Evidence map›Paper›PMID 26979518›Full record

ArticleParasites & vectors2016

Identification of a Tsal152-75 salivary synthetic peptide to monitor cattle exposure to tsetse flies.

Martin Bienvenu Somda, Sylvie Cornelie, Zakaria Bengaly, Françoise Mathieu-Daudé, Anne Poinsignon, Emilie Dama, Jeremy Bouyer, Issa Sidibé, Edith Demettre, Martial Seveno and 3 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. 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

13 authors at 7 institutions in 2 countries.

Martin Bienvenu SomdaCentre International de Recherche-Développement sur l'Elevage en zone Subhumide (CIRDES), 01 BP 454, Bobo-Dioulasso 01, Burkina Faso. somdabienvenu@yahoo.fr.
Sylvie CornelieInstitut de Recherche pour le Développement (IRD), Unité Mixte de Recherche 224, Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution et Contrôle (MIVEGEC), Montpellier, 34394 Cedex 5, France.
Zakaria BengalyCentre International de Recherche-Développement sur l'Elevage en zone Subhumide (CIRDES), 01 BP 454, Bobo-Dioulasso 01, Burkina Faso.
Françoise Mathieu-DaudéInstitut de Recherche pour le Développement (IRD), Unité Mixte de Recherche 224, Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution et Contrôle (MIVEGEC), Montpellier, 34394 Cedex 5, France.
Anne PoinsignonInstitut de Recherche pour le Développement (IRD), Unité Mixte de Recherche 224, Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution et Contrôle (MIVEGEC), Montpellier, 34394 Cedex 5, France.
Emilie DamaCentre International de Recherche-Développement sur l'Elevage en zone Subhumide (CIRDES), 01 BP 454, Bobo-Dioulasso 01, Burkina Faso.
Jeremy BouyerCIRAD, UMR CIRAD-INRA Contrôle des Maladies Animales, Campus International de Baillarguet, F34398, Montpellier, France.
Issa SidibéCentre International de Recherche-Développement sur l'Elevage en zone Subhumide (CIRDES), 01 BP 454, Bobo-Dioulasso 01, Burkina Faso.
Edith DemettreInstitut de Génomique Fonctionnelle, CNRS UMR 5203, INSERM U1191, UM1, UM2, Plate-forme de Protéomique Fonctionnelle CNRS UMS BioCampus 3426, 34094, Montpellier, France.
Martial SevenoInstitut de Génomique Fonctionnelle, CNRS UMR 5203, INSERM U1191, UM1, UM2, Plate-forme de Protéomique Fonctionnelle CNRS UMS BioCampus 3426, 34094, Montpellier, France.
Franck RemouéInstitut de Recherche pour le Développement (IRD), Unité Mixte de Recherche 224, Maladies Infectieuses et Vecteurs: Ecologie, Génétique, Evolution et Contrôle (MIVEGEC), Montpellier, 34394 Cedex 5, France.
Antoine SanonUniversité de Ouagadougou, UFR/SVT, Laboratoire d'Entomologie Fondamentale et Appliquée (LEFA), BP 9499, Ouagadougou 06, Burkina Faso.
Bruno BuchetonInstitut de Recherche pour le Développement, Unité Mixte de Recherche IRD-CIRAD 177, Interactions hôtes-vecteurs-parasites dans les maladies dues aux Trypanosomatidae, Campus International de Baillarguet, Montpellier, 34398 Cedex 5, France.
Maladies Infectieuses et Vecteurs: Écologie, Génétique, Évolution et Contrôle · FRCentre de Coopération Internationale en Recherche Agronomique pour le Développement · FRCentre National de la Recherche Scientifique · FRAgropolis International · FRCentre international de recherche-développement sur l'elevage en zone subhumide · BFNazi Boni University · BFPan African Tsetse and Trypanosomiasis Eradication Campaign · BF

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe saliva of tsetse flies contains a cocktail of bioactive molecules inducing specific antibody responses in hosts exposed to bites. We have previously shown that an indirect-ELISA test using whole salivary extracts from Glossina morsitans submorsitans was able to discriminate between (i) cattle from tsetse infested and tsetse free areas and (ii) animals experimentally exposed to low or high numbers of tsetse flies. In the present study, our aim was to identify specific salivary synthetic peptides that could be used to develop simple immunoassays to measure cattle exposure to tsetse flies.

methodsIn a first step, 2D-electrophoresis immunoblotting, using sera from animals exposed to a variety of bloodsucking arthropods, was performed to identify specific salivary proteins recognised in cattle exposed to tsetse bites. Linear epitope prediction software and Blast analysis were then used to design synthetic peptides within the identified salivary proteins. Finally, candidate peptides were tested by indirect-ELISA on serum samples from tsetse infested and tsetse free areas, and from exposure experiments.

resultsThe combined immunoblotting and bioinformatics analyses led to the identification of five peptides carrying putative linear epitopes within two salivary proteins: the tsetse salivary gland protein 1 (Tsal1) and the Salivary Secreted Adenosine (SSA). Of these, two were synthesised and tested further based on the absence of sequence homology with other arthropods or pathogen species. IgG responses to the Tsal152-75 synthetic peptide were shown to be specific of tsetse exposure in both naturally and experimentally exposed hosts. Nevertheless, anti-Tsal152-75 IgG responses were absent in animals exposed to high tsetse biting rates.

conclusionsThese results suggest that Tsal152-75 specific antibodies represent a biomarker of low cattle exposure to tsetse fly. These results are discussed in the light of the other available tsetse saliva based-immunoassays and in the perspective of developing a simple serological tool for tsetse eradication campaigns to assess the tsetse free status or to detect tsetse reemergence in previously cleared areas.

Indexed as

AnimalsCattleCattle DiseasesEctoparasitic InfestationsEnzyme-Linked Immunosorbent AssayEpitopesImmunoblottingImmunoglobulin GSalivary Proteins and PeptidesTsetse FliesEpitopesImmunoglobulin GSalivary Proteins and PeptidesAfrican Animal TrypanosomosisBiomarker of ExposureCattleSynthetic PeptideTsetse Flies

Identifiers

PMID26979518
PMCPMC4791801
OpenAlexW2296833597

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.