A New Oomycete Metabarcoding Method Using the rps10 Gene

Author:

Foster Zachary S. L.12,Albornoz Felipe E.1,Fieland Valerie J.1,Larsen Meredith M.2,Jones F. Andrew13,Tyler Brett M.14,Nguyen Hai D. T.5,Burgess Treena I.6,Riddell Carolyn7,Voglmayr Hermann8,Martin Frank N.9,Grünwald Niklaus J.2ORCID

Affiliation:

1. Department of Botany and Plant Pathology, Oregon State University, Corvallis, OR 97331, U.S.A.

2. Horticultural Crops Research Unit, United States Department of Agriculture–Agricultural Research Service, Corvallis, OR 97330, U.S.A.

3. Smithsonian Tropical Research Institute, Balboa, Panama

4. Center for Genome Research and Biocomputing (now named Center for Quantitative Life Sciences), Oregon State University, Corvallis, OR 97331, U.S.A.

5. Agriculture and Agri-Food Canada, Ottawa, ON, K1A 0C6, Canada

6. Phytophthora Science and Management, Harry Butler Institute, Murdoch University, Murdoch, Australia

7. Forest Research, Roslin, Edinburgh, EH25 9SY, U.K.

8. Department of Botany and Biodiversity Research, University of Vienna, Rennweg 14, 1030 Wien, Austria

9. Crop Improvement and Protection Research, Agricultural Research Service, USDA, Salinas, CA 93905, U.S.A.

Abstract

Oomycetes are a group of eukaryotes related to brown algae and diatoms, many of which cause plant and animal diseases. Improved methods are needed for rapid and accurate characterization of oomycete communities using DNA metabarcoding. We have evaluated the mitochondrial 40S ribosomal protein S10 ( rps10) gene as a locus for oomycete metabarcoding and provide primers predicted to amplify this region from all oomycetes based on a wide range of available reference sequences. We evaluated its utility relative to the internal transcribed spacer 1 (ITS1), by sequencing environmental samples and a mock community using Illumina MiSeq. Amplified sequence variants (ASVs) and operational taxonomic units (OTUs) were identified per community. Observed sequences and predicted taxonomy of ASVs and OTUs were compared with the known composition of the mock community. Both rps10 and ITS yielded ASVs with sequences matching 21 of the 24 species in the mock community and matching all 24 when allowing for a 1-bp difference. Taxonomic classifications of ASVs included 23 members of the mock community for rps10 and 17 for ITS1. Sequencing results for the environmental samples suggest that the rps10 locus results in substantially less amplification of nontarget organisms than the ITS1 method. The amplified rps10 region also has higher taxonomic resolution than ITS1, allowing for greater discrimination of closely related species. We present a new website with a searchable rps10 reference database for species identification and all protocols needed for oomycete metabarcoding. The rps10 barcode and methods described herein provide an effective tool for metabarcoding oomycetes using short-read sequencing.

Funder

National Science Foundation

United States Department of Agriculture–Agricultural Research Service

Publisher

Scientific Societies

Subject

Plant Science,Agronomy and Crop Science,Molecular Biology,Ecology,Ecology, Evolution, Behavior and Systematics

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