4.7 Article

16S rRNA metabarcoding unearths responses of rare gut microbiome of fathead minnows exposed to benzo[a]pyrene

期刊

SCIENCE OF THE TOTAL ENVIRONMENT
卷 807, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.scitotenv.2021.151060

关键词

Homeostasis; Next-generation sequencing; Freshwater fish; Persistence organics pollution; Molecular ecology; 16S metagenomics

资金

  1. Global Water Futures program, Canada First Research Excellence Fund [419205]
  2. Global Water Futures program
  3. Banting PostDoctoral Fellowship
  4. Canada Research Chairs Program of the Natural Sciences and Engineering Research Council of Canada (NSERC)

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The study investigated the effects of BaP on the active gut microbiome of juvenile fathead minnows, finding that BaP reduces microbiome diversity, alters community composition, and leads to differential proportions of taxa associated with hydrocarbon degradation and fish health. The results also indicated ecological resistance and/or resilience of gut microbiota to BaP exposure.
Activities of gut microbiomes are often overlooked in assessments of ecotoxicological effects of environmental contaminants. Effects of the polycydic aromatic hydrocarbon, benzo[a]pyrene (BaP) on active gut microbiomes of juvenile fathead minnows (Pimephales promelas) were investigated. Fish were exposed for two weeks, to concentrations of 0, 1, 10, 100, or 1000 mu g BaPg(-1) in the diet. The active gut microbiome was characterized using 16S rRNA metabarcoding to determine its response to dietary exposure of BaP. BaP reduced alpha-diversity at the greatest exposure concentrations. Additionally, exposure to BaP altered community composition of active microbiome and resulted in differential proportion of taxa associated with hydrocarbon degradation and fish health. Neighborhood selection networks of active microbiomes were not reduced with greater concentrations of BaP, which suggests ecological resistance and/or resilience of gut microbiota. The active gut microbiome had a similar overall biodiversity as that of the genomic gut microbiota, but had a distinct composition from that of the 165 rDNA profile. Responses of alpha- and beta-diversities of the active microbiome to BaP exposure were consistent with that of genomic microbiomes. Normalized activity of microbiome via the ratio of rRNA to rDNA abundance revealed rare taxa that became active or dormant due to exposure to BaP. These differences highlight the need to assess both 165 rDNA and rRNA metabarcoding to fully derive bacterial compositional changes resulting from exposure to contaminants. (C) 2021 Elsevier B.V. All rights reserved.

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