Evidence map›Paper›PMID 31522684›Full record

ArticleParasites & vectors2019

Mini-FLOTAC as an alternative, non-invasive diagnostic tool for Schistosoma mansoni and other trematode infections in wildlife reservoirs.

Stefano Catalano, Amelia Symeou, Kirsty J Marsh, Anna Borlase, Elsa Léger, Cheikh B Fall, Mariama Sène, Nicolas D Diouf, Davide Ianniello, Giuseppe Cringoli and 3 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Parasites & vectors, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 24 citations in OpenAlex.

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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

13 authors at 6 institutions in 4 countries.

Stefano CatalanoCentre for Emerging, Endemic and Exotic Diseases, Department of Pathobiology and Population Sciences, The Royal Veterinary College, University of London, Hatfield, AL97TA, UK. scatalano@rvc.ac.uk.ORCID http://orcid.org/0000-0001-7827-216X
Amelia SymeouCentre for Emerging, Endemic and Exotic Diseases, Department of Pathobiology and Population Sciences, The Royal Veterinary College, University of London, Hatfield, AL97TA, UK.
Kirsty J MarshCentre for Emerging, Endemic and Exotic Diseases, Department of Pathobiology and Population Sciences, The Royal Veterinary College, University of London, Hatfield, AL97TA, UK.
Anna BorlaseCentre for Emerging, Endemic and Exotic Diseases, Department of Pathobiology and Population Sciences, The Royal Veterinary College, University of London, Hatfield, AL97TA, UK.
Elsa LégerCentre for Emerging, Endemic and Exotic Diseases, Department of Pathobiology and Population Sciences, The Royal Veterinary College, University of London, Hatfield, AL97TA, UK.
Cheikh B FallFaculté de Médecine, de Pharmacie et d'Odonto-Stomatologie, Université Cheikh Anta Diop, BP 5005, Dakar, Senegal.
Mariama SèneUnité de Formation et de Recherche des Sciences Agronomiques, de l'Aquaculture et des Technologies Alimentaires, Université Gaston Berger, BP 234, Saint-Louis, Senegal.
Nicolas D DioufUnité de Formation et de Recherche des Sciences Agronomiques, de l'Aquaculture et des Technologies Alimentaires, Université Gaston Berger, BP 234, Saint-Louis, Senegal.
Davide IannielloDepartment of Veterinary Medicine and Animal Production, University of Naples Federico II, 80137, Naples, Italy.
Giuseppe CringoliDepartment of Veterinary Medicine and Animal Production, University of Naples Federico II, 80137, Naples, Italy.
Laura RinaldiDepartment of Veterinary Medicine and Animal Production, University of Naples Federico II, 80137, Naples, Italy.
Khalilou BâCentre de Biologie et de Gestion des Populations, Institut de Recherche pour le Développement, BP 1386, Dakar, Senegal.
Joanne P WebsterCentre for Emerging, Endemic and Exotic Diseases, Department of Pathobiology and Population Sciences, The Royal Veterinary College, University of London, Hatfield, AL97TA, UK.
University of London · GBUniversity of Naples Federico II · ITUniversité Gaston Berger · SNAgropolis International · FRCheikh Anta Diop University · SNRoyal Veterinary College · GB

Funding

Biotechnology and Biological Sciences Research Council BB/L018985/1Biotechnology and Biological Sciences Research Council BB/N503563/1
6 · The paper itself

Abstract

backgroundSchistosomiasis and food-borne trematodiases are not only of major public health concern, but can also have profound implications for livestock production and wildlife conservation. The zoonotic, multi-host nature of many digenean trematodes is a significant challenge for disease control programmes in endemic areas. However, our understanding of the epidemiological role that animal reservoirs, particularly wild hosts, may play in the transmission of zoonotic trematodiases suffers a dearth of information, with few, if any, standardised, reliable diagnostic tests available. We combined qualitative and quantitative data derived from post-mortem examinations, coprological analyses using the Mini-FLOTAC technique, and molecular tools to assess parasite community composition and the validity of non-invasive methods to detect trematode infections in 89 wild Hubert's multimammate mice (Mastomys huberti) from northern Senegal.

resultsParasites isolated at post-mortem examination were identified as Plagiorchis sp., Anchitrema sp., Echinostoma caproni, Schistosoma mansoni, and a hybrid between Schistosoma haematobium and Schistosoma bovis. The reports of E. caproni and Anchitrema sp. represent the first molecularly confirmed identifications for these trematodes in definitive hosts of sub-Saharan Africa. Comparison of prevalence estimates derived from parasitological analysis at post-mortem examination and Mini-FLOTAC analysis showed non-significant differences indicating comparable results between the two techniques (P = 1.00 for S. mansoni; P = 0.85 for E. caproni; P = 0.83 for Plagiorchis sp.). A Bayesian model, applied to estimate the sensitivities of the two tests for the diagnosis of Schistosoma infections, indicated similar median posterior probabilities of 83.1% for Mini-FLOTAC technique and 82.9% for post-mortem examination (95% Bayesian credible intervals of 64.0-94.6% and 63.7-94.7%, respectively).

conclusionsOur results showed that the Mini-FLOTAC could be applied as an alternative diagnostic technique for the detection of the zoonotic S. mansoni and other trematodes in rodent reservoirs. The implementation of non-invasive diagnostics in wildlife would offer numerous advantages over lethal sampling methodologies, with potential impact on control strategies of zoonotic helminthiases in endemic areas of sub-Saharan Africa and on fostering a framework of animal use reduction in scientific practice.

Indexed as

MurinaeAnimalsDiagnostic Tests, RoutineParasitologyPrevalenceRodent DiseasesSenegalSensitivity and SpecificityTrematodaTrematode InfectionsDiagnosticsMastomys hubertiMini-FLOTACParasitesSchistosomiasisTrematodesWest AfricaWildlifeZoonoses

Identifiers

PMID31522684
PMCPMC6745783
OpenAlexW2972960001

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.