Abstract

Bacterial endosymbionts that produce important phenotypic effects on their hosts are common among plant sap-sucking insects. Aphids have become a model system of insect-symbiont interactions. However, endosymbiont research has focused on a few aphid species, making it necessary to make greater efforts to other aphid species through different regions, in order to have a better understanding of the role of endosymbionts in aphids as a group. Aphid endosymbionts have frequently been studied by PCR-based techniques, using species-specific primers, nevertheless this approach may omit other non-target bacteria cohabiting a particular host species. Advances in high-throughput sequencing technologies are complementing our knowledge of microbial communities by allowing us the study of whole microbiome of different organisms. We used a 16S rRNA amplicon sequencing approach to study the microbiome of aphids in order to describe the bacterial community diversity in introduced populations of the cereal aphids, Sitobion avenae and Rhopalosiphum padi in Chile (South America). An absence of secondary endosymbionts and two common secondary endosymbionts of aphids were found in the aphids R. padi and S. avenae, respectively. Of those endosymbionts, Regiella insecticola was the dominant secondary endosymbiont among the aphid samples. In addition, the presence of a previously unidentified bacterial species closely related to a phytopathogenic Pseudomonad species was detected. We discuss these results in relation to the bacterial endosymbiont diversity found in other regions of the native and introduced range of S. avenae and R. padi. A similar endosymbiont diversity has been reported for both aphid species in their native range. However, variation in the secondary endosymbiont infection could be observed among the introduced and native populations of the aphid S. avenae, indicating that aphid-endosymbiont associations can vary across the geographic range of an aphid species. In addition, we discuss the potential role of aphids as vectors and/or alternative hosts of phytopathogenic bacteria.

Highlights

  • Associations between bacterial endosymbionts and insects are widespread in nature (Gibson & Hunter, 2010)

  • Of the total reads for S. avenae, 98% were classified as Gammaproteobacteria and included mostly bacteria from the Enterobacteriaceae (94.7% of the total reads) (Buchnera aphidicola, Regiella insecticola and Hamiltonella defensa) and to a lesser extent from the Pseudomonadaceae (Pseudomonas) families (3.3% of the total reads)

  • Variation in the secondary endosymbiont infection could be observed among the introduced and native populations of the aphid S. avenae, indicating that aphid-endosymbiont associations can vary across the geographic range of an aphid species

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Summary

Introduction

Associations between bacterial endosymbionts and insects are widespread in nature (Gibson & Hunter, 2010). Secondary or facultative endosymbiotic bacteria are not essential for host survival and reproduction and they are mainly found among the Alphaproteobacteria, Gammaproteobacteria (especially Enterobacteriaceae) and Bacteroidetes (Baumann, 2005; Moran, McCutcheon & Nakabachi, 2008). Secondary endosymbionts may produce ecologically important phenotypic effects on their insect hosts. They can establish facultative mutualistic associations with insects conferring beneficial traits such as protection against natural enemies (review by Oliver et al, 2010; Jaenike et al, 2010; Jiggins & Hurst, 2011), or they can establish parasitic associations that have deleterious effects on host fitness (Werren, Baldo & Clark, 2008)

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