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Maintaining Biological Cultures and Measuring Gene Expression in Aphis nerii: A Non-model System for Plant-insect Interactions
Published on: August 31, 2018
Mobile elements create strain-level variation in the services conferred by an aphid symbiont
Vilas Patel1, Nicole Lynn-Bell1, Germain Chevignon2
1Department of Entomology, University of Georgia, Athens, Georgia, USA.
Mobile genetic elements in Hamiltonella defensa, a bacterial symbiont of pea aphids, drive strain variation and influence aphid defense against parasitoids. This highlights the role of symbiont diversity in arthropod evolution.
Area of Science:
- Microbial Ecology
- Evolutionary Biology
- Insect-Microbe Interactions
Background:
- Heritable, facultative symbionts are prevalent in arthropods, often conferring host defense capabilities.
- Mobile genetic elements (MGEs) are key drivers of genomic variation and phenotypic diversity in symbionts, despite their reduced genomes.
- Strain-level variation in the aphid symbiont Hamiltonella defensa, specifically its bacteriophages (APSEs), is linked to differences in aphid defense against parasitoids.
Purpose of the Study:
- To disentangle the contributions of Hamiltonella defensa genotype and APSE type to aphid anti-parasitoid defense.
- To investigate the evolutionary dynamics of APSEs within H. defensa and their role in rapid adaptation.
- To explore the genomic basis of coinfection with Fukatsuia symbiotica and its potential impact on H. defensa.
Main Methods:
- Comparative genomics of H. defensa isolates with varying APSE types.
- Phenotypic analysis of aphid defense levels correlated with specific APSE virulence modules.
- Genomic analysis to identify genetic elements associated with coinfection by F. symbiotica.
Main Results:
- Aphid protection levels were directly correlated with APSE virulence module type, independent of H. defensa genotype.
- Evidence suggests APSEs undergo repeated horizontal transfer within H. defensa, facilitating rapid evolution of defense mechanisms.
- Genomic data did not support nutritional interactions as the primary driver for coinfection with F. symbiotica, but bacteriocin plasmids were unique to co-infecting strains.
Conclusions:
- Strain diversity within symbionts, coupled with horizontal gene transfer of MGEs and symbionts, significantly contributes to the rapid evolutionary adaptation of arthropods.
- APSEs are crucial in mediating strain-level variation in symbiont-mediated defense.
- The co-evolutionary dynamics of symbionts and their hosts are shaped by mobile genetic elements and horizontal transfer events.
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