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机构地区:[1]郑州大学医学院寄生虫学教研室,河南郑州450052
出 处:《中国病原生物学杂志》2010年第10期746-748,728,共4页Journal of Pathogen Biology
基 金:国家自然科学基金项目(No.30972579);高校博士点专项科研基金项目(No.20094101110004);郑州大学研究生科学研究基金资助项目(No.A119)
摘 要:目的观察旋毛虫肌幼虫在不同培养基中的发育情况。方法将旋毛虫肌幼虫接种在不同培养基中于37℃5%CO2条件下培养18 d,观察幼虫开始蜕皮的时间和蜕皮率,并测量幼虫长度。结果肌幼虫在RPMI-1640、含5%胎牛血清(FBS)的RPMI-1640培养液、PBS和生理盐水中开始蜕皮的时间分别为15、23、19和37 h;肌幼虫在RP-MI-1640与5%FBS+RPMI-1640中分别蜕皮1~4层和1~2层,在PBS与生理盐水中仅蜕皮1层。培养5 d后,RP-MI-1640中培养幼虫的蜕皮率(77.94%)显著高于在其他3种培养液培养的幼虫蜕皮率(39.83%、44.64%和8.84%)(Z1640+5%FBS=-2.268,ZPBS=-2.641,Zsaline=-6.826,P〈0.05);培养18 d后,在RPMI-1640中蜕2~4层皮的幼虫蜕皮率(25.6%、1.32%及0.26%)显著高于在5%FBS+RPMI-1640中培养的幼虫蜕皮率(0.45%、0和0)(Z2=-16.111,Z3=-7.991,Z4=-3.885,P〈0.05);在2种培养液中培养1~18 d的幼虫长度差异无统计学意义(t=0.138,P〉0.05),幼虫长度均随培养时间的延长而减小(F1640=54.639,P〈0.05;F1640+5%FBS=26.928,P〈0.05)。结论绝大多数旋毛虫肌幼虫在RPMI-1640与5%FBS+RPMI-1640培养液中不能蜕下完整表皮,不能发育到成虫阶段。Objective To observe the development of Trichinella spiralis muscle larvae in vitro in different media.Methods The larvae were inoculated in different media and cultured at 37 ℃ in 5%CO2 for 18 days.The molting time and rate of the cultured larvae were observed,and larval length was measured.Results The time when the larvae cultured in RPMI-1640,RPMI-1640+5% fetal bovine serum(FBS),PBS and saline began to molt was 15,19,23 and 37 h,respectively.Larvae with 1-4 and 1-2 sheath(s) were formed in RPMI-1640 and RPMI-1640 +5% FBS medium.Only a single sheath was observed when larvae were cultured in PBS and saline.The molting rate of larvae cultured in RPMI-1640 medium(77.94%) was significantly higher than that in 3 other kinds of media(39.83%,44.64%,and 8.84%) after culturing for 5 days(Z1640+5%FBS=-2.268,ZPBS=-2.641,Zsaline=-6.826,P0.05).After culturing for 18 days,the molting rates of larvae with 2-4 sheaths cultured in RPMI-1640 medium(25.6%,1.32% and 0.26%) were significantly higher than that in RPMI-1640+5% FBS medium(0.45%,0 and 0)(Z2=-16.111,Z3=-7.991,Z4=-3.885,P0.05).There was no statistically significant difference in the length of larvae cultured in RPMI-1640 and RPMI-1640+5% FBS medium for 1-18 days(t=0.138,P0.05),and the length decreased as the culturing time increased(F1640=54.639,F1640+5%FBS=26.928,P0.05).Conclusion The majority of T.spiralis muscle larvae cultured in RPMI-1640 and RPMI-1640+5% FBS medium were unable to completely shed the old cuticle and develop into adults.
分 类 号:R383.15[医药卫生—医学寄生虫学]
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