Host Specificity of the Parasitic Wasp Anaphes flavipes (Hymenoptera: Mymaridae) and a New Defence in Its Hosts (Coleoptera: Chrysomelidae: Oulema spp.)

. 2020 Mar 10 ; 11 (3) : . [epub] 20200310

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid32164339

Grantová podpora
SVV 260434/2019 Ministry of Education, Youth and Sports of the Czech Republic
243-227357 Grant Agency of Charles University
204069 Charles University Research Centre program
MZe-RO0418 Ministry of Agriculture of the Czech Republic
QK1910281 NAZV MZe ČR

The parasitic wasp Anaphes flavipes (Förster, 1841) (Hymenoptera: Mymaridae) is an important egg parasitoid of cereal leaf beetles. Some species of cereal leaf beetle co-occur in the same localities, but the host specificity of the wasp to these crop pests has not yet been examined in detail. A lack of knowledge of host specificity can have a negative effect on the use of this wasps in biological control programs addressed to specific pest species or genus. In this study, laboratory experiments were conducted to assess the host specificity of A. flavipes for three species of cereal leaf beetles (Oulema duftschmidi Redtenbacher, 1874, Oulema gallaeciana Heyden, 1879 and Oulema melanopus Linnaeus, 1758) in central Europe. For the first time, a new host defence against egg parasitoids occurring in O. gallaeciana from localities in the Czech Republic, a strong dark sticky layer on the egg surface, was found and described. The host specificity of A. flavipes was studied in the locality with the presence of this defence on O. gallaeciana eggs (the dark sticky layer) (Czech Republic) and in a control locality (Germany), where no such host defence was observed. Contrary to the idea that a host defence mechanism can change the host specificity of parasitoids, the wasps from these two localities did not display any differences in that. Respectively, even though it has been observed that eggs with sticky dark layer can prevent parasitization, the overall rate of parasitization of the three species of cereal beetles has not been affected. However, in our view, new host defence can influence the effects of biological control, as eggs of all Oulema spp. in the locality are protected against parasitization from the wasps stuck on the sticky layer of the host eggs of O. gallaeciana.

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Strand M.R., Obrycki J.J. Host specifity of insect parasitoids and predators. BioScience. 1996;46:422–429. doi: 10.2307/1312876. DOI

Godfray H.C.J. Parasitoids: Behavioral and Evolutionary Ecology. Princeton University Press; Princeton, NJ, USA: 1994.

Gross P. Insect behavioral and morphological defenses against parasitoids. Annu. Rev. Entomol. 1993;38:251–273. doi: 10.1146/annurev.en.38.010193.001343. DOI

Tylikinais J.M., Tscharntke T., Klein A.M. Diversity, ecosystem function and stability of parasitoid—Host interactions across a tropical habitat gradient. Ecology. 2006;87:3047–3057. PubMed

Giunti G., Canale A., Messing R.H., Donati E., Stefanini C., Michaud J.P., Benelli G. Parasitoid learning: Current knowledge and implications for biological control. Biol. Control. 2015;90:208–219. doi: 10.1016/j.biocontrol.2015.06.007. DOI

Landis D.A., Wratten S.D., Gurr G.M. Habitat management to conserve natural enemies of Arthropod pests in Agriculture. Annu. Rev. Entomol. 2000;45:175–201. doi: 10.1146/annurev.ento.45.1.175. PubMed DOI

Van Lenteren J.C. Quality Control and Production of Biological Control Agents: Theory and Testing Procedures. CABI Publishing; Wallingford, UK: 2003.

Cock M.J., van Lenteren J.C., Brodeur J., Barratt B.I., Bigler F., Bolckmans K., Cônsoli F.L., Haas F., Mason P.G., Parra J.R.P. Do new access and benefit sharing procedures under the convention on biological diversity threaten the future of biological control? BioControl. 2010;55:199–218. doi: 10.1007/s10526-009-9234-9. DOI

González D., Cervenka V., Moratorio M., Pickett C., Wilson T.L. Longterm control of variegated leafhopper in grape IPM programs will depem on fading, rearing, and releasing effective natural enemies. Calif. Agric. 1988;42:23–25.

Altieri M.A. Agroecological foundations of alternative agriculture in California. Agric. Ecosyst. Environ. 1992;39:23–53. doi: 10.1016/0167-8809(92)90203-N. DOI

Altieri M.A., Nicholls C.I. Biodiversity, Ecosystems Function, and Insect pest Management in Agricultural Systems. In: Collins W.W., Qualset C.O., editors. Biodiversity in Agroecosystems. CRC Press; Boca Raton, FL, USA: 1999. pp. 69–84.

Van Lenteren J.C., Bueno V.H. Augmentative biological control of arthropods in Latin America. BioControl. 2003;48:123–139. doi: 10.1023/A:1022645210394. DOI

Grandgirard J., Hoddle M.S., Petit J.N., Roderick G.K., Davies N. Classical biological control of the glassy-winged sharpshooter, Homalodisca vitripennis, by the egg parasitoid Gonatocerus ashmeadi in the Society, Marqesas and Austral archipelagos of French Polynesia. Biol. Control. 2009;48:155–163. doi: 10.1016/j.biocontrol.2008.10.005. DOI

Rivera A.C., Carbone S.S., Andrés J.A. Life cycle and biological control of the Eucalyptus snout beetle [Coleoptera, Curculionidae] by Anaphes nitens [Hymenoptera, Mymaridae] in north-west Spain. Agric. Forest Entomol. 1999;1:103–109. doi: 10.1046/j.1461-9563.1999.00016.x. DOI

Rivera A.C., Carbone S. The effect of three species of eukalyptus on growth and fecundity of the Eucalyptus snout beetle. Forestry. 2000;73:21–29. doi: 10.1093/forestry/73.1.21. DOI

Hoelmer K.A., Kirk A.A. Selecting arthropod biological control agents against arthropod pests: Can the science be improved to decrease the risk of releasing ineffective agents? Biol. Control. 2005;34:255–264. doi: 10.1016/j.biocontrol.2005.05.001. DOI

McEvoy P.B. Host specificity and biological pest control. BioScience. 1996;46:401–405. doi: 10.2307/1312873. DOI

Krombein K.V., Hurd P.D., Smith D.R., Burks B.D. Catalog of Hymenoptera in America north of Mexico. Vol. 1. Smithsonian Institution Press; Washington, WA, USA: 1979.

Vinson S.B. The general host selection behavior of parasitoid Hymenoptera and a comparison of initial strategies utilized by larvaphagous and oophagous species. Biol. Control. 1998;11:79–96. doi: 10.1006/bcon.1997.0601. DOI

Dawkins R., Krebs J.R. Arms races between and within species. Proc. R. Soc. Lond. B. 1979;205:489–511. PubMed

Kraaijeveld A.R., Van Alphen J.J.M., Godfray H.C.J. The coevolution of host resistance and parasitoid virulence. Parasitology. 1998;116:S29–S45. doi: 10.1017/S0031182000084924. PubMed DOI

Anderson R.C., Paschke J.D. The biology and ecology of Anaphes flavipes [Hymenoptera: Mymaridae], an exotic egg parasite of the cereal leaf beetle. Ann. Entomol. Soc. Am. 1968;61:1–5. doi: 10.1093/aesa/61.1.1. DOI

Samková A., Janšta P., Huber J.T. Anaphes flavipes [Foester, 1841] redescription, neotype designation, and comparison with A. nipponicus Kuwayama, 1932 [Hymenoptera: Chalcidoidea: Mymaridae] Acta Ent. Mus. Nat. Pra. 2017;57:677–711.

Samková A., Hadrava J., Skuhrovec J., Janšta P. Reproductive strategy as a major factor determining female body size and fertility of a gregarious parasitoid. J. Appl. Entomol. 2019;143:441–450. doi: 10.1111/jen.12615. DOI

Dysart R.J., Maltby H.L., Brunson M.H. Larval parasites of Oulema melanopus in Europe and their colonization in the United States. Entomophaga. 1973;18:133–167. doi: 10.1007/BF02372026. DOI

Skuhrovec J.O., Douda M., Zouhar M., Maňasová P., Nový P., Božik M., Klouček P. Insecticidal activity of two formulations of essential oils against the cereal leaf beetle. Acta Agric. Scand. B-Soil Plant. 2018;68:489–495. doi: 10.1080/09064710.2018.1432069. DOI

Deutsch C.A., Tewksbury J.J., Tigchelaar M., Battisti D.S., Merrill S.C., Huey R.B., Naylor R.L. Increase in crop losses to insect pests in a warming climate. Science. 2018;361:916–919. doi: 10.1126/science.aat3466. PubMed DOI

Anderson R.C., Paschke J.D. Factors affecting the postrelease dispersal of Anaphes flavipes [Hymenoptera: Mymaridae], with notes on its postrelease development, efficiency, and emergence. Ann. Entomol. Soc. Am. 1970;63:820–828. doi: 10.1093/aesa/63.3.820. DOI

Maltby H.L., Stehr F.W., Anderson R.C., Moorehead G.E., Barton L.C., Paschke J.D. Establishment in the United States of Anaphes flavipes, an egg parasite of the cereal leaf beetle. J. Econ. Entomol. 1971;64:693–697. doi: 10.1093/jee/64.3.693. DOI

Horváth L., Szabolcs J. Parasitoids of cereal leaf beetles, Oulema Goeze spp., in Hungary. Int. St. Crop. 1992;57:585–589.

Maltby H.L., Burger T.L., Holmes M.C., Dewitt P.R. The use of an unnatural host, Lema trilineata trivittata, for rearing the exotic egg parasite Anaphes flavipes. Ann. Entomol. Soc. Am. 1973;66:298–301. doi: 10.1093/aesa/66.2.298. DOI

Bezděk J., Baselga A. Revision of western Palaearctic species of the Oulema melanopus group, with description of two new species from Europe [Coleoptera: Chrysomelidae: Criocerinae] Acta Ent. Mus. Nat. Pra. 2015;55:273–304.

R. Core Team . R. A Language and Environment for Statistical Computing. R Foundation for Statistical Computing. R Core Team; Vienna, Austria: 2017.

Van de Vijver E., Landschoot S., Van Roie M., Temmerman F., Dillen J., De Ceuleners K., Smagghe G., De Baets B., Haesaert G. Inter-and Intrafield Distribution of Cereal Leaf Beetle Species [Coleoptera: Chrysomelidae] in Belgian Winter Wheat. Environ. Entomol. 2019;48:276–283. doi: 10.1093/ee/nvz002. PubMed DOI

Strand M.R., Pech L.L. Immunological basis for compatibility in parasitoid-host relationships. Annu. Rev. Entomol. 1995;40:31–56. doi: 10.1146/annurev.en.40.010195.000335. PubMed DOI

Schaefer P.W. Ivela auripes Butler in Hokkaido: Behavior and morphology of females; host egg defense mechanism against parasitism by Trichogramma sp. nov. Kontyu. 1983;51:298–307.

Damman H., Cappuccino N. Two forms of egg defence in chrysomelid beetle: Egg clumping and excrement cover. Ecol. Entomol. 1991;16:163–167. doi: 10.1111/j.1365-2311.1991.tb00205.x. DOI

Chabo C.S. Biology and phylogeny of the Cassidinae Gyllenhal sensu lato [tortoise and leaf-mining beetles] [Coleoptera: Chrysomelidae] Bull. Am. Mus. Nat. Hist. 2007;305:1–250. doi: 10.1206/0003-0090(2007)305[1:BAPOTC]2.0.CO;2. DOI

Hoffman G.D., Rao S. Oviposition site selection on oats: The effect of plant architecture, plant and leaf age, tissue toughness, and hardness on cereal leaf beetle, Oulema melanopus. Entomol. Exp. Appl. 2011;141:232–244. doi: 10.1111/j.1570-7458.2011.01194.x. DOI

Stone G.N., Cook J.M. The structure of cynipid oak galls: Patterns in the evolution of an extended phenotype. Proc. R. Soc. Lond. B Biol. 1998;265:979–988. doi: 10.1098/rspb.1998.0387. DOI

Stone G.N., Schönrogge K. The adaptive significance of insect gall morphology. Trends. Ecol. Evol. 2003;18:512–522. doi: 10.1016/S0169-5347(03)00247-7. DOI

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