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营养因素对日本血吸虫毛蚴人工转变母胞蚴及体外培养的影响 被引量:2

EFFECTS OF NUTRITIVE FACTORS ON SCHISTOSOMA JAPONICUM MIRACIDIAL TRANSFORMATION AND MOTHER SPOROCYST CULTURE IN VITRO
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摘要 本文报道了4种培养基、4种血清、不同浓度的半乳糖、二巯基苏糖醇及部分三羧酸循环中间产物对日本血吸虫毛蚴体外转变为母胞蚴及其存活的影响。发现稀释一倍的RPMI 1640加10%兔血清为较适宜的培养基。上述添加剂对毛蚴转变和母胞蚴存活均无有益作用,其中柠檬酸可显著抑制毛蚴的转变。文中描述了毛蚴在体外转变成母胞蚴的过程,对血吸虫的糖代谢途径进行了讨论。 This paper observed the effects of several factors on the transformation of miracidia of Schistosoma japonicum and on the culture of young mother sporocysts of S. japonicum in vitro. The results showed: Different media (RPMI 1640, Tc 199, BME, and half strength RPMI 1640) and different serums (calf, sheep, rabbit, and 'O' type human serum) did not affect the transformation. The longest survival seen in half strength RPMI 1640 was 48 days. The development of germinal balls was observed. The length of some parasites was nearly doubled, at 164μm. The serum of rabbit was most beneficial to the survival of the parasites. Galactose and DTT could not promote the transformation and the survival. Citrate, -ketoglutarate, malate and sodium succinate were not helpful to the survival of parasites. They inhibited the transformation and the effect of citrate was significant. The process of miracidial transformation in vitro was discribed and the ways of carbohydrate metabolism in mother sporocysts were discussed. Authors suggested 'Latin square' as an optimum design in studying the composition of medium.
出处 《水生生物学报》 CAS CSCD 北大核心 1989年第4期326-333,T001,共9页 Acta Hydrobiologica Sinica
基金 自家自然科学基金
关键词 日本血吸虫 毛蚴 母胞蚴 体外培养 营养因素 糖代谢 Schistosoma japonicum, miracidium, mother sporocyst, culture in vitro
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参考文献4

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  • 2周述龙,动物学报,1985年,31卷,143页
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同被引文献29

  • 1彭延,董惠芬,蒋明森,钟沁萍,胡世全.β-巯基乙醇与肝基质对日本血吸虫培养细胞的影响[J].中国地方病学杂志,2004,23(4):307-310. 被引量:11
  • 2罗金萍.血吸虫毛蚴孵化法的改进[J].咸宁学院学报(医学版),2005,19(6):464-464. 被引量:3
  • 3Coustau C,Yoshino TP.Flukes without snails:advances in the in vitro cultivation of intramolluscan stages of trematodes[J].Exp Parasitol,2000,94 (1):62-66.
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  • 5Voge M,Seidel JS.Transfomation in vitro of miracidia of Schistosoma mansoni and S.japonicum into young sporocysts[J].J Parasitol,1972,58 (4):699-704.
  • 6Basch PF,DiCoza JJ.The miracidiumsporocyst transition in Schistosoma mansoni:surface changes in vitro with ultrastructural correlation[J].J Parasitol,1974,60(6):935-941.
  • 7DiConza JJ,Hansen EL.Cultivation of Schistosoma mansoni daughter sporocysts in arthropodtissueculture[J].J Parasitol,1973,59(1):211-212.
  • 8DiConza JJ,Basch PF.Axenic cultivation of Schistosoma mansoni daughter sporocysts[J].J Parasitol,1974,60(5):757-763.
  • 9Hansen EL,Peret-Mendez G,Yarwood E,et al.Second-generation daughter sporocysts of Schistosoma mansoni in axenic culture[J].J Parasitol,1974,60(2):371-372.
  • 10Yoshino TP,Laursen JR.Production of Schistosoma mansoni daughter sporocysts from mother sporocysts maintained in synxenic culture with Biomphalaria glabrata embryonic (Bge)cells[J].J Parasitol,1995,81 (5):714-722.

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