Evidence map›Paper›PMID 41641878›Full record

ArticleParasite (Paris, France)2026

Glossina from the Republic of the Congo: species identification by MALDI-TOF MS and research of associated micro-organisms.

Irina Babakana Bemba, Zaina Amirat, Philippe Parola, Christophe Antonio Nkondjio, Arsene Lenga, Lionel Almeras, Adama Zan Diarra

Abstract read
In one paragraph

Article in Parasite (Paris, France), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Irina Babakana Bemba *Marien Ngouabi University, B.P. 69, Brazzaville, Republic of the Congo - Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale (OCEAC), B.P. 288, Yaoundé, Cameroun.ORCID 0000-0002-2524-1084
Zaina Amirat *Aix Marseille Univ, SSA, RITMES, 13005 Marseille, France - IHU-Méditerranée Infection, 13005 Marseille, France.
Philippe ParolaAix Marseille Univ, SSA, RITMES, 13005 Marseille, France - IHU-Méditerranée Infection, 13005 Marseille, France.
Christophe Antonio NkondjioOrganisation de Coordination pour la lutte contre les Endémies en Afrique Centrale (OCEAC), B.P. 288, Yaoundé, Cameroun.
Arsene LengaMarien Ngouabi University, B.P. 69, Brazzaville, Republic of the Congo.
Lionel AlmerasAix Marseille Univ, SSA, RITMES, 13005 Marseille, France - IHU-Méditerranée Infection, 13005 Marseille, France - Unité Parasitologie et Entomologie, Département Microbiologie et Maladies Infectieuses, Institut de Recherche Biomédicale des Armées, 13005 Marseille, France.ORCID 0000-0003-0490-5774
Adama Zan DiarraAix Marseille Univ, SSA, RITMES, 13005 Marseille, France - IHU-Méditerranée Infection, 13005 Marseille, France - IRD, MINES, Maladies Infectieuses, Négligées et Émergentes au Sud, 13005 Marseille, France.ORCID 0000-0002-5476-9590

Funding

IHU ANR-10-IAHU-03
6 · The paper itself

Abstract

Human African trypanosomiasis (HAT) and Animal African trypanosomiasis (AAT), transmitted by Glossina species, remain major health and economic burdens in Africa. Accurate vector identification is essential for effective control strategies. However, current identification methods of Glossina species based on morphological and/or molecular techniques have several limitations that often hinder reliable species-level classification. This study assessed matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) as an alternative or complementary approach to morphological and molecular methods for Glossina species identification and explored its ability to detect infection status. A total of 265 tsetse flies were collected and morphologically classified into the Glossina palpalis group (n = 200) and the Glossina fuscipes group (n = 65), later confirmed by molecular analysis as Glossina palpalis palpalis and Glossina fuscipes quanzensis, respectively. Spectra were generated from wings, legs, and thoraxes to identify the most suitable body parts. For G. p. palpalis, high-quality spectra were obtained from wings (98.0%), legs (96.5%), and thoraxes (93.5%); for G. f. quanzensis, corresponding values were 89.2%, 87.7%, and 72.3%. Blind testing showed that 89.5% of spectra for G. p. palpalis and 95.2% for G. f. quanzensis matched morphological identification, with 87.0% and 94.6%, respectively, reaching relevant score thresholds. Molecular screening detected Trypanosoma congolense DNA in nine specimens, but MALDI-TOF MS spectra could not distinguish infected from uninfected flies. These findings demonstrate that MALDI-TOF MS is a rapid, reliable tool for Glossina species identification, particularly using wings and legs, but is unsuitable for infection status determination.

Indexed as

Insect VectorsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTsetse FliesAnimalsFemaleMaleSpecies SpecificityTrypanosomiasis, AfricanGlossinaMALDI-TOF MSMolecular biologySpecies identificationTrypanosoma

Identifiers

PMID41641878
PMCPMC12875062

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.