Abstract

The Australian sheep blowfly, Lucilia cuprina, is an ecto-parasite that causes significant economic losses in the sheep industry. Emerging resistance to insecticides used to protect sheep from this parasite is driving the search for new drugs that act via different mechanisms. Inhibitors of histone deacetylases (HDACs), enzymes essential for regulating eukaryotic gene transcription, are prospective new insecticides based on their capacity to kill human parasites. The blowfly genome was found here to contain five HDAC genes corresponding to human HDACs 1, 3, 4, 6 and 11. The catalytic domains of blowfly HDACs 1 and 3 have high sequence identity with corresponding human and other Dipteran insect HDACs (Musca domestica and Drosophila melanogaster). On the other hand, HDACs 4, 6 and 11 from the blowfly and the other Dipteran species showed up to 53% difference in catalytic domain amino acids from corresponding human sequences, suggesting the possibility of developing HDAC inhibitors specific for insects as desired for a commercial insecticide. Differences in transcription patterns for different blowfly HDACs through the life cycle, and between the sexes of adult flies, suggest different functions in regulating gene transcription within this organism and possibly different vulnerabilities. Data that supports HDACs as possible new insecticide targets is the finding that trichostatin A and suberoylanilide hydroxamic acid retarded growth of early instar blowfly larvae in vitro, and reduced the pupation rate. Trichostatin A was 8-fold less potent than the commercial insecticide cyromazine in inhibiting larval growth. Our results support further development of inhibitors of blowfly HDACs with selectivity over human and other mammalian HDACs as a new class of prospective insecticides for sheep blowfly.

Highlights

  • The Australian sheep blowfly, Lucilia cuprina, is an important parasite of sheep in Australia

  • In insects the effects of histone deacetylases (HDACs) inhibitors have been reported on gene transcription patterns in Drosophila melanogaster and on the activity of individual recombinant HDAC enzymes (Foglietti et al, 2006; Cho et al, 2005)

  • Examination of the sheep blowfly genome revealed the presence of five HDAC genes with sequences corresponding to human HDAC1, HDAC3, HDAC4 (Class IIa), HDAC6 (Class IIb), and HDAC11 (Class IV)

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Summary

Introduction

The Australian sheep blowfly, Lucilia cuprina, is an important parasite of sheep in Australia. Adult L. cuprina females are attracted to sheep odours, those associated with bacterial infections in damp fleece, or areas of fleece or skin soiled by urine or faeces (Watts et al, 1981; Emmens and Murray, 1983). In these regions of high humidity, each female fly lays approximately 200 eggs per batch. Histone deacetylase (HDAC) enzymes are essential regulators of gene transcription in all eukaryotic organisms, catalysing removal of acetyl groups from lysine sidechains of nucleosomal histone proteins (Kou and Allis, 1998). We were interested in the potential of HDAC inhibitors to be a new class of insecticides

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