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CHARACTERIZATION AND VIRULENCE OF A BRAZILIAN ISOLATE OF METARHIZIUM FLAVOVIRIDE GAMS AND ROZSYPAL (HYPHOMYCETES)

Published online by Cambridge University Press:  31 May 2012

B.P. Magalhães
Affiliation:
Genetic Resources and Biotechnology Research Center, (CENARGEN/EMBRAPA) PO Box 0231210849-970, Brasília, DF, Brazil
M. Faria
Affiliation:
Genetic Resources and Biotechnology Research Center, (CENARGEN/EMBRAPA) PO Box 0231210849-970, Brasília, DF, Brazil
M.S. Tigano
Affiliation:
Genetic Resources and Biotechnology Research Center, (CENARGEN/EMBRAPA) PO Box 0231210849-970, Brasília, DF, Brazil
B.W.S. Sobral
Affiliation:
California Institute of Biological Research (CIBR), 11099 North Torrey Pines Road, Suite 300, La Jolla, California, USA 92037
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Abstract

A new isolate of Metarhizium flavoviride Gams and Rozsypal (Hyphomycetes) (CG 423) found in Northeast Brazil infecting Schistocerca pallens (Thunberg) was identified using arbitrarily primed PCR. Cluster analysis of DNA markers revealed a high level of homogeneity (>83% similarity) among the Brazilian (CG 423) and two other M. flavoviride isolates from Nigeria (CG 366 = IMI 330189) and Australia (CG 291). However, M. flavoviride isolates were very distinct when compared with two isolates of Metarhizium anisopliae (Metschnikoff) Sorokin (6.4% similarity). Bioassays showed that strain CG 423 is as virulent as other isolates of M. flavoviride (CG 291, CG 366), M. anisopliae (CG 087), and Beauveria bassiana (Balsamo) Vuillemin (CG 425) against the grasshopper Rhammatocerus schistocercoides (Rehn) (Orthoptera: Acrididae), an important pest in Central Brazil. However, the Brazilian isolate of M. flavoviride (CG 423) is more virulent than the Brazilian isolate of B. bassiana (CG 250). Because conidia used in bioassays were formulated in soybean oil containing 5% kerosene, the effect of the kerosene present in the oil formulation was tested. Kerosene (0–10%) did not affect the virulence (P > 0.3) of M. flavoviride against R. schistocercoides. The native isolate of M. flavoviride (CG 423) is now being developed as a mycoinsecticide against grasshoppers in Brazil.

Résumé

Un nouvel isolat de Metarhizium flavoviride Gams et Rozsypal (Hyphomycètes) (CG 423), virulent contre Schistocerca pallens (Thunberg), a été identifié dans le nord-est du Brésil au moyen de la réaction en chaîne des polymérases déclenchée arbitrairement. Une analyse des groupements des marqueurs d'ADN a révélé l'existence d'une forte homogénéité (>83%) entre l'isolat brésilien (CG 423) et deux autres isolats de M. flavoviride provenant du Nigeria (CG 366 = IMI 330189) et d'Australie (CG 291). Cependant les isolats de M. flavoviride se sont avérés très distincts de deux isolats de Metarhizium anisopliae (Metschnikoff) Sorokin (6,4% de similarité). Des expériences ont démontré que le CG 423 est aussi virulent contre le criquet Rhammatocerus schistocercoides (Rehn) (Orthoptera: Acrididae), un important ravageur du centre du Brésil, que le CG 366, un agent bioinsecticide en cours de préparation contre les orthoptères d'Afrique. Les conidies utilisées au cours des expériences ont été mises en émulsion dans de l'huile de soja contenant 5% de kérosène. L'effet du kérosène contenu dans la préparation à l'huile a été étudié. Le kérosène (0–10%) n'affecte pas la virulence (P > 0,3) de M. flavoviride contre R. schistocercoides. L'isolat indigène de M. flavoviride (le CG 423) est en cours de raffinement pour être éventuellement utilisé comme mycoinsecticide contre les orthoptères du Brésil. [Traduit par la Rédaction]

Type
Research Article
Copyright
Copyright © Entomological Society of Canada 1997

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References

Bidochka, M.J., McDonald, M.A., St. Leger, R.J. and Roberts, D.W.. 1994. Differentiation of species and strains of entomopathogenic fungi by random amplification of polymorphic DNA (RAPD). Current Genetics 25: 107113.Google Scholar
Bridge, P.D., Williams, M.A.J., Prior, C. and Paterson, R.R.M.. 1993. Morphological, biochemical and molecular characteristics of Metarhizium anisopliae and M. flavoviride. Journal of General Microbiology 139: 11631169.Google Scholar
Cosenza, G.W., Curti, J.B. and Paro, H.. 1990. Comportamento do gafanhoto Rhammatocerus schistocercoides (Rehn, 1906) no Mato Grosso. Pesquisa Agropecuánia Brasileira. 25(2): 173180.Google Scholar
Fegan, M., Maclean, J.M., Irwin, J.A.G., Samuels, K.D.Z., Holdom, D.G. and Li, D.P.. 1993. Random amplified polymorphic DNA markers reveal a high degree of genetic diversity in the entomopathogenic fungus Metarhizium anisopliae var. anisopliae. Journal of General Microbiology 139: 20752081.Google Scholar
Goettel, M.S., Johnson, D.L. and Inglis, G.D.. 1995. The role of fungi in the biological control of grasshoppers. Canadian Journal of Botany 73 (Suppl. 1): S1–S75.Google Scholar
Goettel, M.S., Magalh, B.ães, and Gama, G.. 1995. Palatability and efficacy of a bait formulation of Metarhizium flavoviride against the grasshopper Rhammatocerus schistocercoides. Proceedings of the Society for Invertebrate Pathology Annual Meeting, Ithaca, NY, July 1995 28: 2324.Google Scholar
Greathead, D.J. 1992. Natural enemies of tropical locusts and grasshoppers: Their impact and potential as biological control agents, pp. 4–7 in Lomer, C.J., and Prior, C. (Eds.), Biological Control of Locusts and Grasshoppers. IITA/CAB International, Wallingford, UK. 394 pp.Google Scholar
Jaronski, S.T. and Goettel, M.S.. 1997. Development of Beauveria bassiana for control of grasshoppers and locusts. pp. 225–237 in Goettel, M.S., and Johnson, D.L. (Eds.), Microbial Control of Grasshoppers and Locusts. Memoirs of the Entomological Society of Canada 171: 400 pp.Google Scholar
Lecoq, M. and Pierozzi, I. Jr., 1994. Rhammatocerus schistocercoides (Rhen, 1906), criquet ravageur de l'état du Mato Grosso (Bresil). Essay de synthèse bibliographique. CCE: Bruxelas/CIRAD-GERDAT-PRIFAS: Montpelier/EMBRAPA-NMA: Campinas. 89 pp.Google Scholar
Lomer, C.J., Prior, C. and Kooyman, C.. 1997. Development of Metarhizium spp. for the control of grasshoppers and locusts, pp. 265–286 in Goettel, M.S., and Johnson, D.L. (Eds.), Microbial Control of Grasshoppers and Locusts. Memoirs of the Entomological Society of Canada 171: 400 ppGoogle Scholar
Magalhäes, B.P. 1994. Biological control of grasshoppers, pp. 2327in Simpósio de Controle Biológico, 4, Gramado, RS. Anais: Conferências e Mesas Redondas. EMBRAPA/CPACT.Google Scholar
Milner, R.J. 1997. Metarhizium flavoviride (FI985) as a promising mycoinsecticide for Australian acridids. pp. 287–300 in Goettel, M.S., and Johnson, D.L. (Eds.), Microbial Control of Grasshoppers and Locusts. Memoirs of the Entomological Society of Canada 171: 400 pp.Google Scholar
Rohlf, F.J. 1993. Numerical Taxonomy and Multivariate Analysis System. Applied Biostatistics Inc., Setauket, NY. NTSYS-PC v. 18.Google Scholar
Sneath, P.H.A. and Sokal, R.R.. 1973. Numerical Taxonomy. Freeman, San Francisco, CA.Google Scholar
Sobral, B.W.S. and Honeycutt, R.J.. 1993. High output genetic mapping in polyploids using PCR-generated markers. Theoretical and Applied Genetics 86: 105112.Google Scholar
Tigano-Milani, M.S., Gomes, A.C.M.M. and Sobral, B.W.S.. 1995. Genetic variability of Brazilian isolates of the entomopathogenic fungus Metarhizium anisopliae. Journal of Invertebrate Pathology 65: 206210.Google Scholar
Welsh, J. and McClelland, M.. 1990. Fingerprinting genomes using PCR with arbitrary primers. Nucleic Acids Research 18: 72137218.Google Scholar
Williams, J.G.K., Kubelik, A.R., Livak, K.J., Rafalski, J.A. and Tingey, S.V.. 1990. DNA polymorphism amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Research 18: 65316535.Google Scholar