Park E D, Lightner D V, Park D L
Department of Veterinary Science, University of Arizona, Tucson 85721.
Rev Environ Contam Toxicol. 1994;138:1-20. doi: 10.1007/978-1-4612-2672-7_1.
The consumption of seafood, especially shrimp, increases yearly in the U.S. The U.S. is the second largest importer of shrimp in the world, consuming more than 11% of the total world production. Aquaculture is becoming an increasingly important source of the world's shrimp, currently accounting for approximately 30% of the world's supply. Unfortunately, in this era of international trade deficits, U.S. production of aquacultured shrimp is insignificant (< 0.1%) compared with world production. As shrimp aquaculture expands in the U.S., so does the use of intensive farming techniques. Shrimp aquaculture is like any other animal husbandry industry in that shrimp are subject to disease, especially under intensive farming methods. In penaeid shrimp, the primary diseases associated with mortalities are usually viral or bacterial. The majority of bacterial infections in penaeid shrimp are attributable to Vibrio species, with mortalities ranging from insignificant to 100%. However, the rapid growth of this industry has outpaced efforts by researchers, pharmaceutical companies, and federal regulatory agencies to provide approved therapeutants for shrimp disease management. Approval of drugs and their surveillance for compliance with regulations applicable to seafoods, including aquacultured goods, is the responsibility of the FDA. There are three general areas of concern regarding human health when chemotherapeutants are used in aquaculture: (1) residues of drugs in fish destined for human consumption; (2) development of drug resistance in human pathogenic bacteria; and (3) direct toxic effects to humans from handling of drugs. Currently, there are no antibacterials approved for shrimp aquaculture in the U.S. One of the major obstacles in the development and approval of new drugs for aquaculture is the cost of conducting the required studies. The high cost to pharmaceutical companies discourages investment in shrimp chemotherapeutant research, since the current U.S. market for such products is small. Unfortunately, the U.S. shrimp aquaculture industry will remain small without legal availability of chemotherapeutants. Oxytetracycline (OTC) and Romet-30 are two antibacterials currently approved in the U.S. for catfish and salmonid aquaculture. Shrimp aquaculture facilities outside of the U.S. routinely use these drugs, as well as others, in the treatment of bacterial disease outbreaks. Much of the work required for OTC approval by the FDA for penaeid shrimp has been completed.(ABSTRACT TRUNCATED AT 400 WORDS)
在美国,海产品尤其是虾类的消费量逐年上升。美国是世界第二大对虾进口国,其消费量超过全球总产量的11%。水产养殖正日益成为全球虾类供应的重要来源,目前约占全球供应量的30%。不幸的是,在这个国际贸易存在赤字的时代,与世界产量相比,美国水产养殖虾的产量微不足道(<0.1%)。随着美国对虾养殖业的扩张,集约化养殖技术的使用也在增加。对虾养殖与其他畜牧业一样,虾容易患病,尤其是在集约化养殖方式下。在对虾中,与死亡相关的主要疾病通常是病毒性或细菌性的。对虾中的大多数细菌感染是由弧菌属引起的,死亡率从微不足道到100%不等。然而,该行业的快速发展超过了研究人员、制药公司和联邦监管机构为对虾疾病管理提供经批准治疗剂的努力。药物的批准及其对适用于海产品(包括水产养殖产品)的法规的合规监督是美国食品药品监督管理局(FDA)的职责。在水产养殖中使用化学治疗剂时,关于人类健康有三个普遍关注的领域:(1)供人类食用的鱼类中的药物残留;(2)人类病原菌中耐药性的发展;(3)处理药物对人类的直接毒性作用。目前,美国没有批准用于对虾养殖的抗菌药物。开发和批准水产养殖新药的主要障碍之一是进行所需研究的成本。制药公司的高成本阻碍了对对虾化学治疗剂研究的投资,因为目前此类产品在美国的市场很小。不幸的是,如果没有合法可用的化学治疗剂,美国对虾养殖业将仍然规模较小。土霉素(OTC)和罗美沙星30是目前在美国被批准用于鲶鱼和鲑鱼养殖的两种抗菌药物。美国以外的对虾养殖设施通常使用这些药物以及其他药物来治疗细菌性疾病爆发。FDA批准OTC用于对虾所需的大部分工作已经完成。(摘要截选至400字)