早熟素Ⅱ对德国小蠊生殖的影响

早熟素即昆虫的抗保幼激素,是从菊科熊耳草中分离出的氧杂萘衍生物(2,2-二甲基-6,7-二甲氧杂萘).对某些昆虫具有提前变态、成虫不育等生理效应.人们期望它能成为第四代杀虫剂. 本文以德国小蠊(Blattella germanica)为对象,观察早熟素对其生殖的影响,并对作用机理进行探索,结果如下.     

海葵毒素对心肌钠通道开放模式，动作电位及心电图QT周期的影响

应用膜片箝技术记录游离豚鼠心肌细胞的钠通道电流,细胞内微电极技术记录心室乳头肌的动作电位和心电图机记录豚鼠的心电图,使用与心肌;细胞钠通道有高度亲和力的海葵毒素（sea anemone toxin,ATXⅡ）改变钠通道开放的动力过程,从三个水平来研究钠通道,动作电位,心电图变化的关系,并试图探讨长QT综合征（long QT syndrome,LQTs)的发病机制,结果显示,ATXⅡ使钠通道的开放频率增加,钠通道中“长时间开放模式”的开放时间常数增大,动人电位的持续时间APD50和APD50也分别增加了23％和27％,ATXⅡ使动物心电图QT间期延长18．6％,QTc(校正的QT间期）增大18．9％,这些结果提示,钠通道动力过程的变化对动作电位和心电图QT间期有重要影响,钠通道功能或结构的变异可能是临床上部分长QT综合征产生的原因。     

几种杀虫剂对德国小蠊的毒力测定

德国小煤Btottellagermanica（．）是蜚镰目中分布最广,与人类有着密切关系的一种昆虫。在黑龙江、内蒙和新疆等省区市的宾馆、饭店、医院、仓库和船舶、火车等场所,德国／J‘谦为优势种群’‘’‘’。其食性复杂,除为害各种食品外,还可为害工商业原料及成品等。此外,在居民楼内也普遍发生,其体内可携带痢疾杆菌、沙门氏菌、蜡样芽胞菌、变形杆菌、霉菌、曰tor弧菌、腺病毒、埃柯病毒、脊髓灰质炎病毒、乙型肝炎病毒和寄生虫卵等多种病原体,严重威胁着人类健康［‘,’］。因此,综合防治蜚蛾,对提高工农业生产,改善人民生活环境…     

德国小蠊触角感器的扫描电镜观察

用电子显微镜观察德国小蠊Blattella germanica(L.)雌成虫、雄成虫、老熟若虫和低龄若虫的触角,发现其上分布有大量感器,为刺形感器(Ⅰ、Ⅱ型)、锥形感器、毛形感器、弧形感器、帽形感器、边缘感器和椭圆感器。其中刺形感器(Ⅰ、Ⅱ型)、锥形感器、毛形感器、弧形感器和边缘感器在各种虫态均有分布,帽形感器仅见于成虫触角鞭节上。在各种不同虫态中,雌雄成虫含有所有种类的感器,老熟若虫触角亚节数最多,低龄若虫的各类感器的感毛长度和基部横径普遍较小。     

德国小蠊泛素基因的克隆及序列分析

设计一对简并引物,从德国小蠊Blattellager manica细胞中克隆了泛素基因的编码区,GenBank登录号为AY501003。序列分析表明,该编码区的长度为228 bp,编码的多肽由76个氨基酸残基组成,相对分子质量为8.47 Kd ,其等电点为5.73。同源性比较发现,德国小蠊泛素基因与其他真核生物泛素基因在氨基酸水平上具有94%以上的相似性。     

德国小蠊变应原Bla g 8的克隆表达及进化分析

通过5’-RACE获得德国小蠊变应原Bla g 8基因的全长cDNA序列,进行生物信息学分析,构建原核表达载体,诱导重组蛋白表达,建立系统进化树,为进一步研究奠定基础。通过5’-RACE技术,PCR扩增获取编码德国小蠊变应原Bla g 8蛋白的全长cDNA序列;采用生物信息学方法分析预测Bla g 8蛋白的信号肽、疏水性、跨膜区、二级结构、三级结构;建立系统进化树;构建原核表达载体pET32a-B8,IPTG诱导重组蛋白表达,并用His-tag抗体Western blotting验证。结果显示,获得编码德国小蠊变应原Bla g 8的全长cDNA序列,其完整阅读框含618个碱基,编码205个氨基酸。序列分析显示该蛋白,肌球蛋白轻链,具有EF手蛋白保守功能域。IPTG诱导获得重组蛋白。获得德国小蠊Bla g 8的完整cDNA序列,成功构建重组原核表达质粒pET32a-B8,并表达出融合蛋白。     

光周期与温度对林地德国小蠊生长发育与繁殖的影响

为弄清湖南株洲(北纬27°50′,东经112°54′)栖息于林地的德国小蠊(Blattella germanica)季节生活史策略,研究了光周期和温度对其若虫发育、龄数变异及成虫繁殖的影响。结果表明,德国小蠊的若虫发育明显受光周期的影响。长日条件(LD 16∶8h)下若虫发育最快,中间日长(LD 14∶10h)次之,短日条件(LD 12∶12h)下若虫发育最慢。将孵化后30日的若虫自长日条件向短日条件转移,则若虫发育受到明显抑制,反方向的转移,则若虫发育迅速。说明德国小蠊若虫存在滞育现象,短日条件诱导并维持滞育,长日条件解除滞育。若虫期经历的龄数受光周期和温度的影响,25℃的温度条件下,LD 16∶8h、LD 14∶10h及LD 12∶12h若虫期的龄数分别为7、8和9龄;长日条件下,30℃和25℃的若虫龄数为7龄,而20℃为9龄。根据实验室观察和林地调查结果,德国小蠊在湖南株洲1年发生1代,以滞育若虫越冬。30℃、25℃、20℃的温度条件下,卵鞘成活率分别为14.3%、90.1%和51.9%,高温和低温均不适合德国小蠊的繁殖。因此,可以认为控制若虫发育和龄数的光周期、温度反应的生态意义在于调控繁殖虫态和繁殖的适宜季节保持同步。     

饵料蛋白质水平对德国小蠊营养效应及氮代谢的影响

【目的】本研究旨在探究饵料蛋白质水平对德国小蠊Blattella germanica营养利用及氮代谢的影响,为蟑螂毒饵的研发提供新思路。【方法】采用标准重量分析法评估了取食4种不同蛋白质水平(5%, 25%, 45%和65%)饵料的德国小蠊雄成虫营养效率指数和氮利用率;利用分光光度法测定了取食不同蛋白水平饵料的德国小蠊雄成虫体内黄嘌呤氧化酶(xanthine oxidase, XOD)、谷草转氨酶(glutamic oxaloacetic transaminase, GOT)、谷丙转氨酶(glutamic pyruvic transaminase, GPT)活性及尿酸含量。【结果】取食65%蛋白质饵料组的德国小蠊雄成虫的相对取食量最高,而取食45%蛋白质饵料组的雄成虫食物利用率、食物转化率及相对生长率均显著高于取食5%和65%蛋白质饵料组的雄成虫。且德国小蠊雄成虫体内氮、粪便氮、氮消耗速率、氮排泄率、氮生成率、氮同化效率、黄嘌呤氧化酶活性和尿酸含量均随饵料蛋白质水平的提高而提高,但65%蛋白质饵料组氮利用率最低,45%蛋白质饵料组谷草转氨酶活性最高,25%和45%蛋白质饵料组谷丙转氨酶活性显著高于5%和65%蛋白质饵料组。【结论】适量蛋白质饵料有利于德国小蠊对食物及氮的利用,而高蛋白质含量条件下德国小蠊谷草转氨酶和谷丙转氨酶活性下降,说明高蛋白不利于德国小蠊利用食物,且增加其代谢负担。     

饵料蛋白水平对德国小蠊肠道细菌群落的影响

昆虫肠道微生物在宿主营养代谢、生长发育、免疫以及抵御病原菌等方面具有重要作用。研究不同蛋白水平饵料饲养对德国小蠊（Blattella germanica）雄成虫肠道细菌群落组成及其功能的作用,探究德国小蠊肠道细菌对宿主营养和健康的影响,以期为发展生物防治的诱食性饵料提供理论支持。分别取连续饲喂低蛋白（LP2组：5%）、高蛋白（HP3组：65%）以及正常蛋白水平饵料（CD1组：25%）21 d的德国小蠊雄成虫,饥饿24 h后无菌条件下分离并提取肠道总基因组DNA,采用特异引物扩增细菌16S rDNA的V4可变区并进行高通量测序,分析德国小蠊肠道细菌群落组成及其功能特征。结果表明德国小蠊肠道细菌主要由拟杆菌门（Bacteroidetes）、变形菌门（Proteobacteria）、梭杆菌门（Fusobacteria）和厚壁菌门（Firmicutes）等细菌群落组成。饲喂低蛋白饵料LP2组的德国小蠊肠道细菌中拟杆菌属（Bacteroides）细菌丰度（47.44%）显著高于HP3组（23.97%）和对照CD1（7.04%）。饲喂高蛋白饵料的HP3组梭杆菌门丰度显著高于其他两组。LEfSe物种差异分析也表明HP3组德国小蠊肠道细菌中梭杆菌属（Fusobacterium）细菌与低蛋白饵料LP2组和对照CD1组有显著差异。基于Tax4Fun功能预测显示,HP3高蛋白饵料组的德国小蠊肠道细菌中与能量代谢功能相关基因的相对丰度极显著高于对照组CD1组,外源性物质代谢与降解和其他氨基酸代谢功能基因的相对丰度显著高于低蛋白LP2组。本研究结果表明饵料中蛋白质水平的差异能够显著改变德国小蠊肠道中细菌群落结构组成,并影响其代谢功能。     

保幼激素类似物对德国小蠊卵黄发生及繁殖的影响

应用ELISA、单向免疫扩散法,研究了保幼激素类似物（灭幼宝）对德国小蠊Blattella germanica卵黄发生的影响;同时,观察了灭幼宝对德国小蠊繁殖的影响。灭幼宝促进了德国小蠊脂肪体Vg的合成,使血淋巴Vg的浓度明显增高,出现时间早于对照组;且变化规律不同于对照组,呈双峰模式。灭幼宝处理组昆虫卵巢中Vt的含量在第5天、第7天明显高于对照组,而在第9天明显下降,仅为对照组的50%左右,而此时对照组卵巢的Vt含量则上升到处理组第7天水平。灭幼宝处理新羽化的雌虫,导致不育。     

Peptide Toxins in Sea Anemones: Structural and Functional Aspects

Sea anemones are a rich source of two classes of peptide toxins, sodium channel toxins and potassium channel toxins, which have been or will be useful tools for studying the structure and function of specific ion channels. Most of the known sodium channel toxins delay channel inactivation by binding to the receptor site 3 and most of the known potassium channel toxins selectively inhibit Kv1 channels. The following peptide toxins are functionally unique among the known sodium or potassium channel toxins: APETx2, which inhibits acid-sensing ion channels in sensory neurons; BDS-I and II, which show selectivity for Kv3.4 channels and APETx1, which inhibits human ether-a-go-go-related gene potassium channels. In addition, structurally novel peptide toxins, such as an epidermal growth factor (EGF)-like toxin (gigantoxin I), have also been isolated from some sea anemones although their functions remain to be clarified.     

A new sea anemone peptide, APETx2, inhibits ASIC3, a major acid-sensitive channel in sensory neurons

From a systematic screening of animal venoms, we isolated a new toxin (APETx2) from the sea anemone Anthopleura elegantissima, which inhibits ASIC3 homomeric channels and ASIC3-containing heteromeric channels both in heterologous expression systems and in primary cultures of rat sensory neurons. APETx2 is a 42 amino-acid peptide crosslinked by three disulfide bridges, with a structural organization similar to that of other sea anemone toxins that inhibit voltage-sensitive Na+ and K+ channels. APETx2 reversibly inhibits rat ASIC3 (IC50=63 nM), without any effect on ASIC1a, ASIC1b, and ASIC2a. APETx2 directly inhibits the ASIC3 channel by acting at its external side, and it does not modify the channel unitary conductance. APETx2 also inhibits heteromeric ASIC2b+3 current (IC50=117 nM), while it has less affinity for ASIC1b+3 (IC50=0.9 microM), ASIC1a+3 (IC50=2 microM), and no effect on the ASIC2a+3 current. The ASIC3-like current in primary cultured sensory neurons is partly and reversibly inhibited by APETx2 with an IC50 of 216 nM, probably due to the mixed inhibitions of various co-expressed ASIC3-containing channels.     

Biochemical characterization and purification of esterases from three strains of German cockroach,Blattella germanica (Dictyoptera: Blattellidae)

Three strains of German cockroach, Blattella germanica (L.) showed varying levels of resistance to chlorpyrifos, methyl parathion, propoxur, bendiocarb, and cypermethrin. The general esterase activity was at least twofold higher than susceptible strain. The subcellular distribution studies revealed that the majority of the esterase activity is present in the 100,000g cytosolic fraction. Only a small portion of the activity was membrane bound. Using non-denaturing gel electrophoresis, ten isozymes were identified in German cockroaches. These isozymes were isolated individually from the gels and analyzed for differences in activity. The isozymes E5, E6, and E7 of resistant strains had significantly higher specific activities when compared with the susceptible strain. The purification process using various column chromatography and preparative gel electrophoresis resulted in 9–11% of total esterase recovery. About double the amount of E6 was recovered from the resistant strains when compared with the susceptible strain. Kinetic analyses of E6 did not indicate differences in K_m and V_max values between the resistant and susceptible strains. Also, inhibition of esterase activity by paraoxon, chlorpyrifos, and propoxur did not suggest any structural differences in esterase E6 between strains. The results suggest that the increased production of E6 esterase contributes to insecticide resistance in German cockroaches. The role of E6 may be sequestration of toxic molecules rather than hydrolysis. © 1996 Wiley-Liss, Inc.     

Subconductance states of single sodium channels modified by chloramine-T and sea anemone toxin in neuroblastoma cells

Single channel currents of chloramine-T (Chl-T) and sea anemone toxin (ATX-II) modified sodium channels were studied in neuroblastoma cells. With both substances similar subconductance states have been observed. The conductances of the sublevels were multiples of the unit step which was about onefourth of the most frequently occurring main conductance. Thus, the current levels observed were one fourth, half and five-fourths of the main current size. Both substances caused a slower decay of the averaged current compared to the current of the native channels. The main single-channel conductance was 15.2 pS (T=16°C) for the Chl-T and 10.8 pS (T=12°C) for the ATX-II modified channels. The channel open time was doubled by ATX-II, but was not increased significantly by Chl-T. The existence of the subconductance states suggests that the native channels may also have multiple open conformations.     

Sodium currents in the giant axon of the crabCarcinus maenas

Summary Measurements were made of the kinetics and steady-state properties of the sodium conductance changes in the giant axon of the crabCarcinus maenas. The conductance measurements were made in the presence of small concentrations of tetrodotoxin and as much electrical compensation as possible in order to minimize errors caused by the series resistance. After an initial delay of 10–150 sec, the conductance increase during depolarizing voltage clamp pulses followed the Hodgkin-Huxley kinetics. Values of the time constant for the activation of the sodium conductance lay on a bell-shaped curve with a maximum under 180 sec at –40 mV (at 18°C). Values of the time constant for the inactivation of the sodium conductance were also fitted using a bell-shaped curve with a maximum under 7 msec at –70 mV. The effects of membrane potential on the fraction of Na channels available for activation studied using double pulse protocols suggest that hyperpolarizing potentials more negative than –100 mV lock a fraction of the Na channels in a closed conformation.     

Regulation of cytoplasmic pH of cultured bovine corneal endothelial cells in the absence and presence of bicarbonate

Summary Single sodium-channel currents were measured in neuroblastoma cells after inhibition of inactivation by chloramine-T (CHL-T), sea anemone toxin II (ATX-II) and scorpion toxin (SCT). The decaying phase of the averaged single-channel currents recorded with 90-msec pulses in cell-attached patches was clearly slower than that of the unmodified channels, suggesting inhibition of macroscopic inactivation. Each substance caused repetitive openings and a moderate increase in the channel open time. AtV _m =RP+20 mV andT=12°C, the mean channel open times were 1.4, 1.6 and 1.8 msec for CHL-T, ATX-II and SCT, respectively, as opposed to 1.07 msec for native channels. Open-time histograms could be best fitted by the sum of two exponentials. The time constants of the fits were similar for histograms constructed from single openings and from openings during bursts. This suggests that the population of channels is homogeneous and that in bursts the same open conformations of channels occur as in single openings. Mean burst durations for bursts consisting of more than one opening atV _m =RP+20 mV were 4.9, 5.8 and 6.1 msec for CHL-T, ATX-II and SCT, respectively. Burst open-time histograms constructed from two or three openings were fitted by the gamma function. The different time constants of the fits obtained for ATX-II and SCT suggested multiple open conformations of channels for openings of bursts. However, significantly different open-time histograms constructed from the first, second and third openings of bursts could not be obtained systematically. A positive correlation was found for the dwell time of the first and the second, as well as for the second and the third opening of bursts with each substance, but a negative one for the dwell time of an opening and the neighboring closing of bursts with ATX-II. The results suggest a model with multiple open and inactivated states. In this model the inactivated states are weakly absorbing.     

A New Polypeptide Toxin from the Nematocyst Venom of an Okinawan Sea Anemone Phyllodiscus semoni (Japanese name “unbachi-isoginchaku”)

The venomous sea anemone Phyllodiscus semoni causes cases of severe stinging. We isolated Phyllodiscus semoni toxin 20A (PsTX-20A), a hemolytic and lethal polypeptide (20 kDa), from the nematocyst venom of this species for the first time. Furthermore, we sequenced the cDNA encoding PsTX-20A. The deduced amino acid sequence of PsTX-20A showed that this toxin was a new member of the actinoporin family, which consists of several cytolytic polypeptides originating from sea anemones. PsTX-20A showed lethal toxicity to the shrimp Palaemon paucidens when administered via intraperitoneal injection (LD₅₀, 50 μg/kg) and hemolytic activity toward 0.8% sheep red blood cells (ED₅₀, 80 ng/ml).     

Solution structure of the eukaryotic pore-forming cytolysin equinatoxin II: implications for pore formation

Sea anemones produce a family of 18-20 kDa proteins, the actinoporins, that lyse cells by forming pores in cell membranes. Sphingomyelin plays an important role in their lytic activity, with membranes lacking this lipid being largely refractory to these toxins. The structure of the actinoporin equinatoxin II in aqueous solution, determined from NMR data, consists of two short helices packed against opposite faces of a beta-sandwich structure formed by two five-stranded beta-sheets. The protein core has extensive hydrophobic interfaces formed by residues projecting from the internal faces of the two beta-sheets. 15N relaxation data show uniform backbone dynamics, implying that equinatoxin II in solution is relatively rigid, except at the N terminus; its inferred rotational correlation time is consistent with values for monomeric proteins of similar mass. Backbone amide exchange rate data also support the view of a stable structure, even though equinatoxin II lacks disulfide bonds. As monitored by NMR, it unfolds at around 70 degrees C at pH 5.5. At 25 degrees C the structure is stable over the pH range 2.5-7.3 but below pH 2.5 it undergoes a slow transition to an incompletely unfolded structure resembling a molten globule. Equinatoxin II has two significant patches of positive electrostatic potential formed by surface-exposed Lys and Arg residues, which may assist its interaction with charged regions of the lipid head groups. Tyr and Trp residues on the surface may also contribute by interacting with the carbonyl groups of the acyl chains of target membranes. Data from mutational studies and truncated analogues identify two regions of the protein involved in membrane interactions, the N-terminal helix and the Trp-rich region. Once the protein is anchored, the N-terminal helix may penetrate the membrane, with up to four helices lining the pore, although other mechanisms of pore formation cannot be ruled out.