Abstract

BackgroundGut microbiota affects tephritid (Diptera: Tephritidae) fruit fly development, physiology, behavior, and thus the quality of flies mass-reared for the sterile insect technique (SIT), a target-specific, sustainable, environmentally benign form of pest management. The Queensland fruit fly, Bactrocera tryoni (Tephritidae), is a significant horticultural pest in Australia and can be managed with SIT. Little is known about the impacts that laboratory-adaptation (domestication) and mass-rearing have on the tephritid larval gut microbiome. Read lengths of previous fruit fly next-generation sequencing (NGS) studies have limited the resolution of microbiome studies, and the diversity within populations is often overlooked. In this study, we used a new near full-length (> 1300 nt) 16S rRNA gene amplicon NGS approach to characterize gut bacterial communities of individual B. tryoni larvae from two field populations (developing in peaches) and three domesticated populations (mass- or laboratory-reared on artificial diets).ResultsNear full-length 16S rRNA gene sequences were obtained for 56 B. tryoni larvae. OTU clustering at 99% similarity revealed that gut bacterial diversity was low and significantly lower in domesticated larvae. Bacteria commonly associated with fruit (Acetobacteraceae, Enterobacteriaceae, and Leuconostocaceae) were detected in wild larvae, but were largely absent from domesticated larvae. However, Asaia, an acetic acid bacterium not frequently detected within adult tephritid species, was detected in larvae of both wild and domesticated populations (55 out of 56 larval gut samples). Larvae from the same single peach shared a similar gut bacterial profile, whereas larvae from different peaches collected from the same tree had different gut bacterial profiles. Clustering of the Asaia near full-length sequences at 100% similarity showed that the wild flies from different locations had different Asaia strains.ConclusionsVariation in the gut bacterial communities of B. tryoni larvae depends on diet, domestication, and horizontal acquisition. Bacterial variation in wild larvae suggests that more than one bacterial species can perform the same functional role; however, Asaia could be an important gut bacterium in larvae and warrants further study. A greater understanding of the functions of the bacteria detected in larvae could lead to increased fly quality and performance as part of the SIT.

Highlights

  • Gut microbiota affects tephritid (Diptera: Tephritidae) fruit fly development, physiology, behavior, and the quality of flies mass-reared for the sterile insect technique (SIT), a target-specific, sustainable, environmentally benign form of pest management

  • Of full-length reads generated by dual molecular tagging All of the reads derive from fragments of DNA that underwent dual molecular tagging and amplification

  • The predominant bacteria identified belonged to only three families, suggesting selective factors define what bacteria are present in the gut of B. tryoni larvae

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Summary

Introduction

Gut microbiota affects tephritid (Diptera: Tephritidae) fruit fly development, physiology, behavior, and the quality of flies mass-reared for the sterile insect technique (SIT), a target-specific, sustainable, environmentally benign form of pest management. The Queensland fruit fly, Bactrocera tryoni (Tephritidae), is a significant horticultural pest in Australia and can be managed with SIT. In Australia, the Queensland fruit fly, Bactrocera tryoni (Tephritidae), is a significant economic pest that causes losses due to damage of horticultural produce, while restricting domestic and international market access [1]. B. tryoni originated from tropical and subtropical regions of Australia, its range has expanded further down the east coast of Australia with increasing detections further inland It is established in New South Wales and Victoria, apart from the Greater Sunraysia Pest-Free Area [6]. Over time and with repeated releases of sterile flies, the pest population is suppressed or may be eradicated within the release area

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