渔业科学进展
漁業科學進展
어업과학진전
MARINE FISHERIES RESEARCH
2014年
6期
60-67
,共8页
王蓓%李桂欢%王培%汤菊芬%鲁义善%吴灶和%简纪常
王蓓%李桂歡%王培%湯菊芬%魯義善%吳竈和%簡紀常
왕배%리계환%왕배%탕국분%로의선%오조화%간기상
无乳链球菌%溶血素%原核表达%免疫原性
無乳鏈毬菌%溶血素%原覈錶達%免疫原性
무유련구균%용혈소%원핵표체%면역원성
Streptococcus agalactiae%Hemolysin%Prokaryotic expression%Immunogenicity
为研究罗非鱼源无乳链球菌溶血素(Hemolysin, Hly)对鱼体的免疫保护作用,根据已获得的无乳链球菌ZQ0910全基因组序列设计引物扩增hly基因,定向克隆于原核表达载体pET-28a中,构建原核重组质粒pET-28a-hly,经IPTG诱导表达后,制成亚单位疫苗免疫吉富罗非鱼,并分析疫苗的免疫保护力。结果显示,hly基因产物大小1335 bp,编码444个氨基酸,经测序与GenBank报道的链球菌属Hly氨基酸序列同源性可达99%。经IPTG诱导表达后,SDS-PAGE分析可见一条51.7 kD的特异条带;Western blotting分析结果说明表达的Hly蛋白能与His-Tag单抗特异性结合;制备的亚单位疫苗免疫鱼体后第14天即可检测到抗体产生,并在第28天达到峰值,抗体效价为1∶4096,免疫保护率为70%。由此证实,该亚单位疫苗有望成为预防由无乳链球菌引起的罗非鱼链球菌病的基因工程类疫苗。
為研究囉非魚源無乳鏈毬菌溶血素(Hemolysin, Hly)對魚體的免疫保護作用,根據已穫得的無乳鏈毬菌ZQ0910全基因組序列設計引物擴增hly基因,定嚮剋隆于原覈錶達載體pET-28a中,構建原覈重組質粒pET-28a-hly,經IPTG誘導錶達後,製成亞單位疫苗免疫吉富囉非魚,併分析疫苗的免疫保護力。結果顯示,hly基因產物大小1335 bp,編碼444箇氨基痠,經測序與GenBank報道的鏈毬菌屬Hly氨基痠序列同源性可達99%。經IPTG誘導錶達後,SDS-PAGE分析可見一條51.7 kD的特異條帶;Western blotting分析結果說明錶達的Hly蛋白能與His-Tag單抗特異性結閤;製備的亞單位疫苗免疫魚體後第14天即可檢測到抗體產生,併在第28天達到峰值,抗體效價為1∶4096,免疫保護率為70%。由此證實,該亞單位疫苗有望成為預防由無乳鏈毬菌引起的囉非魚鏈毬菌病的基因工程類疫苗。
위연구라비어원무유련구균용혈소(Hemolysin, Hly)대어체적면역보호작용,근거이획득적무유련구균ZQ0910전기인조서렬설계인물확증hly기인,정향극륭우원핵표체재체pET-28a중,구건원핵중조질립pET-28a-hly,경IPTG유도표체후,제성아단위역묘면역길부라비어,병분석역묘적면역보호력。결과현시,hly기인산물대소1335 bp,편마444개안기산,경측서여GenBank보도적련구균속Hly안기산서렬동원성가체99%。경IPTG유도표체후,SDS-PAGE분석가견일조51.7 kD적특이조대;Western blotting분석결과설명표체적Hly단백능여His-Tag단항특이성결합;제비적아단위역묘면역어체후제14천즉가검측도항체산생,병재제28천체도봉치,항체효개위1∶4096,면역보호솔위70%。유차증실,해아단위역묘유망성위예방유무유련구균인기적라비어련구균병적기인공정류역묘。
Streptococcus is a genus of spherical gram-positive bacteria that can infect a wide range of hosts. Streptococcal diseases of cultured fish caused by Streptococcus agalactiae have been frequently reported in South China, which incurred catastrophic economic losses. Vaccine is one of effective ways to control and eradicate infectious diseases, and so far no effective subunit vaccine for S. agalactiae diseases has been developed. To test whether Hemolysin (Hly) is a potential candidate for vaccine development of Oreochromis niloticus, we cloned hly gene based on bioinformatics analysis and constructed and expressed it. The open reading frame of hly gene contains 1335 bp that encodes 444 amino acid residues. Alignment analysis indicated that the Hly protein was highly homologous to Hly proteins from other Streptococcus(99%). SDS-PAGE confirmed the expression of Hly (51.7 kD) in Escherichia coli BL21(DE3). Then, the recombinant Hly protein was purified by affinity chromatography, which was used for vaccination in Tilapia, O. niloticus. Immunogenicity was confirmed by subsequent western blotting. Enzyme-linked immunosorbent assay (ELISA) analysis demonstrated that Hly produced an observable antibody response in all vaccinated fish, and the maximum antibody titers in the sera reached 1:4096. The RPS value for the Sip vaccine was 70. Tilapia vaccinated with Hly was highly resistant to the infection of the contaminant S. agalactiae. These results indicate that Hly is an effective vaccine candidate against S. agalactiae for tilapia, O. niloticus.