中国血吸虫病防治杂志 ›› 2007, Vol. 19 ›› Issue (05): 321-327.

• 论著 •    下一篇

血吸虫对吡喹酮抗药性的研究Ⅺ日本血吸虫中国大陆现场分离株虫卵毛蚴尾蚴对吡喹酮的敏感性

粱幼生1|戴建荣n|李洪军1|汪伟1|陶永辉1|张键锋1|李伟1|朱荫昌1|G.C.Coles2 |M.J. Doenhoff 3   

  1. 1江苏省血吸虫病防治研究所、卫生部寄生虫病预防和控制技术重点实验室、江苏省寄生虫分子生物学重点实验室(无锡214064);2英国Bristol大学医学院临床兽医系;3英国Wales大学生物科
  • 出版日期:2012-12-26 发布日期:2013-01-05
  • 作者简介:梁幼生(1958-)|男|博士|研究员。研究方向:血吸虫与钉螺的生物学、药理学及血吸虫病防治
  • 基金资助:

    国家自然科学基金(30471516)、江苏省自然科学基金(BK2004024)和江苏省医学领军人才项目

Studies on resistance of Schistosoma to praziquantel XIExperimental investigation on susceptibility of field isolates of Schistosoma japonicum in stages of eggs, miracidia and cercariae to praziquantel

 Liang You-sheng, Dai Jian-rong,  Lii Hong-jun , |Wang Wei| Tao Yong-huil|Zhang Jian- feng| Li  Wei| Zhu Yin-chang, |G. C. Coles, M. J. Doenhoff   

  • Online:2012-12-26 Published:2013-01-05

摘要:

目的测定日本血吸虫中国大陆主要流行区现场分离株虫卵、毛蚴和尾蚴阶段对吡喹酮的敏感性,为建立日本血吸虫吡喹酮敏感性检测技术提供基础。方法分别从中国湖南、湖北、江西、安徽、江苏和云南6省日本血吸虫病流行区病人粪便标本中分离虫卵,建立日本血吸虫现场分离虫株;采用实验室已有的3株曼氏血吸虫株为对照。将各虫株虫卵分别孵育于5×10-6、10-6、5×10-7、l0-7mol/L吡喹酮溶液中24 h后移至清水孵化,观察虫卵的孵化率。将各虫株毛蚴分别暴露于5×10-6、   10-6、5×10-7、10-7mol/L吡喹酮溶液中,0、1、5 min后观察比较毛蚴的运动及形态学变化。将各虫株尾蚴分别暴露于 10-5、6×10-7,4×10-7、10-7 moI/L吡喹酮溶液中,0、20、40、60、80、100 min后,解剖镜下观察尾蚴的泳动、收缩和断尾率的变化。并将结果与曼氏血吸虫株进行比较。结果 经10-6,5×10-7、10-7 mol/L吡喹酮溶液中24 h后,日本血吸虫虫卵的孵化率分别为0. 52%、11. 90%和49.15%,曼氏血吸虫分别为4.17%、31. 37%和92. 53%。当暴露于10-6 mol/L
吡喹酮1 min后,日本血吸虫毛蚴的变形率为100.00%,曼氏血吸虫为55. 73%;当分别暴露于5×10-7、10-7mol/L吡喹酮5 min后,日本血吸虫毛蚴的变形率为96. 82%和21. 80%,曼氏血吸虫毛蚴为21. 80%和0。当暴露于10-5 mol/L吡喹酮中40 min,日本血吸虫尾蚴的断尾率为96. 75%,曼氏血吸虫为28. 30%;暴露于4×10-7mol/L吡喹酮中100 min,日本血吸虫尾蚴的断尾率为95. 82%,曼氏血吸虫为11. 40%;当暴露于l0-7mol/L吡喹酮中80 min,日本血吸虫尾蚴的断尾率为29. 65%,曼氏血吸虫尾蚴为0。结论 日本血吸虫各现场分离株间在虫卵、毛蚴和尾蚴阶段财吡喹酮的敏感性无明显差异,但均明显高于曼氏血吸虫。研究提示,将毛蚴移人5×l0-7mol/L吡喹酮溶液中1 min,镜下观察其变形率,可作为日本血吸虫对吡喹酮敏感性的观察指标,可用于现场判断病人化疗失败的原因是否是由于吡喹酮不敏感株产生所引起。将尾蚴移入 4×10-7 mol/L吡喹酮溶液中80~100 min,镜下观察其断尾率,可用于螺体内虫株吡喹酮敏感性监测。

关键词: 日本血吸虫;曼氏血吸虫;吡喹酮;抗药性;虫卵;毛蚴;尾蚴

Abstract:

 Objective  To establish a test in vitro to monitor the susceptibility of field isolates of Schistosoma japonicum in stages of eggs, miracidia and cercariae to praziquantel. Methods   Six isolates of S. japonicum were collected from the endemic regions in Hunan, Hubei, Jiangxi, Anhui, Jiangsu and Yunan provinces, Cluna and 3 isolates of S. mansoni established in the lab were as the control.  The eggs were incubated in 5×10-6、10-6、5×10-7、l0-7mol/Lmol/L praziquantel for 24 hours, then the eggs were transferred to fresh water to hatch miracidia and the hatch rates were investigated and compared.  The miracidia were exposed t05×10-6、 10-6、5×10-7、10-7 mol/L praziquantel for 0, 1 and 5 min and then the swimming behavior and morphological changes were observed. Thecercariae were exposed in 10-5、6×10-7,4×10-7、10-7mol/L praziquantel for 0, 20, 40, 60, 80,100 min and then the changes in the patterns of behavior, including swimming, contraction and tail shedding were observed under a dissecting microscope. The number of cercariae which had shed tails were counted.  The differences between S. jaPonicum and S. mansoni were compared.  Results Following  the incubation in 10-6, 5X10-7, 10-7 mol/L praziquantel solutions for 24 h, the hatching rates of the eggs of S. japonicum were 0. 52%, 11. 90% and 49.15%, respectively, while thehatching rates of the eggs of S. mansoni which were 4.17%, 31.37% and 92.53%.  When the miracidia were exposed t0 10-6 mol/L praziquante for l min ,100% of miracidia from S. japonicum changed their shape, while only 55. 73% of miracidia from S.mansoni isolates changed their shape. When the miracidia were exposed t0 5 Xl0-7, 10-7mollL praziquantel, respectively, for 5 min,96. 75% and 37. 57% of miracidia from S. japonicum changed their shapes while only 21. 80% and 0
of miracidia from S.mansoniisolates changed their shapes. When the cercariae were exposed t0 10-5
mol/L praziquantel over 40 min,  96. 75% of the cercariae from S. japonicum isolates shed their
tails, while only 28. 30% of the cercariae from S. mansoni isolates shed their tails.  When the cer-
cariae were exposed t0 4X10-7 mol/L praziquantel over 100 min, 95. 82% of the cercariae from S.
 japonicum isolates shed their tails, while only 11. 40% of the cercariae from S. mansoni isolates shed
 their tails.  When the cercariae were exposed t0 10-7 mollL praziquantel over 80 min, 29. 65% of
 the cercariae from S. japonicum isolates shed their tails, while no cercariae from S. mansoni isolates
shed the tails. Conclusions  There were no difference in responses to praziquantel at the egg,
miracidial and cercarial stages among S. japoniczcm isolates, but the in. vitro responses to praziquan-
tel of eggs, miracidia and cercariae of S. japonicum compared with S. mansoni demonstrate that
eggs. miracidia and cercariae of S. japonicum are more sensitive to praziquantel than those of S.
 mansoni.  The percentage of the changes in the shape of miracidia from S. japonicum isolates follow-
 ing the exposure t0 5 Xl0-7mol/L praziquantel for 1 minute may be used to determine whether the
 failed therapy in patients infected  with S. japonicum is due to the presence of praziquantel unsuscep-
tible worms. The tail shedding rates of cercariae of following the exposure t0 4X10-7 mol/L prazi-
quantel for 80-100 minutes could be used to monitor for the presence of praziquantel-resistant
worms in infected snails collected from the field.

Key words:
 Schistosoma japonicum., S. mansoni,
Praz;quantel, Drug-resistance, Egg, Miracidium, Cercariaum, Cercaria

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