Greenway Terrence E, Byars Todd S, Elliot Robert B, Jin Xixuan, Griffin Matt J, Wise David J
a Thad Cochran National Warmwater Aquaculture Center, Mississippi Agricultural and Forestry Experiment Station, Mississippi State University , Post Office Box 197, Stoneville , Mississippi 38776 , USA.
b U.S. Department of Agriculture-Agricultural Research Service-Mid-South Area , Biological Control of Pests Research Unit, National Biological Control Laboratory , Post Office Box 67, Stoneville , Mississippi 38776 , USA.
J Aquat Anim Health. 2017 Jun;29(2):83-88. doi: 10.1080/08997659.2017.1290710.
Mortality associated with Edwardsiella ictaluri infection is a serious impediment to the commercial production of fingerling Channel Catfish Ictalurus punctatus. A patented, live, attenuated, orally delivered vaccine has been developed that offers exceptional protection against E. ictaluri infection in both laboratory and small-scale pond trials. Further vaccine development is contingent on the successful completion of large-scale field trials that accurately reflect industry conditions. This current work focuses on the validation of fermentation protocols and the optimization of downstream processing procedures to produce sufficient quantities of vaccine to conduct commercial-scale field trials. Eight vaccine serials were produced from a master seed stock (S97-773-340X2) in a 50-L floor model fermenter over two consecutive years. Following fermentation, cells were harvested, concentrated 10-fold, and cryogenically stored (-74°C). To assess processing protocols and determine shelf life of cryogenically stored vaccine, serials were tested for cell viability and vaccine potency at various intervals over 24 months. There were no significant differences in cell viability between the fresh vaccine and the stored frozen product. All serials provided a high level of protection (77-100% relative percent survival) against E. ictaluri infection in juvenile Channel Catfish and exhibited excellent poststorage viability. This data demonstrates that the live, attenuated, orally delivered vaccine can be stored at -74°C for at least 2 years with no reduction in cell viability or vaccine potency. Received May 17, 2016; accepted January 19, 2017.
爱德华氏菌感染导致的死亡率是斑点叉尾鮰鱼苗商业化生产的严重阻碍。一种已获专利的、减毒活疫苗通过口服给药方式研发成功,在实验室和小规模池塘试验中,该疫苗对爱德华氏菌感染均提供了卓越的保护。进一步的疫苗研发取决于能否成功完成准确反映行业状况的大规模田间试验。当前这项工作聚焦于发酵方案的验证以及下游加工流程的优化,以生产足够数量的疫苗用于开展商业规模的田间试验。连续两年在一台50升落地式发酵罐中,从主种子库(S97 - 773 - 340X2)生产了八个疫苗批次。发酵后,收获细胞,浓缩10倍,并在低温(-74°C)下储存。为评估加工流程并确定低温储存疫苗的保质期,在24个月内的不同时间间隔对各批次疫苗进行细胞活力和疫苗效力测试。新鲜疫苗和冷冻储存产品之间的细胞活力没有显著差异。所有批次疫苗在斑点叉尾鮰幼鱼中对爱德华氏菌感染均提供了高水平的保护(相对存活率77 - 100%),且储存后活力良好。该数据表明,这种减毒活口服疫苗可在-74°C下储存至少2年,细胞活力和疫苗效力均无下降。2016年5月17日收到;2017年1月19日接受。