文献类型：期刊文献

英文题名：Nanoplastic exposure alters oxidative stress, immunity, and digestive function in Pinctada fucata martensii

作者：Qiu, Jinyu[1];Lu, Fenglan[1];Hao, Ruijuan[2];Liao, Yongshan[3,4,5];Yang, Chuangye[1,4,5];Zheng, Zhe[1,4,5];Deng, Yuewen[1,3,4,5]

机构：[1]Guangdong Ocean Univ, Fisheries Coll, Zhanjiang 524088, Peoples R China;[2]Southern Marine Sci & Engn Guangdong Lab Zhanjiang, Dev & Res Ctr Biol Marine Resources, Zhanjiang 524006, Peoples R China;[3]Guangdong Ocean Univ, Pearl Res Inst, Zhanjiang, Peoples R China;[4]Pearl Breeding & Proc Engn Technol Res Ctr Guangdo, Zhanjiang 524088, Peoples R China;[5]Guangdong Prov Key Lab Aquat Anim Dis Control & Hl, Zhanjiang 524088, Peoples R China

年份：2026

卷号：218

外文期刊名：MARINE ENVIRONMENTAL RESEARCH

收录：SCI-EXPANDED(收录号：WOS:001730749600001)、、EI(收录号：20261320350419)、WOS

基金：This research was funded by Guangdong Basic and Applied Basic Research Foundation (Grant no. 2023A1515030048) , Shellfish & Algae Industry Innovation Team of Guangdong Modern Agricultural Technology System (Grant no. 2025CXTD23) , Research on industrial innovation technology for Guangdong modern marine ranching (Grant no. 2024-MRI-001-03) , and the program for scientific research start-up funds of Guangdong Ocean University (Grant no. 060302022304) .

语种：英文

外文关键词：Pinctada fucata martensii; Nanoplastic toxicity; Oxidative stress; Immune suppression; Transcriptomics

外文摘要：This study investigated the effects of nanoplastic (NP) exposure (0.15, 1.5 and 15 mg/L for 60 days) on Pinctada fucata martensii using integrated biochemical and transcriptomic analyses following exposure and a 7-day recovery period. Results showed that NP exposure induced significant oxidative stress, characterized by concentration- and time-dependent suppression of SOD, GPx, and CAT activities, alongside dynamic alterations in MDA content. A transient rebound in antioxidant enzyme activities was observed on day 15, followed by a significant decline by day 60. Concurrently, immunoenzyme (ACP, AKP) and digestive enzyme (amylase, protease) activities were significantly inhibited. A 7-day recovery period mitigated these disturbances in lower concentration groups (0.15 and 1.5 mg/L), but significant effects persisted in the 15 mg/L group. The differentially expressed genes (DEGs) between CG and EGs at 60 days post-exposure were determined by transcriptome data analysis, which identified 212 upregulated and 95 downregulated DEGs. Similarly, 491 downregulated and 577 upregulated DEGs were identified between the EGs and CG at 67 days post-exposure. Functional analysis revealed that exposure to NPs exerted adverse effects on detoxification, immune response, apoptosis, cytoskeletal dynamics, protein synthesis, and homeostasis in P. f. martensii at 60 days post-exposure. Short-term recovery experiments induced the aberrant expression of an increased number of genes, suggesting that NP exposure exerts long-term effects at a molecular level, potentially resulting in the establishment of a new equilibrium in P. f. martensii. These findings indicate that NP exposure causes substantial physiological and molecular dysregulation, with incomplete recovery at high concentrations, elucidating the underlying toxic mechanisms and potential longterm ecological risks.