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作 者:黄笑 王国浩 董宣 唐琼英[1,3] 段虎 杨国梁 黄倢[2] HUANG Xiao;WANG Guohao;DONG Xuan;TANG Qiongying;DUAN Hu;YANG Guoliang;HUANG Jie(Zhejiang Provincial Key Laboratory of Aquatic Resources Conservation and Development,Key Laboratory of Aquatic Animal Genetic Breeding and Nutrition,Chinese Academy of Fishery Sciences,Huzhou University,Huzhou 313000,China;Yellow Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences,Laboratory for Marine Fisheries Science and Food Production Processes,Qingdao Marine Science and Technology Center,Key Laboratory of Maricultural Organism Disease Control,Ministry of Agriculture and Rural Affairs,Qingdao Key Laboratory of Mariculture Epidemiology and Biosecurity,Qingdao 266071,China;Jiangsu Shufeng Prawn Breeding Co.Ltd.,Gaoyou 225654,China;College of Marine and Environmental Science,Tianjin University of Science and Technology,Tianjin 300457,China)
机构地区:[1]湖州师范学院浙江省水生生物资源养护与开发技术研究重点实验室中国水产科学研究院水生动物繁育与营养重点实验室,浙江湖州313000 [2]中国水产科学研究院黄海水产研究所青岛海洋科技中心海洋渔业科学与食物产出过程功能实验室农业农村部海水养殖病害防治重点实验室青岛市海水养殖流行病学与生物安保重点实验室,山东青岛266071 [3]江苏数丰水产种业有限公司,江苏高邮225654 [4]天津科技大学海洋与环境学院,天津300457
出 处:《渔业科学进展》2024年第4期187-194,共8页Progress in Fishery Sciences
基 金:青岛市市南区科技计划(2022-2-027-ZH);国家现代农业产业技术体系(CARS-48);中国水产科学研究院基本科研业务费(2020TD39)共同资助。
摘 要:细胞平台是研究病原–宿主互作的重要工具,虾类细胞系的缺少严重制约了虾类病毒学研究。传染性早熟病毒(IPV)是近年来发现的能够导致罗氏沼虾(Macrobrachiumrosenbergii)性早熟和生长缓慢的一种新病毒,主要侵染罗氏沼虾神经组织。为建立罗氏沼虾病毒–宿主互作的体外研究平台,本研究采用木瓜蛋白酶消化健康罗氏沼虾的脑、眼柄、胸神经节和腹神经节,获取罗氏沼虾神经细胞,并利用L-15培养基进行离体培养。选择培养效果最佳的脑神经细胞进行IPV体外感染。结果显示,培养的原代细胞在含有谷氨酰胺的L-15培养基中生长良好,其中,从脑组织和眼柄X器官–窦腺复合体中分离出的细胞在体外存活时间可达15d,从胸腹神经节中分离出来的细胞在体外存活时间达9 d。在本研究所采用的感染方式和剂量条件下,脑细胞在感染96 h后检测到高载量的IPV。本研究建立了一种操作简便的罗氏沼虾神经细胞原代培养技术,为罗氏沼虾神经内分泌研究和病毒–宿主互作提供了基础数据和平台。Macrobrachium rosenbergii is one of the most popular species in aquaculture.However,the M.rosenbergii farming industry has been facing an ongoing iron prawn syndrome(IPS)crisis since 2010,resulting in substantial economic losses to the farming industry.Infectious precocity virus(IPV)is a novel virus of Flaviviridae found in recent years that can cause sexual precocity and associated slow growth in healthy M.rosenbergii.It is believed to have a specific correlation with IPS.There are very few cell lines of crustaceans that can be used for studying the response of cells to pathogens.Even though the primary culture technology of blood and muscle cells in M.rosenbergii has gradually matured,there have been few studies on the primary culture of neural cells.Quantitative results of different tissues of IPV-positive M.rosenbergii have indicated that nerve-rich tissues,such as eyestalk,brain,and thoracic ganglion tissues,have a higher viral load,which explains why IPV has neurotropic tissue characteristics.To provide an in vitro cell platform for studying the virus-host interactions of IPV,a simple,stable,and feasible primary culture method was established for the nervous tissue primary cells of M.rosenbergii.In this study,healthy prawns with a body length of about 10–12 cm,healthy appendages,and vitality were selected for the experiments.The body surface of M.rosenbergii was first disinfected with 75%alcohol.On the clean bench,the nervous tissues,including the brain,X organ-sinus gland complex from the eyestalk,thoracic ganglion,and abdominal ganglion tissues,were isolated and washed in PBS buffer containing 100 U/mL penicillin and streptomycin,100 U/mL amphotericin,and 80 U/mL gentamicin,2–3 times.The tissues were then placed in 5 mL of 0.5%papain solution.After digestion at 25℃for 5 min,1×L-15 medium containing 15%FBS,140 mmol/L D-glucose,and antibiotics(100 U/mL penicillin and streptomycin,100 U/mL amphotericin,and 80 U/mL gentamicin)were added to terminate digestion.Next,the cells were seeded onto a 24-well p
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