Egg–larval opiine parasitoids (Hym., Braconidae) of tephritid fruit fly pests do not attack the flowerhead-feeder Trupanea dubautiae (Dipt., Tephritidae)

Abstract:  We investigated the potential impact of three opiine tephritid fruit fly parasitoids: Fopius arisanus (Sonan), Fopius caudatus (Szépligeti) and Fopius ceratitivorus Wharton, on the non-target native Hawaiian tephritid, Trupanea dubautiae (Bryan), infesting flowerheads of the endemic Asteraceae shrub Dubautia raillardioides Hillebrand. The three species are the only known opiine fruit fly parasitoids that attack host eggs (but occasionally attack first instars). F. arisanus , which originated in southeast Asia, is now widely established in Hawaii and elsewhere in the world, while the other two are African species currently in quarantine in Hawaii. In the laboratory, field-collected flowerheads of D. raillardioides containing T. dubautiae eggs and first instar larvae were exposed to naïve female wasps of each of the three Fopius species in the absence (no-choice test) or presence (choice test) of papaya fruit infested with eggs of the Mediterranean fruit fly Ceratitis capitata (Wiedemann), the parasitoids' normal host. All three Fopius species visited the papaya fruit much more often than the flowerheads, and displayed normal ovipositional responses (probing and stinging) on the fruit in the choice test. None of the three parasitoid species showed ovipositional responses to flowerheads in either choice or no-choice tests. As a result, not a single T. dubautiae egg or larva was attacked by any of the three parasitoids, indicating that these parasitoids of pest tephritids are unable to recognize the microhabitats of flowerhead-feeding tephritids. The results suggest minimal risk of non-target impact in these biological control agents.     

Extraordinary conservation of entire chromosomes in insects over long evolutionary periods

Comparison of the genomes of different Drosophila species has shown that six different chromosomes, the so‐called ‘‘Muller elements,” constitute the building blocks for all Drosophila species. Here, we confirm previous results suggesting that this conservation of the Muller elements extends far beyond Drosophila, to at least tephritid fruit flies, thought to have diverged from drosophilids 60–70 mYr ago. Less than 10 percent of genes differ in chromosome location between the two insect groups. Within chromosomes, however, the order is highly scrambled, as expected from the comparison between Drosophila species. The data also support the notion that the sex chromosomes of tephritid flies originated from an ancestor of the dot chromosome 4 of Drosophila. Overall, therefore, no new chromosome has been created for perhaps a billion generations over the two evolutionary lines. This stability at the chromosome level, which appears to extend to all Diptera including mosquitoes, is in stark contrast to other groups such as mammals, birds, fish and plants, in which chromosome numbers and organization vary enormously among species that have diverged over much fewer generations.     

CRISPR/Cas9‐mediated mutagenesis of the white gene in the tephritid pest Bactrocera tryoni

The Queensland fruit fly, Bactrocera tryoni (Froggatt), is a polyphagous horticultural pest in Australia that is capable of causing significant damage to more than 100 different host fruits and vegetables. Chemical applications and ecological control strategies, such as the sterile insect technique (SIT), are commonly used to suppress established populations and eradicate invasive outbreaks following migration. The recently published B. tryoni draft genome provides new opportunities to identify candidate genes for targeted genome modification in order to generate advanced genetic strains for management using sterile insect strategies. Here, we demonstrate CRISPR/Cas‐mediated mutagenesis in B. tryoni through generating a series of frame‐shift mutations in the ATP‐dependent binding cassette transporter, white, causing a classic white‐eye phenotype. This work establishes methods for CRISPR/Cas genome editing in tephritids and demonstrates its potential for developing genetic sexing strains which could be used for SIT‐based pest control.