Gut microbiota modulates aversive learning and memory of honeybees (Apis mellifera)

Growing evidence indicates that host behaviors are regulated by the gut-brain interaction. In honeybees (Apis mellifera), a critical defensive behavior is the sting extension reflex. However, it remains unclear how the gut microbiota affects aversive learning and memory of this behavior. Here we demonstrate that the normal gut microbiota contributes to aversive learning and memory of the sting extension reflex in honeybees. Metabolomics analysis reveals that the gut microbiota affects tyrosine metabolism of the gut and hemolymph. Oral reintroduction of Enterococcus faecium or Enterococcus faecalis restores aversive learning and memory of microbiota-free honeybees, with an increase in their brain dopamine levels by supplying exogenous tyrosine. Conversely, applying fluphenazine, which decreases brain dopamine levels, weakens aversive learning and memory of honeybees in normal hives. These findings provide insights into the role of gut bacteria in regulating aversive learning and memory in honeybees, highlighting beneficial effects of the gut microbiota on the cognitive behaviors of social insects.

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Publication Details

Journal
Nature Communications
Published
2025-12-18
DOI
https://doi.org/10.1038/s41467-025-67586-8
Citations
1
Primary Topic
Insect and Pesticide Research
Type
article
Field-Weighted Citation Impact
1.67

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article

Gut microbiota modulates aversive learning and memory of honeybees (Apis mellifera)

Pingli Dai, David C. Lyon, Tong An, Hongyang Zhao et al.
1 citations
Nature Communications
Insect and Pesticide Research
1.67
article

Gut microbiota modulates aversive learning and memory of honeybees (Apis mellifera)

Pingli Dai, David C. Lyon, Tong An, Hongyang Zhao, Yuan Ge, Wangjiang Feng, Li Zhang, Yong‐Jun Liu, Danyang Zhao, Jing Li
article en
1 citations

Abstract

Growing evidence indicates that host behaviors are regulated by the gut-brain interaction. In honeybees (Apis mellifera), a critical defensive behavior is the sting extension reflex. However, it remains unclear how the gut microbiota affects aversive learning and memory of this behavior. Here we demonstrate that the normal gut microbiota contributes to aversive learning and memory of the sting extension reflex in honeybees. Metabolomics analysis reveals that the gut microbiota affects tyrosine metabolism of the gut and hemolymph. Oral reintroduction of Enterococcus faecium or Enterococcus faecalis restores aversive learning and memory of microbiota-free honeybees, with an increase in their brain dopamine levels by supplying exogenous tyrosine. Conversely, applying fluphenazine, which decreases brain dopamine levels, weakens aversive learning and memory of honeybees in normal hives. These findings provide insights into the role of gut bacteria in regulating aversive learning and memory in honeybees, highlighting beneficial effects of the gut microbiota on the cognitive behaviors of social insects.

Nature CommunicationsVol. 16(1)
Chinese Academy of Sciences (CN), University of California, Irvine (US), Chinese Academy of Agricultural Sciences (CN), Research Center for Eco-Environmental Sciences (CN), Institute of Apiculture Research (CN), University of Chinese Academy of Sciences (CN), China Agricultural University (CN)
Chinese Academy of Agricultural Sciences
Openalex Percentile: Top 12%
Insect and Pesticide Research
1.67
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