中国农业科学 ›› 2007, Vol. 40 ›› Issue (5): 1042-1049 .

• 畜牧·兽医·资源昆虫 • 上一篇    下一篇

抗浓核病毒中国株家蚕品系中肠羧酸酯酶活力变化和基因表达差异的研究

高贵田,陈克平,姚 勤,陈慧卿,王林玲,徐家萍,赵 远,王永杰   

  1. 江苏大学生命科学研究院
  • 收稿日期:2006-03-16 修回日期:1900-01-01 出版日期:2007-05-10 发布日期:2007-05-10
  • 通讯作者: 陈克平

The activity of carboxylesterase in the midgets of Bombyx mori against BmDNV-Z

  1. 江苏大学生命科学研究院
  • Received:2006-03-16 Revised:1900-01-01 Online:2007-05-10 Published:2007-05-10

摘要: 【目的】探讨家蚕中肠羧酸酯酶活力变化及羧酸酯酶基因表达差异与家蚕抗浓核病毒之间的关系,阐明其抗性的分子机理。【方法】以易感浓核病毒中国株家蚕品系华八和完全抗性品系BC8(华八的近等基因系)为材料,用BIO-TEK SYNERGY测定经口接种病毒(以下简称接种)后12 h、36 h、72 h 2个品系中肠的羧酸酯酶活力,并用实时荧光定量PCR研究接种后12 h、36 h、72 h中肠羧酸酯酶基因的表达差异。【结果】接种后12 h中肠羧酸酯酶活力BC8接种组分别是BC8对照组、华八接种组和华八对照组的3.28倍、2.26倍和3.02倍,差异达到极显著水平(P<0.01)其它时间段的供试组之间无统计学差异;接种后12 h中肠羧酸酯酶基因的相对表达量BC8接种组分别是华八接种组、华八对照组、BC8对照组的17.714倍、21.76倍和15.09倍,差异达到极显著水平(P<0.01),其它时间段的供试组之间也无统计学差异。【结论】接种后12 h抗性品系BC8中肠羧酸酯酶活力升高及中肠羧酸酯酶基因表达水平升高可能与家蚕品系是否有抗性基因(nsd/nsd)有关,也与浓核病毒中国株的感染刺激有关;抗性品系BC8中肠羧酸酯酶活力升高的分子基础可能是羧酸酯酶基因表达水平的改变。

关键词: 家蚕, 抗性, 浓核病毒中国株, 中肠, 羧酸酯酶, 酶活力, 表达差异

Abstract: We dectected the activity of Bombyx mori carboxylesterase (BmCarE)in the midgetss by BIO-TEK SYNERGY between the silkworm strains HUABA which is susceptible to BmDNV-Z and BC8 which is resistant to the same virus. The expression differential of the BmCar was investigated after infecting 12,36 and 72 hours by Real-time fluorescence quantitative PCR. The results showed that : 1).The activity of BmCarE in the midgut of BC8 infecting virus after 12 hours was 3.28,2.26 and 3.02 times of that in the BC8 (water), HUABA (DNV)and HUABA (water) respectively (P<0.01), and therer was no statistic difference among the three treatments BC8 (water), HUABA (DNV)and HUABA (water); 2).The quantity of BmCarE in the midgut of BC8 infecting virus after 12 hours was 17.714, 21.76 and 15.09 times of that in the BC8 (water), HUABA (DNV)and HUABA (water) respectively (P<0.01), and therer was no statistic difference among the three treatments BC8 (water), HUABA (DNV)and HUABA (water); 3). The increase of BmcarE activity and the expression level related to the resistant gene (nsd/nsd) and the stimulation of BmDNV-Z; 4). The molecular base of the increase of BmcarE activity in the resistant strain BC8 was the change of carboxylesterase in the transcription level.