Transcriptome Analysis of the Brain and Gnathal Ganglion Reveals Feeding-Mediated Genes in Helicoverpa armigera Larvae

Despite the central role of the gustatory nervous system in regulating feeding behavior in the larvae of the major agricultural pest <i>Helicoverpa armigera</i>, the systemic molecular basis of this process is largely unknown. To investigate the molecular basis, we performed RNA-seq on dissected brains and gnathal ganglion (GNG) from fifth-instar larvae, revealing 944 differentially expressed genes (DEGs) that are potentially involved in feeding behaviors. Bioinformatic analyses revealed significant enrichment of these DEGs in pathways including "taste transduction", "neuroactive ligand-receptor interaction", and "feeding behavior". Furthermore, 41 candidate genes closely associated with feeding behaviors were screened, including neuropeptides, neuropeptide receptors, gustatory receptors, and feeding-mediated proteins. Phylogenetic analyses demonstrated that these key genes are evolutionarily conserved. Quantitative real-time PCR (qPCR) results confirmed that most of these candidate genes were significantly upregulated during the fifth instar stage, and their expression was further enhanced under starvation conditions (<i>p</i> < 0.05). Our study presents the first systemic feeding-mediated transcriptomic profile in the insect central nervous system and identifies key feeding-mediated genes in <i>H. armigera</i> larvae. These findings advance our understanding of the molecular basis of feeding in Lepidopteran pests and offer potential target genes for developing gustatory-based pest control strategies.

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Publication Details

Journal
Biomolecules
Published
2026-02-04
DOI
https://doi.org/10.3390/biom16020250
Primary Topic
Neurobiology and Insect Physiology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Transcriptome Analysis of the Brain and Gnathal Ganglion Reveals Feeding-Mediated Genes in Helicoverpa armigera Larvae

Guiying Xie, Rongmei Lin, Xinyu Zhao, Shuting Chen et al.
Biomolecules
Neurobiology and Insect Physiology Research
article

Transcriptome Analysis of the Brain and Gnathal Ganglion Reveals Feeding-Mediated Genes in Helicoverpa armigera Larvae

Guiying Xie, Rongmei Lin, Xinyu Zhao, Shuting Chen, Longlong Sun, Qingbo Tang, Wenbo Chen
article en

Abstract

Despite the central role of the gustatory nervous system in regulating feeding behavior in the larvae of the major agricultural pest <i>Helicoverpa armigera</i>, the systemic molecular basis of this process is largely unknown. To investigate the molecular basis, we performed RNA-seq on dissected brains and gnathal ganglion (GNG) from fifth-instar larvae, revealing 944 differentially expressed genes (DEGs) that are potentially involved in feeding behaviors. Bioinformatic analyses revealed significant enrichment of these DEGs in pathways including "taste transduction", "neuroactive ligand-receptor interaction", and "feeding behavior". Furthermore, 41 candidate genes closely associated with feeding behaviors were screened, including neuropeptides, neuropeptide receptors, gustatory receptors, and feeding-mediated proteins. Phylogenetic analyses demonstrated that these key genes are evolutionarily conserved. Quantitative real-time PCR (qPCR) results confirmed that most of these candidate genes were significantly upregulated during the fifth instar stage, and their expression was further enhanced under starvation conditions (<i>p</i> < 0.05). Our study presents the first systemic feeding-mediated transcriptomic profile in the insect central nervous system and identifies key feeding-mediated genes in <i>H. armigera</i> larvae. These findings advance our understanding of the molecular basis of feeding in Lepidopteran pests and offer potential target genes for developing gustatory-based pest control strategies.

BiomoleculesVol. 16(2)
Henan Academy of Agricultural Sciences (CN), Henan Agricultural University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Henan Province
Zero hunger
Openalex Percentile: Top 68%
Neurobiology and Insect Physiology Research
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