4.7 Article

Methodological Approaches Frame Insights into Endophyte Richness and Community Composition

Journal

MICROBIAL ECOLOGY
Volume 82, Issue 1, Pages 21-34

Publisher

SPRINGER
DOI: 10.1007/s00248-020-01654-y

Keywords

Ascomycota; Diversity; Illumina; Media; Metabarcoding; Magnoliophyta; Pinophyta; Pteridophyta

Funding

  1. National Science Foundation [DEB-1541496, DEB-1541538]
  2. Funai Overseas Scholarship
  3. Japanese Student Service Organization
  4. School of Plant Sciences at the University of Arizona
  5. College of Agriculture and Life Sciences at the University of Arizona

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The study found that endophyte richness and composition were consistent across different cultivation media types and largely robust to differences in storage period. Differences in endophyte richness, composition, and taxonomic diversity between culturing and NGS were significant, but both methods revealed host-structured communities. Comparing studies with variations in cultivation media or storage period can help estimate endophyte diversity at larger scales.
Isolating microbes is vital to study microbiomes, but insights into microbial diversity and ecology can be constrained by recalcitrant or unculturable strains. Culture-free methods (e.g., next-generation sequencing, NGS) have become popular in part because they detect greater richness than culturing alone. Both approaches are used widely to characterize microfungi within healthy leaves (foliar endophytes), but methodological differences among studies can constrain large-scale insights into endophyte ecology. We examined endophytes in a temperate plant community to quantify how certain methodological factors, such as the choice of cultivation media for culturing and storage period after leaf collection, affect inferences regarding endophyte communities; how such effects vary among plant taxa; and how complementary culturing and NGS can be when subsets of the same plant tissue are used for each. We found that endophyte richness and composition from culturing were consistent across five media types. Insights from culturing and NGS were largely robust to differences in storage period (1, 5, and 10 days). Although endophyte richness, composition, and taxonomic diversity identified via culturing vs. NGS differed markedly, both methods revealed host-structured communities. Studies differing only in cultivation media or storage period thus can be compared to estimate endophyte richness, composition, and turnover at scales larger than those of individual studies alone. Our data show that it is likely more important to sample more host species, rather than sampling fewer species more intensively, to quantify endophyte diversity in given locations, with the richest insights into endophyte ecology emerging when culturing and NGS are paired.

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