Responses of zebrafish (Danio rerio) cells to antibiotic erythromycin stress at the subcellular levels

Meng Yang, Hongbing Fu, Wen-Xiong Wang*

*Corresponding author for this work

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

16 Citations (Scopus)

Abstract

Erythromycin (ERY) is one of the most used antibiotics frequently detected in different aquatic environments and may bring burdens to aquatic ecosystems. However, the impacts of antibiotics on aquatic systems other than the antibiotic resistance genes remain largely unknown. In the present study, the responses to ERY exposure at the subcellular-organelle levels were for the first time investigated and imaged over 24 h. Exposure to ERY hampered the zebrafish (Danio rerio) cell growth and decreased the cell viability in a time-dependent mode. Meanwhile, exposure to a low concentration of ERY (73.4 μg L−1) induced reactive oxygen species (ROS) overproduction and lysosomal damage following lysosomal alkalization and swelling. In turn, the lysosomal stress was the major driver of altering the ROS level, superoxide dismutase (SOD) activity, and glutathione (GSH) content. Subsequently, mitochondria displayed dysfunction such as increased mitochondrial ROS, impaired mitophagy, and induced mitochondria-driven apoptosis, as well as impaired mitochondrial electron transport chain and loss of membrane potential. These results collectively demonstrated the subcellular sensitive machinery responses to ERY stress at environmentally relevant and slightly higher sub-lethal concentrations. ERY may induce switching from autophagy to apoptosis with corresponding changes in lysosomal activity, antioxidant activity, and mitochondrial activity. The findings provided important information on the physiological and subcellular responses of fish cells to ERY.
Original languageEnglish
Article number158727
JournalScience of the Total Environment
Volume853
Online published13 Sept 2022
DOIs
Publication statusPublished - 20 Dec 2022

Funding

We thank the anonymous reviewers for their comments. This study was supported by the Hong Kong Research Grants Council (T21-604/19-R, C6014-20W) and the Natural Science Foundation of China (No. 22076159).

Research Keywords

  • Apoptosis
  • ERY toxicity
  • Lysosomal pH
  • Mitophagy
  • Subcellular response

RGC Funding Information

  • RGC-funded

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