Laboratory for Earth Surface Processes, College of Urban and Environmental Sciences, Peking University, Beijing, China.
Environ Toxicol Chem. 2011 Jun;30(6):1252-60. doi: 10.1002/etc.508. Epub 2011 Apr 11.
The presence of antibiotics in the environment is of great concern because of their potential for resistance selection among pathogens. In the present study we investigated the occurrence of 19 sulfonamides, five N-acetylated sulfonamide metabolites, and trimethoprim in the Liao River basin and adjacent Liaodong Bay, China, as well as 10 human/agricultural source samples. Within the 35 river samples, 12 sulfonamides, four acetylated sulfonamides, and trimethoprim were detected, with the dominant being sulfamethoxazole (66.6 ng/L), N-acetylsulfamethoxazole (63.1 ng/L), trimethoprim (29.0 ng/L), sulfadiazine (14.0 ng/L), and sulfamonomethoxine (8.4 ng/L); within the 36 marine samples, 10 chemicals were detected, with the main contributions from sulfamethoxazole (25.2 ng/L) and N-acetylsulfamethoxazole (28.6 ng/L). Sulfamethoxazole (25.9%), N-acetylsulfamethoxazole (46.6%), trimethoprim (22.9%), and sulfapyridine (1.4%) were the main chemicals from human sources, while sulfamonomethoxine, sulfamethazine, sulfaquinoxaline, sulfaguanidine, sulfadiazine, sulfanilamide, and sulfamethoxypyridazine were dominant in the animal husbandry sources, specifically, swine and poultry farms, and sulfamethoxazole (91%) was dominant in the mariculture source. A principal component analysis with multiple linear regression was performed to evaluate the source apportionment of total sulfonamides in Liaodong Bay. It was found that animal husbandry contributed 15.2% of total sulfonamides, while human sources contributed 28.5%, and combined human and mariculture sources contributed 56.3%. In addition, the mariculture contribution was 24.1% of total sulfonamides into the sea based on mass flux estimation. The present study is the first report that the environmental levels of sulfonamide metabolites were comparable to the corresponding parents; therefore, we should pay attention to their environmental occurrence. Source apportionment showed human discharge (60.7%) significantly contributed to these antibiotics in Liaodong Bay, which provides important information for environmental management.
本研究调查了中国辽河流域及其毗邻的辽东湾地区的 19 种磺胺类药物、5 种 N-乙酰化磺胺类代谢物和甲氧芐啶的环境浓度,并采集了 10 个人类/农业源样品。在 35 个河流样品中,检测到 12 种磺胺类药物、4 种乙酰化磺胺类药物和甲氧芐啶,其中磺胺甲恶唑(66.6ng/L)、N-乙酰磺胺甲恶唑(63.1ng/L)、甲氧芐啶(29.0ng/L)、磺胺嘧啶(14.0ng/L)和磺胺二甲氧嘧啶(8.4ng/L)为主要污染物;在 36 个海洋样品中,检测到 10 种磺胺类药物,其中磺胺甲恶唑(25.2ng/L)和 N-乙酰磺胺甲恶唑(28.6ng/L)为主要污染物。人类源中磺胺甲恶唑(25.9%)、N-乙酰磺胺甲恶唑(46.6%)、甲氧芐啶(22.9%)和磺胺吡啶(1.4%)为主要污染物,而畜牧源中磺胺二甲氧嘧啶、磺胺甲嘧啶、磺胺喹恶啉、磺胺胍、磺胺嘧啶、磺胺酰胺和磺胺甲噁唑为主要污染物,水产养殖源中以磺胺甲恶唑(91%)为主。采用主成分分析与多元线性回归相结合的方法对辽东湾地区磺胺类药物的来源进行了评估。结果表明,畜牧源对磺胺类药物的贡献率为 15.2%,人类源为 28.5%,人类和水产养殖源的综合贡献率为 56.3%。此外,根据质量通量估算,水产养殖向海洋输入的磺胺类药物总量的 24.1%。本研究首次报道了磺胺类代谢物的环境浓度与相应母体相当,因此应关注其环境行为。来源分析表明,人类排放(60.7%)对辽东湾磺胺类抗生素的贡献最大,为环境管理提供了重要信息。