4.7 Article

Integrative analysis uncovers response mechanism of Pirata subpiraticus to chronic cadmium stress

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 29, Issue 60, Pages 90070-90080

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-022-22043-7

Keywords

Cadmium pollution; Pirata subpiraticus; Enzyme; Gene expression; Protein interaction

Funding

  1. Natural Science Foundation of Hunan Province [2020JJ4427]
  2. Key Project of Education Department of Hunan Province [18A024]

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This study explored the impact of chronic cadmium exposure on a wolf spider and its molecular mechanism. The findings revealed that the spider fed with cadmium-accumulated flies showed reduced enzyme activity and increased malondialdehyde content. Transcriptomic analysis identified differentially expressed genes and down-regulated genes encoding enzymatic indicators. The study also suggested that cadmium stress inhibited the expression of certain genes involved in cuticle and chitin production, and affected hedgehog and FoxO signaling pathways. The interactive network showed that cadmium exposure repressed key biological processes in the spider.
Soil cadmium (Cd) pollution is global environmental pollution and adversely affects paddy field organisms. Wolf spider grants a new insight to evaluate the toxicity triggered by Cd, yet the impact of chronic Cd exposure on the spider and its molecular mechanism remains unclear. The present study found that the wolf spider Pirata subpiraticus fed with Cd-accumulated flies for 5 weeks presented lower catalase, peroxidase, and acetylcholinesterase activities and higher malonaldehyde content than the control spiders (p < 0.05). An in-depth transcriptomic analysis yielded a total of 5995 differentially expressed genes (DEGs, with 3857 up-regulated and 2138 down-regulated genes) from the comparison, and 19 DEGs encoding three enzymatic indicators were down-regulated. Further enrichment analysis indicated that Cd stress could inhibit the expression of cuticle and chitin-encoding genes via the down-regulation of several key enzymes, such as chitin synthase, glutamine-fructose-6-phosphate transaminase, and chitinase. In addition, our findings suggested that hedgehog and FoxO signaling pathways might play an essential role in regulating survival, cell cycle, and autophagy process in spiders, which were primarily down-regulated under Cd stress. An intensely interactive network displayed that Cd exposure could repress key biological processes in P. subpiraticus, particularly peptide metabolic process and peptide biosynthetic process. To sum up, this integrative investigation confirmed an effective bioindicator for assessing Cd-induced toxicity; provided a mass of genes, proteins, and enzymes for further validation; and granted novel perspectives to uncover the molecular responses of spiders to Cd pollution.

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