Evidence map›Paper›PMID 34780575›Full record

ArticlePLoS pathogens2021

Raman spectroscopic analysis of skin as a diagnostic tool for Human African Trypanosomiasis.

Alexandre Girard, Anneli Cooper, Samuel Mabbott, Barbara Bradley, Steven Asiala, Lauren Jamieson, Caroline Clucas, Paul Capewell, Francesco Marchesi, Matthew P Gibbins and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 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

17 authors at 4 institutions in 2 countries.

Alexandre GirardWellcome Centre for Integrative Parasitology, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-6825-765X
Anneli CooperWellcome Centre for Integrative Parasitology, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-1159-142X
Samuel MabbottDepartment of Biomedical Engineering, Texas A&M University, College Station, Texas, United States of America.
Barbara BradleyWellcome Centre for Integrative Parasitology, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.
Steven AsialaDepartment of Pure and Applied Chemistry, University of Strathclyde, Glasgow, United Kingdom.ORCID 0000-0002-3517-9915
Lauren JamiesonDepartment of Pure and Applied Chemistry, University of Strathclyde, Glasgow, United Kingdom.
Caroline ClucasWellcome Centre for Integrative Parasitology, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0001-5592-6810
Paul CapewellWellcome Centre for Integrative Parasitology, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-8803-5034
Francesco MarchesiVeterinary Diagnostic Services, School of Veterinary Medicine, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0003-1179-5788
Matthew P GibbinsWellcome Centre for Integrative Parasitology, Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-7166-044X
Franziska HentzschelWellcome Centre for Integrative Parasitology, Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-9812-0128
Matthias MartiWellcome Centre for Integrative Parasitology, Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0003-1040-9566
Juan F QuintanaWellcome Centre for Integrative Parasitology, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-5092-5576
Paul GarsideInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.
Karen FauldsDepartment of Pure and Applied Chemistry, University of Strathclyde, Glasgow, United Kingdom.
Annette MacLeodWellcome Centre for Integrative Parasitology, Institute of Biodiversity Animal Health and Comparative Medicine, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-0150-5049
Duncan GrahamDepartment of Pure and Applied Chemistry, University of Strathclyde, Glasgow, United Kingdom.ORCID 0000-0002-6079-2105
Wellcome Centre for Molecular Parasitology · GBUniversity of Strathclyde · GBUniversity of Glasgow · GBTexas A&M University · US

Funding

Wellcome Trust 209511/Z/17/Z
6 · The paper itself

Abstract

Human African Trypanosomiasis (HAT) has been responsible for several deadly epidemics throughout the 20th century, but a renewed commitment to disease control has significantly reduced new cases and motivated a target for the elimination of Trypanosoma brucei gambiense-HAT by 2030. However, the recent identification of latent human infections, and the detection of trypanosomes in extravascular tissues hidden from current diagnostic tools, such as the skin, has added new complexity to identifying infected individuals. New and improved diagnostic tests to detect Trypanosoma brucei infection by interrogating the skin are therefore needed. Recent advances have improved the cost, sensitivity and portability of Raman spectroscopy technology for non-invasive medical diagnostics, making it an attractive tool for gambiense-HAT detection. The aim of this work was to assess and develop a new non-invasive diagnostic method for T. brucei through Raman spectroscopy of the skin. Infections were performed in an established murine disease model using the animal-infective Trypanosoma brucei brucei subspecies. The skin of infected and matched control mice was scrutinized ex vivo using a confocal Raman microscope with 532 nm excitation and in situ at 785 nm excitation with a portable field-compatible instrument. Spectral evaluation and Principal Component Analysis confirmed discrimination of T. brucei-infected from uninfected tissue, and a characterisation of biochemical changes in lipids and proteins in parasite-infected skin indicated by prominent Raman peak intensities was performed. This study is the first to demonstrate the application of Raman spectroscopy for the detection of T. brucei by targeting the skin of the host. The technique has significant potential to discriminate between infected and non-infected tissue and could represent a unique, non-invasive diagnostic tool in the goal for elimination of gambiense-HAT as well as for Animal African Trypanosomiasis (AAT).

Indexed as

AnimalsFemaleMiceMice, Inbred BALB CMice, Inbred C57BLSkinSpectrum Analysis, RamanTrypanosoma brucei bruceiTrypanosoma brucei gambienseTrypanosomiasis, African

Identifiers

PMID34780575
PMCPMC8629383
OpenAlexW3212413085

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.