School of Life and Environmental Sciences, Hangzhou Normal University, Hangzhou, 311121, China.
Zhejiang Qiushi Environmental Monitoring Co., Ltd, Hangzhou, 310018, China.
Environ Pollut. 2022 Nov 1;312:120029. doi: 10.1016/j.envpol.2022.120029. Epub 2022 Aug 28.
Pollution caused by per- and polyfluoroalkyl substances (PFASs) has become a major global concern. The association between PFAS-induced hepatotoxicity and gut microbiota in amphibians, particularly at environmentally relevant concentrations, remains elusive. Herein we exposed male black-spotted frogs (Rana nigromaculata) to 1 and 10 μg/L waterborne perfluorooctanoic acid (PFOA), perfluorooctanesulfonic acid (PFOS), and 6:2 chlorinated polyfluorinated ether sulfonate (6:2 Cl-PFESA) for 21 days; subsequently, liver histopathological, oxidative stress, molecular docking, gene/protein expression, and gut microbiome analyses were conducted. PFOS and 6:2 Cl-PFESA exposure enhanced serum alanine aminotransferase and aspartate aminotransferase activities, and markedly increased hepatic area of vacuoles and inflammatory cell infiltration, while PFOA exposure increased serum alanine aminotransferase but not aspartate aminotransferase activities and affected hepatic area of vacuoles and inflammatory cell infiltration to a lesser extent. All three PFASs elevated catalase, glutathione S-transferase, and glutathione peroxidase activities and glutathione and malondialdehyde contents in the liver, suggesting the induction of oxidative stress. Further, PFASs could bind to mitogen-activated protein kinases (p38, ERK, and JNK), upregulating not only their expression but also the expression of downstream oxidative stress-related genes and that of P-p38, P-ERK, and Nrf2 proteins. In addition, PFAS exposure significantly increased the relative abundance of Proteobacteria and Delftia and decreased that of Firmicutes and Dietzia, Mycoplasma, and Methylobacterium-Methylorubrum in the order of PFOS ≈ 6:2 Cl-PFESA > PFOA. Altogether, it appears that PFOS and 6:2 Cl-PFESA are more toxic than PFOA. Finally, microbiota function prediction, microbiota co-occurrence network, and correlation analysis between gut microbiota and liver indices suggested that PFAS-induced hepatotoxicity was associated with gut microbiota dysbiosis. Our data provide new insights into the role of gut microbiota in PFAS-induced hepatotoxicity in frogs.
全氟和多氟烷基物质(PFASs)造成的污染已成为一个主要的全球性问题。在环境相关浓度下,PFAS 诱导的两栖类动物肝毒性与肠道微生物组之间的关联仍然难以捉摸。在此,我们将雄性黑斑蛙暴露于水中的 1 和 10μg/L 全氟辛酸(PFOA)、全氟辛烷磺酸(PFOS)和 6:2 氯代多氟醚磺酸(6:2 Cl-PFESA)中 21 天;随后进行了肝组织病理学、氧化应激、分子对接、基因/蛋白表达和肠道微生物组分析。PFOS 和 6:2 Cl-PFESA 暴露增加了血清丙氨酸氨基转移酶和天冬氨酸氨基转移酶的活性,并显著增加了肝空泡面积和炎症细胞浸润,而 PFOA 暴露仅增加了血清丙氨酸氨基转移酶的活性,而对肝空泡面积和炎症细胞浸润的影响较小。三种 PFAS 均提高了肝组织中的过氧化氢酶、谷胱甘肽 S-转移酶和谷胱甘肽过氧化物酶的活性,以及肝组织中的谷胱甘肽和丙二醛的含量,提示氧化应激的诱导。此外,PFAS 可以与丝裂原活化蛋白激酶(p38、ERK 和 JNK)结合,不仅上调它们的表达,还上调下游氧化应激相关基因和 P-p38、P-ERK 和 Nrf2 蛋白的表达。此外,PFAS 暴露显著增加了变形菌门和德氏菌属的相对丰度,降低了厚壁菌门和迪茨氏菌属、支原体属和甲基杆菌属-甲基红菌属的相对丰度,按 PFOS ≈ 6:2 Cl-PFESA > PFOA 的顺序。总的来说,PFOS 和 6:2 Cl-PFESA 比 PFOA 更具毒性。最后,微生物组功能预测、微生物组共生网络以及肠道微生物组与肝指数之间的相关性分析表明,PFAS 诱导的肝毒性与肠道微生物组失调有关。我们的数据为肠道微生物组在 PFAS 诱导的青蛙肝毒性中的作用提供了新的见解。