Conference Agenda

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Session Overview
Session
CP16.1: Ectoparasites & Vectors 5 min talks
Time:
Thursday, 29/Aug/2024:
4:15pm - 4:30pm

Session Chair: Abdul Ghafar, The University of Melbourne
Session Chair: Kate Mounsey, University of the Sunshine Coast
Location: Plenary Lecture Theatre 1, Uni of Auckland Engineering Complex Bldg, LT 405-470

Lecture Theatre 405-470

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Presentations

Characterization and Comparative Analysis of the Nuclear Genomes of Lucilia cuprina dorsalis and Lucilia cuprina cuprina (Diptera: Calliphoridae).

Shilpa Kapoor1,2, Allison N. Dickey3, Ezra Bailey3, Leticia Baldassio4, Vernon M. Bowles2, Ross S. Hall2, Paul V. Hickner5, Aaron R. Jex6, Brian Wiegmann3, Tatiana T. Torres4, Trent Perry1, Maxwell J. Scott3, Clare A. Anstead2

1Bio21 Molecular Science and Biotechnology Institute, Faculty of Science, The University of Melbourne, Parkville, VIC, Australia; 2Department of Veterinary Biosciences, Faculty of Science, The University of Melbourne, Parkville, VIC, Australia; 3Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, North Carolina, USA; 4Departamento de Genética e Biologia Evolutiva, Instituto de Biociências, Universidade de São Paulo (USP), São Paulo, Brazil; 5USDA-ARS Knipling-Bushland U.S. Livestock Insects Research Laboratory and Veterinary Pest Genomics Center, Kerrville, Texas, USA; 6Population Health and Immunity, Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia

Lucilia cuprina dorsalis is a parasitic blowfly that causes flystrike (myiasis) in many countries worldwide. In Australasia alone, flystrike costs in excess of $320 million each year resulting from production losses and costs of control that rely heavily on the use of insecticides. As a result, resistance in blowfly to almost all insecticides in current use will require the development of further intervention strategies. In contrast, the closely related subspecies, Lucilia cuprina cuprina, is primarily found in urban areas and exhibits limited parasitic behavior. In the present study, the nuclear genomes of Lucilia cuprina dorsalis (Australia) and Lucilia cuprina cuprina (USA) were sequenced and annotated. Comparative genomic analyses revealed important differences in blowfly biology, host interactions and insecticide resistance between the two subspecies. This comparative data will form the basis for downstream analyses investigating novel blowfly specific gene targets for the design of new methods for improved control of flystrike.



Microbiome of the bush tick (Haemaphysalis longicornis): the current state of play revisited

Abdul Ghafar1, Zainab Umar Abdullahi1, Bahar E Mustafa1, Ghazanfar Abbas1, Charles Gauci1, Ard M Nijhof2, Robin Gasser1, Abdul Jabbar1

1Department of Veterinary Biosciences, Melbourne Veterinary School, University of Melbourne, Werribee, 3030, Victoria, Australia; 2Institute of Parasitology and Tropical Veterinary Medicine, Freie Universität Berlin, 10117, Berlin, Germany

Haemaphysalis longicornis is an important vector of several bacterial, protozoal and viral pathogens, and is distributed in Australasia, eastern Asia and the USA. We systematically reviewed the literature on the microbiome of H. longicornis using PRISMA guidelines, with an inclusion criterion focused on studies employing next-generation sequencing techniques. We identified 46 studies from four databases (Web of Science, PubMed, Scopus and CAB Direct) published from six countries. These studies primarily characterised the bacterial components of the tick microbiome, detecting potentially pathogenic bacteria such as Anaplasma, Borrelia, Bartonella, Coxiella, Ehrlichia, Francisella, and Rickettsia as well as endosymbionts, including Arsenophonus-like, Coxiella-like and Rickettsia-like organisms. The virome studies revealed a diverse array of novel viruses, enhancing our understanding of the viral diversity within this tick species. Moreover, few studies have reported significant changes in the microbiome composition due to tick life stage, feeding status and infection. Our findings suggest that the microbiome of H. longicornis plays a potential role in the tick’s life cycle and its vectorial capability. Future investigations should encompass the “non-pathogen” microbiome components of H. longicornis to understand their role in tick biology and the transmission of pathogens to develop sustainable strategies for controlling ticks and tick-borne diseases.



Assessment of the in vitro acaricidal activity of Bravecto® (fluralaner) and a proposed orange oil-based formulation vehicle for the treatment of Sarcoptes scabiei

Kate Mounsey1, Kotaro Takano1, Scott Carver2, Yolandi Vermaak3, Katja Fischer4, Robert Harvey1

1University of the Sunshine Coast, Australia; 2Odum School of Ecology, University of Georgia, Georgia, USA; 3Wombat Support and Rescue NSW/ACT Inc., ACT, Australia; 4Infection and Inflammation Program, QIMR Berghofer Medical Research Institute, QLD, Australia

Sarcoptic mange is a serious animal welfare concern in bare-nosed wombats (Vombatus ursinus). While fluralaner is a promising new treatment, the ‘spot-on’ formulation of fluralaner can limit in-situ treatment delivery. Dilution to a volume for ‘pour-on’ delivery is one solution. This study investigated the acaricidal activity of Bravecto, a proposed essential oil-based diluent (Orange Power®), and two of its active constituents, limonene and citral, against Sarcoptes scabiei. In vitro assays determined the lethal concentration (LC50) and survival time of the mites when exposed to test solutions. All compounds were highly effective at killing mites in vitro. The LC50 values of Bravecto, Orange Power, limonene and citral at 1 hour were 14.61 mg/mL, 4.50%, 26.53% and 0.76%, respectively. A pilot survival assay of mites collected from a mange affected wombat showed survival times of <10 minutes when exposed to Bravecto and Orange Power, and 20 minutes when exposed to moxidectin. These results confirm the acaricidal properties of Bravecto, demonstrate acaricidal properties of Orange Power and support the potential suitability of Orange Power and its active constituents as a diluent for Bravecto. Further research evaluating the physiochemical properties and modes of action of Orange Power constituents would be of value.