Most caterpillars, the larvae of butterflies and moths(Lepidoptera), are herbivorous. Even though their major role in the ecosystem, details of biology are poorly known for most species. This study has been carried out to identify larvae and to acquire useful biological information of insect larvae through rearing from 1997 to 2015 in HECRI(Holoce Ecosystem Conservation Research Institution). From 2012, 2013, 2014 we are carrying out ‘Larvae Identification and Specimen Security of Primary Endemic Moths in Korea Peninsula through Rearing’ supported by National Institute of Biological Resources(NIBR). Of these this study is the list about special caterpillars feeding on the foliage wild peach (Prunus spp.) Total 209 species belonging to 15 families were collected and 52 species belonging to 13 families identified. Among them wild peach dependent monophagous caterpillars are 17 species belonging to 9 families, oligophagous 1 species belonging to 1 families and polyphagous 34 species belonging to 9 families. The dominant family is Geometridae(65 species), second is Noctuidae(57 species) and followed by Pyralidae(21 species).

Regarding therapies for treatment of corneal wounds, ex vivo corneal culture is the most effective for minimizing expensive animal studies. Eighteen porcine enucleated eyes were soaked in 0.2% povidone iodine solution for disinfection prior to cornea excision. Subsequently, corneas were excised from whole eyes and filled with an agar/medium mixture. Corneas were transferred into culture dishes, after which culture medium was added until the limbus was covered. Cultures were then placed onto a plate rocker to mimic blinking action, followed by incubation at 37°C and 5% CO2. Corneas were harvested on Days 0, 3, and 7 after incubation, and optical coherence tomography (OCT) was performed on Day 7. Two eyes from each group were fixed in 2% glutaraldehyde/4% paraformaldehyde for low-vacuum scanning electron microscopy (LV-SEM), and four eyes from each group were fixed in 10% neutral-buffered formalin for histological analysis. OCT results showed that central corneal thickness significantly increased by Day 7 compared to Day 0 (P<0.05). Using LV-SEM, gaps between endothelial cells were detected on Day 7 of ex vivo culture. In the histological evaluation, four to five stratified squamous cell layers, wing cells, and basal cells in the epithelium as well as flat-shaped keratocytes in the stroma were found on Day 0. By Day 7, stratified squamous cells and basal cells had decreased in number, and slightly round-shaped keratocytes were observed; however, the number of keratocytes was similar to that on Day 0. In this short-term ex vivo culture, epithelium and endothelium were sensitive to culture, whereas stroma and keratocytes were well maintained. An additional deswelling method will be needed to obtain more successful results in porcine corneal ex vivo culture.

Riptortus pedestris (F.) (Hemiptera: Alydidae) attacks several leguminous crops and its reproductive success is found to be affected by the leguminous host types. Ooencyrtus nezarae Ishii (Hymenoptera: Encyrtidae) is an egg parasitoid of R. pedestris and its quality attributes depend on the host egg quality. We, thus, investigated the performance of O. nezarae on eggs of R. pedestris fed on different leguminous seeds. Eggs collected from R. pedestris female adults obtained from rearing on one of the four hosts such as soybean, adzuki bean, mung bean, and cowpea seeds were exposed as a batch (n=15) to a single 4 to 5 day-old mated female O. nezarae. The eggs exposed were collected after 24 h. Number of parasitized eggs, sex ratio, development times, and adult emergence were recorded. The maximum number of eggs parasitized by O. nezarae were the eggs of mung bean fed R. pedestris. Eggs produced from the adzuki bean fed bugs had the lowest parasitization. There was no difference recorded in the developmental time of parasitoids emerged from the eggs of R. pedestris fed on different legumes. Proportion of male O. nezarae was highest on the eggs of cowpea seed fed adult bugs (26%); the lowest of that was found on the eggs of mung bean fed bugs (22.4%). Ooencyrtus nezarae can successfully parasitize eggs of R. pedestris regardless of hosts food sources. However, eggs of mung bean fed R. pedestris, among the tested legumes, were found to be of the best quality for reproductive success of O. nezarae.

Antibiotics have been used to prevent disease, promote growth rate, and improve feed efficiency. However, the use of antibiotics in livestock has been restricted worldwide due to problems such as bacterial resistance. Therefore, probiotics among alternatives to antibiotics have gained attention in the livestock feed industry these days. This study was conducted to investigate the effects of dietary supplementation with probiotic 379D on safety, growth rate, and feed efficiency. In this study, bacterial strain 379D was isolated from soil and identified as a Bacillus sp. according to 16S rRNA sequence analysis. In an in vitro test, in-gel activity assay and antimicrobial susceptibility test were conducted to evaluate 379D. In an in vivo study, 379D was administered at concentrations of 0.1% and 1% to broiler chickens for 28 days. The results of in-gel activity assay and antimicrobial susceptibility test showed that strain 379D had broad spectrum antimicrobial activity. Furthermore, no adverse 379D-related effects were observed in 0.1% and 1% groups. Feed efficiency was higher in the 379D-treated groups than in the control group. In conclusion, 379D is expected to be used as a safe alternative to antibiotics in a feed supplement and will improve feed efficiency in broiler chickens.

Twenty Inter simple sequence repeat (ISSR) and 30 SSR primers were used to assess genetic diversity of 64 Agaricus strains including 45 A. bisporus strains and other 19 Agaricus spp. Of them, four ISSR primers, (GA)₈T, (AG)₈YC, (GA)₈C and (CTC)₆and seven SSR markers produced PCR polymorphic bands between the Agaricus species or within A. bisporus strains. PCR polymorphic bands were inputted for UPGMA cluster analysis. Forty five strains of A. bisporus are genetically clustered into 6 groups, showing coefficient similarity from 0.75 to 0.9 among them. The varieties, Saea, saedo, Saejeong and Saeyeon that have recently been developed in Korea were involved in the same group with closely genetic relationship of coefficient similarity over 0.96, whereas, other strains were genetically related to A. bisporus strains that were introduced from USA, Eroupe and Chinese.

Methyl Bromide (MB) has been regulated by montreal protocol due to ozone depletion since 1992, and there is a need to develop MB alternative fumigation methods. To find out the efficacies and tolerance in developmental stages of citrus mealybugs (Planococcus citri) which frequently infested in imported pineapples, phosphine(PH3) gas was tested in different exposure times (2~24 hr) and concentrations (0.1∼2g/m3) in small desiccators at 8℃. Based on Lethal 99% concentration × time products (LCTP 99%) of PH3 gas to target developmental insect, 2g/m3 PH3 was applied for 24 hr in 300 m3 fumigation facility, which was designed in well sealed and evacuation system (5 air exchange/min). We monitored PH3 gas in fumigation facility to confirm CTP and checked PH3 gas in atmospheres in air ventiliation process after fumigations to make quarantine guideline and protocol for worker safety as well as efficacy to target pest.

Porphyromonas gingivalis is one of the most important periodontal pathogens and has been to known to invade various types of cells, including endothelial cells. The present study investigated the mechanisms involved in the internalization of P. gingivalis in human umbilical vein endothelial cells (HUVEC). P. gingivalis internalization was reduced by clathrin and lipid raft inhibitors, as well as a siRNA knockdown of caveolin-1, a principal molecule of lipid raft-related caveolae. The internalization was also reduced by perturbation of actin rearrangement, while microtubule polymerization was not required. Furthermore, we found that Src kinases are critical for the internalization of P. gingivalis into HUVEC, while neither Rho family GTPases nor phosphatidylinositol 3-kinase are required. Taken together, this study indicated that P. gingivalis internalization into endothelial cells involves clathrin and lipid rafts and requires actin rearrangement associated with Src kinase activation

본 연구는 방울토마토의 MA 저장시 저장기간 연장과 품질 유지를 위한 비천공 breathable 필름 종류를 구명하고자 진행되었다. 강원도에 위치한 플라스틱 하우스에서 수경재배한 토마토를 담적색기에 수확하여 5oC, 11oC, 그리고 24oC에서 산소투과도가 각기 다른 비천공 breathable 필름(10,000; 20,000; 40,000; 60,000; 80,000; 100,000 cc/m2.day.atm)과 천공필름으로 포장하여 저장하였다. 저장 중 생체중 감소율은 세가지 온도 모두에서 모든 비천공 breathable 필름처리구에서는 0.6%미만이었으나, 천공필름은 5oC는 2.93%, 11oC는 13.29%, 그리고 24oC에서는 27.24%에 달하였다. 포장내 이산화탄소와 산소 농도를 볼 때 5oC와 11oC에서 20,000 cc 필름, 24oC에서 40,000 cc 필름이 MA 조건에 근접한 수치를 보였다. 에틸렌 농도는 산소투과도가 가장 낮은 10,000 cc에서 모든 온도에서 가장 높았다. 저장 중 외관상 품질과 최종일에 측정한 경도와 당도는 5oC와 11oC의 20,000 cc 필름, 24oC의 40,000 cc 필름이 높은 수치를 나타내었다. 그러나 산도와 비타민 C 함량은 필름처리에 대한 일정한 경향을 보이지 않았다. 이상의 결과로 보았을 때, MA 저장시 포장내 대기조성과 저장 종료일의 과실 품질 등을 비교한 결과 방울토마토는 5oC와 11oC에서 20,000 cc 필름, 24oC에서는 40,000 cc 필름이 적합하였다.

Renal dysplasia is a developmental disorder of the renal parenchyma involving anomalous differentiation. It is characterized by persistent metanephric ducts surrounded by primitive mesenchyme, fetal or immature glomeruli, fetal or immature tubules, interstitial fibrosis, and dysontogenic metaplasia involving tissues such as cartilage. Renal dysplasia has been rarely reported in rats. Here, we observed a small left kidney in a rat used in a short-term repeat toxicity study. The rat showed no clinical signs throughout the study. All parameters, including those reflecting kidney functions, were normal upon hematological examination and urinalysis. Grossly, the kidney was small (5 × 8 mm) and its surface appeared normal. Histological examination revealed that the cortex and medulla were poorly demarcated and contained immature/atrophic glomeruli, immature renal tubules, and mesenchymal cells. The cortex contained immature glomeruli, atrophic glomeruli with cystic dilatation of Bowman’s capsular space, and some atypical tubules. Primitive metanephric tubules in the medulla were larger in diameter than normal collecting ducts, lined by a tall columnar epithelium with pale cytoplasm and basal nucleus, and surrounded by loose mesenchymal cells. Occasional tubules contained pale eosinophilic homogenous material in the lumen. Thus, this was diagnosed as a case of renal dysplasia on the basis of histologic features and is the first reported case of renal dysplasia in Sprague Dawley rats.

The current study was conducted to evaluate the biocompatibility of α-1,3 galactosyltransferase knockout pig bone graft in a rat calvarial defect model. Porcine cancellous bones were harvested from general and alpha-gal KO pigs and washed with 70% ethanol solution and normal saline. Bone pieces of the alpha-gal KO pig underwent a chemical treatment process to delipidize and deproteinize the bone. Bone graft particles were freeze-dried and stored at −70°C until use. Each bone graft was implanted into the rat calvarial defect in a fresh general pig, fresh transgenic pig, and chemical-treated pig bone group. There was no systemic adverse effect on hematology or necropsy findings in all groups at 1 week and 4 weeks. In the microcomputed tomography analysis, bone volume increased significantly in the chemical-treated transgenic pig bone group, whereas bone mineral density decreased significantly in the fresh general pig bone group compared with other groups. Histological evaluation showed cellular infiltration located at the margin of the bone graft particles, especially in the fresh general pig bone group. These results indicate that fresh general pig bone can elicit a greater local inflammatory response than fresh transgenic pig bone. Further, chemical-treated transgenic pig bone graft was less immunogenic than fresh bone graft. In conclusion, transgenic pig bone is a more biocompatible graft material. In addition, chemical treatment can reduce bone graft immunogenicity by delipidizing and deproteinizing bone.

The specific genetic modification in porcine somatic cells by gene targeting has been very difficult because of low efficiency of homologous recombination. To improve gene targeting, we designed three kinds of knock-out vectors with α1,3-galactosyltransferase gene (α1,3-GT gene), DT-A/pGT5’/neo/pGT3’, DT-A/NLS/pGT5’/neo/pGT3’ and pGT5’/neo/ pGT3’/NLS. The knock-out vectors consisted of a 4.8-kb fragment as the 5’ recombination arm (pGT5’) and a 1.9-kb fragment as the 3’ recombination arm (pGT3’). We used the neomycin resistance gene (neo) as a positive selectable marker and the diphtheria toxin A (DT-A) gene as a negative selectable marker. These vectors have a neo gene insertion in exon 9 for inactivation of α1,3-GT locus. DT-A/pGT5’/neo/pGT3’ vector contain only positive-nega-tive selection marker with conventional targeting vector. DT-A/NLS/pGT5’/neo/pGT3’ vector contain positive-negative selection marker and NLS sequences in upstream of 5’ recombination arm which enhances nuclear transport of foreign DNA into bovine somatic cells. pGT5’/neo/pGT3’/NLS vector contain only positive selection marker and NLS sequence in downstream of 3’ recombination arm, not contain negative selectable marker. For transfection, linearzed vectors were introduced into porcine ear fibroblasts by electroporation. After 48 hours, the transfected cells were selected with 300 μg/ml G418 during 12 day. The G418-resistant colonies were picked, of which 5 colonies were positive for α1,3-GT gene disruption in 3´ PCR and southern blot screening. Three knock-out somatic cells were obtained from DT-A/NLS/ pGT5’/neo/pGT3’ knock-out vector. Thus, these data indicate that gene targeting vector using nuclear localization signal and negative selection marker improve targeting efficiency in porcine somatic cells.

This study evaluated the possibility of clinical application using matrigel-based bioceramic/polymer scaffolds treated with bone morphogenetic protein, angiogenic factor, and mesenchymal stem cells (MSCs) for new bone formation. In the in vitro study, bone morphogenetic protein (BMP-2) and vascular endothelial growth factor (VEGF) containing matrigel, which is a basement membrane gel, was injected into HA/PCL scaffolds to estimate the release rates of growth factors. In the in vivo study, BMP-2, VEGF, and MSCs with matrigel-based scaffolds were implanted into rat femoral segmental defects, and new bone formation was evaluated at 4 and 8 weeks. In the results, the release rates of BMP-2 and VEGF explosively increased by day 5. For the in vivo study results, radiological evaluation revealed that the matrigel-based HA/PCL scaffolds with BMP-2 and VEGF grafted (M+B+V) and matrigel-based HA/PCL scaffolds with BMP-2, VEGF, and MSC grafted (MSC) groups showed increased bone volume and bone mineral density. Moreover, in the histological evaluation, large new bone formation was observed in the M+B+V group, and high cellularity in the scaffold was observed in the MSC group. In conclusion, grafted matrigel-based HA/PCL scaffolds with BMP-2, angiogenic factor, and MSCs increased new bone formation, and in clinical cases, it may be effective and useful to enhance healing of delayed fractures.

The differences in adult lifetime among various silkworm strains has been suggested that the adult lifetime may be genetically controlled. In this experiment, using J037 and Daizo strains we investigated genetic factors related to the adult lifetime of silkworm. We constructed the full-length cDNA library from the adult male of the J037 strain. A total of 2,688 clones were randomly selected, and we performed a differential display hybridization with cDNA probes generated from J037 and Daizo adult males. In conclusion, 193 clones were identified as differential expressed genes, and 154 unique genes were generated after the assembly of 193 clones. Of the 154 unique genes, the most abundant genes were cytochrome oxidase subunit-1 gene(9 times) and unknown(clone ID; 1-50) gene(5 times). The functional groups of these unique genes with matches in the AmiGo database were constructed according to their putative molecular functions. Among thirteen functional categories, the largest group was unclassified protein(24%). In addition, We analyzed the nucleotide and deduced amino acid sequences of the most highly occurred gene(1-50, EF434397), which consisted of 240 amino acids. However, it is confirmed yet that these genes really have an affected on the silkworms longevity.

7 new sericinjams are in breeding by the hybridization of silkworm genetic resource, that is, ND strain and the parent silkworm, and the feature of new sericinjam was classified by a cocoon color. According to cocoon color, sericinjam showed two kind of color including the light green and yellow. D601, D704 and D707 with the light green silk were a difference to density of color. Also D703, D705, D751 and D752 with the yellow silk showed a difference to density of color. As investigating the pupation rate which means the healthiness of the silkworm, D601 was highest with 93%, and D703 was lowest with 65.6%. The ratio of the sericin silk showed some difference every breed, and D601 among them was highest with 91%. There is close correlation between sericin cocoon quantity and the dried silkgrand weight. The weight of the dried silkgrand for sericinjams which were compared with baeokjam was low about 2.5 ~ 7.9 times. Among sericinjams, D601 was lowest, and D707 was highest. The pure sericin content of sericinjams was an above 96%, and sericin content of per one cocoon was low 1.4 ~ 2.5 times than baeokjam. Blood of silkworm which makes the light green silk exhibited anti bacterial activity against Gram-negative bacteria.