Testing and optimizing metabarcoding of iDNA from dung beetles to sample mammals in the hyperdiverse Neotropics

Author:

Saranholi Bruno H.12ORCID,França Filipe M.34ORCID,Vogler Alfried P.15ORCID,Barlow Jos6ORCID,Vaz de Mello Fernando Z.7ORCID,Maldaner Maria E.8ORCID,Carvalho Edrielly9ORCID,Gestich Carla C.2ORCID,Howes Benjamin1ORCID,Banks‐Leite Cristina1ORCID,Galetti Pedro M.2ORCID

Affiliation:

1. Department of Life Sciences Imperial College London Ascot UK

2. Departamento de Genética e Evolução Universidade Federal de São Carlos São Carlos Brazil

3. School of Biological Sciences University of Bristol Bristol UK

4. Graduate Program in Ecology, Biological Sciences Institute Federal University of Pará Belém Pará Brazil

5. Department of Life Sciences Natural History Museum London UK

6. Lancaster Environment Centre Lancaster University Lancaster UK

7. Departamento de Biologia e Zoologia Universidade Federal de Mato Grosso, Instituto de Biociências Cuiabá MT Brazil

8. Programa de Pós‐Graduação Em Ecologia e Conservação da Biodiversidade (PPGECB) Universidade Federal de Mato Grosso (UFMT) Cuiabá Brazil

9. Programa de Pós‐Graduação Em Entomologia Instituto Nacional de Pesquisas da Amazônia INPA Manaus Amazonas Brazil

Abstract

AbstractOver the past few years, insects have been used as samplers of vertebrate diversity by assessing the ingested‐derived DNA (iDNA), and dung beetles have been shown to be a good mammal sampler given their broad feeding preference, wide distribution and easy sampling. Here, we tested and optimized the use of iDNA from dung beetles to assess the mammal community by evaluating if some biological and methodological aspects affect the use of dung beetles as mammal species samplers. We collected 403 dung beetles from 60 pitfall traps. iDNA from each dung beetle was sequenced by metabarcoding using two mini‐barcodes (12SrRNA and 16SrRNA). We assessed whether dung beetles with different traits related to feeding, nesting and body size differed in the number of mammal species found in their iDNA. We also tested differences among four killing solutions in preserving the iDNA and compared the effectiveness of each mini barcode to recover mammals. We identified a total of 50 mammal OTUs (operational taxonomic unit), including terrestrial and arboreal species from 10 different orders. We found that at least one mammal‐matching sequence was obtained from 70% of the dung beetle specimens. The number of mammal OTUs obtained did not vary with dung beetle traits as well as between the killing solutions. The 16SrRNA mini‐barcode recovered a higher number of mammal OTUs than 12SrRNA, although both sets were partly non‐overlapping. Thus, the complete mammal diversity may not be achieved by using only one of them. This study refines the methodology for routine assessment of tropical mammal communities via dung beetle ‘samplers’ and its universal applicability independently of the species traits of local beetle communities.

Funder

University of Bristol

Fondation BNP Paribas

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Natural Environment Research Council

Medical Research Council

Publisher

Wiley

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