Jin Kyo Jung

We investigated several characteristics of the development and reproduction of the aphid Aulacorthum solani raised on soybean (Glycine max) at 10 constant temperatures between 2.5 and 30 °C, and described the relationship between temperature and several critical biological characteristics using mathematical models. We found that A. solani could survive and reproduce on soybean at temperatures ranging from 5 to 27.5 °C. High fecundity was observed at temperatures from 12.5 to 20 °C. The lower developmental threshold and thermal constant for this species’ nymphal stages were estimated to be 5.02 °C and 131.2 degree-days, respectively, using a linear model. The upper developmental threshold was estimated to be 33.9 °C using the Lactin-2 model. The optimum temperature for nymphal development was estimated to be 26.9 °C. The maximum total fecundity was estimated as ca. 76.9 nymphs per adult at 18.1 °C. The daily fecundity sharply increased at earlier adult ages, and slowly decreased thereafter until final parthenogenesis occurred, over a range of temperatures from 12.5 to 25 °C. The maximum daily fecundity was estimated to be ca. 6.1 nymphs per adult per day for a 5.2 day old of adult at 21.3 °C using an age- and temperature-dependent model of adult fecundity. In terms of life table statistics, the intrinsic rates of increase and the finite rate of increase were both highest at 25 °C, while the net reproductive rate was highest at 20 °C.

Insulin/insulin-like growth peptide signaling (IIS) down-regulates hemolymph sugar level and facilitates larval growth in the soybean pod borer, Maruca vitrata. The objective of this study is to determine whether IIS of M. vitrata can mediate ovarian development of adult females. A pair of ovaries consists of 8 ovarioles, each of which is separated into distal germarium and proximal vitellarium in M. vitrata. In the germarium, oocyte development occurred with active mitotic activity which was visible by incorporating bromodeoxyribose uridine. Previtellogenic development and subsequent vitellogenesis began soon after adult emergence. They continued with increase of female age. Oocyte development was facilitated by up-regulation of vitellogenin (Vg) and Vg receptor (VgR) gene expression. Larval diets significantly influenced on ovarian development of M. vitrata because oocyte development varied with pupal size derived from larvae treated with different nutritional diets. Its ovarian development was dependent on endocrine signal(s) from the head because decapitation soon after adult emergence prevented oogenesis and subsequent vitellogenesis along with marked reduction of Vg and VgR expression. Topical application of juvenile hormone (JH) significantly recovered its ovarian development whereas farnesoic acid (a precursor of JH biosynthesis) or 20-hydroxyecdysone treatment did not. JH stimulated vitellogenesis and choriogenesis, but not previtellogenic development. In contrast, insulin injection to decapitated females stimulated oocyte differentiation and vitellogenesis along with increase of Vg and VgR expression. To further analyze the effect of insulin on ovarian development, expression of four IIS components (InR, FOXO, Akt, and TOR) genes was manipulated by RNA interference. Hemocoelic injection of gene-specific double stranded RNAs significantly reduced their target gene mRNA levels and interfered with ovarian development. An addition of insulin to JH treatment against decapitated females enhanced the gonadotropic effect of JH by stimulating oogenesis. IIS plays crucial role in mediating previtellogenic development of M. vitrata in response to nutrient signal. It also enhances the gonadotropic effect of JH II on vitellogenesis.

This study was conducted to develop temperature-dependent postdiapause development models of overwintering larvae of the Asian corn borer, Ostrinia furnacalis Guenée (Lepidoptera: Crambidae), and to evaluate the models’ forecasting accuracy using spring adult emergence data. Overwintering larvae were collected at three different times: 24 February (first), 23 March (second), and 25 April (third), 2005. The developmental periods of each collection colony were measured at eight constant temperatures, and those developmental rates were modeled with linear and nonlinear regression. One linear and three nonlinear models provided good fits of developmental rate to temperature across all colonies (r² = 0.96–0.99). The distribution of development completion time was modeled with a Weibull equation that fit data from the second (r² = 0.92) and third (r² = 0.97) colonies better than the first (r² = 0.87). A Lactin 2 model based on data from the first colony was statistically the best model to describe the relationship between temperature and the postdiapause development rate of O. furnacalis (r²_adj = 0.99). However, validation results based on the field data showed that the Logan 6 model combined with the Weibull model (based on the second colony) was well describing spring adult emergence patterns up to 50% cumulative emergence date.

A subtropical insect, Maruca vitrata (F.) (Lepidoptera: Crambidae), is invasive to temperate zones, in which low temperatures during winter would be a serious challenge for colonization. This study assessed cold tolerance and cold-hardening of M. vitrata to understand its overwintering mechanism. Supercooling capacity was confirmed in all developmental stages exhibiting body freezing points at lower than −10°C, in which supercooling points (SCPs) were significantly different among developmental stages, with eggs having the lowest SCP (at −22.5°C). However, all developmental stages suffered significant mortality after being exposed to low temperatures much higher than SCPs. Furthermore, nonfreezing injury increased with elapsed time at 25°C after cold shock. One of the nonfreezing symptoms was a darkening on thorax, which was explained by uncontrolled prophenoloxidase activation. Pre-exposure to 8°C for 1 h significantly increased the survival of both young and old larvae to a low-temperature treatment (−5°C for 1 h). Rapid cold-hardening (RCH) was accompanied by significant increase in hemolymph trehalose concentration. During RCH, trehalose-6-phosphate synthase was significantly upregulated in its expression level. These results suggest that M. vitrata is a freeze-susceptible species and becomes cold-hardy via hypertrehalosemia.

A viral histone H4 (CpBV-H4) is encoded in a polydnavirus, Cotesia plutellae bracovirus (CpBV). It plays a crucial role in parasitism of an endoparasitoid wasp, C. plutellae, against diamondback moth, Plutella xylostella, by altering host gene expression in an epigenetic mode by its N-terminal tail after joining host nucleosomes. Comparative transcriptomic analysis between parasitized and nonparasitized P. xylostella by RNA-Seq indicated that 1,858 genes were altered at more than two folds in expression levels at late parasitic stage, including 877 up-regulated genes and 981 down-regulated genes. Among parasitic factors altering host gene expression, CpBV-H4 alone explained 16.3% of these expressional changes. To characterize the joining sites of CpBV-H4 on host chromosomes, ChIP-Seq (chromatin immunoprecipitation followed by deep sequencing) was applied to chromatins extracted from parasitized larvae. It identified specific 538 ChIP targets. Joining sites were rich (60.2%) in AT sequence. Almost 40% of ChIP targets included short nucleotide repeat sequences presumably recognizable by transcriptional factors and chromatin remodeling factors. To further validate these CpBV-H4 targets, CpBV-H4 was transiently expressed in nonparasitized host at late larval stage and subjected to ChIP-Seq. Two kinds of ChIP-Seqs shared 51 core joining sites. Common targets were close (within 1 kb) to genes regulated at expression levels by CpBV-H4. However, other host genes not close to CpBV-H4 joining sites were also regulated by CpBV-H4. These results indicate that CpBV-H4 joins specific chromatin regions of P. xylostella and controls about one sixth of the total host genes that were regulated by C. plutellae parasitism in an epigenetic mode.