CN110115759A - 一种提高鱼类抗病毒免疫力的方法 - Google Patents
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- Peptides Or Proteins (AREA)
Abstract
本发明提供一种提高鱼类抗病毒免疫力的方法,通过上调Bmp8a蛋白的表达量来增强鱼类的抗病毒免疫力。本发明首先提供Bmp8a蛋白的一种用途,是在制备提高鱼类抗病毒免疫力的制品中的应用。本发明证明bmp8a基因敲除后的斑马鱼的抗病毒能力显著下降,而过表达Bmp8a可显著上调干扰素等抗病毒相关基因的表达,显示Bmp8a在抗病毒免疫中具有重要作用。通过在鱼类中注射Bmp8a成熟肽,增强鱼类的抗病毒免疫力,从而达到防治鱼类病毒性疾病的目的。
Description
技术领域
本发明属于鱼类免疫技术领域,具体涉及一种提高鱼类抗病毒免疫力的方法。
背景技术
鱼类病毒性疾病传染性强、传播速度快、死亡率高,严重危害水产养殖业,能够造成重大经济损失。国内外已经研发和生产了少数鱼类病毒性疾病的疫苗,但仍存在免疫效果差、血清型差异等问题,难以在生产实践中应用。因此,目前鱼类病毒性疾病的治疗还存在相当大难度,主要以预防为主。
骨形态发生蛋白(Bone Morphogenetic Protein,BMP)家族是一类疏水性糖蛋白家族,属于Transforming Growth Factor Beta(TGF-β)超家族。BMP8是BMP家族的众多成员之一,在斑马鱼中,Bmp8只有Bmp8a一种形式。斑马鱼Bmp8a首先形成一个含有433个氨基酸的前肽,活性的Bmp8a成熟肽由羧基端的137个氨基酸组成。
发明内容
本发明的目的是提供一种提高鱼类抗病毒免疫力的方法,通过上调Bmp8a蛋白的表达量来增强鱼类的抗病毒免疫力,从而弥补现有技术的不足。
本发明首先提供Bmp8a蛋白的一种用途,是在制备提高鱼类抗病毒免疫力的制品中的应用;所述的制品,为注射用液体蛋白制剂;
本发明还提供Bmp8a蛋白的另一种用途,是通过检测Bmp8a蛋白的表达量来筛选抗病毒能力强的亲鱼;
所述的Bmp8a蛋白,其氨基酸序列为SEQ ID NO:1;其成熟肽的氨基酸序列为SEQID NO:2;
编码上述的Bmp8a蛋白的基因,其核苷酸序列为SEQ ID NO:3。
本发明另一个方面还提供一种提高鱼类抗病毒免疫力的方法,通过上调bmp8a蛋白的表达量来增强鱼类的抗病毒免疫力。
本发明将bmp8a基因敲除后的斑马鱼抗病毒能力显著下降,显示Bmp8a在抗病毒免疫中具有重要作用。通过在饲料中添加Bmp8a成熟肽或在鱼类中注射Bmp8a成熟肽,增强鱼类的抗病毒免疫力,从而达到防治鱼类病毒性疾病的目的。
附图说明
图1:斑马鱼bmp8a基因的组织表达图;
图2:斑马鱼bmp8a基因TALEN靶位点设计图;
图3:斑马鱼bmp8a基因TALEN靶位点上下游嵌套PCR电泳图。M:DL 2000Maker;1:外侧PCR产物;2:内侧PCR产物。
图4:斑马鱼bmp8a基因TALEN靶位点突变检测结果。(A):Hph Ⅰ酶切PCR产物电泳图。M:DL 2000Maker;1-9:注射TALEN mRNA胚胎;WT:未注射TALEN mRNA的野生型胚胎。(B):图(A)中1、2、8号胚胎bmp8a基因突变测序结果。
图5:利用TALEN技术对斑马鱼bmp8a基因进行敲除示意图。
图6:斑马鱼bmp8a基因敲除后,MHC1基因表达显著下降图。
图7:GCRV病毒刺激可显著上调斑马鱼组织中bmp8a基因表达图。
图8:GCRV病毒刺激可显著上调斑马鱼ZFL细胞中bmp8a基因的表达图。
图9:过表达斑马鱼Bmp8a可显著上调抗病毒相关基因的表达图。
图10:过表达斑马鱼Bmp8a可显著抑制病毒基因VP5的表达图。
图11:bmp8a突变体斑马鱼更易受到病毒感染图。
具体实施方式
下面结合实施例和附图对本发明进行详细的描述。
实施例1:bmp8a基因敲除实验
斑马鱼Bmp8a蛋白DE氨基酸序列为SEQ ID NO:1,其对应的成熟肽的氨基酸序列为SEQ ID NO:2,编码上述Bmp8a蛋白的基因的核苷酸序列为SEQ ID NO:3。斑马鱼bmp8a基因主要表达在斑马鱼的精巢、肠和皮肤组织中,脑组织中表达次之,心脏、肌肉组织中表达量相对较低(图1)。
运用TALEN技术对斑马鱼bmp8a基因进行敲除。具体方法如下:
1)靶位点设计:
利用Submit TALEN Targeter(https://tale-nt.cac.cornell.edu/node/add/talen)网站,根据TALEN技术靶位点设计原则,对斑马鱼BMP8a基因每个外显子进行分析,结合zBMP8a基因结构域特点,设计靶位点,并通过NEB公司网站找到高效率酶切位点。选择在第4个外显子上设计靶位点,Spacer为斑马鱼BMP8a cDNA的833-849bp,左臂为816-832bp,右臂为850-866bp,Spacer上含有Hph Ⅰ酶切位点,用于后续突变体检验,且Hph Ⅰ酶效率很高,可直接切割PCR产物(图2)。
2)靶位点确认
在靶位点上下游设计嵌套PCR扩增外侧引物P5和内侧引物P6。以外侧引物P5、基因组粗提液进行第一轮PCR扩增,外侧PCR扩增产物大小为957bp;以内侧引物P6、第一轮PCR产物进行二轮PCR扩增,内侧PCR扩增产物大小为556bp(图3)。Hph Ⅰ酶切内侧PCR产物分别产生227bp、339bp两条带。
引物序列如下:
P5-F:5'-GGAACTCTGAATCTGCGTCT-3'
P5-R:5'-TCACAGGAGGGCGAATAG-3'
P6-F:5'-GACAGACATTCAGGCACGTA-3'
P6-R:5'-GCCGTCCACTGCTATGAT-3'
3)构建TALEN表达载体及体外转录、纯化mRNA
利用Golden Gate方法构建TALEN表达载体,并测序。提取含有TALEN表达载体菌液质粒,通过NotⅠ酶将质粒线性化。体外转录合成编码TALEN的mRNA。体外转录结束后,加入1μl DNase Ⅰ,37℃水浴孵育15min,以出去mRNA中的DNA模板,并电泳检测。-80℃保存备用。
4)显微注射
(1)性成熟的野生型斑马鱼雌雄交配产卵,体外受精后收集胚胎。
(2)将左臂、右臂TALEN mRNA混合,显微注射到单细胞期或2细胞期斑马鱼受精卵中,得到F0胚胎。
5)突变检测
取2dpf注射后斑马鱼胚胎,粗提基因组。进行嵌套PCR。HPh Ⅰ酶酶切PCR产物,37℃反应2h。酶切结束后,将10μl酶切产物进行电泳检测。如果有完整的、没有被切开的条带,则靶位点可能发生突变,将未切开的条带回收纯化,回收纯化的PCR产物连接到pGEM-T载体,转化到trans5α克隆菌种,涂布到蓝白斑筛选平板上,挑选出重组子,并测序。将测序结果与野生型BMP8a基因组比对分析,确认基因敲除成功(图4),获得F0代突变体斑马鱼。
6)经过几代的筛选和养殖,获得了在靶位点内缺失7bp的F3代纯合子突变体(图5)。
进一步利用Real-time PCR技术检测发现,斑马鱼bmp8a基因敲除后,MHC1基因表达显著下降(图6)。MHCⅠ在提呈病毒抗原给细胞毒性T细胞(cytotoxic T cell,Tc或CTL)的细胞免疫中发挥着关键作用。由此推断Bmp8a蛋白与抗病毒免疫有关。
实施例2:GCRV病毒刺激可显著上调斑马鱼bmp8a基因的表达
用草鱼呼肠孤病毒(Grass carp reovirus,GCRV)腹腔注射斑马鱼,分别用Real-time PCR技术检测对脾、肠、肝脏和肾脏组织中bmp8a基因表达的影响,发现GCRV病毒刺激可显著上调斑马鱼bmp8a基因的表达(图7)。同样,用GCRV病毒处理斑马鱼肝脏细胞系(ZFL),也发现bmp8a基因的表达显著上调(图8)。结果表明斑马鱼bmp8a对病毒刺激有明显的应答反应,Bmp8a在鱼类抗病毒免疫中具有重要作用。
实施例3:过表达斑马鱼Bmp8a可显著上调抗病毒相关基因的表达
在斑马鱼ZFL细胞系中,过表达斑马鱼Bmp8a,用Real-time PCR技术检测抗病毒相关基因IFNφ1、IFNφ3和Mx的表达,发现过表达斑马鱼Bmp8a可显著上调抗病毒相关基因IFNφ1、IFNφ3和Mx的表达(图9),进一步证明Bmp8a在鱼类抗病毒免疫中具有重要作用。
在EPC细胞系中,过表达斑马鱼Bmp8a。用GCRV病毒感染细胞,用Real-time PCR技术检测病毒基因VP5的表达,发现过表达斑马鱼Bmp8a可显著下调病毒基因VP5的表达(图10),证明Bmp8a具有抑制病毒在EPC细胞中的复制的功能。
实施例4:bmp8a突变体斑马鱼更易受到病毒感染
采取腹腔注射的方法用大菱鲆皮疣病毒感染斑马鱼,成年野生型和bmp8a突变体各10条,注射剂量是20μl,108TCID 50/ml。结果发现,大菱鲆皮疣病病毒感染后相同时间,突变体的病害症状程度更为严重(图11A);另外,野生型比突变体的生存率要高,在感染后5d,突变体开始死亡,直到6d多后全部死亡,在此期间,野生型斑马鱼一直没有出现死亡(图11B)。这说明Bmp8a参与了斑马鱼的抗病毒免疫,可提高斑马鱼对病毒感染的抵抗力。
本发明提供的Bmp8a蛋白可用于制备提高鱼类抗病毒免疫力的制品。例如饲料添加剂,但优选制备成能注射使用的液体制剂;通过注射方式来提供鱼体内Bmp8a蛋白的含量提升,从而提高鱼类抗病毒的能力。
序列表
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<120> 一种提高鱼类抗病毒免疫力的方法
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Claims (6)
1.一种Bmp8a蛋白的用途,其特征在于,是在制备提高鱼类抗病毒免疫力的制品中的应用。
2.如权利要求1所述的用途,其特征在于,所述的制品为饲料添加剂或注射用液体蛋白制剂。
3.本发明还提供bmp8a蛋白的另一种用途,是通过检测bmp8a蛋白的表达量来筛选抗病毒能力强的亲鱼。
4.如权利要求1-3任一项所述的用途,其特征在于,所述的Bmp8a蛋白的氨基酸序列为SEQ ID NO:1;其成熟肽的氨基酸序列为SEQ ID NO:2。
5.如权利要求1-3任一项所述的用途,其特征在于,所述的Bmp8a蛋白的编码基因,其核苷酸序列为SEQ ID NO:3。
6.一种提高鱼类抗病毒免疫力的方法,其特征在于,所述的方法是通过上调Bmp8a蛋白的表达量来增强鱼类的抗病毒免疫力。
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