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Effects of the European hornet ( Vespa crabro Linnaeus 1761) crude venom on its own species

Abstract

Background

Lethal dose 50% is a classical index of toxicity that usually employs small rodents as experimental animals. Therefore, scarce data are available on the effects of venom on invertebrates, particularly the impact of wasp venom on its own species.

Findings

In the present study, the lethality of Vespa crabro venom on its own species was studied. Lethal dose 50% values of crude venom on workers of hornet Vespa crabro were estimated to be 4.0 mg/kg of body weight.

Conclusions

Wasps can use their venom apparatus effectively when attacking foreign workers that appear in the immediate vicinity of their nest. The toxins released during stinging are potent enough to kill. The result of this study eliminates the popular myth that venomous animals can be resistant to their own venom.

European hornet; Vespa crabro; Hornet venoms; LD50


Findings

The classical method of determining the toxicity of a substance is the lethal dose 50% (LD50), which is often used in analysis of different animal toxins [ 1Bayram A, Yigit N, Danisman T, Corak I, Sancak Z, Ulasoglu D. Venomous spiders of Turkey (Araneae) J Applied Biol Sciences. 2007;19(3):33–36. - 6Schmidt JO, Yamane S, Matsuura M, Starr CK. Hornet venoms: lethalities and lethal capacities. Toxicon. 1986;19(9):950–954. doi: 10.1016/0041-0101(86)90096-6.
https://doi.org/10.1016/0041-0101(86)900...
]. Almost all studies about venom activity are based on the lethality of small rodents including mice and rats. There is little published data on the effects of venom on invertebrates [ 7Sak O, Ergin E, Uçkan F, Rivers DB, Aylin ER. Changes in the hemolymph total protein of Galleria mellonella (Lepidoptera: Pyralidae) after parasitism and envenomation by Pimpla turionellae (Hymenoptera: Ichneumonidae) Turk J Biol. 2011;19(4):425–432. ]. Only a few studies on the lethal activity of a venom on its own species demonstrated significant results [ 8Nadolski J. Zróżnicowanie własności toksycznych jadu wybranych żądłówek społecznych (Hymenoptera, Aculeata) Acta Univ Lodz Folia zool. 2000;19:3–24. ]. In addition, the degree of toxicity of venoms on individuals of their own species is unknown.

In the present study the toxicity of the European hornet Vespa crabro (Linnaeus, 1758) venom in relation to workers of its own species was assessed. Based on the author’s own personal observations, it can be stated that hornets also sting to defend their nest against intruders of their own species, but from alien colonies. Thus, this study attempted, for the first time, to answer the following questions: did natural selection create defense mechanisms to protect these insects against their own toxins and how hornets are sensitive to their own venom?

The analysis of the toxic activity of Vespa crabro venom was carried out on workers from two colonies of hornets established in Łódź city in Central Poland. Hornet venom was obtained by irritating insects with tweezers on their torso and abdomen, resulting in stinging reaction. The secreted venom was collected on watch glasses [ 8Nadolski J. Zróżnicowanie własności toksycznych jadu wybranych żądłówek społecznych (Hymenoptera, Aculeata) Acta Univ Lodz Folia zool. 2000;19:3–24. ]. Then, frozen dried venom was stored in the dark at −20°C until used. In order to obtain percent values of dry matter from liquid venom, specified quantities of venom were weighed [ 6Schmidt JO, Yamane S, Matsuura M, Starr CK. Hornet venoms: lethalities and lethal capacities. Toxicon. 1986;19(9):950–954. doi: 10.1016/0041-0101(86)90096-6.
https://doi.org/10.1016/0041-0101(86)900...
]. The final venom concentration was adjusted with PBS (137 mM NaCl, 10 mM phosphate, 2.7 mM KCl, pH 7.4) [ 7Sak O, Ergin E, Uçkan F, Rivers DB, Aylin ER. Changes in the hemolymph total protein of Galleria mellonella (Lepidoptera: Pyralidae) after parasitism and envenomation by Pimpla turionellae (Hymenoptera: Ichneumonidae) Turk J Biol. 2011;19(4):425–432. ].

After weighing, each hornet worker received, into the abdomen, the appropriate amount of venom by using a 1 μL Hamilton microsyringe (USA). LD50 values for hornet workers (twenty workers per dose) at 24 hours were determined by the standard statistic method based on probit analysis [ 9Reed LJ, Muench HA. A simple method for the estimated fifty percent end points. Amer J Hyg. 1938;19:493–495. - 14Throne JE, Weaver DK, Baker JE. Probit analysis: assessing goodness-of-fit based on back transformation and residuals. J Economic Entomol. 1995;19(5):1513–1516. ]. Controls consisted o hornets injected only with PBS.

Table  1 displays the toxicity of Vespa crabro venom assessed on representatives of its own species. The obtained results underwent statistical analysis, including probit transformation, and the final value of LD50 is presented in Table  2 .

Table 1

Analysis of probit-transformed mortality of European hornet Vespa crabro workers provoked by their own venom


Table 2

Estimated 95 % confidence interval for the LD 50 of hornet’s workers Vespa crabro L. and standard error (SE) of LD 50


The LD50 of several aculeate venoms has been determined, including toxins of different hornet species, ranging from 1.6 mg/kg for Vespa luctuosa Saussure venom, 2.8 mg/kg for Vespa tropica L., 3.1-3.8 mg/kg for Vespa simillima Smith, 4.1-6.1 mg/kg for Vespa mandarinia Smith venom, to 8.7-10.9 mg/kg for the venom of Vespa crabro [ 5Schmidt JO. In: Venoms of the Hymenoptera: biochemical, pharmacological and behavioral aspects. Piek T, editor. London: Academic; 1986. Chemistry, pharmacology, and chemical ecology of ant venoms; pp. 425–508. , 8Nadolski J. Zróżnicowanie własności toksycznych jadu wybranych żądłówek społecznych (Hymenoptera, Aculeata) Acta Univ Lodz Folia zool. 2000;19:3–24. ]. However, all these values refer only to the mortality on experimental rodents, especially mice and rats. As shown by a previous study carried out on Calliphora sp. larvae, the toxicity of Vespa crabro venom is increased on these insects when compared to vertebrates, and is approximately about 2.7-7.6 mg/kg [ 8Nadolski J. Zróżnicowanie własności toksycznych jadu wybranych żądłówek społecznych (Hymenoptera, Aculeata) Acta Univ Lodz Folia zool. 2000;19:3–24. ]. Thus, these results support the hypothesis of greater toxicity of hornet venom on its potential prey (other insects), than on mammal aggressors. Other hymenopterans have more potent venoms, such as the solitary wasp Bracon hebetor Say. Its LD50 on lepidopterous larvae was found to be less than 0.3 mg/kg [ 15Quistad GB, Nguyen Q, Bernasconi P, Leisy DJ. Purification and characterization of insecticidal toxins from venom glands of the parasitic wasp, Bracon hebetor. Insect Biochem Mol Biol. 1994;19(10):955–961. doi: 10.1016/0965-1748(94)90132-5.
https://doi.org/10.1016/0965-1748(94)901...
].

Venoms of arthropods, including insects, comprise a source of numerous bioactive compounds, which evolved for prey capture and defense against predators and microorganisms. The antimicrobial, insecticidal, and hemolytic properties of peptides isolated from arthropod venoms are well known, especially concerning arachnids (scorpions and spiders) and hymenopterans (ants, wasps and bees) [ 15Quistad GB, Nguyen Q, Bernasconi P, Leisy DJ. Purification and characterization of insecticidal toxins from venom glands of the parasitic wasp, Bracon hebetor. Insect Biochem Mol Biol. 1994;19(10):955–961. doi: 10.1016/0965-1748(94)90132-5.
https://doi.org/10.1016/0965-1748(94)901...
- 19Ross DC, Crim JW, Brown MR, Herzog GA, Lea AO. Toxic and antifeeding actions of melittin in the corn earworm, heliothis zea (boddie): comparisons to bee venom and the insecticides chlorpyriphos and cyromazine. Toxicon. 1987;19(3):307–313. doi: 10.1016/0041-0101(87)90259-5.
https://doi.org/10.1016/0041-0101(87)902...
]. Many of these peptides have been purified and their amino acid sequences have already been characterized.

The composition and properties of the several aculeate venoms, including those of wasps and hornets, have been extensively studied [ 4Habermehl GG. Venomous animals and their toxins. Berlin-New York: Springer; 1981. - 6Schmidt JO, Yamane S, Matsuura M, Starr CK. Hornet venoms: lethalities and lethal capacities. Toxicon. 1986;19(9):950–954. doi: 10.1016/0041-0101(86)90096-6.
https://doi.org/10.1016/0041-0101(86)900...
, 20Habermann E. In: Venomous animals and their venoms: Biochemical, pharmacological and behavioral aspects. 3. Bücherl W, Buckley E, editor. New York: Academic; 1971. Chemistry, pharmacology, and toxicology of bee, wasp and hornet venoms; pp. 61–93. - 25Yang H, Xu X, Ma D, Zhang K, Lai R. A phospholipase A1 platelet activator from the wasp venom of Vespa magnifica (Smith) Toxicon. 2008;19(2):289–296. doi: 10.1016/j.toxicon.2007.10.003.
https://doi.org/10.1016/j.toxicon.2007.1...
]. On mammals, vespid venoms provoke prolonged pain, local edema and erythema due to increased permeability of blood vessels in the skin. Besides these direct outcomes of hornet stings, allergic reactions have also been observed in numerous cases. The generalized allergic reaction may be lethal.

In addition to their systemic effects, wasp and hornet venoms act kinetically on isolated smooth muscle and reduce blood pressure. They release endogenous histamines from granulocytes including mast cells and basophilic leucocytes; and also release catecholamines from adrenal chromaffin cells. Such toxins may also provoke cytolysis, including hemolysis and chemotaxis to macrophages and polymorphonuclear leukocytes.

The overall action of wasp and hornet venoms is complicated and may be described as an accumulation of active principles of venoms. Compounds of several wasp venoms, including venom toxins from social wasps and hornets, have been isolated and investigated. Such venoms consist of complex mixtures of active amines (serotonin, histamine, tyramine, dopamine noradrenaline and adrenaline), peptides (pain-producing peptides such as kinins, and chemotactic peptides like mastoparan or crabrolin) and proteins including many types of hydrolases (i.e. proteases, hyaluronidases, phosphatases, nucleotidases and phospholipase A), as well as allergens and neurotoxins.

Many social insects have developed defensive systems that prevent infections within their colonies. For example, bee propolis and royal jelly present antimicrobial properties and the fecal pellets of termites inhibit the development of fungal pathogens [ 26Anderson KE, Eckholm B, Mott BM, Sheehan TH, Hoffman GD. An emerging paradigm of colony health: microbial balance of the honey bee and hive (Apis mellifera) Insectes Sociaux. 2011;19(4):431–444. doi: 10.1007/s00040-011-0194-6.
https://doi.org/10.1007/s00040-011-0194-...
, 27Rosengaus RB, Guldin MR, Traniello JFA. Inhibitory effect of termite fecal pellets on fungal spore germination. J Chem Ecol. 1998;19(10):1697–1706. doi: 10.1023/A:1020872729671.
https://doi.org/10.1023/A:1020872729671...
]. Concerning ants, most species possess metapleural glands on the thorax whose secretions, spread over individuals and throughout the nest, have a broad spectrum of antimicrobial action. The antibacterial property of ant venom has been demonstrated, for example, in the fire ant, whose venom alkaloids inhibit bacterial growth and presumably act as an antibiotic [ 28Blum MS, Walker JR, Callahan PS, Novak AF. Chemical, insecticidal and antibiotic properties of fire ant venom. Science. 1958;19(3319):306–307. ]. Venoms of honey bees, wasps and hornets, including Vespa crabro , possess antimicrobial peptides; however, their natural functions must be further clarified [ 26Anderson KE, Eckholm B, Mott BM, Sheehan TH, Hoffman GD. An emerging paradigm of colony health: microbial balance of the honey bee and hive (Apis mellifera) Insectes Sociaux. 2011;19(4):431–444. doi: 10.1007/s00040-011-0194-6.
https://doi.org/10.1007/s00040-011-0194-...
, 29Monteiro MC, Romao PR, Soares AM. Pharmacological perspectives of wasp venom.Protein Pept Lett. 2009;19(8):944–952. doi: 10.2174/092986609788923275.
https://doi.org/10.2174/0929866097889232...
, 30Banks BEC, Shipolini RA. In: Venoms of the Hymenoptera: Biochemical, pharmacological and behavioral aspects. Piek T, editor. London: Academic; 1986. Chemistry and pharmacology of honey bee venom; pp. 329–416. ].

In addition to the development of social behavior, aculeate venom composition underwent evolution towards producing toxins that would be more effective against potential attackers. Usually solitary wasp venoms are employed primarily to paralyze and then kill prey [ 23Piek T, Spanjer W. In: Venoms of the Hymenoptera: Biochemical, pharmacological and behavioral aspects. Piek T, editor. London: Academic; 1986. Chemistry and pharmacology of solitary wasp venoms; pp. 161–307. ]. Although Vespinae subfamily produces venoms that are efficient for hunting and self-defense, the most effective venom regarding defense is that of Apis mellifera [ 8Nadolski J. Zróżnicowanie własności toksycznych jadu wybranych żądłówek społecznych (Hymenoptera, Aculeata) Acta Univ Lodz Folia zool. 2000;19:3–24. , 22O’Connor R, Henderson G, Nelson D, Parker R, Peck ML. In: Animal Toxins. Russell FE, Saunders PR, editor. Oxford: Pergamon Press; 1967. The venom of the honey bee (Apis mellifera) pp. 17–22. ]. Its main component is melittin, a powerful detergent that provokes hemolysis of red blood cells [ 30Banks BEC, Shipolini RA. In: Venoms of the Hymenoptera: Biochemical, pharmacological and behavioral aspects. Piek T, editor. London: Academic; 1986. Chemistry and pharmacology of honey bee venom; pp. 329–416. , 31Nabil ZI, Hussein AA, Zalat SM, Rakha MK. Mechanism of action of honey bee (Apis mellifera L.) venom on different types of muscles. Hum Exp Toxicol. 1998;19(3):185–190. doi: 10.1191/096032798678908396.
https://doi.org/10.1191/0960327986789083...
].

Aculeate venoms are used not only to attack prey, but also to defend the colony against foreign individuals [ 32Dijkstra KDB, Rivera AC, Andrés JA. Repeated predation of Odonata by the hornet Vespa crabro (Hymenoptera: Vespidae) Inter J Odonatology. 2001;19(1):17–21. doi: 10.1080/13887890.2001.9748154.
https://doi.org/10.1080/13887890.2001.97...
]. Observations by the present author demonstrate the importance of hornet sting in nest defense against other colonies. Wasps use their venom apparatus effectively when attacking foreign workers that appear in the immediate vicinity of their nest. The toxins released in such cases are potent enough to kill (LD50 = 4.0 mg/kg of hornet body weight – Table  2 ). The determination of LD50 eliminates the popular myth that venomous animals can be resistant to their own venom.

The present results indicate that Vespa crabro venom is toxic for its own species as well as to other insects. Therefore, although both are predators, wasps and hornets as are natural allies against different pest insects and the effectiveness of their venom is proven by the relatively high values of LD50.

Potent venoms represent a source of new insecticidal compounds because they act selectively on their molecular targets. Such toxins affect the invertebrate nervous system and several insecticidal compounds that belong to the class of peptides or polyamine-like compounds have been purified and characterized from the venom of several hymenopterans. Numerous studies are focused on isolating and assessing the lethality of insecticidal toxins from wasps. Their venoms are expected to be used for manufacture of bioinsecticides with high selectivity for different groups of insects [ 29Monteiro MC, Romao PR, Soares AM. Pharmacological perspectives of wasp venom.Protein Pept Lett. 2009;19(8):944–952. doi: 10.2174/092986609788923275.
https://doi.org/10.2174/0929866097889232...
].

Animal venoms have been employed in the analysis of different physiopathological processes, and have also been involved in the design of new therapeutic drugs. Wasp toxins, due to their biological effects, may constitute potential sources of pharmacologically active compounds particularly for neuropharmacology [ 33Schwartz EF, Mourão CB, Moreira KG, Camargos TS, Mortari MR. Arthropod venoms: a vast arsenal of insecticidal neuropeptides. Pept Sc. 2012;19(4):385–405. doi: 10.1002/bip.22100.
https://doi.org/10.1002/bip.22100...
]. Finally, it is worth noting that various components of venoms from wasps and bees can be used for human therapy. A classic example is the honeybee venom, which is widely employed in natural medicine (apitherapy).

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    » https://doi.org/10.1016/j.toxicon.2007.10.003
  • Anderson KE, Eckholm B, Mott BM, Sheehan TH, Hoffman GD. An emerging paradigm of colony health: microbial balance of the honey bee and hive (Apis mellifera) Insectes Sociaux. 2011;19(4):431–444. doi: 10.1007/s00040-011-0194-6.
    » https://doi.org/10.1007/s00040-011-0194-6
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    » https://doi.org/10.1023/A:1020872729671
  • Blum MS, Walker JR, Callahan PS, Novak AF. Chemical, insecticidal and antibiotic properties of fire ant venom. Science. 1958;19(3319):306–307.
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    » https://doi.org/10.2174/092986609788923275
  • Banks BEC, Shipolini RA. In: Venoms of the Hymenoptera: Biochemical, pharmacological and behavioral aspects. Piek T, editor. London: Academic; 1986. Chemistry and pharmacology of honey bee venom; pp. 329–416.
  • Nabil ZI, Hussein AA, Zalat SM, Rakha MK. Mechanism of action of honey bee (Apis mellifera L.) venom on different types of muscles. Hum Exp Toxicol. 1998;19(3):185–190. doi: 10.1191/096032798678908396.
    » https://doi.org/10.1191/096032798678908396
  • Dijkstra KDB, Rivera AC, Andrés JA. Repeated predation of Odonata by the hornet Vespa crabro (Hymenoptera: Vespidae) Inter J Odonatology. 2001;19(1):17–21. doi: 10.1080/13887890.2001.9748154.
    » https://doi.org/10.1080/13887890.2001.9748154
  • Schwartz EF, Mourão CB, Moreira KG, Camargos TS, Mortari MR. Arthropod venoms: a vast arsenal of insecticidal neuropeptides. Pept Sc. 2012;19(4):385–405. doi: 10.1002/bip.22100.
    » https://doi.org/10.1002/bip.22100

Publication Dates

  • Publication in this collection
    2013

History

  • Received
    19 Nov 2012
  • Accepted
    15 Mar 2013
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