Dae-Weon Lee

AN ENTOMOPATHOGENIC BACTERIUM, Xenorhabdus nematophila, SUPPRESSES EXPRESSION OF ANTIMICROBIAL PEPTIDES CONTROLLED BY TOLL AND IMD PATHWAYS BY BLOCKING EICOSANOID BIOSYNTHESIS

Immune-associated genes of the beet armyworm, Spodoptera exigua, were predicted from 454 pyrosequencing transcripts of hemocytes collected from fifth instar larvae challenged with bacteria. Out of 22,551 contigs and singletons, 36% of the transcripts had at least one significant hit (E-value cutoff of 1e-20) and used to predict immune-associated genes implicated in pattern recognition, prophenoloxidase activation, intracellular signaling, and antimicrobial peptides (AMPs). Immune signaling and AMP genes were further confirmed in their expression patterns in response to different types of microbial challenge. To discriminate the AMP expression signaling between Toll and Imd pathways, RNA interference was applied to specifically knockdown each signal pathway; the separate silencing treatments resulted in differential suppression of AMP genes. An entomopathogenic bacterium, Xenorhabdus nematophila, suppressed expression of most AMP genes controlled by Toll and Imd pathways, while challenge with heat-killed X. nematophila induced expression of all AMPs in experimental larvae. Benzylideneacetone (BZA), a metabolite of X. nematophila, suppressed the AMP gene inductions when it was co-injected with the heat-killed X. nematophila. However, arachidonic acid, a catalytic product of PLA2 , significantly reversed the inhibitory effect of BZA on the AMP gene expression. This study suggests that X. nematophila suppresses AMP production controlled by Toll and Imd pathways by inhibiting eicosanoid biosynthesis in S. exigua.

A Viral Histone H4 Joins to Eukaryotic Nucleosomes and Alters Host Gene Expression

ABSTRACT A viral histone H4 (CpBV-H4) is encoded in a polydnavirus, Cotesia plutellae bracovirus. Its predicted amino acid sequence is highly homologous to that of host insect histone H4 except for an extended N-terminal tail containing 38 amino acids with nine lysine residues. Its expression induces an immunosuppression of target insects by suppressing immune-associated genes, presumably through an epigenetic control. This study analyzed its molecular interaction with eukaryotic host nucleosomes and subsequent regulation of host gene expression. Purified recombinant CpBV-H4 could associate with nucleosomal components (H2A, H2B, H3, and H4) and form an octamer. Transient expression of CpBV-H4 in an insect, Tribolium castaneum, was performed by microinjection of a recombinant expression vector and confirmed by both reverse transcriptase PCR (RT-PCR) and immunoblotting assays. Under this transient expression condition, total RNAs were extracted and read by a deep-sequencing technique. Annotated transcripts were classified into different gene ontology (GO) categories and compared with those of control insects injected with a truncated CpBV-H4. Target genes manipulated by CpBV-H4 expression showing significant differences (fold changes > 109) included all GO categories, including development and immune-associated genes. When the target genes were physically mapped, they were found to be scattered on entire chromosomes of T. castaneum. In addition, chromatin immunoprecipitation against CpBV-H4 determined 16 nucleosome sites (P < 10−5) of the viral histone incorporation, which were noncoding regions near DNA-binding and inducible genes. These findings suggest that the viral histone H4 alters host gene expression by a direct molecular interaction with insect nucleosomes.

Protein tyrosine phosphatase encoded in Cotesia plutellae bracovirus suppresses a larva-to-pupa metamorphosis of the diamondback moth, Plutella xylostella

Parasitization by an endoparasitoid wasp, Cotesia plutellae, inhibits a larva-to-pupa metamorphosis of the diamondback moth, Plutella xylostella. This study tested an inhibitory effect of C. plutellae bracovirus (CpBV) on the metamorphosis of P. xylostella. Parasitized P. xylostella exhibited significantly reduced prothoracic gland (PTG) development at the last instar compared to nonparasitized larvae. Expression of the ecdysone receptor (EcR) was markedly suppressed during the last instar larvae parasitized by C. plutellae. By contrast, expression of the insulin receptor (InR) significantly increased in the parasitized larvae. Microinjection of CpBV significantly inhibited the larva-to-pupa metamorphosis of nonparasitized larvae in a dose-dependent manner. Injection of CpBV also inhibited the expression of the EcR and increased the expression of the InR. Individual CpBV segments were transiently expressed in its encoded genes in nonparasitized larvae and screened to determine antimetamorphic viral gene(s). Out of 21 CpBV segments, two viral segments (CpBV-S22 and CpBV-S27) were proved to inhibit larva-to-pupa metamorphosis by transient expression assay. RNA interference of each gene encoded in the viral segments was applied to determine antimetamorphic gene(s). Protein tyrosine phosphatase, early expressed gene, and four hypothetical genes were selected to be associated with the antimetamorphic activity of CpBV. These results suggest that antimetamorphosis of P. xylostella parasitized by C. plutellae is induced by inhibiting PTG development and subsequent ecdysteroid signaling with viral factors of CpBV.

Teratocyte-secreting proteins of an endoparasitoid wasp, Cotesia plutellae, prevent host metamorphosis by altering endocrine signals.

An endoparasitoid wasp, Cotesia plutellae, parasitizes young larvae of the diamondback moth, Plutella xylostella, with its parasitic factors of polydnavirus, venom, ovarian proteins, and teratocytes (TCs). TCs are originated from embryonic serosal membrane at hatch of C. plutellae egg. Injection of in vitro cultured TCs significantly prolonged a larval period of nonparasitized P. xylostella and impaired a larva-to-pupa metamorphosis. This developmental alteration was also induced by injection of TC-cultured medium (TCM). However, heat-treated TCM significantly lost the inhibitory activity against larval development of P. xylostella. Larvae treated with TC or TCM appeared to undergo abnormal endocrine conditions. Juvenile hormone esterase activity was significantly suppressed at early last instar by injection of TC or TCM. In addition, expression of ecdysone receptor at final instar was lost, but that of insulin receptor was maintained until the end of the larval period in TC or TCM treatment. A proteomic analysis of TCM predicted several teratocyte-secreting proteins (TSPs). The inhibitory effect of host development by TCs was significantly enhanced by an addition of another parasitic factor, C. plutellae bracovirus. These results suggest that C. plutellae TC plays a crucial role in alteration of host development by secreting TSPs.

Rapid Cold-Hardening of a Subtropical Species, Maruca vitrata (Lepidoptera: Crambidae), Accompanies Hypertrehalosemia by Upregulating Trehalose-6-Phosphate Synthase.

Abstract 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.

Overwintering Conditions of the Diamondback Moth and Genetic Variation of Overwintering Populations

ABSTRACT: It has been unclear whether the diamondback moth, Plutella xylostella can overwinter in Korean field conditions. This study determined overwintering conditions of P. xylostella by conducting field exposure tests based on its cold tolerance and monitoring overwintering populations by direct examination of overwintering larval habitats and capturing adults with sex pheromone traps. In addition, the overwintering populations were analyzed using polymorphic genetic markers to trace their sources. When all immatu re stage sof P. xylostella were exposed to -5 ℃, which was the temperature much above their supercooling points, they significantly suffered with direc tcold injuries, where larval stage was most tolerant to the cold injury. However, the exposure to 5 ℃ for a long period (4 weeks) did not giv eany significant cold injury to nonfeeding stages, while this treatment gave lethality to larval stage without diet. When all developmenta lstages of P. xylostella were exposed to open field conditions during winter, they exhibited significant decreases of survival rates. However,some protected and indoor conditions reduced the cold injuries and the diet provision significantly increased larval survival r ates. Adultmonitoring with sex pheromone during winter period indicated that the first captures were observed at similar periods at differ ent locations (≈ 260 Km apart). The overwintering adults were captured until early April. Genetic variation of these overwintering populations was analyzed with polymorphic molecular markers, indicating significant genetic divergences among the overwintering populations. This study indicates that P. xylostella can overwinter in southern Korean fields or some protected greenhouses with host plants.Key words: Plutella xylostella, Overwintering, Cold injury, Cold hardiness, Genetic variation초 록: 배추좀나방(Plutella xylostella)이 국내에서 월동이 가능한 지 명확하지 않았다. 본 연구는 배추좀나방의 내한성에 기초한 야외 노출 실험을 실시하여 월동 환경 조건을 결정하고, 동계 야외 지역의 배추좀나방 유충 서식지 관찰 및 성페로몬을 이용한 성충 모니터링을 통해 월동이 가능한 지 조사하였다. 또한 이들 월동집단의 유래를 추적하기 위해 다형유전좌위를 이용한 집단 분석을 실시하였다 . 배추좀나방의 체내빙결점 보다 높은 -5℃로 처리한 결과 모든 미성숙 발육태에서 뚜렷한 생존력 저하를 보여 직접적 냉해 피해를 주었다 . 여기서 유충발육태는 가장 낮은 냉해 피해를 받았다. 그러나 5℃로 장기간(4 주) 처리한 결과 냉해 피해는 없었지만, 유충의 경우 먹이가 없는 상태에서 치사율이 증가했다 . 모든 발육태의 배추좀나방을 대상으로 겨울 기간 동안 야외조건에 노출시킨 결과 모든 발육태에서 생존력 저하를 나타냈다 . 그러나 비가온 실내조건에서저온 피해를 줄였으며 유충의 경우 먹이가 공급되면 생존력이 뚜렷하게 증가하였다 . 동계 성페로몬 모니터링 결과 2014년도 최초의 성충발생일은 유사한 시기에 서로 다른 지역(약 260 Km 거리)에서 나타났으며 월동집단의 성충은 4월 상순까지 포획되었다. 지역간 이들 월동집단의 유전적 거리는 다형분자마커를 이용하여 분석되었으며 이들 월동집단들 사이에 뚜렷한 유전적 분화가 있는 것을 나타냈다 . 본 연구는 배추좀나방의 국내 월동이 남쪽 지역 또는 기주 식물이 있는 시설재배지에서 가능한 것으로 제시하고 있다 .검색어: 배추좀나방, 월동, 냉해, 내한성, 유전분화*Corresponding author: hosanna@andong.ac.krReceived June 17 2014; Revised September 15 2014Accepted October 2 2014

Effect of Chloride-deicers on Growth of Wheat, Barley and Spinach

Received: 28 October 2014 / Revised: 11 November 2014 / Accepted: 26 November 2014 Copyright c 2014 The Korean Society of Environmental Agriculture This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Juvenile hormone regulates an expression of a late gene encoded in a polydnavirus, Cotesia plutellae bracovirus

An endoparasitoid wasp Cotesia plutellae encodes two host translation inhibitory factors (HTIFs) that are expressed in late larval stage of Plutella xylostella parasitized by C. plutellae. The late expressions of HTIFs seemed to be associated with decreasing titer of juvenile hormone (JH) at the last larval instar because an addition of pyriproxyfen (PYR, a JH analog) inhibited the late expression pattern of two HTIF genes. To understand their late expression control, promoter region of an HTIF gene called CpBV15α was cloned by inverse PCR. The cloned HTIF upstream region (1113 bp) possessed a putative JH response element (JHRE) and other promoter elements. The putative promoter region was rejoined with an open reading frame of enhanced green fluorescence protein (EGFP). When the recombinant vector construct was injected into early third instar larvae of nonparasitized P. xylostella, it was expressed in fourth larval instar at 72 h after injection, compared to relatively early expression in 24 h after injection of control construct containing a baculovirus immediate-early promoter. However, recombinant EGFP construct lost the late expression pattern when its promoter region was incomplete by truncating JHRE region. PYR application inhibited EGFP expression of the recombinant construct, but gave little influence on truncated constructs. Interestingly, when the complete promoter construct was injected to pupal stage, its late expression pattern was lost and showed early expression pattern. However, an addition of PYR to pupae, which had been injected with the complete promoter construct, inhibited the reporter gene expression. These results suggest that late expression of a HTIF (CpBV15α) is controlled by its promoter, which is sensitive to host JH titer.