TY - JOUR
T1 - Integrative analyses of transcriptomics and metabolomics in Raphidocelis subcapitata treated with clarithromycin
AU - Peng, Jianglin
AU - Guo, Jiahua
AU - Lei, Yuan
AU - Mo, Jiezhang
AU - Sun, Haotian
AU - Song, Jinxi
PY - 2021/3
Y1 - 2021/3
N2 - 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.
AB - 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.
KW - Macrolide antibiotic
KW - Multi-omics
KW - Oxidative phosphorylation
KW - Photosynthesis
KW - Xenobiotic metabolism
KW - Macrolide antibiotic
KW - Multi-omics
KW - Oxidative phosphorylation
KW - Photosynthesis
KW - Xenobiotic metabolism
KW - Macrolide antibiotic
KW - Multi-omics
KW - Oxidative phosphorylation
KW - Photosynthesis
KW - Xenobiotic metabolism
UR - http://www.scopus.com/inward/record.url?scp=85096561371&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85096561371&origin=recordpage
U2 - 10.1016/j.chemosphere.2020.128933
DO - 10.1016/j.chemosphere.2020.128933
M3 - RGC 21 - Publication in refereed journal
SN - 0045-6535
VL - 266
JO - Chemosphere
JF - Chemosphere
M1 - 128933
ER -