Evidence map›Paper›PMID 31924169›Full record

ArticleBMC genomics2020

Venomics of the ectoparasitoid wasp Bracon nigricans.

Andrea Becchimanzi, Maddalena Avolio, Hamed Bostan, Chiara Colantuono, Flora Cozzolino, Donato Mancini, Maria Luisa Chiusano, Pietro Pucci, Silvia Caccia, Francesco Pennacchio

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.6field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Lipid Metabolism in Parasitoids and Parasitized Hosts.Advances in experimental medicine and biology · 2026
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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

10 authors at 3 institutions in 2 countries.

Andrea BecchimanziDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy.
Maddalena AvolioDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy.
Hamed BostanDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy.
Chiara ColantuonoDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy.
Flora CozzolinoDepartment of Chemical Sciences and CEINGE Biotecnologie Avanzate, University of Napoli Federico II, Napoli, Italy.
Donato ManciniDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy.
Maria Luisa ChiusanoDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy.
Pietro PucciDepartment of Chemical Sciences and CEINGE Biotecnologie Avanzate, University of Napoli Federico II, Napoli, Italy.
Silvia CacciaDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy. silvia.caccia@unina.it.
Francesco PennacchioDepartment of Agricultural Sciences, University of Napoli Federico II, Portici, NA, Italy. f.pennacchio@unina.it.
Federico II University Hospital · ITCeinge Biotecnologie Avanzate (Italy) · ITDavid H. Murdock Research Institute · US

Funding

Horizon 2020 (research and innovation programme) grant agreement no. 773554
6 · The paper itself

Abstract

backgroundVenom is one of the most important sources of regulation factors used by parasitic Hymenoptera to redirect host physiology in favour of the developing offspring. This has stimulated a number of studies, both at functional and "omics" level, which, however, are still quite limited for ectophagous parasitoids that permanently paralyze and suppress their victims (i.e., idiobiont parasitoids).

resultsHere we present a combined transcriptomic and proteomic study of the venom of the generalist idiobiont wasp Bracon nigricans, an ectophagous larval parasitoid of different lepidopteran species, for which we recently described the host regulation strategy and the functional role of the venom in the induction of physiological changes in parasitized hosts. The experimental approach used led to the identification of the main components of B. nigricans venom involved in host regulation. Enzymes degrading lipids, proteins and carbohydrates are likely involved in the mobilization of storage nutrients from the fat body and may concurrently be responsible for the release of neurotoxic fatty acids inducing paralysis, and for the modulation of host immune responses.

conclusionThe present work contributes to fill the gap of knowledge on venom composition in ectoparasitoid wasps, and, along with our previous physiological study on this species, provides the foundation on which to develop a functional model of host regulation, based both on physiological and molecular data. This paves the way towards a better understanding of parasitism evolution in the basal lineages of Hymenoptera and to the possible exploitation of venom as source of bioinsecticidal molecules.

Indexed as

AnimalsHost-Parasite InteractionsInsect ProteinsProteomicsTranscriptomeWaspsWasp VenomsInsect ProteinsWasp VenomsHost-parasitoid interactionsHost regulationIdiobiont parasitoidsVenom proteomeVenom transcriptome

Identifiers

PMID31924169
PMCPMC6954513
OpenAlexW3000627049

What OpenQuestion 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 OpenQuestion graph.