Integrative analyses of transcriptomics and metabolomics in Raphidocelis subcapitata treated with clarithromycin

Jianglin Peng, Jiahua Guo*, Yuan Lei, Jiezhang Mo, Haotian Sun, Jinxi Song*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

45 Citations (Scopus)

Abstract

As a macrolide antibiotic, clarithromycin (CLA) has a high detection rate in surface water and sewage treatment plant effluents worldwide, posing a considerably high ecological risk to aquatic ecosystem. However, algal transcriptome and metabolome in response to CLA remains largely unknown. In this study, a model alga Raphidocelis subcapitata (R. subcapitata), was exposed to CLA at the concentrations of 0, 3, 10, and 15 μg L−1. Transcriptomic analysis was performed for all the treatment groups, whereas metabolomics was merely applied to 0, 3, and 10 μg L−1 groups because of the limited amount of algal biomass. After 7 d cultivation, the growth of R. subcapitata was significantly hindered at the concentrations above 10 μg L−1. A total of 115, 1833, 2911 genes were differentially expressed in 3, 10, and 15 μg L−1 groups, respectively; meanwhile, 134 and 84 differentially accumulated metabolites (DAMs) were found in the 3 and 10 μg L−1 groups. Specifically, expression levels of DEGs and DAMs related to xenobiotic metabolism, electron transport and energy synthesis were dysregulated, leading to the produced reactive oxygen species (ROS). To confront the CLA-induced injury, the biosynthesis of unsaturated fatty acids and carotenoids of R. subcapitata in 3 μg L−1 were up-regulated; although the photosynthesis was up-regulated in both 10 μg L−1 and 15 μg L−1 groups, the energy synthesis and the ability to resist ROS in these two groups were down-regulated. Overall, this study shed light on the mechanism underlying the inhibitory effects of macrolide antibiotics in algae.
Original languageEnglish
Article number128933
JournalChemosphere
Volume266
Online published11 Nov 2020
DOIs
Publication statusPublished - Mar 2021

Research Keywords

  • Macrolide antibiotic
  • Multi-omics
  • Oxidative phosphorylation
  • Photosynthesis
  • Xenobiotic metabolism

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