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Genetic variability among Paecilomyces fumosoroseus isolates from various geographical and host insect origins based on the rDNA-ITS regions

Published online by Cambridge University Press:  13 November 2002

Jacques FARGUES
Affiliation:
Centre de Biologie et de Gestion des Populations (CBGP), Institut National de la Recherche Agronomique (INRA), Campus International de Baillarguet, CS 30 016, 34988 Montferrier-sur-Lez Cedex, France
Marie-Claude BON
Affiliation:
European Biological Control Laboratory, USDA-ARS, Campus International Agropolis de Montferrier-Baillarguet, 34980 Montferrier-sur-Lez, France
Sylvie MANGUIN
Affiliation:
Centre de Biologie et de Gestion des Populations (CBGP), Institut de Recherche pour le Developpement (IRD), Campus International de Baillarguet, CS 30 016, 34988 Montferrier-sur-Lez Cedex, France
Yvonne COUTEAUDIER
Affiliation:
Unité de Recherche en Lutte Biologique, INRA-Versailles, La Minière, 78285 Guyancourt, France Present address: INRA, Direction scientifique Plante et Produits du Végétal, 147 rue de l'Université, 75338, Paris Cedex 07, France.
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Abstract

The entomopathogenic hyphomycete Paecilomyces fumosoroseus is a promising candidate for biocontrol of economically important agricultural pests. Assessment of genetic relatedness of this species appears to be essential to gain insight into the monitoring of such biocontrol products. Intraspecific variation within the internal transcribed spacer region of the ribosomal RNA gene (rDNA-ITS) was studied in 48 isolates of P. fumosoroseus. These strains were isolated from different geographical and biological origins, more particularly from the silverleaf whitefly, Bemisia tabaci-argentifolii (Homoptera: Aleyrodidae), a major insect pest in field and greenhouse crops. PCR amplification of the ITS1-5.8S-ITS2 rDNA region followed by restriction analysis of the PCR products underlined the overall highly variable nature of this region. Digestion with the six endonucleases AluI, HaeIII, Hin6I, HpaII, NdeII, and SmaI allowed the separation of the isolates into three distinct groups. The group 1, representing 25 isolates, is composed of strains isolated only from the host B. tabaci-argentifolii. By contrast, the group 3 is more diffuse as it included strains from various insect host and geographical origins. Phylogenetic analysis of rDNA-ITS sequence data strongly supported the conclusions of the PCR-RFLP analysis and recognized three monophyletic groups within the P. fumosoroseus complex. The high level of polymorphism within the P. fumosoroseus species is discussed in the light of their biological origin.

Type
Research Article
Copyright
© The British Mycological Society 2002

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