Evidence map›Paper›PMID 27090566›Full record

ArticleScientific reports2016

A protease-based biosensor for the detection of schistosome cercariae.

A J Webb, R Kelwick, M J Doenhoff, N Kylilis, J T MacDonald, K Y Wen, C McKeown, G Baldwin, T Ellis, K Jensen and 1 more

Open access · goldAbstract readValidation Study
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. 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

11 authors at 2 institutions in 1 country.

A J WebbCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
R KelwickCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
M J DoenhoffSchool of Life Sciences, University of Nottingham, Nottingham, UK.
N KylilisCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
J T MacDonaldCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
K Y WenCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
C McKeownSection of Structural Biology, Department of Medicine, Imperial College London, London, UK.
G BaldwinCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
T EllisCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
K JensenCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
P S FreemontCentre for Synthetic Biology and Innovation, Imperial College London, London, UK.
Imperial College London · GBUniversity of Nottingham · GB

Funding

Wellcome Trust 084369/Z/07/Z
6 · The paper itself

Abstract

Parasitic diseases affect millions of people worldwide, causing debilitating illnesses and death. Rapid and cost-effective approaches to detect parasites are needed, especially in resource-limited settings. A common signature of parasitic diseases is the release of specific proteases by the parasites at multiple stages during their life cycles. To this end, we engineered several modular Escherichia coli and Bacillus subtilis whole-cell-based biosensors which incorporate an interchangeable protease recognition motif into their designs. Herein, we describe how several of our engineered biosensors have been applied to detect the presence and activity of elastase, an enzyme released by the cercarial larvae stage of Schistosoma mansoni. Collectively, S. mansoni and several other schistosomes are responsible for the infection of an estimated 200 million people worldwide. Since our biosensors are maintained in lyophilised cells, they could be applied for the detection of S. mansoni and other parasites in settings without reliable cold chain access.

Indexed as

Biosensing TechniquesLarvaAnimalsEndopeptidasesFreeze DryingSchistosoma mansoniEndopeptidasesTEV protease

Identifiers

PMID27090566
PMCPMC4835807
OpenAlexW2339364309

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.