RNAi分析舞毒蛾谷胱甘肽S-转移酶(GST)基因对黄酮和槲皮素胁迫响应

为了明确舞毒蛾Lymantria dispar谷胱甘肽S-转移酶家族基因对生长发育影响及对次生物质的响应机制,采用RNAi技术分别沉默LdGSTe2、LdGSTs1、LdGSTs2和LdGSTz1基因,分析对舞毒蛾3龄幼虫体重、存活率、营养利用等生理指标的影响以及次生物质黄酮和槲皮素胁迫响应.结果表明,dsRNA可有效抑制LdGSTe2、LdGSTs1、LdGSTs2和LdGSTz1基因表达,分别注射dsLdGSTe2、dsLdGSTs1、dsLdGSTs2和dsLdGSTz1处理组舞毒蛾幼虫的相对生长率、相对取食量、食物利用率、食物转化率均低于对照组,但对幼虫的存活率无影响,表明LdGSTe2、LdGSTs1、LdGSTs2和LdGSTz1影响舞毒蛾幼虫生长发育;次生物质黄酮和槲皮素胁迫下,沉默LdGSTe2、LdGSTs1、LdGSTs2和LdGSTz1后舞毒蛾幼虫存活率显著下降,体重显著降低.沉默LdGSTe2、LdGSTs1、LdGSTs2和LdGSTz1基因对舞毒蛾幼虫的生长发育、食物利用具有抑制作用,同时影响了舞毒蛾幼虫对黄酮和槲皮素的适应能力.     

外源茉莉酸诱导的青杨叶片保护性酶活性变化及其对舞毒蛾幼虫生长发育的影响

为探讨外源茉莉酸对青杨Populus cathayana的诱导抗性及其对舞毒蛾Lymantria dispar的影响, 室内对青杨扦插苗喷施不同浓度的茉莉酸（对照为0.17%丙酮）, 分别在喷施后1, 5和10 d采集叶片分析其保护性酶活性的变化, 并接舞毒蛾幼虫于青杨苗木上观测其长发育情况。结果表明： 0.1 和0.001 mmol/L两种浓度的茉莉酸（JA）处理均使青杨叶过氧化物酶（POD）、 多酚氧化酶（PPO）、 苯丙氨酸解氨酶（PAL）、 胰凝乳蛋白酶抑制剂（CI）和胰蛋白酶抑制剂（TI）活性较对照增加(P<0.05)。取食茉莉酸诱导的青杨苗木后, 舞毒蛾幼虫的发育历期延长, 体重降低。0.1 mmol/L茉莉酸诱导的青杨苗木5 d后接虫, 使舞毒蛾幼虫的发育历期显著延长, 较对照长8 d; 接虫21 d后称重时, 取食茉莉酸诱导的青杨叶片的幼虫体重较对照组降低了50%~100%, 该结果说明外源茉莉酸诱导青杨产生了对舞毒蛾明显的抗虫性。     

绿原酸提高舞毒蛾核型多角体病毒(LdNPV)的致病力

【目的】明确绿原酸(chlorogenic acid,CA)对舞毒蛾核型多角体病毒Lymantria dispar necleopolyhydrovirus(Ld NPV)致病力的影响,为舞毒蛾的防治提供参考依据。【方法】采用食料给毒法进行生物测定,测定舞毒蛾2龄幼虫对单独Ld NPV及添加绿原酸的Ld NPV(CA+Ld NPV)的剂量及致死时间响应。【结果】CA+Ld NPV与单独Ld NPV对舞毒蛾2龄幼虫的剂量及时间响应间有显著差异,二者对舞毒蛾2龄幼虫的致死中浓度(LC50)分别为161.8 OBs/μL(95%的置信区间为105.6~235.3 OBs/μL)和264.4 OBs/μL(95%的置信区间为178.6~384.0 OBs/μL),前者对舞毒蛾的致病力较后者强。CA+Ld NPV对舞毒蛾2龄幼虫的致死中时间(LT_(50))较Ld NPV的短,当Ld NPV浓度为590 OBs/μL,CA+Ld NPV及Ld NPV对舞毒蛾2龄幼虫的LT_(50)分别为9.9 d和12.3 d;当Ld NPV浓度为5 900 OBs/μL时,则LT_(50)分别为6.9 d和8.0 d。绿原酸降低了Ld NPV对舞毒蛾幼虫的致死中浓度,缩短了致死中时间。【结论】绿原酸可提高Ld NPV对舞毒蛾2龄幼虫的致病力,其机理有待进一步研究。     

舞毒蛾卵寄生蜂大蛾卵跳小蜂发育与温度的关系及利用替代寄主柞蚕卵繁育的子代品质评价

舞毒蛾Lymantria dispar (L.)是国际性检疫害虫。大蛾卵跳小蜂Ooencyrtus kuwanae (Howard)是舞毒蛾卵的重要寄生蜂, 对舞毒蛾有一定的控制作用。为了在规模化繁育大蛾卵跳小蜂时控制小蜂的发育进度, 设置不同的温度梯度研究了该蜂发育与温度的关系; 同时, 为了对替代寄主繁育出的天敌质量进行评价, 对利用其自然寄主舞毒蛾卵和替代寄主柞蚕Antheraea pernyi卵繁育出的子代成蜂的寿命、 胸宽、 雌雄性比进行了比较。结果显示： 大蛾卵跳小蜂的发育起点温度和有效积温分别为10.50±1.41℃和260.74±25.09日·度, 温度与发育速率的关系为T=10.50+260.74V。当采用30%的蜂蜜水饲喂成蜂时, 柞蚕卵繁育出的大蛾卵跳小蜂雌、 雄蜂的平均寿命分别为15.01和10.38 d, 采用原寄主舞毒蛾卵繁育出的雌、 雄蜂平均寿命分别为20.94和15.95 d, 两者差异显著; 采用柞蚕卵繁育出的雌蜂个体显著大于用舞毒蛾卵繁育出的雌蜂个体; 柞蚕卵和舞毒蛾卵繁育出的大蛾卵跳小蜂雌雄性比没有显著差异, 分别为2.42∶1和2.57∶1。结果表明, 在野外开展舞毒蛾的生物防治时, 释放利用柞蚕卵繁育出的大蛾卵跳小蜂具有可行性。     

Putrescine--an inhibitor of the reaction of carbon dioxide hydration in hemolymph of lepidoptera

Using high-voltage electrophoresis, thin-layer chromatography and chemical analysis tetramethylene diamine was found in hemolymph of 8 Lepidoptera species (Bombyx mori L., Ocneria dispar L., Euproctis chrysorrhoea L., Yponomeuta malinella L., Pieris brassicae L., Aporia crataegi L., Melacosoma neustria L., Mamestra brassicae L.). Its content reaches 11 mM 1 l of hemolymph. The absence of tetramethylene diamine in the intestine wall and Malpighian vessels and its presence in the fat body permits suggesting its synthesis in the fat body. Ion-selective H-electrodes were used to show the function of tetramethylene diamine as an inhibitor of the CO2 hydration reaction in the insects hemolymph.     

Attachment and germination of Entomophaga maimaiga conidia on host and non-host larval cuticle

The lepidopteran-specific fungal pathogen Entomophaga maimaiga is highly virulent against Lymantria dispar (gypsy moth) larvae, and other members of the family Lymantriidae. Numerous species in the subfamily Cuculliinae (Family Noctuidae) are not susceptible to E. maimaiga due to the inability of this fungus to penetrate the larval cuticle. Conidial attachment and germination were compared among five cuculliine species and L. dispar using bioassays and scanning electron microscopy. Although conidia were showered evenly across larvae during bioassays, on L. dispar conidia were most abundant on segments, where they adhered well to the cuticle and germinated at high percentages. Conidia on cuculliine cuticles were predominantly found in large, loose aggregations in intersegmental areas. Few conidia on cuculliine cuticle germinated and scanning electron microscopy revealed a thick film of mucous enveloping conidia. We hypothesize that the conidia on cuculliines become coated by this film and were only loosely attached to the larval cuticle. No such film was seen on L. dispar larvae where individual conidia appeared well attached. On L. dispar larvae many conidia also adhered to setae. To determine if hydrophobicity affected the ability of E. maimaiga conidia to attach and germinate on a substrate, a goniometer was used to determine relative hydrophobicity of larval cuticles. L. dispar cuticle was more hydrophobic than cuculliine cuticle, suggesting that a high level of hydrophobicity could be a required characteristic for hosts. Cuticles from four cuculliine species and L. dispar were sequentially extracted using hexane, chloroform, and methanol. Conidia were showered onto glass slides coated with the different extracts and germination was quantified. Methanol extracts of cuculliine cuticle consistently decreased germination, compared to all extracts of L. dispar cuticle. For all L. dispar extracts, the majority of conidia produced germ tubes, which is a normal prerequisite for cuticular penetration. For the cuculliines, conidia exposed to hexane and chloroform extracts produced secondary conidia as did all controls, but the conidia exposed to cuculliine methanol extracts that germinated produced germ tubes. These studies demonstrated that a range of factors act in concert to prevent E. maimaiga infection of the cuculliine species investigated.     

Conversion of 3-dehydroecdysone by a ketoreductase in post-diapause, pre-hatch eggs of the gypsy moth Lymantria dispar

The prothoracic glands (PGs) of Lymantria dispar (day-5 female, last-stage larvae) produce both ecdysone and an ecdysteroid which has the same retention time on reverse-phase liquid chromatography (RPLC) as a known standard of 3-dehydroecdysone. The latter ecdysteroid can be converted by a heat-labile factor in extracts of post-diapause, pre-hatch L. dispar eggs to an ecdysteroid which has the same retention time on RPLC as ecdysone. Purified 3-dehydroecdysone, similarly treated with egg extract, also gives the same retention time on RPLC as ecdysone. Taken together, these data suggest that, like Manduca sexta, a major product of the PGs in L. dispar is 3-dehydroecdysone. Furthermore, these data suggest that L. dispar eggs, which contain mature embryos, possess ecdysteroid ketoreductase activity capable of converting 3-dehydroecdysone to ecdysone. This is the first report of ecdysteroid ketoreductase activity in embryonated eggs.     

Response of beech (Fagus sylvatica) to elevated CO2 and N: Influence on larval performance of the gypsy moth Lymantria dispar (Lep., Lymantriidae)

Two-year-old beech seedlings were kept from germination to bioassays with Lymantria dispar under the following conditions: ambient CO₂/low N, elevated CO₂/low N, ambient CO₂/elevated N, and elevated CO₂/elevated N. The effect of these growing conditions of the trees on the performance of the defoliator L. dispar was studied 2 years after initiating the tree cultivation. The developmental success of third-instar larvae of L. dispar was characterized by the weight gained, percentage of weight gain, relative growth rate (RGR), relative consumption rate (RCR), and efficiency of conversion of ingested food into body substance (ECI). Contrary to our expectations, additional N-fertilization did not increase and elevated CO₂ did not delay larval growth rate. However, the environmental treatments of the beech seedlings were found to affect the larval performance. Larvae consumed significantly higher amounts of foliage (RCR) on beech trees under controlled conditions (ambient CO₂ and low N) compared to those under elevated CO₂ and enhanced N. The opposite was true for ECI. The lowest efficacy to convert consumed food to body substance was observed under control conditions and the highest when the larvae were kept on beech trees grown under elevated CO₂ and additional N-fertilization. These opposite effects resulted in the weight gain-based parameters (absolute growth, percentage of growth, and RGR) of the gypsy moth larvae remaining unaffected. The results indicate that the gypsy moth larvae are able to change their ECI and RCR to obtain a specific growth rate. This is discussed as an adaptation to specific food qualities.     

ALLOCATION OF CYSTEINE FOR GLUTATHIONE PRODUCTION IN CATERPILLARS WITH DIFFERENT ANTIOXIDANT DEFENSE STRATEGIES: A COMPARISON OF Lymantria dispar AND Malacosoma disstria

Sulfur amino acids [cysteine (Cys) and methionine (Met)] play two major roles during animal development: protein synthesis for growth and glutathione synthesis for defense. For caterpillars, the levels of sulfur amino acids found in foliar protein can be especially low relative to their nutritional needs. Previous work has measured concentrations of glutathione (GSH; containing Cys) in specific animal tissues, but has not examined whole‐body levels to ascertain the costliness of this defense in terms of Cys allocation. This study examined whether the production of GSH varies between species and within individuals in accordance with an insect's need for antioxidant defense. Secondly, we quantified the allocation of total Cys (peptide‐bound plus free Cys) to GSH in caterpillars as an estimate of its cost. Two contrasting species were compared: Lymantria dispar (Lymantriidae), a species that is highly defended, and Malacosoma disstria (Lasiocampidae), a species that is less defended. As expected, GSH levels were significantly higher in L. dispar than in M. disstria. Consistent with the function of the midgut as a first line of defense against ingested toxins, GSH levels were significantly higher in these tissues than in the whole bodies of both species. A major finding in this study was that a large fraction of total Cys is used to produce GSH: GSH in the midguts of L. dispar and M. disstria contained 23 and 21%, respectively, of the total Cys in these tissues, and the GSH in their remaining body tissues contained 19 and 17% of the total Cys in these tissues. Levels of total Cys in caterpillar tissues followed the same pattern of distribution as did GSH, producing a strong association between GSH and total Cys (R² = 0.794). We conclude that GSH is a costly defense, especially in generalist tree‐feeding species such as L. dispar. These results further suggest that the large allocation of Cys to GSH in highly defended species might produce a tradeoff by limiting the amount of Cys available for rapid growth.     

外源茉莉酸诱导的青杨生化抗性及其对舞毒蛾幼虫食物利用的影响

【目的】为探讨外源茉莉酸(jasmonic acid, JA)诱导的青杨 Populus cathayana Rehd.抗性对舞毒蛾 Lymantria dispar (L.)幼虫食物利用的影响。【方法】在室内对青杨苗木喷施0.001和0.1 mmol/L两种浓度的茉莉酸,对照喷0.2%的丙酮水溶液,喷施后1, 5和10 d分别采集叶片,分析其初生和次生物质含量的变化。另选喷施0.1 mmol/L茉莉酸的青杨苗木,喷施后1, 5和10 d分别接舞毒蛾2龄幼虫,单头饲养,测定其取食量、体重和排粪量及发育历期,统计分析其食物消化率、转化率和利用率。【结果】两种浓度茉莉酸处理均使青杨叶片中的蛋白质和可溶性糖含量降低,而木质素、单宁、黄酮和酚类物质含量增加。蛋白质和可溶性糖在处理第10天时含量最低,其中高浓度茉莉酸处理较对照分别降低46.5%和49.1%,低浓度处理分别降低30.6%和22.8%。叶片中酚类物质含量在高浓度处理第10 天时增幅最大,较对照增加102%。木质素、黄酮和单宁酸在处理第5天时的含量最高,其中高浓度处理分别较对照增加113%, 75%和57%。用0.1 mmol/L茉莉酸诱导处理后,舞毒蛾2龄幼虫对叶片的消化率、转化率和利用率均有所降低, 取食处理后1, 5和10 d的青杨叶片的食物利用率较对照分别降低了29.4%, 27.6%和28.2%,且幼虫体重降低、发育历期延长。【结论】结果提示外源茉莉酸诱导青杨可对舞毒蛾产生明显的生化抗性,实践中可利用这种生化抗性防治舞毒蛾的危害。     

Inhibition of juvenile hormone esterase activity in Lymantria dispar (Lepidoptera, Lymantriidae) larvae parasitized by Glyptapanteles liparidis (Hymenoptera, Braconidae)

Glyptapanteles liparidis is a gregarious, polydnavirus (PDV)-carrying braconid wasp that parasitizes larval stages of Lymantria dispar. In previous studies we showed that parasitized hosts dramatically increase juvenile hormone (JH) titers, whereas JH degradation is significantly inhibited in the hemolymph. Here we (i) quantified the effects of parasitism on JH esterase (JHE) activity in hemolymph and fat body of penultimate and final instars of L. dispar hosts and (ii) assessed the relative contribution of individual and combined wasp factors (PDV/venom, teratocytes, and wasp larvae) to the inhibition of host JHE activity. The effects of PDV/venom was investigated through the use of gamma-irradiated wasps, which lay non-viable eggs (leading to pseudoparasitization), while the effects of teratocytes and wasp larvae were examined by injection or insertion of these two components in either control or pseudoparasitized L. dispar larvae. Parasitism strongly suppressed host JHE activity in both hemolymph and fat body irrespective of whether the host was parasitized early (premolt-third instar) or late (mid-fourth instar). Down-regulation of JHE activity is primarily due to the injection of PDV/venom at the time of oviposition, with only very small additive effects of teratocytes and wasp larvae under certain experimental conditions. We compare the results with those reported earlier for L. dispar larvae parasitized by G. liparidis and discuss the possible role of JH alterations in host development disruption.     

舞毒蛾谷胱甘肽S-转移酶对杨树次生物质协同溴氰虫酰胺的胁迫响应

为了明确舞毒蛾Lymantria dispar谷胱甘肽S-转移酶(GST)对杨树次生物质协同溴氰虫酰胺的胁迫响应机制,选择3种杨树次生物质(黄酮、槲皮素、芦丁)以及新型邻二苯甲酰胺类杀虫剂溴氰虫酰胺作为胁迫外源化合物,以舞毒蛾2龄幼虫为研究对象,通过人工饲料添加次生物质和溴氰虫酰胺的单剂和混剂,测定对舞毒蛾存活率、谷胱甘肽S-转移酶活性及其基因表达影响。结果表明,处理48 h后,3种联合处理组舞毒蛾幼虫的存活率显著低于对照组和各杨树次生物质单剂处理组,存活率依次为53.33%、60.00%和53.33%,各联合处理组幼虫存活率与溴氰虫酰胺处理组差异不显著。除处理6 h外,不同杨树次生物质单剂处理后GST活性均诱导增加。溴氰虫酰胺处理组在48 h内GST活性显著高于单剂处理组和对照组。除联合处理1在6 h、12 h的GST诱导活性低于溴氰虫酰胺处理组外,各联合处理组的GST诱导活性均高于溴氰虫酰胺处理组。舞毒蛾2龄幼虫取食含有不同处理的人工饲料后,其体内LdGSTe2、LdGSTs1、LdGSTs2和LdGSTz1均有所表达,且不同处理的诱导程度呈现差异。以上研究结果为杨树次生物质协同溴...     

The metabolism of [14C]nicotine in the cat

The metabolism of [2'-(14)C]nicotine given as an intravenous injection in small doses to anaesthetized and unanaesthetized cats has been studied. A method is described for the quantitative determination of [(14)C]nicotine and [(14)C]cotinine in tissues and body fluids. Nanogram amounts of these compounds have been detected. After a single dose of 40mug. of [(14)C]nicotine/kg., 55% of the injected radioactivity was excreted in the urine within 24hr., but only 1% of this radioactivity was unchanged nicotine. [(14)C]Nicotine is metabolized extremely rapidly, [(14)C]cotinine appearing in the blood within 2.5min. of intravenous injection. [(14)C]Nicotine accumulates rapidly in the brain and 15min. after injection 90% of the radioactivity still represents [(14)C]nicotine. Metabolites of [(14)C]nicotine have been identified in liver and urine extracts. [(14)C]Nicotine-1'-oxide has been detected in both liver and urine.     

Aminopeptidase N purified from gypsy moth brush border membrane vesicles is a specific receptor for Bacillus thuringiensis CryIAc toxin.

We have evaluated the binding of Bacillus thuringiensis Cry toxins to aminopeptidase N (APN) purified from Lymantria dispar (gypsy moth) brush border membrane vesicle (BBMV). CryIAc toxin bound strongly to APN, while either the structurally related CryIAa and CryIAb toxins or CryIC, CryIIA, and CryIIIA toxins showed weak binding to APN. An in vitro competition binding study demonstrated that the binding of CryIAc to L. dispar BBMV was inhibited by APN. Inhibition of short circuit current for CryIAc, measured by voltage clamping of whole L. dispar midgut, was substantially reduced by addition of phosphatidylinositol-specific phospholipase C, which is known to release APN from the midgut membrane. In contrast, addition of phosphatidylinositol-specific phospholipase C had only a marginal effect on the inhibition of short circuit current for CryIAa. These data suggest that APN is the major functional receptor for CryIAc in L. dispar BBMV. A ligand blotting experiment demonstrated that CryIAc recognized a 120-kDa peptide (APN), while CryIAa and CryIAb recognized a 210-kDa molecule in L. dispar BBMV. In contrast, CryIAa and CryIAb bound to both the 120- and 210-kDa molecules in Manduca sexta BBMV, while CryIAc recognized only the 120-kDa peptide. The 120-kDa peptide (APN) in L. dispar BBMV reacted with soybean agglutinin, indicating that N-acetylgalactosamine is a component of this glycoprotein.     

向小黑杨转化蜘蛛杀虫毒素基因（英文）

近年来,危害小黑杨Populus simonii×Ｐ.nigra的害虫发生严重,给林业生产造成很大损失。为了提高小黑杨的抗虫能力,避免使用杀虫剂带来的污染,用农杆菌介导法将澳大利亚漏斗蛛Atrax robustus的毒蛋白基因和苏云金芽孢杆菌CryⅠA（b）基因C末端的融合基因BGT转化入小黑杨。PCR 和Southern印记分析转基因植株,结果表明,BGT杀虫基因已经整合在小黑杨基因组上。活性实验表明,取食转基因杨树6天和9天后,舞毒蛾Lymantria dispar 2龄幼虫的校正死亡率分别是37.0%和92.6%。方差分析表明取食转基因和对照杨树的舞毒蛾幼虫体重差异显著。这些结果显示转基因杨树上的舞毒蛾的发育速率受到影响。     

Discrimination of pheromone enantiomers by two pheromone binding proteins from the gypsy moth Lymantria dispar

The gypsy moth, Lymantria dispar, uses (7R, 8S)-cis-2-methyl-7, 8-epoxyoctadecane, (+)-disparlure, as a sex pheromone. The (-) enantiomer of the pheromone is a strong behavioral antagonist. Specialized sensory hairs, sensillae, on the antennae of male moths detect the pheromone. Once the pheromone enters a sensillum, the very abundant pheromone binding protein (PBP) transports the odorant to the sensory neuron. We have expressed the two PBPs found in gypsy moth antennae, PBP1 and PBP2, and we have studied the affinity of these recombinant PBPs for the enantiomers of disparlure. To study pheromone binding under equilibrium conditions, we developed and validated a binding assay. We have addressed the two major problems with hydrophobic ligands in aqueous solution: (1) concentration-dependent adsorption of the ligand on vial surfaces and (2) separation of the protein-bound ligand from the material remaining free in solution. We used this assay to demonstrate for the first time that pheromone binding to PBP is reversible and that the two PBPs from L. dispar differ in their enantiomer binding preference. PBP1 has a higher affinity for the (-) enantiomer, while PBP2 has a higher affinity for the (+) enantiomer. The PBP from the wild silk moth, Antheraea polyphemus (Apol-3) bound the disparlure enantiomers more weakly than either of the L. dispar PBPs, but Apol-3 was also able to discriminate the enantiomers. We have observed extensive aggregation of both L. dispar PBPs and an increase in pheromone binding at high (>2 microM) PBP concentrations. We present a model of disparlure binding to the two PBPs.     

Growth-promoting effect on iron-sulfur proteins on axenic cultures of Entamoeba dispar

A growth-promoting factor (GPF) that promotes the growth of Entamoeba dispar under axenic culture conditions was found in fractions of mitochondria (Mt), hydrogenosomes (Hg) and chloroplasts (Cp) obtained from cells of six different protozoan, mammalian and plant species. We were able to extract the GPF from the Cp-rich leaf cells of a plant (spiderwort: Commelina communis L.) in an acetone-soluble fraction as a complex of chlorophyll with low molecular weight proteins (molecular weight [MW] approximately 4,600). We also found that on treatment with 0.6% complexes of 2-mercapthoethanol (2ME), complexes of chlorophyll-a with iron-sulphur (Fe-S) proteins (e.g., ferredoxins [Fd] from spinach and Clostridium pasteurianum) and noncomplex rubredoxin (Rd) from C. posteurianum have a growth-promoting effect on E. dispar. These findings suggest that E. dispar may lack a sufficient quantity of some essential components of Fe-S proteins, such as Fe-S center.     

Food utilization values of gypsy moth Lymantria dispar (Lepidoptera: Lymantriidae) larvae infected with the microsporidium Vairimorpha sp. (Microsporidia: Burenellidae)

Infection of the gypsy moth, Lymantria dispar, with the microsporidium Vairimorpha sp. strongly influences the development of the host in ways typical of many species of terrestrial entomopathogenic Microsporidia; growth is reduced while development time is extended in infected insects. The appearance of the different stages of the parasite in the host relative to the elapsed time after oral infection, as well as the influence of the parasite proliferation on food utilization of the host, were examined. At 3 days postinfection, midgut muscle cells were infected with primary spores, and the fat body tissues contained meronts, sporonts, and primary spores. Many more fat body cells contained vegetative stages and primary spores at 4 and 5 days postinfection, and diplokaryotic spores and immature octospores were also present. Approximate digestibility of infected larvae increased during this time period, whereas the conversion of ingested and digested food to body substance decreased. The relative growth rate of infected and uninfected groups did not differ significantly between 4 and 5 days postinfection, although the relative consumption rate in infected L. dispar larvae was higher. Between 8 and 10 days postinfection, the relative growth rate of uninfected larvae increased. The infected group did not demonstrate this increase at a time period characterized by maturation of diplokaryotic spores and octospores in larval fat body tissues. Total body weight of uninfected larvae remained higher than that of infected larvae after 8 days postinfection.     

不同光照强度下兴安落叶松对舞毒蛾幼虫生长发育及防御酶的影响

为了探讨舞毒蛾对光照环境变化引起的落叶松抗性的变化是如何响应的,分析了不同光照强度处理的兴安落叶松对舞毒蛾幼虫生长发育状况和生理指标变化的影响。研究发现,取食50%和25%光照强度下生长的落叶松后,舞毒蛾幼虫平均体重、蛹重、化蛹率和羽化率与对照组相比均显著下降（P<0.05）。幼虫体内保护酶SOD、POD、CAT和解毒酶ACP、AKP、CarE、GSTs、MFO活性与对照组(100% 光照)相比均显著降低（P<0.05）且除CAT外在50%光照强度下降低最为显著（P<0.05）;4龄和5龄幼虫取食同一光强处理的落叶松后,SOD、POD、CarE、GSTs和MFO活性5龄显著低于4龄（P<0.05）,ACP和AKP活性5龄却显著高于4龄（P<0.05）,表明昆虫在不同的发育阶段启用不同的排毒酶系。光照差异对取食人工饲料的舞毒蛾生长发育和排毒代谢酶活性均没有显著影响,说明舞毒蛾生长发育和酶活性的变化是因寄主植物抗性的影响而非光照强度的作用。本研究结果表明,采取适当的营林措施调节林分内的光照条件,可以提高落叶松的自主抗虫性,增强其抵御害虫危害的能力,有效控制害虫危害,减少化学农药的施用量。