Transcriptome Analysis and Identification of Chemosensory Genes in the Galleria mellonella Larvae

The greater wax moth <i>Galleria mellonella</i> (Lepidoptera: Galleriinae) represents a ubiquitous apicultural pest that poses significant threats to global beekeeping industries. The larvae damage honeybee colonies by consuming wax combs and tunneling through brood frames, consequently destroying critical hive infrastructure including brood-rearing areas, honey storage cells, and pollen reserves. Larval feeding behavior is critically dependent on chemosensory input for host recognition and food selection. In this study, we conducted a transcriptome analysis of larval heads and bodies in <i>G. mellonella</i>. We identified a total of 25 chemosensory genes: 9 odorant binding proteins (OBPs), 1 chemosensory protein (CSP), 5 odorant receptors (ORs), 4 gustatory receptors (GRs), 4 ionotropic receptors (IRs) and 2 sensory neuron membrane proteins (SNMPs). TPM normalization was employed to assess differential expression patterns of chemosensory genes between heads and bodies. Nine putative chemosensory genes were detected as differentially expressed, suggesting their potential functional roles. Subsequently, we quantified expression dynamics via reverse transcription quantitative PCR in major chemosensory tissues (larval heads, adult male and female antennae), revealing adult antennal-biased expression for most chemosensory genes in <i>G. mellonella</i>. Notably, two novel candidates (GmelOBP22 and GmelSNMP3) exhibited particularly high expression in larval heads, suggesting their crucial functional roles in larval development and survival. These findings enhance our understanding of the chemosensory mechanisms in <i>G. mellonella</i> larvae and establish a critical foundation for future functional investigations into its olfactory mechanisms.

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Publication Details

Journal
Insects
Published
2025-09-27
DOI
https://doi.org/10.3390/insects16101004
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Transcriptome Analysis and Identification of Chemosensory Genes in the Galleria mellonella Larvae

Yuan Guo, Chenyang Li, Peng Wang, Lele Sun et al.
Insects
Neurobiology and Insect Physiology Research
article

Transcriptome Analysis and Identification of Chemosensory Genes in the Galleria mellonella Larvae

Yuan Guo, Chenyang Li, Peng Wang, Lele Sun, Jiaoxin Xie, Huiman Zhang
article en

Abstract

The greater wax moth <i>Galleria mellonella</i> (Lepidoptera: Galleriinae) represents a ubiquitous apicultural pest that poses significant threats to global beekeeping industries. The larvae damage honeybee colonies by consuming wax combs and tunneling through brood frames, consequently destroying critical hive infrastructure including brood-rearing areas, honey storage cells, and pollen reserves. Larval feeding behavior is critically dependent on chemosensory input for host recognition and food selection. In this study, we conducted a transcriptome analysis of larval heads and bodies in <i>G. mellonella</i>. We identified a total of 25 chemosensory genes: 9 odorant binding proteins (OBPs), 1 chemosensory protein (CSP), 5 odorant receptors (ORs), 4 gustatory receptors (GRs), 4 ionotropic receptors (IRs) and 2 sensory neuron membrane proteins (SNMPs). TPM normalization was employed to assess differential expression patterns of chemosensory genes between heads and bodies. Nine putative chemosensory genes were detected as differentially expressed, suggesting their potential functional roles. Subsequently, we quantified expression dynamics via reverse transcription quantitative PCR in major chemosensory tissues (larval heads, adult male and female antennae), revealing adult antennal-biased expression for most chemosensory genes in <i>G. mellonella</i>. Notably, two novel candidates (GmelOBP22 and GmelSNMP3) exhibited particularly high expression in larval heads, suggesting their crucial functional roles in larval development and survival. These findings enhance our understanding of the chemosensory mechanisms in <i>G. mellonella</i> larvae and establish a critical foundation for future functional investigations into its olfactory mechanisms.

InsectsVol. 16(10)
Shanxi Agricultural University (CN)
Shanxi Agricultural University
Openalex Percentile: Top 71%
Neurobiology and Insect Physiology Research
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