Engineered gut symbiont targets mite and microsporidian parasites and improves honey bee survival

Honey bees (Apis mellifera) have been suffering high annual losses worldwide, in part owing to parasitism. Both the ectoparasite Varroa destructor and the intracellular parasite Nosema ceranae can cause failure of honey bee colonies. Colonies rarely survive when heavily infested by the two parasites simultaneously, and both parasites have developed resistance to small-molecule treatments. Thus, an alternative long-term strategy to combat the parasites is urgently needed. We engineered the honey bee gut symbiont Snodgrassella alvi, inducing self-destruction of parasites by activating their own RNA interference systems. First, we identified genes essential for mite survival and verified these by measuring mite mortality following symbiont-mediated dsRNA delivery. We then engineered S. alvi to express dsRNA targeting Varroa and Nosema concurrently. The symbiont targeting both parasites improves the number of honey bees surviving by 45.6% when bees are simultaneously challenged by Varroa and Nosema parasites in lab conditions. Additionally, the engineered symbiont was transferred to 52% of young and 16% of old honey bees through co-housing with inoculated individuals. Thus, the engineered symbiont offers a potential solution against multiple parasites.

Authors

Institutions

Publication Details

Journal
Proceedings of the Royal Society B Biological Sciences
Published
2025-12-17
DOI
https://doi.org/10.1098/rspb.2025.1743
Primary Topic
Insect and Pesticide Research
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Engineered gut symbiont targets mite and microsporidian parasites and improves honey bee survival

Nancy A. Moran, Xiuxiu Wei, Qiang Huang, Lian Zang et al.
Proceedings of the Royal Society B Biological Sciences
Insect and Pesticide Research
article

Engineered gut symbiont targets mite and microsporidian parasites and improves honey bee survival

Nancy A. Moran, Xiuxiu Wei, Qiang Huang, Lian Zang, Jenkyn Elijah Powell
article en

Abstract

Honey bees (Apis mellifera) have been suffering high annual losses worldwide, in part owing to parasitism. Both the ectoparasite Varroa destructor and the intracellular parasite Nosema ceranae can cause failure of honey bee colonies. Colonies rarely survive when heavily infested by the two parasites simultaneously, and both parasites have developed resistance to small-molecule treatments. Thus, an alternative long-term strategy to combat the parasites is urgently needed. We engineered the honey bee gut symbiont Snodgrassella alvi, inducing self-destruction of parasites by activating their own RNA interference systems. First, we identified genes essential for mite survival and verified these by measuring mite mortality following symbiont-mediated dsRNA delivery. We then engineered S. alvi to express dsRNA targeting Varroa and Nosema concurrently. The symbiont targeting both parasites improves the number of honey bees surviving by 45.6% when bees are simultaneously challenged by Varroa and Nosema parasites in lab conditions. Additionally, the engineered symbiont was transferred to 52% of young and 16% of old honey bees through co-housing with inoculated individuals. Thus, the engineered symbiont offers a potential solution against multiple parasites.

Proceedings of the Royal Society B Biological SciencesVol. 292(2061)
Jiangxi Agricultural University (CN), The University of Texas at Austin (US)
National Natural Science Foundation of China, National Institutes of Health
Openalex Percentile: Top 31%
Insect and Pesticide Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.