The diapriid wasp Trichopria drosophilae Perkins (Hymenoptera:Diapriidae) attacks and develops in puparia of the common fruit fly, Drosophila melanogaster Meigen (Diptera: Drosophilidae). Host recognition of T. drosophilae was studied using both a morphological and behavioural approach. Scanning and electron microscopical observations of female parasitoid antennae showed the presence of two types of sensilla, which we named MGS1 and MGS2. The former are present on the ventral side of both the apical (A11) and sub-apical (A12) antennomeres, while the latter occur only on A12. Ultrastructural features suggest a gustatory function for these sensilla. Arena bioassays using intact or antennaectomised females and intact host puparia showed that MGS2 are necessary for achieving host acceptance. Further bioassays, where the host’s anterior spiracles were covered with wax, led to a very low level of host acceptance. We suggest that the secretion produced by glands associated with the anterior spiracles act as a contact kairomone, which has to be perceived by MGS2 in order to elicit host recognition. The removal of both the female apical antennomeres (A12) led to the failure of the parasitoid to recognize its host.
Host recognition in the pupal parasitoid Trichopria drosophilae: a morpho-functional approach
ROMANI, Roberto;ISIDORO, Nunzio;BIN, Ferdinando;
2002
Abstract
The diapriid wasp Trichopria drosophilae Perkins (Hymenoptera:Diapriidae) attacks and develops in puparia of the common fruit fly, Drosophila melanogaster Meigen (Diptera: Drosophilidae). Host recognition of T. drosophilae was studied using both a morphological and behavioural approach. Scanning and electron microscopical observations of female parasitoid antennae showed the presence of two types of sensilla, which we named MGS1 and MGS2. The former are present on the ventral side of both the apical (A11) and sub-apical (A12) antennomeres, while the latter occur only on A12. Ultrastructural features suggest a gustatory function for these sensilla. Arena bioassays using intact or antennaectomised females and intact host puparia showed that MGS2 are necessary for achieving host acceptance. Further bioassays, where the host’s anterior spiracles were covered with wax, led to a very low level of host acceptance. We suggest that the secretion produced by glands associated with the anterior spiracles act as a contact kairomone, which has to be perceived by MGS2 in order to elicit host recognition. The removal of both the female apical antennomeres (A12) led to the failure of the parasitoid to recognize its host.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
