Effects of sulfamethazine and tetracycline at molecular, cellular and tissue levels in Eisenia fetida earthworms.

IF 5.4 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS
C F Rutkoski, I Vergara-Luis, E Urionabarrenetxea, N García-Velasco, B Zaldibar, M Anza, M Olivares, A Prieto, L Epelde, C Garbisu, E A Almeida, M Soto
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Abstract

Soil contamination by antibiotics is a global issue of great concern that contributes to the rise of bacterial antibiotic resistance and can have toxic effects on non-target organisms. This study evaluated the variations of molecular, cellular, and histological parameters in Eisenia fetida earthworms exposed to sulfamethazine (SMZ) and tetracycline (TC), two antibiotics commonly found in agricultural soils. The earthworms were exposed for 14 days to a series of concentrations (0, 10, 100, and 1000 mg/kg) of both antibiotics. SMZ and TC did not affect the survival of E. fetida, however, other effects at different levels of biological complexity were detected. The two highest concentrations of SMZ reduced the viability of coelomocytes. At the highest TC concentration, there was a noticeable decline in cell viability, acetylcholinesterase activity (neurotoxicity), and the relative presence of mucopolysaccharides in the epidermis (mucous production). Glutathione S-transferase activity decreased in all TC treatments and at the highest SMZ concentration. However, levels of malondialdehyde and protein carbonyls did not change, suggesting an absence of oxidative stress. Tetracycline was neurotoxic to E. fetida and changed the integrity of the epidermis. Both antibiotics altered the intestinal microbiota of E. fetida, leading to a reduction in the relative abundance of bacteria from the phyla Proteobacteria and Bacteroidetes, while causing an increase in the phylum Actinobacteroidota. All observed changes indicate that both SMZ and TC can disrupt the earthworms' immune system and gut microbiome, while fostering the growth of bacteria that harbour antibiotic resistance genes. Finally, both antibiotics exerted additional metabolic and physiological effects that increased the vulnerability of E. fetida to pathogens.

磺胺甲基嘧啶和四环素在分子、细胞和组织水平上对费氏蚯蚓的影响
抗生素对土壤的污染是一个备受关注的全球性问题,它导致了细菌抗药性的增加,并可能对非目标生物产生毒性影响。本研究评估了暴露于磺胺甲基嘧啶(SMZ)和四环素(TC)这两种农业土壤中常见抗生素的蚯蚓分子、细胞和组织学参数的变化。蚯蚓在一系列浓度(0、10、100 和 1000 毫克/千克)的两种抗生素中暴露 14 天。SMZ和TC不影响E. fetida的存活,但在不同的生物复杂性水平上检测到了其他影响。两种最高浓度的 SMZ 会降低腹腔细胞的存活率。在最高浓度的 TC 中,细胞活力、乙酰胆碱酯酶活性(神经毒性)和表皮中粘多糖的相对存在(粘液生成)都明显下降。在所有 TC 处理中,以及在 SMZ 浓度最高时,谷胱甘肽 S 转移酶活性都会降低。然而,丙二醛和蛋白质羰基的水平没有变化,表明没有氧化应激。四环素对E. fetida有神经毒性,并改变了表皮的完整性。这两种抗生素都改变了E. fetida的肠道微生物群,导致变形菌门和类杆菌门细菌的相对丰度降低,而放线菌门的细菌则有所增加。所有观察到的变化都表明,SMZ 和 TC 都会破坏蚯蚓的免疫系统和肠道微生物群,同时促进携带抗生素耐药基因的细菌的生长。最后,这两种抗生素还产生了额外的代谢和生理效应,增加了E. fetida对病原体的脆弱性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Biomaterials Science & Engineering
ACS Biomaterials Science & Engineering Materials Science-Biomaterials
CiteScore
10.30
自引率
3.40%
发文量
413
期刊介绍: ACS Biomaterials Science & Engineering is the leading journal in the field of biomaterials, serving as an international forum for publishing cutting-edge research and innovative ideas on a broad range of topics: Applications and Health – implantable tissues and devices, prosthesis, health risks, toxicology Bio-interactions and Bio-compatibility – material-biology interactions, chemical/morphological/structural communication, mechanobiology, signaling and biological responses, immuno-engineering, calcification, coatings, corrosion and degradation of biomaterials and devices, biophysical regulation of cell functions Characterization, Synthesis, and Modification – new biomaterials, bioinspired and biomimetic approaches to biomaterials, exploiting structural hierarchy and architectural control, combinatorial strategies for biomaterials discovery, genetic biomaterials design, synthetic biology, new composite systems, bionics, polymer synthesis Controlled Release and Delivery Systems – biomaterial-based drug and gene delivery, bio-responsive delivery of regulatory molecules, pharmaceutical engineering Healthcare Advances – clinical translation, regulatory issues, patient safety, emerging trends Imaging and Diagnostics – imaging agents and probes, theranostics, biosensors, monitoring Manufacturing and Technology – 3D printing, inks, organ-on-a-chip, bioreactor/perfusion systems, microdevices, BioMEMS, optics and electronics interfaces with biomaterials, systems integration Modeling and Informatics Tools – scaling methods to guide biomaterial design, predictive algorithms for structure-function, biomechanics, integrating bioinformatics with biomaterials discovery, metabolomics in the context of biomaterials Tissue Engineering and Regenerative Medicine – basic and applied studies, cell therapies, scaffolds, vascularization, bioartificial organs, transplantation and functionality, cellular agriculture
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