Rhizobacteria regulate colonising <scp> <i>Sitobion avenae</i> </scp> aphid populations through induced host resistance and alter plant volatiles promoting early parasitoid recruitment on barley ( <scp> <i>Hordeum vulgare</i> </scp> )

BACKGROUND: Soil rhizobacteria can enhance crop resistance to insect herbivores and influence higher trophic interactions, offering potential for sustainable pest management. Aphids are sap-feeding pests that alter plant physiology, reduce yields and transmit plant viruses. Previous work has shown that inoculation with specific rhizobacterial strains can reduce aphid fitness in short-term trials. Here, we extend this approach by testing effects across three plant growth stages in glasshouse experiments, monitoring natural colonisation by aphids and their natural enemies in an outdoor pot study, and conducting host-choice and volatile profile assays. RESULTS: Under glasshouse conditions, rhizobacterial inoculation consistently suppressed aphid populations, although the magnitude of effects varied with plant variety, bacterial strain and aphid genotype. In our experiments, suppression was strongest when aphids were confined to individual plants, consistent with enhanced host resistance. In outdoor trials, inoculated plants were colonised earlier by parasitoid wasps and harboured more parasitised aphids, independent of aphid density. Volatile assays confirmed that bacterial inoculation altered plant volatile profiles, suggesting a mechanism for enhanced parasitoid attraction. One aphid genotype showed a preference for uninoculated plants in host-choice assays, indicating potential genotype-specific avoidance of induced defences. CONCLUSION: These findings demonstrate that rhizobacteria can influence both bottom-up and top-down regulation of aphid populations through plant-mediated mechanisms. By simultaneously enhancing host resistance and natural enemy attraction, rhizobacterial inoculants offer a promising biological tool for integrated pest management. Understanding context dependency among plant, microbe and insect genotypes will be crucial for translating these interactions into effective and predictable field applications. © 2026 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Authors

Institutions

Publication Details

Journal
Pest Management Science
Published
2026-04-10
DOI
https://doi.org/10.1002/ps.70783
Primary Topic
Insect-Plant Interactions and Control
Type
article
Field-Weighted Citation Impact
0.00

Funders

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

Rhizobacteria regulate colonising Sitobion avenae aphid populations through induced host resistance and alter plant volatiles promoting early parasitoid recruitment on barley ( Hordeum vulgare )

Angharad M. R. Gatehouse, Sharon E. Zytynska, Megan Parker
Pest Management Science
Insect-Plant Interactions and Control
article

Rhizobacteria regulate colonising Sitobion avenae aphid populations through induced host resistance and alter plant volatiles promoting early parasitoid recruitment on barley ( Hordeum vulgare )

Angharad M. R. Gatehouse, Sharon E. Zytynska, Megan Parker
article en

Abstract

BACKGROUND: Soil rhizobacteria can enhance crop resistance to insect herbivores and influence higher trophic interactions, offering potential for sustainable pest management. Aphids are sap-feeding pests that alter plant physiology, reduce yields and transmit plant viruses. Previous work has shown that inoculation with specific rhizobacterial strains can reduce aphid fitness in short-term trials. Here, we extend this approach by testing effects across three plant growth stages in glasshouse experiments, monitoring natural colonisation by aphids and their natural enemies in an outdoor pot study, and conducting host-choice and volatile profile assays. RESULTS: Under glasshouse conditions, rhizobacterial inoculation consistently suppressed aphid populations, although the magnitude of effects varied with plant variety, bacterial strain and aphid genotype. In our experiments, suppression was strongest when aphids were confined to individual plants, consistent with enhanced host resistance. In outdoor trials, inoculated plants were colonised earlier by parasitoid wasps and harboured more parasitised aphids, independent of aphid density. Volatile assays confirmed that bacterial inoculation altered plant volatile profiles, suggesting a mechanism for enhanced parasitoid attraction. One aphid genotype showed a preference for uninoculated plants in host-choice assays, indicating potential genotype-specific avoidance of induced defences. CONCLUSION: These findings demonstrate that rhizobacteria can influence both bottom-up and top-down regulation of aphid populations through plant-mediated mechanisms. By simultaneously enhancing host resistance and natural enemy attraction, rhizobacterial inoculants offer a promising biological tool for integrated pest management. Understanding context dependency among plant, microbe and insect genotypes will be crucial for translating these interactions into effective and predictable field applications. © 2026 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Pest Management Science
University of Liverpool (GB), Newcastle College (GB), Newcastle University (GB)
Biotechnology and Biological Sciences Research Council, Natural Environment Research Council
Openalex Percentile: Top 17%
Insect-Plant Interactions and Control
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.