Evidence map›Paper›PMID 30940213›Full record

ArticleParasites & vectors2019

The composition and abundance of bacterial communities residing in the gut of Glossina palpalis palpalis captured in two sites of southern Cameroon.

Jean Marc Tsagmo Ngoune, Julie Reveillaud, Guilhem Sempere, Flobert Njiokou, Trésor T Melachio, Luc Abate, Majoline T Tchioffo, Anne Geiger

Abstract read
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.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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.

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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

8 authors.

Jean Marc Tsagmo NgouneINTERTRYP, Institut de Recherche pour le Développement, University of Montpellier, Montpellier, France.
Julie ReveillaudASTRE, INRA, CIRAD, University of Montpellier, Montpellier, France.
Guilhem SempereINTERTRYP, Institut de Recherche pour le Développement, University of Montpellier, Montpellier, France.
Flobert NjiokouFaculty of Science, University of Yaoundé I, P.O. Box 812, Yaoundé, Cameroon.
Trésor T MelachioFaculty of Science, University of Yaoundé I, P.O. Box 812, Yaoundé, Cameroon.
Luc AbateUMR Maladies Infectieuses Et Vecteurs Écologie, Génétique, Évolution Et Contrôle, IRD 224-Centre National de la Recherche Scientifique, 5290-UM1-UM2, Montpellier, France.
Majoline T TchioffoUMR Maladies Infectieuses Et Vecteurs Écologie, Génétique, Évolution Et Contrôle, IRD 224-Centre National de la Recherche Scientifique, 5290-UM1-UM2, Montpellier, France.
Anne GeigerINTERTRYP, Institut de Recherche pour le Développement, University of Montpellier, Montpellier, France. anne.geiger@libertysurf.fr.

Funding

Aix-Marseille Université (FR) ANR-10-INBS-0009-10CIRAD AGAP HPC Data Center of the South Green Bioinformatics platformConseil Régional Languedoc-Roussillon Chercheur d'Avenir 2011Institut de Recherche pour le Développement Bourse ARTS
6 · The paper itself

Abstract

backgroundA number of reports have demonstrated the role of insect bacterial flora on their host's physiology and metabolism. The tsetse host and vector of trypanosomes responsible for human sleeping sickness (human African trypanosomiasis, HAT) and nagana in animals (African animal trypanosomiasis, AAT) carry bacteria that influence its diet and immune processes. However, the mechanisms involved in these processes remain poorly documented. This underscores the need for increased research into the bacterial flora composition and structure of tsetse flies. The aim of this study was to identify the diversity and relative abundance of bacterial genera in Glossina palpalis palpalis flies collected in two trypanosomiasis foci in Cameroon.

methodsSamples of G. p. palpalis which were either negative or naturally trypanosome-positive were collected in two foci located in southern Cameroon (Campo and Bipindi). Using the V3V4 and V4 variable regions of the small subunit of the 16S ribosomal RNA gene, we analyzed the respective bacteriome of the flies' midguts.

resultsWe identified ten bacterial genera. In addition, we observed that the relative abundance of the obligate endosymbiont Wigglesworthia was highly prominent (around 99%), regardless of the analyzed region. The remaining genera represented approximately 1% of the bacterial flora, and were composed of Salmonella, Spiroplasma, Sphingomonas, Methylobacterium, Acidibacter, Tsukamurella, Serratia, Kluyvera and an unidentified bacterium. The genus Sodalis was present but with a very low abundance. Globally, no statistically significant difference was found between the bacterial compositions of flies from the two foci, and between positive and trypanosome-negative flies. However, Salmonella and Serratia were only described in trypanosome-negative flies, suggesting a potential role for these two bacteria in fly refractoriness to trypanosome infection. In addition, our study showed the V4 region of the small subunit of the 16S ribosomal RNA gene was more efficient than the V3V4 region at describing the totality of the bacterial diversity.

conclusionsA very large diversity of bacteria was identified with the discovering of species reported to secrete anti-parasitic compounds or to modulate vector competence in other insects. For future studies, the analyses should be enlarged with larger sampling including foci from several countries.

Indexed as

AnimalsBacteriaCameroonGastrointestinal MicrobiomeMolecular TypingRNA, BacterialRNA, Ribosomal, 16STsetse FliesRNA, BacterialRNA, Ribosomal, 16SBacterial floraGlossinaMetabarcodingNaganaSleeping sicknessTrypanosome

Identifiers

PMID30940213
PMCPMC6444424

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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 OpenQuestion graph.