苦皮藤素Ⅴ对东方粘虫肌细胞的影响

苦皮藤素Ⅴ是从杀虫植物苦皮藤Celustrus angulatus Max.根皮中分离的一种对昆虫具毒杀活性的新化合物。采用电子显微镜技术研究了苦皮藤素Ⅴ对东方粘虫Mythimna separata（Walker）肌肉系统的作用。电镜观察发现,苦皮藤素Ⅴ对东方粘虫成虫飞行肌和幼虫体壁肌均具致毒作用,中毒试虫肌细胞特别是肌细胞的质膜及内膜系统发生明显病变：肌膜破坏,脱落;线粒体肿胀,空泡化,崩解;肌原纤维与线粒体间间隙增大;肌质网扩张,产生髓鞘样结构;细胞核肿胀,核质浓缩,核膜破坏;微气管与肌细胞之间间隙增大;肌小节弥散、排列紊乱。这些结果表明,肌细胞质膜及内膜系统可能是苦皮藤素Ⅴ的一个作用部位。     

粘虫飞行肌中与能量代谢有关的酶活性研究

该文报道粘虫Mythimna separata (Walker ) 蛹及不同日龄成虫飞行肌中与3 种代谢途径有关的5 种酶,即3-磷酸甘油醛脱氢酶(GAPDH)、3-磷酸甘油脱氢酶(GDH)、乳酸脱氢酶(LDH)、3-羟酰辅酶A 脱氢酶(HOAD)、柠檬酸合成酶(CS)活性的变化。成虫羽化后,这5 种酶的活性大多数都高于蛹期,表明成虫飞行肌与能量代谢有关的活动比蛹期高。不同日龄成虫飞行肌的能量代谢特点为：成虫羽化后糖酵解循环的活性增加;1 日龄进行糖酵解的能力较强,2 日龄即具备较强的脂肪代谢能力,2～5日龄糖及脂肪代谢的能力基本相当,但7日龄脂肪代谢的能力较强。1～7日龄粘虫蛾飞行肌具有较高的GDH 和LDH活性,这既是粘虫蛾飞行肌能进行高度有氧代谢的重要标志,也是其具有一定无氧代谢能力的最好说明,而飞行肌中较高的CS活性则是粘虫蛾具有较强飞行能力的重要保证。对成虫GAPDH∶HOAD 活性进行分析比较的结果还显示,粘虫蛾持续飞行的能源物质既有脂类也有糖类,而不仅仅只限于脂类。     

雷公藤总生物碱对粘虫生长发育及几种代谢酶系的影响

雷公藤生物碱是雷公藤Tripterygium wilfordii Hook f.中的主要杀虫活性物质。为进一步深入了解雷公藤总生物碱的杀虫作用,本研究采用小叶碟添加法测定了雷公藤总生物碱对粘虫Mythimna separate (Walker)5龄幼虫生长发育及几种代谢酶系的影响。结果表明：雷公藤总生物碱对粘虫5龄幼虫生长发育有明显抑制作用,表现为体重、体重增加量和相对生长率显著下降,幼虫龄期延长,幼虫存活率、化蛹率和成虫羽化率显著降低;可显著激活酯酶、羧酸酯酶; 明显抑制酸性磷酸酯酶和碱性磷酸酯酶的活性;对谷胱甘肽S-转移酶表现为先激活后抑制的趋势;细胞色素P450酶系的O-脱甲基酶在处理后3 h活性变化不明显,12和24 h后被激活,36 h后接近同期对照。     

基于黏虫转录组的几丁质酶基因筛选和表达分析

昆虫的几丁质酶对昆虫的生长发育致关重要,是生物农药的重要靶标。本研究使用高通量测序技术对迁飞性害虫黏虫Mythimna separata的中肠和表皮组织进行了转录组测序、序列组装、功能注释及差异表达基因分析。对转录组数据库中鉴定出的几丁质酶基因进行了理化性质的预测,包括cDNA长度、蛋白质分子量、氨基酸序列、等电点、不稳定系数、跨膜结构和蛋白结构域等。使用MEGA软件构建了黏虫和其他昆虫几丁质酶的系统进化树,并通过q-PCR验证了黏虫基因在不同组织和发育阶段的表达模式。通过中肠与表皮的转录组测序,获得了19.42 Gb的数据,在COG、GO、KEGG、KOG、Pfam、Swissprot、eggNOG、nr数据库注释到了25 236个Unigene;基因表达分析结果表明,中肠和表皮的差异表达基因共有3 137个,其中中肠高表达基因有1 872个,表皮高表达基因有1 265个。从转录组数据中鉴定出9个几丁质酶基因,其中7个是新的几丁质酶基因,这些基因的cDNA长度在1 362~9 816 bp,SMART结构预测表明几丁质酶含有1个或多个催化结构域。构建的系统进化树将昆虫几丁质酶基因分为9个亚家族。q-PCR结果表明〖STBX〗MsCht2、MsCht5、MsCht6、MsCht7、MsIDGF1在表皮中表达量较高,MsCht4、MsCht11和MsChi-H在中肠中表达量较高,与转录组数据一致;多数几丁质酶基因在蛹期或预蛹期表达量最高,而MsCht4〖STBZ〗在5龄期表达量最高,在蛹期表达量很低。黏虫几丁质酶基因表达上存在不同的差异,不同的几丁质酶基因可能具有不同的功能。本研究筛选出了7个新的几丁质酶基因,为黏虫的生物防治提供了新的靶标。研究结果为进一步研究黏虫几丁质酶的功能奠定了基础。     

The combined effect of photoperiod and temperature on the calling behaviour of the true army worm, Pseudaletia unipuncta

ABSTRACT. Pseudaletia unipuncta (Haw.) (Lepidoptera: Noctuidae) virgin females, maintained at either 10 or 25d?C under LD 12:12 or 16:8 h, started calling at different ages. For a given photoperiod, calling was initiated 11 days later at 10d?C than at 25d?C, while for a given temperature, calling at LD 12:12 h was 3–4 days later than at LD 16:8 h. At 10d?C 50.8% of females did not call within 35 days at LD 12:12 h compared with 30.8% at LD 16:8 h. Calling started earlier in the scotophase at 10d?C than at 25d?C and at LD 16:8 h than at LD 12:12 h. Under all treatments calling generally advanced on successive nights. The time elapsed between the mean onset time of calling and the mid-scotophase was relatively constant under both photoperiod conditions at 25d?C, but at 10d?C was more variable. The mean time spent calling increased significantly with calling age but did not differ significantly between the four experimental conditions tested. Older (15 days) females transferred from 10d?C, LD 16:8 h to 25d?C at either LD 163 or 12:12 h, required less time to initiate calling than younger (5 days) ones. Those transferred from 10d?C, LD 12:12 h took the same time, regardless of their age at the time of the transfer. Females experiencing either a decrease or increase in daylength as well as a temperature increase, required respectively more or less time to initiate calling, compared with individuals that only experienced an increase in temperature. If temperature was the only parameter changed females that initiated calling soon after the transfer immediately adjusted their calling periodicity to prevailing conditions. When both temperature and photoperiod were altered, it took several days before calling periodicity adjusted to the new regime. The ecological implications of temperature and photoperiodic conditions on the possible autumn migration of P. unipuncta are discussed.     

The clock gene,period, influences migratory flight and reproduction of the oriental armyworm,Mythimna separata (Walker)

The oriental armyworm, Mythimna separata, is a major long-distance migratory insect pest of grain crops in China and other Asian countries. Migratory flights and reproductive behavior usually occur at night, regulated by a circadian rhythm. However, knowledge about the linkages between adult flight, reproduction, and clock genes is still incomplete. To fill this important gap in our knowledge, a clock gene (designated Msper) was identified and phylogenetic analysis indicated that the encoded protein (MsPER) was highly similar to PER proteins from other insect species. Quantitative RT-PCR assays demonstrated that significantly different spatiotemporal and circadian rhythmic accumulations of mRNA encoding MsPER occurred during development under steady 14 h : 10 h light : dark conditions. The highest mRNA accumulation occurred in adult antennae and the lowest in larvae. Msper was expressed rhythmically in adult antennae, relatively less in photophase and more entering scotophase. Injecting small interference RNA (siRNA) into adult heads effectively knocked down Msper mRNA levels within 72 h. Most siRNA-injected adults reduced their evening flight activity significantly and did not exhibit a normal evening peak of flight activity. They also failed to mate and lay eggs within 72 h. Adult mating behavior was restored to control levels by 72 h post injection. We infer that Msper is a prominent clock gene that acts in regulating adult migratory flight and mating behaviors of M. separata. Because of its influence on migration and mating, Msper may be a valuable gene to target for effective management of this migratory insect.     

Flight capacity: genetic determination and physiological constraints in a migratory moth Mythimna separata

Abstract. Flight capacity of the oriental armyworn Mythimna separata (Walker) (Lepidoptera: Noctuidae) was estimated by a new tethered flight technique. Samples of a migrant population showed a substantial proportion of 'long fliers'. Heritability of flight capacity was found to be significant ( h ²= 0.27). Female moths from a line selected for long pre-reproductive period (PRP) showed greater flight capacity than those from a short PRP line. This difference was not apparent among males. Onset of calling behaviour inhibited the expression of flight capacity in females showing a clear 'oogenesis-flight syndrome'. These results are discussed in relation to seasonal migration in eastern China and the mechanisms involved in the migratory strategy of this species.     

Interaction between Neoaplectana carpocapsae (Nematoda: Steinernematidae) and Apanteles militaris (Hymenoptera: Bracondiae), a parasitoid of the armyworm, Pseudaletia unipuncta

The DD-136 strain of Neoaplectana carpocapsae adversely affected the development of immature stages of Apanteles militaris, a gregarious internal parasitoid of the armyworm, Pseudaletia unipuncta. The adverse effect of the nematode-bacterium complex was indirect, i.e., the infection by the nematode killed the host before A. militaris could complete its development. However, if armyworms containing 10- or 11-day-old A. militaris were exposed to dauer juveniles in Petri dishes, 48.1 and 94.4%, respectively, produced normal cocoons. If hosts containing 9- or 10-day-old A. militaris were fed dauer juveniles, 42.6 and 73.4% of the armyworms, respectively, produced A. militaris which formed normal cocoons. Cocoon-spinning A. militaris larvae were infected by the nematode. After cocoon formation was completed, the dauer juveniles could not penetrate the cocoon and infect the pupa. However, pupae in cocoons which had been deliberately cut open at one end became infected. A. militaris adults were infected when exposed to dauer juveniles in Petri dishes. After 3 days of exposure to dauer juveniles, 25.0, 44.2, and 7.0% of the adults in three trials were alive, whereas 100, 100, and 96.7% of the control adults were alive. Examination of dead adults in the nematode treatment showed that 67.6% contained nematodes. N. carpocapsae developed and reproduced in unparasitized armyworms, in armyworms containing 9-day-old A. militaris, and in those from which A. militaris had emerged. Production of dauer juveniles was significantly higher in unparasitized armyworms and in armyworms containing 9-day-old A. militaris than in those from which A. militaris had emerged.     

Chromosome-level genomes of two armyworms,Mythimna separata and Mythimna loreyi,provide insights into the biosynthesis and reception of sex pheromones

Mythimna separata and Mythimna loreyi are global pests of gramineous cereals, heavily controlled with synthetic insecticides. Here, we generated two high-quality chromosome-level genome assemblies for M. separata (688 Mb) and M. loreyi (683 Mb). Our analysis identified Z and W chromosomes, with few genes and abundant transposable elements (TEs) found on the W chromosome. We also observed a recent explosion of long interspersed nuclear elements (LINEs), which contributed to the larger genomes of Mythimna. The two armyworms diverged ~10.5 MYA, with only three chromosomes have intrachromosomal rearrangements. Additionally, we observed a tandem repeat expansion of α-amylase genes in Mythimna, which may promote the digestion of carbohydrates and exacerbate their damage to crops. Furthermore, we inferred the sex pheromone biosynthesis pathway for M. separata, M. loreyi and Spodoptera frugiperda. We discovered that M. loreyi and S. frugiperda synthesized the same major constituents of sex pheromones through different pathways. Specifically, the double bonds in the dominant sex pheromone components of S. frugiperda were generated by Δ9- and Δ11-desaturase, while they were generated by Δ11-desaturase and chain-shortening reactions in M. loreyi. We also identified pheromone receptor (PR) genes and inferred their corresponding components. These findings provide a better understanding of sex pheromone communication and promote the development of a new pest control strategy involving pheromone traps, which are more effective and environmentally friendly than current strategies.