ArticleFrontiers in microbiology2015
Phenotype MicroArrays as a complementary tool to next generation sequencing for characterization of tree endophytes.
Article in Frontiers in microbiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed.
- Role of metabolism, resistance, and/or antagonism as drivers of endomicrobiomes assemblage in Origanum heracleoticum L.Communications biology · 2025Article
- Phenothiazines Rapidly Induce Laccase Expression and Lignin-Degrading Properties in the White-Rot FungusJournal of fungi (Basel, Switzerland) · 2023Article
- Differences in the endophytic fungal community and effective ingredients in root of threePeerJ · 2021Article
- How DoInternational journal of molecular sciences · 2020Article
- Assessment of Phenotype Microarray plates for rapid and high-throughput analysis of collateral sensitivity networks.PloS one · 2019Article
- Identification of a Novel Small RNAFrontiers in microbiology · 2018Article
- Pedunculate Oaks (Frontiers in microbiology · 2018Article
- Genome mining of Streptomyces scabrisporus NF3 reveals symbiotic features including genes related to plant interactions.PloS one · 2018Article
- An Endohyphal Bacterium (Frontiers in microbiology · 2017Article
- Article
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5 authors.
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Abstract
There is an increasing need to calibrate microbial community profiles obtained through next generation sequencing (NGS) with relevant taxonomic identities of the microbes, and to further associate these identities with phenotypic attributes. Phenotype MicroArray (PM) techniques provide a semi-high throughput assay for characterization and monitoring the microbial cellular phenotypes. Here, we present detailed descriptions of two different PM protocols used in our recent studies on fungal endophytes of forest trees, and highlight the benefits and limitations of this technique. We found that the PM approach enables effective screening of substrate utilization by endophytes. However, the technical limitations are multifaceted and the interpretation of the PM data challenging. For the best result, we recommend that the growth conditions for the fungi are carefully standardized. In addition, rigorous replication and control strategies should be employed whether using pre-configured, commercial microwell-plates or in-house designed PM plates for targeted substrate analyses. With these precautions, the PM technique is a valuable tool to characterize the metabolic capabilities of individual endophyte isolates, or successional endophyte communities identified by NGS, allowing a functional interpretation of the taxonomic data. Thus, PM approaches can provide valuable complementary information for NGS studies of fungal endophytes in forest trees.
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