Evidence map›Paper›PMID 28939989›Full record

ReviewGenetica2017

The Cotesia sesamiae story: insight into host-range evolution in a Hymenoptera parasitoid and implication for its use in biological control programs.

L Kaiser, S Dupas, A Branca, E A Herniou, C W Clarke, C Capdevielle Dulac, J Obonyo, R Benoist, J Gauthier, P A Calatayud and 2 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Genetica, 2017. 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
3.3field-weighted citation impact, top 9% 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

5 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
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

12 authors at 7 institutions in 2 countries.

L KaiserLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France. laure.kaiser-arnauld@egce.cnrs-gif.fr.
S DupasLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France.
A BrancaLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France.
E A HerniouInstitut de Recherche sur la Biologie de l'Insecte (UMR CNRS 7261), Université François-Rabelais, UFR Sciences et Techniques, Parc Grandmont, Avenue Monge, 37200, Tours, France.
C W Clarkeicipe: African Insect Science for Food and Health, Duduville Campus, Kasarani, P.O. Box 11, 30772-00100, Nairobi, Kenya.
C Capdevielle DulacLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France.
J Obonyoicipe: African Insect Science for Food and Health, Duduville Campus, Kasarani, P.O. Box 11, 30772-00100, Nairobi, Kenya.
R BenoistLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France.
J GauthierInstitut de Recherche sur la Biologie de l'Insecte (UMR CNRS 7261), Université François-Rabelais, UFR Sciences et Techniques, Parc Grandmont, Avenue Monge, 37200, Tours, France.
P A CalatayudLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France.
J F SilvainLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France.
B P Le RuLaboratoire Evolution, Génome, Comportement et Ecologie (UMR CNRS-Univ. Paris-Sud- IRD ; Univ. Paris-Saclay), 1 Avenue de la Terrasse, 91198, Gif-sur-Yvette Cedex, France.
Université Paris-Sud · FRCentre National de la Recherche Scientifique · FRÉvolution, Génomes, Comportement, Écologie · FRInternational Centre of Insect Physiology and Ecology · KEInstitut de Recherche pour le Développement · FRUniversité de Tours · FRUniversité Paris-Saclay · FR

Funding

Agence Nationale de la Recherche ANR-12-ADAP-0001
6 · The paper itself

Abstract

This review covers nearly 20 years of studies on the ecology, physiology and genetics of the Hymenoptera Cotesia sesamiae, an African parasitoid of Lepidoptera that reduces populations of common maize borers in East and South Africa. The first part of the review presents studies based on sampling of C. sesamiae from maize crops in Kenya. From this agrosystem including one host plant and three main host borer species, studies revealed two genetically differentiated populations of C. sesamiae species adapted to their local host community, and showed that their differentiation involved the joint evolution of virulence genes and sensory mechanisms of host acceptance, reinforced by reproductive incompatibility due to Wolbachia infection status and natural inbreeding. In the second part, we consider the larger ecosystem of wild Poales plant species hosting many Lepidoptera stem borer species that are potential hosts for C. sesamiae. The hypothesis of other host-adapted C. sesamiae populations was investigated based on a large sampling of stem borer larvae on various Poales across sub-Saharan Africa. The sampling provided information on the respective contribution of local hosts, biogeography and Wolbachia in the genetic structure of C. sesamiae populations. Molecular evolution analyses highlighted that several bracovirus genes were under positive selection, some of them being under different selection pressure in C. sesamiae populations adapted to different hosts. This suggests that C. sesamiae host races result from co-evolution acting at the local scale on different bracovirus genes. The third part considers the mechanisms driving specialization. C. sesamiae host races are more or less host-specialized. This character is crucial for efficient and environmentally-safe use of natural enemies for biological control of pests. One method to get an insight in the evolutionary stability of host-parasite associations is to characterize the phylogenetic relationships between the so-called host-races. Based on the construction of a phylogeny of C. sesamiae samples from various host- and plant species, we revealed three main lineages. Mechanisms of differentiation are discussed with regard to the geography and ecology of the samples. One of the lineage presented all the hallmarks of a distinct species, which has been morphologically described and is now studied in the perspective of being used as biological control agent against Sesamia nonagrioides Lefèbvre (Lepidoptera: Noctuidae), a major maize pest in West Africa and Mediterranean countries (see Benoist et al. 2017). The fourth part reviews past and present use of C. sesamiae in biological control, and points out the interest of such molecular ecology studies to reconcile biodiversity and food security stakes in future biological control.

Indexed as

Biological Control AgentsBiological EvolutionAdaptation, BiologicalAnimalsGenetic SpeciationHost-Parasite InteractionsKenyaPlantsWaspsBiological Control AgentsAfricaMaizeParasitic waspSpecializationStem borer larvaeVirulence genes

Identifiers

PMID28939989
OpenAlexW2757927368

What OpenQuestion holds

Textmetadata
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.