菜粉蝶蛹血细胞体外细胞免疫反应及蝶蛹金小蜂毒液的影响

为探明蝶蛹金小蜂Pteromalus puparum毒液对其寄主菜粉蝶Pieris rapae蛹颗粒血细胞和浆血细胞的包囊与吞噬能力的影响, 本研究分别采用Na₂-EDTA处理和尼龙毛法对菜粉蝶蛹颗粒血细胞与浆血细胞进行分离纯化; 再采用离体细胞培养方法, 研究了菜粉蝶蛹颗粒血细胞、 浆血细胞各自在包囊和吞噬反应中的作用, 以及蝶蛹金小蜂毒液对其所产生的影响。结果表明： 颗粒血细胞和浆血细胞均参与了包囊反应, 其中前者包囊作用明显, 后者作用微弱, 但两者同时存在时包囊作用最为明显; 血淋巴浆质对颗粒血细胞和浆血细胞包囊反应均无显著影响。毒液对颗粒血细胞和浆血细胞的包囊能力均存在显著的抑制作用, 且抑制作用具有明显的剂量效应特征。此外, 菜粉蝶蛹颗粒血细胞和浆血细胞均具吞噬能力, 其中前者吞噬能力显著强于后者; 毒液对颗粒血细胞与浆血细胞的吞噬能力亦均存在显著的抑制作用, 且该抑制作用亦具有显著的剂量效应特征。结果说明, 菜粉蝶蛹颗粒血细胞及浆血细胞均参与寄主的细胞免疫反应, 蝶蛹金小蜂毒液对其寄主颗粒血细胞和浆血细胞的包囊与吞噬能力均存在显著的抑制作用。     

蝶蛹金小蜂毒液蛋白不同提取分离方法的比较

为了建立蝶蛹金小蜂Pteromalus puparum毒液抑制寄主血细胞免疫活性组分合适的分离纯化方法,就等电点沉淀法、乙醇沉淀法、75%硫酸铵沉淀法、75%硫酸铵沉淀法+40℃加热处理法,以及75%硫酸铵沉淀法分别与3种不同滤膜的分子大小截留法的组合等7种方法对毒液蛋白分离效果及活性的影响进行了比较。结果表明：等电点沉淀法获得的组分抑制寄主菜粉蝶Pieris rapae离体血细胞延展和包囊的活性最强,乙醇沉淀法次之,75%硫酸铵沉淀法最弱。从蛋白组分的SDS-PAGE图谱来看,等电点沉淀法获得毒液组分相对最纯,仅有3条主要谱带,分子量大小在45～116.2 kDa范围内;乙醇沉淀法次之,有5条主要谱带,分子量大小在24～116.2 kDa范围内;硫酸铵沉淀法的谱带组成与毒液蛋白粗提液相似。3种分子大小截留法获得的毒液组分的活性分析表明,强活性组分分子量大小可能都大于100 kDa。综合认为,7种方法中以等电点沉淀法提取分离蝶蛹金小蜂毒液蛋白相对为最适。     

菜粉蝶蛹体型大小对蝶蛹金小蜂后代数量、性比及体型大小的影响

为检验“寄主体型大小-质量假说”,采取饥饿方法处理菜粉蝶(Pieris rapae)高龄幼虫,以获得体型大小(用体质量表示)差异大于同一自然地理种群内个体间差异的寄主蛹,然后供聚寄生蜂-蝶蛹金小蜂(Pteromalus puparum)寄生,观察寄生蜂在不同大小寄主蛹内的后代数量、性比以及体型大小。结果表明,蝶蛹金小蜂1次攻击产出的后代蜂数随寄主蛹体质量增加而显著增多,蛹中平均出蜂314.97头·g^-1。蝶蛹金小蜂后代的雌性比例随寄主蛹质量的增大而显著提高,后代雌蜂和雄蜂的体型大小(后足胫节长度)均随寄主蛹质量的增大而显著增大。可见,蝶蛹金小蜂母蜂能够根据寄主蛹质量来调整后代数量和性比,以使后代适应度最大化。最后,就蝶蛹金小蜂产卵策略及其影响因素进行了讨论。     

蝶蛹金小蜂寄生对菜粉蝶体液免疫反应的影响(英文)

以蝶蛹金小蜂及其寄主菜粉蝶为研究对象 ,研究了内寄生蜂对寄主体液免疫反应的影响。当寄主蛹被寄生后 1 2h或第 4和 5d时 ,血淋巴中酚氧化酶活性明显增高。寄生蛹血淋巴中血细胞凝集素活性始终高于针刺和未寄生蛹 ;同样 ,寄生蛹血淋巴的抗菌活性也明显增强 ,而后两者处理蛹的活性则很微弱。由此可知 ,该蜂寄生能引起寄主体液免疫因子活性的不同程度的变化     

蝶蛹金小蜂寄生对菜粉蝶血细胞骨架相关蛋白基因的转录调控

为揭示蝶蛹金小蜂Pteromalus puparum抑制寄主菜粉蝶Pieris rapae血细胞免疫反应的分子机制, 克隆了菜粉蝶肌动蛋白、肌动蛋白解聚因子及微管蛋白cDNA, 并研究了蝶蛹金小蜂寄生对其转录水平的影响。结果显示： 菜粉蝶肌动蛋白cDNA ORF为1 131 bp, 编码377 aa, 预测分子量为41.78 kDa, pI为5.29, 与其他昆虫肌动蛋白的相似性非常高, 在90%以上。氨基酸组成特点和系统进化分析表明, 克隆到的菜粉蝶肌动蛋白基因属细胞质型肌动蛋白。菜粉蝶肌动蛋白解聚因子cDNA全长为1 243 bp, ORF为 447 bp, 编码149 aa, 预测分子量为16.97 kDa, pI为7.11,与家蚕Bombyx mori、赤拟谷盗Tribolium castaneum、意大利蜜蜂Apis mellifera和桑粉介壳虫Maconellicoccus hirsutus肌动蛋白解聚因子的相似性分别为97%, 87%, 89%和72%。菜粉蝶微管蛋白cDNA全长为1 757 bp, ORF为1 344 bp, 编码448 aa, 预测分子量为50.38 kDa, pI为4.86, 与家蚕β型微管蛋白1, 2, 3和4的相似性分别为97%, 97%, 87%和93%。系统进化分析表明, 克隆到的菜粉蝶微管蛋白基因属β型微管蛋白。RT-PCR分析表明, 蝶蛹金小蜂寄生能抑制肌动蛋白、肌动蛋白解聚因子及微管蛋白基因在菜粉蝶蛹血细胞中的转录水平。由此推断蝶蛹金小蜂调控寄主血细胞骨架相关蛋白基因的转录是该蜂抑制寄主血细胞免疫反应的分子机制之一。     

蝇蛹俑小蜂、丽蝇蛹集金小蜂触角感器的扫描电镜观察

本文利用扫描电镜首次对蝇蛹俑小蜂(Spalangia endius)触角及其感器进行了研究.共观察到七类感器:触觉毛类感器、板状感器、薄壁化学感受器、锥形乳头状感器、鬃形感器、短刺形感器和棒状感器.同时在丽蝇蛹集金小蜂(Nasonia Vitripennis)触角上观察到七种感器.比较研究发现,在两种小蜂间.同种小蜂异性间.感器的种类、数量、排列及分布均有差异,并对此进行了讨论.     

丽蝇蛹集金小蜂寄生对寄主蛹可溶性蛋白与芳基蛋白组成与含量的影响

为了探讨蛹期寄生蜂对寄主蛋白代谢的寄生生理效应,利用Bradford蛋白含量测定法、Western免疫印迹法及酶联免疫吸附检测法研究了棕尾别麻蝇Boettcherisca peregrina蛹被丽蝇蛹集金小蜂Nasonia vitripennis寄生后其脂肪体和血淋巴中可溶性蛋白及芳基蛋白组成与含量的变化。结果表明：寄生蛹脂肪体和血淋巴中可溶性蛋白的组成与未寄生相比基本无明显差异; 不论寄生与否寄主蛹脂肪体和血淋巴中芳基蛋白亚基分子量均为80 kDa,该亚基在脂肪体中未出现降解现象,而在血淋巴中仅于寄生后12 h的寄主蛹中呈现2条分子量相近的Western免疫印迹带,说明其降解可能先于未寄生对照。就含量而言,寄生蛹脂肪体中可溶性蛋白含量除寄生后24 h外均显著低于未寄生对照,芳基蛋白含量除寄生后48 h外也均显著低于未寄生对照,其中寄生后12 h的含量仅为未寄生的32.0%。寄生蛹血淋巴中可溶性蛋白含量多低于未寄生蛹,且寄生后2,12,24 h的差异达显著水平;芳基蛋白的含量均有低于未寄生的趋势,其中寄生后12 h的含量为未寄生的17.0%。综合认为,丽蝇蛹集金小蜂的寄生可导致寄主脂肪体和血淋巴中可溶性蛋白及芳基蛋白含量下降。     

白蛾周氏啮小蜂毒液对美国白蛾蛹血细胞免疫的影响

【目的】明确白蛾周氏啮小蜂Chouioia cunea毒液对其寄主美国白蛾Hyphantria cunea蛹细胞免疫的影响。【方法】采用Na_2-EDTA分离美国白蛾蛹颗粒细胞,尼龙毛法分离浆血细胞,再利用细胞离体培养法,测评了白蛾周氏啮小蜂毒液对寄主美国白蛾两种血细胞包囊作用和吞噬作用的影响。【结果】美国白蛾颗粒细胞的包囊指数强于浆血细胞。白蛾周氏啮小蜂毒液对颗粒细胞和浆血细胞的包囊指数均有明显的抑制作用,毒液浓度越大,抑制作用越强,两种血细胞的包囊作用均呈先增长后降低的趋势。在所有浓度毒液处理下,颗粒细胞的包囊指数在12 h时最强。未经小蜂毒液处理的浆血细胞包囊指数在15 h时达到最强,但经浓度为0.01~0.03 VRE/μL的毒液处理后浆血细胞的包囊指数在12 h时达到最强,而经浓度为0.04~0.10 VRE/μL的毒液处理后包囊指数在9 h时最强。白蛾周氏啮小蜂毒液对美国白蛾蛹颗粒细胞的吞噬作用强于浆血细胞。毒液对两种血细胞的吞噬能力均有明显的抑制作用,但毒液处理对浆血细胞的吞噬作用影响较小。【结论】白蛾周氏啮小蜂毒液可以抑制美国白蛾蛹颗粒细胞和浆血细胞的包囊作用和吞噬作用,且随着毒液浓度的增加,两种血细胞的免疫作用显著下降。     

棉铃虫血细胞对葡聚糖凝胶珠的包囊反应

研究了棉铃虫Helicoverpa armigera(Hübner)血细胞对葡聚糖凝胶珠的包囊反应。结果表明:棉铃虫血细胞对不同类型的葡聚糖凝胶珠具有不同的包囊能力,其中对SephadexA-25葡聚糖凝胶珠具有很强的包囊能力;棉铃虫血细胞启动对SephadexA-25葡聚糖凝胶珠的包囊反应是较迅速的,而包囊的完成大概是在凝胶珠进入棉铃虫体内12h之后;在离体的情况下,棉铃虫血细胞仍然能包囊葡聚糖凝胶珠。     

去除Wolbachia 对丽蝇蛹集金小蜂繁殖适合度和成蜂寿命的影响

【目的】明确内共生菌 Wolbachia 对丽蝇蛹集金小蜂 Nasonia vitripennis 繁殖适合度和成蜂寿命的影响。【方法】通过给自然感染 Wolbachia 的丽蝇蛹集金小蜂成蜂喂食不同浓度的利福平来消除其体内的 Wolbachia,然后进行10个世代的连续饲养,探究不同浓度利福平对丽蝇蛹集金小蜂体内 Wolbachia 的去除效果和去除 Wolbachia 后对丽蝇蛹集金小蜂繁殖力、性比（雌蜂占子代数量的比值）和成蜂寿命的影响。【结果】低浓度利福平（0.1~0.5 mg/mL）对丽蝇蛹集金小蜂的毒害作用较小,而高浓度利福平（0.7~10.0 mg/mL）对丽蝇蛹集金小蜂的毒害作用较大,但二者均能去除丽蝇蛹集金小蜂体内的 Wolbachia;去除 Wolbachia 后丽蝇蛹集金小蜂的出蜂量显著下降（P <0.01）,子代中性比显著下降（P <0.01）,但寿命无明显差异。【结论】不同浓度利福平均能去除丽蝇蛹集金小蜂体内Wolbachia,但效果不一致;Wolbachia 对丽蝇蛹集金小蜂的出蜂量和子代性比均有显著影响,对成蜂寿命无显著影响。     

Venom of Pteromalus puparum (Hymenoptera: Pteromalidae) induced endocrine changes in the hemolymph of its host,Pieris rapae (Lepidoptera: Pieridae)

Pteromalus puparum is a predominant endoparasitoid wasp of Pieris rapae. Its venom is the only active factor injected into host associated with oviposition. In this report, we explored whether the venom alone from this wasp affects the endocrine system of its host or not. We monitored the changes of hemolymph juvenile hormone (JH; only JH III detected), ecdysteroid, and juvenile hormone esterase activity (JHE) over 72 h in parasitized and venom‐microinjected P. rapae pupae. Non‐parasitized and PBS‐microinjected P. rapae served as controls. Results showed that JH titers were significantly higher in parasitized and venom‐microinjected pupae than that in control pupae during 24 to 72 h. After 12 h, JH titers were significantly promoted by parasitization and venom microinjection. JHE activities of non‐parasitized and PBS‐microinjected pupae were significantly higher than that of parasitized and venom‐microinjected pupae, which was with a peak at 12 h (parasitized pupae) or 24 h (venom‐microinjected pupae) during 6 to 48 and 12 to 36 h, respectively. The hemolymph titers of ecdysteroid in non‐parasitized and PBS‐microinjected pupae increased rapidly during 12 to 36 h with a peak at 36 h, and were higher than treatments before 48 h, while presenting a significant difference at 24 to 48 h between the treatments and controls. The results demonstrate that venom alone of this parasitoid wasp can disrupt its host's endocrine system. © 2009 Wiley Periodicals, Inc.     

Parasitism of Pieris rapae (Lepidoptera: Pieridae) by the endoparasitic wasp Pteromalus puparum (Hymenoptera: Pteromalidae): Effects of parasitism on differential hemocyte counts,micro‐ and ultra‐structures of host hemocytes

Abstract Parasitism by the endoparasitic wasp Pteromalus puparum (Hymenoptera: Pteromalidae) by using only its associated venom, can suppress the immunal responses of Pieris rapae (Lepidoptera: Pieridae). However, up to now, current knowledge of the mechanisms has been limited. The response of host hemocytes to parasitism was investigated using a combination of light and transmission electron microscopy (TEM). Five hemocyte types, prohemocytes (PRs), granulocytes (GRs), plasmatocytes (PLs), oenocytoids (OEs) and coagulocytes (COs), were observed and characterized from both unparasitized and parasitized Pieris rapae pupae. Light microscopy showed that both GRs and PLs became more round and spread abnormally after parasitism, whereas the shape of other types of hemocytes remained unaffected. In addition, the size of PRs and PLs became larger while OEs became smaller. The proportion of PRs significantly increased after parasitism and that of PLs decreased by 43.9%, but there was no significant increase of GRs and OEs. TEM showed that all types of hemocytes except COs were damaged to various degrees after parasitism, especially resulting in electron opaque cytoplasm and nucleus, fewer cell organelles of rough endoplasmic reticulum, mitochondria and vesicles. Our results indicate that parasitism by P. puparum affects differential hemocyte counts and structures of host hemocytes, particularly for GRs and PLs, which may be the main cause of the parasitoid suppressing host cellular immune responses.     

Parasitism of Pieris rapae (Lepidoptera: Pieridae) by a pupal endoparasitoid, Pteromalus puparum (Hymenoptera: Pteromalidae): effects of parasitization and venom on host hemocytes

In contrast to the situation with egg-larval and larval endoparasitic wasps, little is known about the effects of pupal endoparasitoids and their secretions on the hemocytes of their insect hosts. This study focuses on the pupal endoparasitoid, Pteromalus puparum, and its host, the small white butterfly, Pieris rapae. Parasitism by P. puparum, resulted in a significant increase in the total number of host hemocytes up to day five after parasitization. From day one to day four after parasitization, the percentage of plasmatocytes significantly decreased, and the proportion of granular cells increased. Moreover, from 12 h to day three after parasitization, hemocyte mortality in parasitized pupae was noticeably higher. When P. rapae pupae were parasitized by adult females of P. puparum irradiated by gamma-ray (pseudoparasitization), it was clear that the treated wasps could induce similar hemocyte changes. However, such phenomena did not occur in punctured host pupae (mimic-parasitization). After treatment with P. puparum venom, both the percentages of spreading plasmatocytes and encapsulated Sephadex G-25 beads were lessened significantly in vitro. Electron microscopy analysis and visualization of hemocyte F-actin with phalloidin-FITC showed that hemocytes treated with venom had a rounded configuration and neither spread nor extended pseudopods, while there was no marked alteration of hemocyte cytoskeletons after venom treatment. The results suggested that venom of P. puparum could actively suppress the hemocyte immune response of its host, but not by destroying the host hemocyte cytoskeleton.     

蝶蛹金小蜂热激蛋白家族基因表达与热保护功能

作为分子伴侣, 热激蛋白可起修复变性蛋白与阻止其他蛋白质聚集的作用。为进一步理解蝶蛹金小蜂Pteromalus puparum热激蛋白家族的分子伴侣功能, 本研究对来自该寄生蜂的热激蛋白Pphsp90, Pphsp70, Pphsc70, Pphsp60, Pphsp40和Pphsp20的基因在大肠杆菌Escherichia coli BL21菌株中进行了过表达。结果表明： 除Pphsp40外, 其余5个基因均得到高效表达, 且表达的重组热激蛋白在高温下（80℃）具可溶性与热稳定性。其中, Pphsp20与Pphsp90在大肠杆菌中的表达显著提高了高温下（50℃, 1 h）细胞的存活率。离体活性实验证实, 利用纯化的融合蛋白Pphsp20可减少高温下荧光素酶的聚集现象。据此认为, Pphsp20与Pphsp90均具有大肠杆菌细胞的热保护功能, 但Pphsp20可以单独发挥作用, 而Pphsp90可能需其他因子协同作用才有保护活性。     

Effects of starvation on the vitellogenesis,ovarian development and fecundity in the ectoparasitoid,Nasonia vitripennis (Hymenoptera: Pteromalidae)

A female‐specific protein, vitellogenin (Vg), and its corresponding egg vitellin (Vt) are identified in the ectoparasitic wasp Nasonia vitripennis. Both native Vt and Vg have a molecular mass of about 350 kDa, which is composed of two subunits of approximately 190 kDa and 165 kDa under reducing and denaturing conditions (sodium dodecyl sulfate—polyacrylamide gel electrophoresis). An indirect sandwich enzyme‐linked immunosorbent assay developed with both monoclonal and polyclonal antibodies against N. vitripennis Vt. Vg was first detected in the hemolymph on the 10th day after parasitism, and was first observed in oocytes on the 12th day. In adults deprived of food, the highest hemolymph Vg level occurred at the time of adult eclosion and the highest level of Vt in ovaries was found at 30 h after eclosion. In contrast, feeding adults with 20% sucrose resulted in the reduction of Vt uptake by ovaries and the extension of life span, but had little effect on Vg production. Deprived of hosts, starvation of female wasps had no significant effects on ovariole growth and oocyte maturation before the wasps died. However, starvation of female wasps supplied with hosts accelerated the wasps laying progeny into hosts, but resulted in a decrease of total progeny production by comparison with wasps fed with 20% sucrose.