中国寄生虫学与寄生虫病杂志

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蚊龄对斯氏按蚊感染伯氏疟原虫能力的影响

宋秀梅,王敬文*   

  1. 复旦大学生命科学学院微生物与微生物工程系,上海200433
  • 出版日期:2016-12-30 发布日期:2017-01-10
  • 基金资助:

    国家自然科学基金(No. 31472039)

Influence of Age on the Susceptibility of  Anopheles stephensi to Plasmodium berghei Infection

SONG Xiu-mei, WANG Jing-wen*   

  1. 1 Department of Microbiology and Microbial Engineering, School of Life Sciences, Fudan University, Shanghai 200433, China
  • Online:2016-12-30 Published:2017-01-10
  • Supported by:

    Supported by the National Natural Science Foundation of China(No. 31472039)

摘要:

目的 研究不同日龄斯氏按蚊(Anopheles stephensi)传播伯氏疟原虫(Plasmodium berghei)能力的变化以及可能机制。 方法 选取4日龄和25日龄雌性斯氏按蚊,用原虫血疟为4%~8%的伯氏疟原虫感染BALB/c小鼠饲喂蚊虫,感染后8 d解剖蚊虫肠道,镜检计数蚊虫肠道中疟原虫卵囊数,比较4日龄和25日龄蚊虫对疟原虫易感性的变化。选取感染前4日龄和25日龄雌性斯氏按蚊,采用LB平板培养法检测其体内可培养共生菌的量,用实时定量PCR(real-time quantitative PCR,qPCR)方法检测其体内的共生菌总量。选取感染前4日龄和25日龄雌性斯氏按蚊,采用qPCR检测其体内天蚕抗菌肽1(cecropin,CEC1)、CEC3、防御素(defensin,DEF;gambicin,GAM)、攻击素(attacin,ATT)以及一氧化氮合成酶(nitric oxide synthase,NOS)、双氧化酶(dual oxidase,DUOX)和含硫酯蛋白1(thioester protein 1,TEP1)等主要免疫效应因子的表达水平。 结果 感染伯氏疟原虫后8 d,4日龄斯氏按蚊中肠道疟原虫卵囊中位数是139,25日龄按蚊卵囊数中位数是3,4日龄按蚊伯氏疟原虫的感染密度是25日龄的46倍(P<0.01)。qPCR结果显示,25日龄蚊虫体内共生菌总量为4日龄蚊虫的1.5倍,差异有统计学意义(P<0.05 );LB平板培养法结果显示,25日龄肠道可培养共生菌平均为28 889个菌落形成单位(colony forming units,cfu),是4日龄(3 200 cfu)的9倍,差异有统计学意义(P<0.01)。25日龄斯氏按蚊体内NOS基因表达量是4日龄的2.4倍(P<0.01),抗菌肽ATT、DEF、CEC3、CEC1的表达量分别为4日龄的27%、48%、14%、61%,差异均有统计学意义(P<0.05);4日龄与25日龄斯氏按蚊体内GAM、DUOX、TEP1的表达量均未发生显著变化。 结论 随斯氏按蚊日龄增加,斯氏按蚊抗菌肽水平发生显著下调,体内共生菌增多,NOS表达量上调,按蚊抵抗疟原虫的能力增强。

关键词: 年龄, 免疫反应, 共生菌, 伯氏疟原虫

Abstract:

Objective To investigate the ability of Anopheles stephensi at different ages to transmit Plasmodium berghei and elucidate the possible mechanisms. Methods To study and compare the susceptability of A. stephensi of different ages to P. berghei, 4-day and 25-day female A. stephensi were fed with P. berghei infected BALB/c mouse blood with parasitaemia 4%-8%. At 8 days after infection, the mosquitoes were dissected and the number of intestinal Plasmodium oocysts was counted under microscope. Difference in the susceptability to Plasmodium infection was analyzed between the two age groups. To study the intestinal bacteria load in A. stephensi, LB plate culture was used to detect the intestinal bacteria in the mosquitoes of the two groups before infection, and real-time quantitative PCR(qPCR) was performed to check the culturable bacteria and the total bacteria load. The expression levels of major immune response effectors cecropin(CEC1, CEC3), defensin(DEF), gambicin(GAM), attacin(ATT), nitric oxide synthase(NOS), dual oxidase(DUOX), and thioester protein 1(TEP1) in 4-day and 25-day mosquitoes were determined by qPCR. Results At 8 days after infection, the median of oocyst number in 4-day mosquitoes was 139, which was nearly 46 times of that in 25-day mosquitoes(median, 3)(P<0.01). There was a significant difference in the intestinal bacteria load between 4-day and 25-day mosquitoes. The results of qPCR showed that the total bacteria load in 25-day mosquitoes was 1.5 times of that in 4-day mosquitoes(P<0.05). By LB plate culture, proliferation of 28 889 colony forming units(cfu) bacteria was found for 25-day mosquitoes, which was 9 times of that for 4-day mosquitoes(3 200 cfu)(P<0.05). In addition, the NOS expression level in 25-day mosquitoes was 2.4 times of that in 4-day mosquitoes(P<0.01), while the expression levels of antimicrobiota peptides ATT, DEF, CEC3, and CEC1 in 25-day mosquitoes were only 27%, 48%, 14%, and 61% of those in 4-day mosquitoes, respectively(P<0.05). The expression levels of GAM, DUOX, TEP1 showed no difference between the two groups. Conclusion The antimicrobiota peptides in A. stephensi are significantly downregulated with age increase, together with increased intestinal bacteria load and NOS expression, resulting in enhanced resistance to Plasmodium.

Key words: Age, Immune response, Microbiota, Plasmodium berghei