Abstract

Characterizing trophic networks is fundamental to many questions in ecology, but this typically requires painstaking efforts, especially to identify the diet of small generalist predators. Several attempts have been devoted to develop suitable molecular tools to determine predatory trophic interactions through gut content analysis, and the challenge has been to achieve simultaneously high taxonomic breadth and resolution. General and practical methods are still needed, preferably independent of PCR amplification of barcodes, to recover a broader range of interactions. Here we applied shotgun-sequencing of the DNA from arthropod predator gut contents, extracted from four common coccinellid and dermapteran predators co-occurring in an agroecosystem in Brazil. By matching unassembled reads against six DNA reference databases obtained from public databases and newly assembled mitogenomes, and filtering for high overlap length and identity, we identified prey and other foreign DNA in the predator guts. Good taxonomic breadth and resolution was achieved (93% of prey identified to species or genus), but with low recovery of matching reads. Two to nine trophic interactions were found for these predators, some of which were only inferred by the presence of parasitoids and components of the microbiome known to be associated with aphid prey. Intraguild predation was also found, including among closely related ladybird species. Uncertainty arises from the lack of comprehensive reference databases and reliance on low numbers of matching reads accentuating the risk of false positives. We discuss caveats and some future prospects that could improve the use of direct DNA shotgun-sequencing to characterize arthropod trophic networks.

Highlights

  • Understanding the complexity of trophic interactions and their causes and consequences has been a major focus of ecology since Elton [1] developed the concept, continuing to the present with about 250 scientific papers each year

  • The shotgun-sequencing of the DNA in the gut of predators enabled the identification of a set of taxonomically and functionally diverse foreign taxa, and this information was used to infer a qualitative trophic interaction network (Fig 1)

  • The results provided similar taxonomic breadth but higher taxonomic resolution for prey identification compared to other works using multiplex-PCR or metabarcoding on insect gut contents (Table 3)

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Summary

Introduction

Understanding the complexity of trophic interactions and their causes and consequences has been a major focus of ecology since Elton [1] developed the concept, continuing to the present with about 250 scientific papers each year. Molecular analyses of predator gut contents have become the dominant approach to identify arthropod trophic interactions [3,4,5,6], especially PCR-based methods. Several studies have combined classic single DNA barcoding with next-generation sequencing, referred to as metabarcoding, which has overcome the limitations of Sanger sequencing when working with mixtures of templates, as those present in the gut [7,8]. These PCR-based methods have various limitations that restrict their general applicability and overall scope. Taxonomic biases and inaccurate estimation of the relative abundance of some taxa are common due to marker choice and variation in primer efficiency [11,12,13,14,15,16,17,18]

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