4.6 Article

Comparing microscopy and DNA metabarcoding techniques for identifying cyanobacteria assemblages across hundreds of lakes

Journal

HARMFUL ALGAE
Volume 113, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.hal.2022.102187

Keywords

Cyanobacteria; Microscopy; 16s rRNA gene metabarcoding; eDNA; Freshwater lakes; Trophic status; Microcystis genotypes

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC) Canadian Lake Pulse Network
  2. Genome Canada/Genome Quebec
  3. NSERC
  4. Fonds de recherche du Quebec en nature et technologies (FRQNT)
  5. FRQNT
  6. Groupe de recherche interuniversitaire en limnologie (GRIL), McGill University
  7. Liber Ero
  8. Canada Research Chair awards

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Accurate identification of species in an ecosystem is crucial for lake managers and bioassessment programs, especially when monitoring cyanobacteria. DNA-based techniques like metabarcoding offer advantages over traditional light microscopy methods, and can be used to measure aquatic biodiversity more efficiently. A comparison of cyanobacteria assemblages generated by light microscopy and DNA metabarcoding from a dataset of 379 lakes revealed moderate congruence between the two methods at the order level, supporting the use of either method for monitoring eutrophication. The biggest difference between the methods was the detection of picocyanobacteria, which are often underestimated by light microscopy. This suggests that a combined-method strategy should be employed when monitoring trophic systems.
Accurately identifying the species present in an ecosystem is vital to lake managers and successful bioassessment programs. This is particularly important when monitoring cyanobacteria, as numerous taxa produce toxins and can have major negative impacts on aquatic ecosystems. Increasingly, DNA-based techniques such as metabarcoding are being used for measuring aquatic biodiversity, as they could accelerate processing time, decrease costs and reduce some of the biases associated with traditional light microscopy. Despite the continuing use of traditional microscopy and the growing use of DNA metabarcoding to identify cyanobacteria assemblages, methodological comparisons between the two approaches have rarely been reported from a wide suite of lake types. Here, we compare planktonic cyanobacteria assemblages generated by inverted light microscopy and DNA metabarcoding from a 379-lake dataset spanning a longitudinal and trophic gradient. We found moderate levels of congruence between methods at the broadest taxonomic levels (i.e., Order, RV=0.40, p < 0.0001). This comparison revealed distinct cyanobacteria communities from lakes of different trophic states, with Microcystis, Aphanizomenon and Dolichospermum dominating with both methods in eutrophic and hypereutrophic sites. This finding supports the use of either method when monitoring eutrophication in lake surface waters. The biggest difference between the two methods was the detection of picocyanobacteria, which are typically underestimated by light microscopy. This reveals that the communities generated by each method currently are complementary as opposed to identical and promotes a combined-method strategy when monitoring a range of trophic systems. For example, microscopy can provide measures of cyanobacteria biomass, which are critical data in managing lakes. Going forward, we believe that molecular genetic methods will be increasingly adopted as reference databases are routinely updated with more representative sequences and will improve as cyanobacteria taxonomy is resolved with the increase in available genetic information.

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