Evidence map›Paper›PMID 27467595›Full record

ArticlePloS one2016

Characterization of Venom and Oviduct Components of Parasitoid Wasp Asobara japonica.

Shunsuke Furihata, Takashi Matsumura, Makiko Hirata, Tetsuya Mizutani, Noriyo Nagata, Michiyo Kataoka, Yukie Katayama, Tsutomu Omatsu, Hitoshi Matsumoto, Yoichi Hayakawa

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

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  4. Parasitoid wasp venoms degradeScience advances · 2025
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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 1 country.

Shunsuke FurihataDepartment of Applied Biological Sciences, Saga University, Saga 840-8502, Japan.
Takashi MatsumuraDepartment of Applied Biological Sciences, Saga University, Saga 840-8502, Japan.
Makiko HirataDepartment of Applied Biological Sciences, Saga University, Saga 840-8502, Japan.
Tetsuya MizutaniResearch and Education Center for Prevention of Global Infectious Diseases of Animals, Tokyo University of Agriculture and Technology, Fuchu, Tokyo, 183-8509, Japan.
Noriyo NagataDepartment of Virology II, National Institute of Infectious Diseases, Tokyo, 280-0011, Japan.
Michiyo KataokaDepartment of Virology II, National Institute of Infectious Diseases, Tokyo, 280-0011, Japan.
Yukie KatayamaResearch and Education Center for Prevention of Global Infectious Diseases of Animals, Tokyo University of Agriculture and Technology, Fuchu, Tokyo, 183-8509, Japan.
Tsutomu OmatsuResearch and Education Center for Prevention of Global Infectious Diseases of Animals, Tokyo University of Agriculture and Technology, Fuchu, Tokyo, 183-8509, Japan.
Hitoshi MatsumotoDepartment of Applied Biological Sciences, Saga University, Saga 840-8502, Japan.
Yoichi HayakawaDepartment of Applied Biological Sciences, Saga University, Saga 840-8502, Japan.
Saga University · JPTokyo University of Agriculture and Technology · JPNational Institute of Infectious Diseases · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During natural parasitization, Asobara japonica wasps introduce lateral oviduct (LO) components into their Drosophila hosts soon after the venom injection to neutralize its strong toxicity; otherwise, the host will die. Although the orchestrated relationship between the venom and LO components necessary for successful parasitism has attracted the attention of many researchers in this field, the molecular natures of both factors remain ambiguous. We here showed that precipitation of the venom components by ultracentrifugation yielded a toxic fraction that was inactivated by ultraviolet light irradiation, boiling, and sonication, suggesting that it is a virus-like entity. Morphological observation of the precipitate after ultracentrifugation showed small spherical heterogeneous virus-like particles 20-40 nm in diameter. The venom's detrimental effect on D. melanogaster larvae was not directly neutralized by the LO components but blocked by a hemolymphal neutralizing factor activated by the LO factor. Furthermore, we found that A. japonica venom and LO components acted similarly on the larvae of the common cutworm Spodoptera litura: the venom injection caused mortality but coinjection of the LO factor protected S. litura larvae from the venom's toxicity. In contrast, D. ficusphila and D. bipectinata, which are closely related to D. melanogaster but non-habitual host species of A. japonica, were not negatively affected by A. japonica venom due to an intrinsic neutralizing activity in their hemolymph, indicating that these species must have acquired a neutralizer of A. japonica venom during evolution. These results give new insights into the characteristics of both the venom and LO components: A. japonica females have utilized the virus-like toxic venom factor to exploit a wider range of host species after the evolutionary process enabled them to use the LO factor for activation of the host hemolymph neutralizer precursor, although the non-habitual host Drosophila species possess an active intrinsic neutralizer in their hemolymph.

Indexed as

AnimalsDrosophila melanogasterFemaleHost-Parasite InteractionsOviductsSpodopteraSurvival RateWaspsWasp VenomsWasp Venoms

Identifiers

PMID27467595
PMCPMC4965004
OpenAlexW2504480381

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.