit BhuvaCenter for Infection & Immunity, Columbia University, New York, New York, USA.
Florian LaubscherLaboratory of Virology, University Hospitals of Geneva, Geneva, Switzerland.
Mary-Anne HartleyDepartment of Ambulatory Care and Community Medicine, University of Lausanne, Lausanne, Switzerland.
Noémie Boillat-BlancoSwiss Tropical and Public Health Institute, University of Basel, Lausanne, Switzerland.
Zainab MbarackMwananyamala Hospital, Dar es Salaam, United Republic of Tanzania.
Josephine SamakaIfakara Health Institute, Dar es Salaam, United Republic of Tanzania.
Tarsis MlaganileIfakara Health Institute, Dar es Salaam, United Republic of Tanzania.
Komal JainCenter for Infection & Immunity, Columbia University, New York, New York, USA.
Valerie d'AcremontDepartment of Ambulatory Care and Community Medicine, University of Lausanne, Lausanne, Switzerland.
Laurent KaiserLaboratory of Virology, University Hospitals of Geneva, Geneva, Switzerland.
W Ian LipkinCenter for Infection & Immunity, Columbia University, New York, New York, USA wil2001@cumc.columbia.edu.

Funding

Translational CoreU19AI109761 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BARIC, RALPH S · 2014 to 2018
$32.6M
NIAID NIH HHS U19 AI109761
6 · The paper itself

Abstract

High-throughput sequencing can provide insights into epidemiology and medicine through comprehensive surveys of viral genetic sequences in environmental and clinical samples. Here, we characterize the plasma virome of Tanzanian patients with unexplained febrile illness by using two high-throughput sequencing methods: unbiased sequencing and VirCapSeq-VERT (a positive selection system). Sequences from dengue virus 2, West Nile virus, human immunodeficiency virus type 1, human pegivirus, and Epstein-Barr virus were identified in plasma. Both sequencing strategies recovered nearly complete genomes in samples containing multiple viruses. Whereas VirCapSeq-VERT had better sensitivity, unbiased sequencing provided better coverage of genome termini. Together, these data demonstrate the utility of high-throughput sequencing strategies in outbreak investigations.

Indexed as

FeverGenome, ViralHigh-Throughput Nucleotide SequencingHumansPlasmaTanzaniaVirus DiseasesVirusesfebrile illnesssequencingUHTSVirCapSeq-VERTvirology

Identifiers

PMID30135221
PMCPMC6106054

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.