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. 2022 Dec 19:9:1066793.
doi: 10.3389/fmolb.2022.1066793. eCollection 2022.

Stings on wings: Proteotranscriptomic and biochemical profiling of the lesser banded hornet (Vespa affinis) venom

Affiliations

Stings on wings: Proteotranscriptomic and biochemical profiling of the lesser banded hornet (Vespa affinis) venom

Kartik Sunagar et al. Front Mol Biosci. .

Abstract

Distinct animal lineages have convergently recruited venoms as weaponry for prey capture, anti-predator defence, conspecific competition, or a combination thereof. Most studies, however, have been primarily confined to a narrow taxonomic breadth. The venoms of cone snails, snakes, spiders and scorpions remain particularly well-investigated. Much less explored are the venoms of wasps (Order: Hymenoptera) that are infamous for causing excruciating and throbbing pain, justifying their apex position on Schmidt's pain index, including some that are rated four on four. For example, the lesser banded wasp (V. affinis) is clinically important yet has only been the subject of a few studies, despite being commonly found across tropical and subtropical Asia. Stings from these wasps, especially from multiple individuals of a nest, often lead to clinically severe manifestations, including mastocytosis, myasthenia gravis, optic neuropathy, and life-threatening pathologies such as myocardial infarction and organ failure. However, their venom composition and activity remain unexplored in the Indian subcontinent. Here, we report the proteomic composition, transcriptomic profile, and biochemical and pharmacological activities of V. affinis venom from southern India. Our findings suggest that wasp venoms are rich in diverse toxins that facilitate antipredator defence. Biochemical and pharmacological assessments reveal that these toxins can exhibit significantly higher activities than their homologues in medically important snakes. Their ability to exert potent effects on diverse molecular targets makes them a treasure trove for discovering life-saving therapeutics. Fascinatingly, wasp venoms, being evolutionarily ancient, exhibit a greater degree of compositional and sequence conservation across very distant populations/species, which contrasts with the patterns of venom evolution observed in evolutionarily younger lineages, such as advanced snakes and cone snails.

Keywords: V. affinis; arthropod venom; venom gland transcriptome; venom proteome; wasp venom.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
The lesser banded hornet and its venom composition. Images of V. affinis and its nest are shown (panel A) alongside the SDS-PAGE profile of the venom (panel B). Red boxes in panel B are indicative of the bands that were excised for mass spectrometric analysis.
FIGURE 2
FIGURE 2
Comparative venom gland transcriptome and venom proteome of the lesser banded hornet. The venom gland transcriptome and venom proteome of V. affinis are shown as doughnut charts in panels (A) and (B), respectively. Each toxin is uniquely colour coded, and its relative abundance is mentioned in percentages: ACP: acid phosphatase; AP: aminopeptidase; AK: arginine kinase; CAP: antigen 5, and pathogenesis-related one proteins; CP: carboxypeptidase; CHI: chitinase; CRISP: cysteine-rich secretory proteins; DPP: dipeptidyl peptidase; HYL: hyaluronidase; LAAO: L-amino acid oxidases; NEP: neprilysin; PER: peroxiredoxin; PLA1: phospholipase A1; PLB: phospholipase B; SP: serine protease; TRY: trypsin.
FIGURE 3
FIGURE 3
Functional profile of Vespa venom. Graphs in panels (A) and (B) represent the hyaluronidase (TRU·mg−1·min−1) and phospholipase (nmol·ng−1·min−1) activity of V. affinis venom in comparison to the venoms of the “big four” Indian snakes. Here, the error bars represent the standard deviation, and PC denotes the positive control. Heatmaps depict the anomalies caused by wasp venom on the blood coagulation cascade via (C) intrinsic and (D) extrinsic pathways. The colour scales in these panels represent the time in seconds, while the time required to form the first fibrin clot is denoted within each cell. Panel (E) depicts the haemolytic potential of V. affinis venom as a percentage relative activity to the positive control (0.5% Triton X). The numbers within cells show the percentage of haemolysis.
FIGURE 4
FIGURE 4
Insect specific toxicity. This Kaplan-Meier survival plot depicts the survival probability of crickets injected with the V. affinis venom (2 per dose group), where the x-axis depicts the time in hours, and the y-axis the probability of survival. Curves represent various doses of venoms administered into crickets. Experimental animals were monitored over a period of 24 h.

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