Haikun Zhang , Yingchun Han , Suyun Fang , Shenghui Zhang , Manman Cheng , Xingyue Lin , Xiaoke Hu
{"title":"卵形沙眼的短期深海网箱培养增加了抗生素抗性基因的流动性","authors":"Haikun Zhang , Yingchun Han , Suyun Fang , Shenghui Zhang , Manman Cheng , Xingyue Lin , Xiaoke Hu","doi":"10.1016/j.aquaeng.2025.102591","DOIUrl":null,"url":null,"abstract":"<div><div>Antibiotic resistance genes (ARGs) have been extensively studied in offshore mariculture areas, yet their profiles in deep-sea cage culture environments remain largely unexplored. In this study, the proliferation, hosts and spread risks of ARGs before and after deep-sea cage mariculture activities were investigated, employing environmental parameter measurements, metagenomic assembly, and binning approaches. Our results showed that following aquaculture activity, the abundances of fosmidomycin- (an antibiotic targeting the MEP pathway), MLS (Macrolides, lincosamides, streptogramines), phenicol-, and triclosan-related ARGs decreased, while diaminopyrimidine- (interfere with the folic acid metabolism of bacteria), rifamycin-, aminoglycoside- (prevent bacterial protein synthesis), multidrug-, and mupirocin-related ARGs increased, thereby increasing the likelihood of microorganisms acquiring resistance. The hosts of these ARGs were classified into 38 classes across 19 phyla, with Gammaproteobacteria accounting for over 36.29 % of all ARG hosts, and Alphaproteobacteria contributing an additional 16.9 %. This information can guide us in targeting specific types of microorganisms for controlling particular ARGs. Certain ARGs were predominantly located on plasmids, indicating enhanced mobility and an increased risk of horizontal gene transfer. Additionally, the presence of plasmids, viruses, or mobile genetic elements in aquaculture-affected water showed a general increase, further highlighting the environmental risk of ARG spread. Overall, this study deepens our understanding of the environmental impacts of deep-sea cage aquaculture.</div></div>","PeriodicalId":8120,"journal":{"name":"Aquacultural Engineering","volume":"111 ","pages":"Article 102591"},"PeriodicalIF":3.6000,"publicationDate":"2025-06-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Short-term deep-sea cage culture of Trachinotus ovatus increases mobility of antibiotic-resistance genes\",\"authors\":\"Haikun Zhang , Yingchun Han , Suyun Fang , Shenghui Zhang , Manman Cheng , Xingyue Lin , Xiaoke Hu\",\"doi\":\"10.1016/j.aquaeng.2025.102591\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Antibiotic resistance genes (ARGs) have been extensively studied in offshore mariculture areas, yet their profiles in deep-sea cage culture environments remain largely unexplored. In this study, the proliferation, hosts and spread risks of ARGs before and after deep-sea cage mariculture activities were investigated, employing environmental parameter measurements, metagenomic assembly, and binning approaches. Our results showed that following aquaculture activity, the abundances of fosmidomycin- (an antibiotic targeting the MEP pathway), MLS (Macrolides, lincosamides, streptogramines), phenicol-, and triclosan-related ARGs decreased, while diaminopyrimidine- (interfere with the folic acid metabolism of bacteria), rifamycin-, aminoglycoside- (prevent bacterial protein synthesis), multidrug-, and mupirocin-related ARGs increased, thereby increasing the likelihood of microorganisms acquiring resistance. The hosts of these ARGs were classified into 38 classes across 19 phyla, with Gammaproteobacteria accounting for over 36.29 % of all ARG hosts, and Alphaproteobacteria contributing an additional 16.9 %. This information can guide us in targeting specific types of microorganisms for controlling particular ARGs. Certain ARGs were predominantly located on plasmids, indicating enhanced mobility and an increased risk of horizontal gene transfer. Additionally, the presence of plasmids, viruses, or mobile genetic elements in aquaculture-affected water showed a general increase, further highlighting the environmental risk of ARG spread. Overall, this study deepens our understanding of the environmental impacts of deep-sea cage aquaculture.</div></div>\",\"PeriodicalId\":8120,\"journal\":{\"name\":\"Aquacultural Engineering\",\"volume\":\"111 \",\"pages\":\"Article 102591\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-06-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Aquacultural Engineering\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0144860925000809\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"AGRICULTURAL ENGINEERING\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquacultural Engineering","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0144860925000809","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"AGRICULTURAL ENGINEERING","Score":null,"Total":0}
Short-term deep-sea cage culture of Trachinotus ovatus increases mobility of antibiotic-resistance genes
Antibiotic resistance genes (ARGs) have been extensively studied in offshore mariculture areas, yet their profiles in deep-sea cage culture environments remain largely unexplored. In this study, the proliferation, hosts and spread risks of ARGs before and after deep-sea cage mariculture activities were investigated, employing environmental parameter measurements, metagenomic assembly, and binning approaches. Our results showed that following aquaculture activity, the abundances of fosmidomycin- (an antibiotic targeting the MEP pathway), MLS (Macrolides, lincosamides, streptogramines), phenicol-, and triclosan-related ARGs decreased, while diaminopyrimidine- (interfere with the folic acid metabolism of bacteria), rifamycin-, aminoglycoside- (prevent bacterial protein synthesis), multidrug-, and mupirocin-related ARGs increased, thereby increasing the likelihood of microorganisms acquiring resistance. The hosts of these ARGs were classified into 38 classes across 19 phyla, with Gammaproteobacteria accounting for over 36.29 % of all ARG hosts, and Alphaproteobacteria contributing an additional 16.9 %. This information can guide us in targeting specific types of microorganisms for controlling particular ARGs. Certain ARGs were predominantly located on plasmids, indicating enhanced mobility and an increased risk of horizontal gene transfer. Additionally, the presence of plasmids, viruses, or mobile genetic elements in aquaculture-affected water showed a general increase, further highlighting the environmental risk of ARG spread. Overall, this study deepens our understanding of the environmental impacts of deep-sea cage aquaculture.
期刊介绍:
Aquacultural Engineering is concerned with the design and development of effective aquacultural systems for marine and freshwater facilities. The journal aims to apply the knowledge gained from basic research which potentially can be translated into commercial operations.
Problems of scale-up and application of research data involve many parameters, both physical and biological, making it difficult to anticipate the interaction between the unit processes and the cultured animals. Aquacultural Engineering aims to develop this bioengineering interface for aquaculture and welcomes contributions in the following areas:
– Engineering and design of aquaculture facilities
– Engineering-based research studies
– Construction experience and techniques
– In-service experience, commissioning, operation
– Materials selection and their uses
– Quantification of biological data and constraints