中国寄生虫学与寄生虫病杂志

• 论著 • 上一篇    下一篇

过继转移RNA干扰日本血吸虫的发育表型评价技术的建立

柳建发1,李健2,任怡静3,张瑞祥2,方芳3,胡薇2,4*   

  1. 1 宁波大学医学院,宁波 315211;2 复旦大学生命科学学院,上海 200438;3 广西大学动物科学技术学院,南宁 530004;4 中国疾病预防控制中心寄生虫病预防控制所,国家热带病研究中心,世界卫生组织热带病合作中心,科技部国家级热带病国际联合研究中心,卫生部寄生虫病原与媒介生物学重点实验室,上海 200025
  • 出版日期:2018-06-30 发布日期:2018-07-02

Establishment of developmental phenotype evaluation technique for adoptive RNAi schistosomula transfer

LIU Jian-fa1, LI Jian2, REN Yi-jing3, ZHANG Rui-xiang2, FANG Fang3, HU Wei2,4*   

  1. 1 Medical School of Ningbo University, Ningbo 315211; 2 School of Life Science, Fudan University, Shanghai 200438, China; 3 School of Animal Science and Technology, Guangxi University, Nanning 530004, China; 4 National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention; Chinese Center for Tropical Diseases Research; WHO Collaborating Centre for Tropical Diseases; National Center for International Research on Tropical Diseases, Ministry of Science and Technology; Key Laboratory of Parasite and Vector Biology, Ministry of Health, Shanghai 200025, China
  • Online:2018-06-30 Published:2018-07-02

摘要:

目的 建立RNA干扰后的日本血吸虫转移至小鼠体内发育情况的评价技术,为后组学时代功能基因研究提供工具。 方法 设计引物扩增日本血吸虫组织蛋白酶B1(SjCB1)基因dsRNA、绿色荧光蛋白(GFP)dsRNA。用日本血吸虫尾蚴感染小鼠,收集14 d的日本血吸虫童虫。用6 mg/L SjCB1 dsRNA体外培养浸泡法对日本血吸虫童虫的SjCB1基因进行特异性敲低(SjCB1干扰组),对照组加6 mg/L GFP dsRNA(GFP干扰组)。采用外科手术将干扰后的童虫过继转移至小鼠肠系膜静脉(SjCB1干扰组、GFP干扰组各3只小鼠,40条/鼠),待虫体发育至性成熟时收集虫体。统计分析雌雄虫回收数量、合抱率、虫体回收率以及虫体长度,观察虫体生长发育情况。采用荧光定量PCR检测干扰后的14 d雌、雄童虫以及回收的雌、雄成虫SjCB1基因的表达情况。 结果 SjCB1干扰组、GFP干扰组回收的雌、雄虫数量,合抱率,虫体回收率分别为(9.0 ± 1.4)、(9.0 ± 2.1)条,(13.0 ± 2.9)、(11.3 ± 2.5)条,100%、100%和58.60%、54.67%。两组雌、雄虫数量,合抱率,虫体回收率差异均无统计学意义(P > 0.05)。SjCB1干扰组过继转移前雌、雄童虫SjCB1基因的相对表达量为1.022 ± 0.019、0.643 ± 0.105,均低于GFP干扰组的2.880 ± 0.297、2.753 ± 0.164(t = 0.000、0.000,P < 0.01);SjCB1干扰组回收的雌、雄虫SjCB1基因相对表达量分别为1.286 ± 0.211、1.182 ± 0.287,均低于GFP干扰组的5.506 ± 0.326、4.986 ± 1.230 (t = 0.013、0.000,P < 0.01)。SjCB1干扰组、GFP干扰组雌虫长分别为(7.059 ± 1.255) 、(8.433 ± 0.749) cm,雄虫长分别为(6.993 ± 2.734)、(10.561 ± 1.375) cm,两组间雌、雄虫差异有统计学意义(t = 0.003、0.001,P < 0.01)。SjCB1干扰组、GFP干扰组虫体外观形态及内部的生殖系统、消化系统未见差异,两组雌虫在卵模与子宫中均有成形的虫卵。 结论 建立了干扰特异性基因后观察虫体体内发育表型的技术,体外培养浸泡干扰后日本血吸虫童虫、成虫SjCB1基因表达水平被显著敲低,该方法可用于研究发育相关基因的表型。

关键词: 日本血吸虫, RNA干扰, 过继转移

Abstract:

Objective To establish an approach for evaluating the development of Schistosoma japonicum receiving RNA interference, after being transferred to mice, in order to provide a tool for studying functional genes in the post-genomics era. Methods The primers of S. japonicum cathepsin B1(SjCB1) and green fluorescent protein(GFP) genes were designed to amplify  dsRNA. The 14-day-old schistosomula were collected from infected mice, and cultured by in vitro soaking with 6 mg/L SjCB1 dsRNA to specifically knock down the SjCB1 gene (SjCB1 interference group). In the control group, 6 mg/L green fluorescent protein (GFP) dsRNA was used instead (GFP interference group). The schistosomula after interference were surgically transferred back to the mouse mesenteric vein (3 mice in each group, 40 schistosomula/mouse). The adult worms were then collected after growing to sexual maturity. The numbers of male and female worms recovered, the pairing rate, the recovery rate, and the body length were analyzed. The growth and development of the adult worms were assessed. The relative expression level of SjCB1 gene in 14-day schistosomula and in recovered adult worms was detected by real-time PCR.  Results The recovered numbers of female and male worms, the pairing rate and the recovery rate in the SjCB1 interference group were (9.0 ± 1.4), (13.0 ± 2.9), 100% and 58.60%, and those in the GFP interference group were (9.0 ± 2.1), (11.3 ± 2.5), 100% and 54.67%, respectively. None was significantly different between the two groups (P > 0.05). The relative expression levels of SjCB1 in male and female schistosomula before adoptively transferred were 1.022 ± 0.019 and 0.643 ± 0.105, respectively, in the SjCB1 interference group, and both were significantly lower than those in the GFP interference group (2.880 ± 0.297 and 2.753 ± 0.164) (t = 0.000, 0.000; P < 0.01). The relative expression levels of SjCB1 in female and male worms recovered from the SjCB1 interference group were 1.286 ± 0.211 and 1.182 ± 0.287, respectively, which were significantly lower than those in the GFP interference group (5.508 ± 0.326 and 4.896 ± 1.230) (t = 0.013, 0.000; P < 0.01). The lengths of females in the SjCB1 interference group and the GFP interference group were (7.059 ± 1.255) and (8.433 ± 0.749) cm (t = 0.003, P < 0.01), and the lengths of males were (6.993 ± 2.734) and (10.561 ± 1.375) cm, respectively (t = 0.001, P < 0.01). There were no differences in the appearance, the internal reproductive system and the digestive system between the SjCB1 interference group and the GFP interference group. Females in both groups had eggs with a clear shape in the egg molds and the uterus.  Conclusion A standard procedure has been established to observe the developmental phenotypes in vivo of S. japonicum with RNA interference, and the SjCB1 gene has been knocked down by a soaking method. This procedure can be used to study the phenotypes of development-related genes.

Key words: Schistosoma japonicum, RNA interference, Adoptive transfer