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Development of a piggyBac transgenic system in Bactrocera dorsalis and its potential for research on olfactory molecular targets

Jie Zhang1, Qi Wang1, Jinxi Yuan2, Zhen Tian1, Shanchun Yan1( ), Wei Liu2( )
School of Forestry/Key Laboratory of Sustainable Forest Ecosystem Management of Ministry of Education, Northeast Forestry University, Harbin 150040, China
Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture/Key Laboratory of Synthetic Biology of Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen 518120, China
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Highlights

  • A stable transgenic system based on piggyBac was developed in Bactrocera dorsalis.

  • The transgenic system can drive the expression of reporter genes in the olfactory organs of B. dorsalis while maintaining normal antennal electrophysiological responses.

  • The transgenic system significantly affects certain olfactory-related behaviors.

Abstract

Chemicals that modify pest behavior are developed to reduce crop damage by altering pest behavior, using specific genes within the olfactory system as molecular targets. The identification of these molecular targets in Bactrocera dorsalis, also known as the functional study of key olfactory genes, relies on CRISPR/Cas9-mediated gene knockout techniques. However, these techniques face limitations when applied to lethal genes. Transgenic technology offers a solution since it enables precise manipulation of gene expression in specific tissues or during certain developmental stages. Consequently, this study developed a piggyBac-mediated transgenic system in B. dorsalis to investigate reporter gene expression in olfactory organs, and assessed the olfactory behavior and antennal electrophysiological responses in transgenic lines. The goal was to assess the potential of this approach for future research on olfactory gene function. A universally expressed housekeeping gene from the BdorActin family was identified using the developmental transcriptome dataset. Its candidate promoter region (BdorActinA3a-1P–2k) was then cloned into the piggyBac plasmid. We subsequently established two stable transgenic lines with specific TTAA insertion sites on chromosomes 4 and 5, consistent with the characteristics of piggyBac transposition. The transgenic strains exhibited essentially normal survival, with hatchability and adult lifespan unaffected, although there were slight reductions in the emergence rate and oviposition capacity. The fluorescent reporter has been successfully expressed in olfactory-related organs, such as the antennae, proboscis, maxillary palp, legs, external genitalia, and brain. The antennal electrophysiological responses to representative chemicals in the transgenic lines were consistent with those of the wild type. However, some olfactory-related behaviors, such as pheromone response and mating, were significantly affected in the transgenic lines. These findings suggest that our system could potentially be applied in future olfactory research, such as driving the expression of exogenous elements that are effective in olfactory organs. However, caution is advised regarding its impact when applied to some olfactory-related behavioral phenotypes.

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Journal of Integrative Agriculture (JIA)
Pages 2311-2326

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Cite this article:
Zhang J, Wang Q, Yuan J, et al. Development of a piggyBac transgenic system in Bactrocera dorsalis and its potential for research on olfactory molecular targets. Journal of Integrative Agriculture (JIA), 2025, 24(6): 2311-2326. https://doi.org/10.1016/j.jia.2024.07.021

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Received: 07 May 2024
Revised: 03 June 2024
Accepted: 13 June 2024
Published: 18 July 2024
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