4.7 Article

Tylosin toxicity in the alga Raphidocelis subcapitata revealed by integrated analyses of transcriptome and metabolome: Photosynthesis and DNA replication-coupled repair

期刊

AQUATIC TOXICOLOGY
卷 239, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.aquatox.2021.105964

关键词

Macrolide antibiotic; Omics; Chlorophyll metabolism; Photosynthesis; DNA replication; Energy metabolism

资金

  1. Second Tibetan Plateau Scientific Expedition and Research Program [2019QZKK1003]
  2. National Natural Science Foundation of China [42101077]
  3. Key Research and Development Plan of Shaanxi Province [2020SF-387, 2020SF-400]
  4. ShaanXi Thousand Talent Program for Young Outstanding Scientists [334041900007]
  5. Scientific Research Foundation of the Water Conservancy Department of Shaanxi Province [2020slkj-13]

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This study elucidated the molecular mechanisms of Tylosin toxicity in Raphidocelis subcapitata, revealing impacts on pathways related to photosynthesis, DNA replication, and energy metabolism. Photosynthesis was identified as the most sensitive target of Tylosin toxicity in the algae species.
Tylosin (TYN) is widely used in veterinary prophylactic as a macrolide and frequently detected in the surface water. Previous studies showed that exposure to TYN caused suppression of chlorophyll biosynthesis and inhibition of photosynthesis at the physiological level, associated with reduced growth performances in algae, but the molecular mechanisms remain unknown, especially at environmental exposure levels. The present study elucidated the underlying molecular mechanism(s) of TYN toxicity in a model green alga Raphidocelis subcapitata using approaches of transcriptomics and metabolomics. Following a 7-day exposure, algal growth performances were reduced by 26.3% and 58.3% in the 3 (an environmentally realistic level) and 400 mu g L-1 TYN treatment group, respectively. A total of 577 (99) and 5438 (180) differentially expressed genes (differentially accumulated metabolites) were identified in algae treated with 3 and 400 mu g L-1 TYN, respectively. Signaling pathways including photosynthesis - antenna protein, porphyrin and chlorophyll metabolism, carbon fixation in photosynthetic organisms, and DNA replication were altered in the 400 mu g L-1 TYN treatment, while photosynthesis and DNA replication were the shared pathways in both TYN treatments. The metabolomic data further suggest that molecular pathways related to photosynthesis, DNA replication-coupled repair and energy metabolism were impaired. Photosynthesis was identified as the most sensitive target of TYN toxicity in R. subcapitata, in contrast to protein synthesis inhibition caused by TYN in bacteria. This study provides novel mechanistic information of TYN toxicity in R. subcapitata.

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