Evidence map›Paper›PMID 38829379›Full record

ArticleMicrobial ecology2024

Shaping the Microbial Landscape: Parasitoid-Driven Modifications of Bactrocera dorsalis Microbiota.

Rehemah Gwokyalya, Jeremy K Herren, Christopher W Weldon, Shepard Ndlela, Joseph Gichuhi, Nehemiah Ongeso, Anne W Wairimu, Sunday Ekesi, Samira A Mohamed

Abstract read
In one paragraph

Article in Microbial ecology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 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

9 authors.

Rehemah GwokyalyaInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya. remysuffy2@gmail.com.
Jeremy K HerrenInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Christopher W WeldonDepartment of Zoology and Entomology, University of Pretoria, Private Bag X20, Pretoria, South Africa.
Shepard NdlelaInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Joseph GichuhiInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Nehemiah OngesoInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Anne W WairimuInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Sunday EkesiInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya.
Samira A MohamedInternational Centre of Insect Physiology and Ecology, P.O. Box 30772-00100, Nairobi, Kenya. sfaris@icipe.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Koinobiont endoparasitoids regulate the physiology of their hosts through altering host immuno-metabolic responses, processes which function in tandem to shape the composition of the microbiota of these hosts. Here, we employed 16S rRNA and ITS amplicon sequencing to investigate whether parasitization by the parasitoid wasps, Diachasmimorpha longicaudata (Ashmaed) (Hymenoptera: Braconidae) and Psyttalia cosyrae (Wilkinson) (Hymenoptera: Braconidae), induces gut dysbiosis and differentially alter the gut microbial (bacteria and fungi) communities of an important horticultural pest, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae). We further investigated the composition of bacterial communities of adult D. longicaudata and P. cosyrae to ascertain whether the adult parasitoids and parasitized host larvae share microbial taxa through transmission. We demonstrated that parasitism by D. longicaudata induced significant gut perturbations, resulting in the colonization and increased relative abundance of pathogenic gut bacteria. Some pathogenic bacteria like Stenotrophomonas and Morganella were detected in both the guts of D. longicaudata-parasitized B. dorsalis larvae and adult D. longicaudata wasps, suggesting a horizontal transfer of microbes from the parasitoid to the host. The bacterial community of P. cosyrae adult wasps was dominated by Arsenophonus nasoniae, whereas that of D. longicaudata adults was dominated by Paucibater spp. and Pseudomonas spp. Parasitization by either parasitoid wasp was associated with an overall reduction in fungal diversity and evenness. These findings indicate that unlike P. cosyrae which is avirulent to B. dorsalis, parasitization by D. longicaudata induces shifts in the gut bacteriome of B. dorsalis larvae to a pathobiont-dominated community. This mechanism possibly enhances its virulence against the pest, further supporting its candidacy as an effective biocontrol agent of this frugivorous tephritid fruit fly pest.

Indexed as

BacteriaGastrointestinal MicrobiomeLarvaRNA, Ribosomal, 16STephritidaeWaspsAnimalsDysbiosisFungiHost-Parasite InteractionsMicrobiotaRNA, Ribosomal, 16SBacteriaDiachasmimorpha longicaudataFruit flyGut microbiomeParasitisationPsyttalia cosyraeTephritid

Identifiers

PMID38829379
PMCPMC11147917

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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 OpenQuestion graph.