Metabolomic Profiling Reveals Heat-Responsive Metabolic Markers in Honey Bee Workers Under Contrasting Diets
- 1Department of SmartBio, College of Life and Health Science, Kyungsung University, Busan 48434, Republic of Korea
- 2Department of Life Sciences and Convergence Research Center for Insect Vectors (CRCIV), Incheon National University R&D Complex, 265 Harmony-ro, Yeonsu-gu, Incheon 22014, Republic of Korea
- 3College of Fisheries Science, Pukyong National University, 45 Yongso-ro, Nam-gu, Busan 48513, Republic of Korea
Abstract
Acute heat exposure challenges honey bee (Apis mellifera) workers, yet the associated small-molecule response and its relationship to nutritional status remain incompletely resolved. Workers were conditioned for 7 days on bee bread plus sucrose (B+S) or sucrose alone (S), maintained at 37 °C or exposed to 45 °C for 3 h, and thorax–abdomen metabolites were profiled by untargeted Ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF/MS). Three independent cages were used per diet × temperature group, with 15 workers per cage pooled to generate one cage-level biological replicate (n = 3 per group). Putative metabolite annotation used accurate-mass (10 ppm) and isotope-pattern matching against METLIN and the Agilent Personal Compound Database and Library (PCDL), followed by manual curation, without tandem mass spectrometry (MS/MS) o or authentic-standard confirmation. After statistical filtering and biological curation, 149 heat-responsive metabolite annotations were retained under B+S and 123 under S. Targeted re-extraction of proteinogenic amino acids from the same raw files recovered 16 common peaks across all samples. Fifteen increased at 45 °C in both diets, whereas proline decreased; 14 of 16 showed a larger fold change under B+S. Phenylalanine-related metabolism showed the strongest convergence across targeted amino-acid analysis, untargeted phenylpyruvate detection, and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment. Lipid-class responses also differed descriptively between diets, with a bias toward decreased free fatty acyls under B+S and decreased phospholipids under S. These findings define coordinated metabolic markers of acute heat exposure in worker bees and show that, within the targeted amino-acid dataset, response magnitudes were generally larger under B+S while retaining the same overall direction.
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BibTeX
@article{jang2026metabolomic,
title = {{Metabolomic Profiling Reveals Heat-Responsive Metabolic Markers in Honey Bee Workers Under Contrasting Diets}},
author = {Hyeonji Jang and Hyunjee Kim and Olga Frunze and Hyung-Wook Kwon and Boyun Kim and Jewon Jung},
journal = {International Journal of Molecular Sciences},
year = {2026},
month = oct,
doi = {10.3390/ijms27209237},
url = {https://www.mdpi.com/1422-0067/27/20/9237},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Metabolomic Profiling Reveals Heat-Responsive Metabolic Markers in Honey Bee Workers Under Contrasting Diets
AU - Hyeonji Jang
AU - Hyunjee Kim
AU - Olga Frunze
AU - Hyung-Wook Kwon
AU - Boyun Kim
AU - Jewon Jung
PY - 2026
DA - 2026/10/01
JO - International Journal of Molecular Sciences
DO - 10.3390/ijms27209237
UR - https://www.mdpi.com/1422-0067/27/20/9237
AB - Acute heat exposure challenges honey bee (Apis mellifera) workers, yet the associated small-molecule response and its relationship to nutritional status remain incompletely resolved. Workers were conditioned for 7 days on bee bread plus sucrose (B+S) or sucrose alone (S), maintained at 37 °C or exposed to 45 °C for 3 h, and thorax–abdomen metabolites were profiled by untargeted Ultra-performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UPLC-QTOF/MS). Three independent cages were used per diet × temperature group, with 15 workers per cage pooled to generate one cage-level biological replicate (n = 3 per group). Putative metabolite annotation used accurate-mass (10 ppm) and isotope-pattern matching against METLIN and the Agilent Personal Compound Database and Library (PCDL), followed by manual curation, without tandem mass spectrometry (MS/MS) o or authentic-standard confirmation. After statistical filtering and biological curation, 149 heat-responsive metabolite annotations were retained under B+S and 123 under S. Targeted re-extraction of proteinogenic amino acids from the same raw files recovered 16 common peaks across all samples. Fifteen increased at 45 °C in both diets, whereas proline decreased; 14 of 16 showed a larger fold change under B+S. Phenylalanine-related metabolism showed the strongest convergence across targeted amino-acid analysis, untargeted phenylpyruvate detection, and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment. Lipid-class responses also differed descriptively between diets, with a bias toward decreased free fatty acyls under B+S and decreased phospholipids under S. These findings define coordinated metabolic markers of acute heat exposure in worker bees and show that, within the targeted amino-acid dataset, response magnitudes were generally larger under B+S while retaining the same overall direction.
SN - 1422-0067
ER -