Interactions between the entomopathogenic fungus Beauveria bassiana and the Neotropical predator Eriopis connexa (Coleoptera: Coccinellidae): Implications in biological control of pest

• Autorzy: Scorsetti A.C. , Pelizza S. , Fogel M.N. , Vianna F. , Schneider M.I.
• Języki publikacji: EN

Abstrakty

EN

Aphids (Hemiptera: Aphididae) are serious pests of crops causing direct damage by feeding and indirect by the transmission of plant viruses. The use of conventional insecticides for controlling aphids has caused different problems and insecticide resistance. Accordingly, there is more interest in alternative control methods such as biological control by natural enemies for sustainable agricultural management. Among biological control agents, entomopathogenic fungi are one of the most significant microbial pathogens of insects. Also, Coccinellidae, as a major group, is a serious natural enemy. Both larval and adult stages of Coccinellidae feed on different soft-body pests, such as aphids. Eriopis connexa (Germar) (Coleoptera: Coccinellidae) is a common species in agroecosystems of the Neotropical region where it is considered to be a potential control agent. Pathogens and arthropod natural enemies may contribute to the control of phytophagous pests; however, it is important to assess potential interactions within biological control agents that share hosts (intraguild interaction) to evaluate their combined use for pest control. Therefore, the aim of this study was to evaluate the compatibility and interaction (lethal and sublethal effects) between E. connexa and the entomopathogenic fungus Beauveria bassiana (Bals.-Criv.) Vuill. (Ascomycota: Hypocreales). Both are important biological control agents of aphids. The pathogenicity of B. bassiana against larvae, pupae and adults of the predator E. connexa was evaluated, and results showed, that B. bassiana infected the coleopteran. On the other hand, interaction between B. bassiana and the predator was evaluated through infected-prey. The effects of fungus on larvae survival were significantly different when we analyzed the accumulated survival (from first larval instar to adulthood). The daily fecundity was significantly reduced at five days compared to control group. By contrast, no significant differences were observed between the five oviposition days in the rate of hatched eggs. This study shows that despite having received a single dose of the fungus in its life cycle, the population parameters of the predator E. connexa are affected. More studies would be necessary to help identify interactions between microbes and natural enemies to increase and enhance opportunities and further develop biological pest control programs.

Słowa kluczowe

EN

interaction; entomopathogenic fungi; Beauveria bassiana; pathogen-predator interaction; Eriopis connexa; Coleoptera; Coccinellidae; biological control; pest; aphid; Hemiptera; Aphididae

• Wydawca: -
• Czasopismo: Journal of Plant Protection Research
• Rocznik: 2017
• Tom: 57
• Numer: 4
• Opis fizyczny: p.389-395,fig.,ref.

Twórcy

autor

Scorsetti A.C.

• Botanical Institute Carlos Spegazzini (FCNyM-UNLP), Calle 53#477, 1900 La Plata, Buenos Aires, Argentina

autor

Pelizza S.

• Centre of Parasitological and Vector Studies (CEPAVE), CCT La Plata-CONICET-UNLP, Boulevard 120 s/n between 61 and 64, 1900 La Plata, Buenos Aires, Argentina

autor

Fogel M.N.

• Laboratory of Ecotoxicology: Pesticides and Biological Control, Centre of Parasitological and Vector Studies (CEPAVE-CONICET-UNLP), Boulevard 120 s/n between 61 and 64, 1900 La Plata, Buenos Aires, Argentina

autor

Vianna F.

• Botanical Institute Carlos Spegazzini (FCNyM-UNLP), Calle 53#477, 1900 La Plata, Buenos Aires, Argentina

autor

Schneider M.I.

• Laboratory of Ecotoxicology: Pesticides and Biological Control, Centre of Parasitological and Vector Studies (CEPAVE-CONICET-UNLP), Boulevard 120 s/n between 61 and 64, 1900 La Plata, Buenos Aires, Argentina

Bibliografia

• Addinsoft. 2009. XLstat for Excel. Available on: https://www.xlstat.com/es/descargar [Accessed: July 20, 2009].
• Bayissa W., Ekesia S., Mohameda S.A., Kaayab G.P., Wagachab J.M., Hannac R., Maniania N.K. 2016. Interactions among vegetable infesting aphids, the fungal pathogen Metarhizium anisopliae (Ascomycota: Hypocreales) and the predatory coccinellid Cheilomenes lunata (Coleoptera: Coccinellidae). Biocontrol Science and Technology 26 (2): 274–290.DOI: 10.1080/09583157.2015.1099148
• Biddinger D.J., Weber D.C., Hull L.A. 2009. Coccinellidae as predators of mites: Stethorini in biological control. Biological Control 51 (2): 268–283. DOI: https://doi.org/10.1016/j.biocontrol.2009.05.014
• Chen B., Li Z.Y., Feng M.G. 2008. Occurrence of entomopathogenic fungi in migratory alate aphids in Yunnan province of China. BioControl 53: 317–326.
• Cottrell T.E., Shapiro-Ilan D.I. 2003. Susceptibility of a native and an exotic lady beetle (Coleoptera: Coccinellidae) to Beauveria bassiana. Journal of Invertebrate Pathology 84 (2): 137–144. DOI: https://doi.org/10.1016/j.jip.2003.09.003
• Cottrell T.E., Shapiro-Ilan D.I. 2008. Susceptibility of endemic and exotic North American ladybirds (Coleoptera: Coccinellidae) to endemic fungal entomopathogens. European Journal of Entomology 105 (3): 455–460. DOI: 10.14411/eje.2008.058
• de Faria M.R., Wraight S.P. 2007. Mycoinsecticides and mycoacaricides: a comprehensive list with worldwide coverage and international classification of formulation types. Biological Control 43 (3): 237–256. DOI: https://doi.org/10.1016/j.biocontrol.2007.08.001
• Draganova S., Donkova R., Georgieva D. 2008. Impact of strains of entomopathogenic fungi on some main groups of soil microorganisms. Journal of Plant Protection Research 48 (2):169–179. DOI: https://doi.org/10.2478/v10045-008-0020-y
• Duarte Gómez W., Zenner de Polanía I. 2009. Tabla de vida del cucarrón depredador Eriopis connexa (Germar). Revista U.D.C.A Actualidad & Divulgación Científica 12: 147–155.
• Fogel M.N. 2012. Selectividad de insecticidas utilizados en cultivos hortícolas del Cinturón Hortícola Platense sobre el depredador Eriopis connexa en el marco del Manejo Integrado de Plagas. P.Th. Doctoral, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Argentina, 146 pp.
• Fogel M.N., Schneider M.I., Desneux N., Gonzalez B., Ronco A.E. 2013. Impact of the neonicotinoid acetamiprid on immature stages of the predator Eriopis connexa (Coleoptera: Coccinellidae). Ecotoxicology 22 (6): 1063–1071. DOI:10.1007/s10646-013-1094-5
• Foster S.P., Devine G., Devonshire A.L. 2007. Insecticide resistance. p. 261–278. In: “Aphids as Crop Pests” (H.F. Van Emden, R. Harrington, eds.). CAB International, London, UK, 716 pp.
• Goettel M.S., Inglis G.D. 1997. Fungi: Hyphomycetes. p. 213–248. In: “Manual of Techniques in Insect Pathology” (L.A. Lacey, ed.). Academic Press, San Diego, USA.
• Gonzalez F., Tkaczuk C., Dinu M.M., Fiedler Z., Vidal S., Zchori-Fein E., Messelink G.J. 2016. New opportunities for the integration of microorganisms into biological pest control systems in greenhouse crops. Journal of Pest Science 89 (2): 295–311. DOI: 10.1007/s10340-016-0751-x
• Hajek A.E., Butler L. 2000. Predicting the host range of entomopathogenic fungi. p. 263–273. In: “Nontarget Effects of Biological Control” (P.A. Follett, J.J. Duan, eds.). Kluwer Academic Publisher, Dordrecht, NL.
• Hogenhout S.A., Ammar E.D., Whitfield A.E., Redinbaugh M.G. 2008. Insect vector interactions with persistently transmitted viruses. Annual Review of Phytopathology 46: 327–359.
• Jaber L.R., Araj S.E. 2017. Interactions among endophytic fungal entomopathogens (Ascomycota: Hypocreales), the green peach aphid Myzus persicae Sulzer (Homoptera: Aphidi dae), and the aphid endoparasitoid Aphidius colemani Viereck (Hymenoptera: Braconidae). Biological Control. DOI:10.1016/j.biocontrol.2017.04.005
• Jarrahi A., Safavi S.E. 2016. Sublethal effects of Metarhizium anisopliae on life table parameters of Habrobracon hebetor parasitizing Helicoverpa armigera larvae at different time intervals. BioControl 61 (2): 167–175. DOI 10.1007/s10526-015-9707-y
• Lacey L.A., Brooks W.M. 1997. Initial handling and diagnosis of diseased insects. p. 1–15. In: “Manual of Techniques in Insect Pathology” (L.A. Lacey, ed.). Academic Press, San Diego, USA.
• Lacey L.A., Grzywacz D., Shapiro-Ilan D.I., Frutos R., Brownbridge M., Goettel M.S. 2015. Insect pathogens as biological control agents: Back to the future. Journal of Invertebrate Pathology 132: 1–41. DOI: 10.1016/j.jip.2015.07.009
• Martins I.C.F., Silva R.J., Alencar J.R.D., Silva K.P., Cividanes F.J., Duarte R.T., Agostini L.T., Polanczyk C. 2014. Interactions between the entomopathogenic fungi Beauveria bassiana (Ascomycota: Hypocreales) and the aphid parasitoid Diaeretiella rapae (Hymenoptera: Braconidae) on Myzus persicae (Hemiptera: Aphididae). Journal of Economic Entomology 107 (3): 933–938. DOI: https://doi.org/10.1603/EC13542
• Mesquita A.L.M., Lacey L.A. 2001. Interactions among the entomopathogenic fungus, Paecilomyces fumosoroseus (Deuteromycotina: Hyphomycetes), the parasitoid, Aphelinus asychis (Hymenoptera: Aphelinidae) and their aphid host. Biological Control 22 (1): 51–59. DOI: https://doi.org/10.1006/bcon.2001.0950
• Mohammed A.A., Hatcher P.E. 2017. Combining entomopathogenic fungi and parasitoids to control the green peach aphid Myzus persicae. Biological Control 110: 44–55. DOI: http://dx.doi.org/10.1016/j.biocontrol.2017.03.012
• Nalepa C.A., Weir A. 2007. Infection of Harmonia axyridis (Coleoptera: Coccinellidae) by Hesperomyces virescens (Ascomycetes: Laboulbeniales): role of mating status and aggregation behavior. Journal of Invertebrate Pathology 94 (3): 196–203. DOI: 10.1016/j.jip.2006.11.002
• Obrycki J.J., Harwood J.D., Kring T.J., O’Neil R.J. 2009. Aphidophagy by Coccinellidae: application of biological control in agroecosystems. Biological Control 51 (2): 244–254. DOI:https://doi.org/10.1016/j.biocontrol.2009.05.009
• Ormond E., Thomas A.P.M., Pell J.K., Freeman S.N., Roy H.E. 2011. Avoidance of a generalist entomopathogenic fungus by the ladybird, Coccinella septempunctata. FEMS Microbiology Ecology 77: 229–237. DOI: 10.1111/j.1574-6941.2011.01100.x
• Pelizza S.A., Elíades L.A., Saparrat M.C.N., Cabello M.N., Scorsetti A.C., Lange C.E. 2012. Screening of argentine native fungal strains for biocontrol of the grasshopper Tropidacris collaris: relationship between fungal pathogenicity and chitinolytic enzyme activity. World Journal of Microbiology and Biotechnology 28 (4): 1359–1366. DOI: 10.1007/s11274-011-0935-8
• Pell J.K., Eilenberg J., Hajek A.E., Steinkraus D.C. 2001. Biology, ecology, and pest management potential of Entomophthorales. p. 71–153. In: “Fungal Biological Control Agents: Progress, Problems and Potential” (T.M. Butt, C. Jackson, N. Magan, eds.). CAB International. Wallingford, Oxon.
• Pell J.K., Vandenberg J.D. 2002. Interactions among the aphid Diuraphis noxia, the entomopathogenic fungus Paecilomyces fumosoroseus and the coccinellid Hippodamia convergens. Biocontrol Science and Technology 12 (2): 217–224.DOI: http://dx.doi.org/10.1080/09583150120124478
• Powell W., Pell J.K. 2007. Biological Control. p. 469–513. In: “Aphids as Crop Pests” (R. Harrington, H. van Emden, eds.). CABI International, 717 pp.
• Rashki M., Kharazi-pakdel A., Allahyari H., van Alphen J.J.M. 2009. Interactions among the entomopathogenic fungus, Beauveria bassiana (Ascomycota: Hypocreales), the parasitoid, Aphidius matricariae (Hymenoptera: Braconidae), and its host, Myzus persicae (Homoptera: Aphididae). Biological Control 50 (3): 324–328. DOI: https://doi.org/10.1016/j.biocontrol.2009.04.016
• Riddick E.W., Cottrell T.E., Kidd K.A. 2009. Natural enemies of the Coccinellidae: Parasites, pathogens, and parasitoids. Biological Control 51 (2): 306–312. DOI: https://doi.org/10.1016/j.biocontrol.2009.05.008
• Roy H., Pell J.K. 2000. Interactions between entomopathogenic fungi and other natural enemies: Implications for biological control. Biocontrol Science and Technology 10 (6): 737–752.DOI: http://dx.doi.org/10.1080/09583150020011708
• Roy H., Steinkraus D.C., Eilinberg J., Hajek A.E., Pell J.K. 2006. Bizarre interactions and endgames: entomopathogenic fungi and their arthropod hosts. Annual Review of Entomology 51: 331–357.
• Sarmento R.A., Pallini A., Venzon M., Fonseca de Souza F., Molina-Rugama A.J., Lima de Olivera C. 2007. Functional response of the predator Eriopis connexa (Coleoptera Coccinellidae) to different prey types. Brazilian Archives of Biology and Technology 50: 121–126.
• Scorsetti A.C., Humber R.A., García J.J., López Lastra C.C. 2007. Natural occurrence of entomopathogenic fungi (Zygomycetes: Entomophthorales) of aphid (Hemiptera: Aphididae) pests of horticultural crops in Argentina. BioControl 52: 641–655. DOI 10.1007/s10526-006-9045-1
• Scorsetti A.C., Maciá A., Steinkraus D.C., López Lastra C.C. 2010. Prevalence of Pandora neoaphidis (Zygomycetes: Entomophthorales) infecting Nasonovia ribisnigri (Hemiptera: Aphididae) on lettuce crops in Argentina. Biological Control 52: 46–50. DOI: https://doi.org/10.1016/j.biocontrol.2009.09.005
• Scorsetti A.C., Pelizza S., Cabello M.N. 2012. New records of hypocrealean fungi infecting aphids and whiteflies: pathogenicity against Myzus persicae and interaction with its predator Eriopis connexa. Biocontrol Science and Technology 22 (9): 1099–1105. DOI: http://dx.doi.org/10.1080/09583157.2012.710320
• Silva R.B., Cruz I., Zanuncio J.C., Figueiredo M.L.C., Canevari G.C., Pereira A.G., Serrão J.E. 2013. Biological aspects of Eriopis connexa (Germar) (Coleoptera: Coccinellidae) fed on different insect pests of maize (Zea mays L.) and sorghum [Sorghum bicolor L. (Moench.)]. Brazilian Journal of Biology 73 (2): 419–424. DOI: 10.1590/S1519-69842013000200025
• Simelane D.O., Steinkraus D.C., Kring T.J. 2008. Predation rate and development of septempunctata L. influenced by Neozygites fresenii-infected cotton aphid prey. Biological Control 44: 128–135. DOI: https://doi.org/10.1016/j.biocontrol.2007.10.004
• Steenberg T., Harding S. 2009. Entomopathogenic fungi recorded from the harlequin ladybird, Harmonia axyridis. Journal of Invertebrate Pathology 102: 88–89. DOI: https://doi.org/10.1016/j.jip.2009.07.002
• Toledo A.V., Remes Lenicov A.M.M., López Lastra C.C. 2008. Host range findings on Beauveria bassiana and Metarhizium anisopliae (Ascomycota: Hypocreales) in Argentina. Boletín de la Sociedad Argentina de Botánica 43 (3–4): 211–220.

Identyfikatory

DOI

10.1515/jppr-2017-0053