Acute toxicity of binary mixtures for quorum sensing inhibitors and sulfonamides against Aliivibrio fischeri: QSAR investigations and joint toxic actions

IF 2.9 Q2 TOXICOLOGY
Zhenheng Long , Jingyi Yao , Minghong Wu , Shu-shen Liu , Liang Tang , Bo Lei , Jiajun Wang , Haoyu Sun
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引用次数: 0

Abstract

Quorum sensing inhibitors (QSIs), as a kind of ideal antibiotic substitutes, have been recommended to be used in combination with traditional antibiotics in medical and aquaculture fields. Due to the co-existence of QSIs and antibiotics in environmental media, it is necessary to evaluate their joint risk. However, there is little information about the acute toxicity of mixtures for QSIs and antibiotics. In this study, 10 QSIs and 3 sulfonamides (SAs, as the representatives for traditional antibiotics) were selected as the test chemicals, and their acute toxic effects were determined using the bioluminescence of Aliivibrio fischeri (A. fischeri) as the endpoint. The results indicated that SAs and QSIs all induced S-shaped dose-responses in A. fischeri bioluminescence. Furthermore, SAs possessed greater acute toxicity than QSIs, and luciferase (Luc) might be the target protein of test chemicals. Based on the median effective concentration (EC50) for each test chemical, QSI-SA mixtures were designed according to equitoxic (EC50(QSI):EC50(SA) = 1:1) and non-equitoxic ratios (EC50(QSI):EC50(SA) = 1:10, 1:5, 1:0.2, and 1:0.1). It could be observed that with the increase of QSI proportion, the acute toxicity of QSI-SA mixtures enhanced while the corresponding TU values decreased. Furthermore, QSIs contributed more to the acute toxicity of test binary mixtures. The joint toxic actions of QSIs and SAs were synergism for 23 mixtures, antagonism for 12 mixtures, and addition for 1 mixture. Quantitative structure–activity relationship (QSAR) models for the acute toxicity QSIs, SAs, and their binary mixtures were then constructed based on the lowest CDOCKER interaction energy (Ebind-Luc) between Luc and each chemical and the component proportion in the mixture. These models exhibited good robustness and predictive ability in evaluating the toxicity data and joint toxic actions of QSIs and SAs. This study provides reference data and applicable QSAR models for the environmental risk assessment of QSIs, and gives a new perspective for exploring the joint effects of QSI-antibiotic mixtures.

Abstract Image

定量感应抑制剂和磺胺类药物二元混合物对弗氏阿里维氏菌的急性毒性:QSAR 研究和联合毒性作用
法定量感应抑制剂(QSIs)作为一种理想的抗生素替代品,已被推荐在医疗和水产养殖领域与传统抗生素结合使用。由于 QSIs 和抗生素同时存在于环境介质中,因此有必要对它们的共同风险进行评估。然而,有关 QSIs 和抗生素混合物急性毒性的信息很少。本研究选择了 10 种 QSIs 和 3 种磺胺类药物(SAs,传统抗生素的代表)作为测试化学品,并以弗氏阿里弧菌(A. fischeri)的生物发光为终点测定了它们的急性毒性效应。结果表明,SAs 和 QSIs 都能诱导鱼腥藻生物发光的 S 型剂量反应。此外,SAs 的急性毒性高于 QSIs,而荧光素酶(Luc)可能是测试化学品的靶蛋白。根据每种测试化学品的中位有效浓度(EC50),按照等毒性(EC50(QSI):EC50(SA) = 1:1)和非等毒性(EC50(QSI):EC50(SA) = 1:10、1:5、1:0.2 和 1:0.1)比例设计了 QSI-SA 混合物。可以看出,随着 QSI 比例的增加,QSI-SA 混合物的急性毒性增强,而相应的 TU 值降低。此外,QSI 对试验二元混合物急性毒性的影响更大。在 23 种混合物中,QSIs 和 SAs 的共同毒性作用是协同作用,在 12 种混合物中是拮抗作用,在 1 种混合物中是相加作用。然后,根据 Luc 与每种化学品之间的最低 CDOCKER 相互作用能(Ebind-Luc)以及混合物中的成分比例,构建了急性毒性 QSIs、SAs 及其二元混合物的定量结构-活性关系(QSAR)模型。这些模型在评估 QSIs 和 SAs 的毒性数据和联合毒性作用时表现出良好的稳健性和预测能力。这项研究为 QSIs 的环境风险评估提供了参考数据和适用的 QSAR 模型,并为探索 QSI- 抗生素混合物的联合效应提供了一个新的视角。
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来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
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