Brucellosis is a notorious zoonotic disease with global implications. Efforts to control the spread of the disease have been restricted to the agricultural livestock. Increasing incidences of accidental human infection have motivated researches to start working on alternative vaccines. At present, live attenuated vaccines are the only accepted type of vaccines used in developed countries for the prevention of brucellosis. Although serodiagnosis is occasionally unreliable, some countries have already claimed to have eradicated the disease, based on this testing. Live attenuated vaccines are not suitable for use in pregnant and immune-depressed animals. Moreover, these vaccines are not tolerated in humans. Therefore, many researches have been striving to discover alternative methods of vaccination. Most research has focused on the generation of subcellular, subunit, and DNA vaccines that are as efficient as the live attenuated vaccines. At present, none of the available vaccines has been able to replace the live attenuated vaccines. Therefore, additional research is necessary in order to discover a new brucellosis vaccine that is suitable for human use.

The aim of the present study was to evaluate the use of an immunochromatographic test (ICT) strip using recombinant MPB70 (rMPB70) protein as a complementary tool for the diagnosis of naturally occurring tuberculosis in cattle. The study was performed on 249 cattle from populations known to be free from Mycobacterium bovis (M. bovis) and 119 cattle with M. bovis infection, confirmed postmortem. Compared to reference standards (culture isolation and/or visible lesion), the sensitivity of ICT was 94.12% (95% CI: 89.89∼98.35%) while the specificity was 96.80% (95% CI; 94.62∼96.82%). The findings indicate that the ICT strip is efficient for diagnosing bovine tuberculosis in cattle from Korea.

A long term monitoring was carried out to compare altitudinal effects on insect community structures on high mountains and evaluate responses the monitoring and changed of insect communities induced by the climate change. These mountains were choose for Mt. Jeombong for northern part, Mt. Ilwol for middle and Mt. Beakun for southern. Each mountain was divided into three altitudinal gradients. They were collected three times a season from spring to autumn, using pitfall traps for ground beetles and UV light trap for moths. The present study presents preliminary results of analysis for the first year monitoring. In total 41beetle species and 326 moths were collected from the monitoring sites in 2012. abundance of ground beetles and moths were the highest in Mt. Baekun followed by Mt. Ilwol and lowest in Mt. Jeombong. Analysis of variance (ANOVA) results showed statistically significant differences among sampling area, species evenness and Shannon’s diversity index with altitude in species abundance as a response variable. Also we found statistically significant differences to three species of ground beetle and six species of moths with altitude. Although we expected a distinct cluster with the difference of altitude at each study site. one of ordination analysis, nonmetric multidimensional scaling (NMS), showed distinct clusters with the ground beetles assemblage at some altitude and moths assemblage at sampling date.

The larvicidal and repellent activities of 33 plant extracts against two mosquitoes as Culex pipiens and Aedes albopictus were examined using direct contact application for larva and a patch test for adult. Chrysanthemum zawadskii var. alpinum, Cnidium officinale, Ginkgo biloba, Magnolia kobus, and Magnolia denudate at 1,000 ppm caused 100% mortality to Cx. pipiens larva within 24 hr. Ailanthus altissima, Dryopteris crassirhizoma, Houttuynia cordata, Mentha arvensis, Phyllostachys nigra, and Parthenocissus tricuspidata showed over 90% mortality to Cx. pipiens. C. zawadskii var. alpinum, C. officinale, G. biloba, M. kobus, M. denudate, and P. nigra gave 100% mortality at 1,000 ppm to Ae. albopictus. Acorus gramineus, Campanula takesimana, and D. crassirhizoma, showed 97.8%, 94.5%, and 94.4% mortality to Ae. albopictus at 24 hr, respectively. Five plant extracts (C. zawadskii var. alpinum, C. officinale, G. biloba, M. kobus, and M. denudate) showed 100% mortality both Cx. pipiens and Ae. albopictus. However, A. altissima gave 90% larvicidal activity to Cx. pipiens, whereas 7.8% mortality to Ae. albopictus. Several plant extracts which have highly larvicidal activities, were determined repellency against two mosquitoes species.

The insecticidal activities of materials derived from the rhizomes of turmeric, Curcuma longa L., against third instar larva of Culex pipiens and Aedes albopictus were evaluated using a direct contact mortality bioassay. Curcuma longa L. hexane extraction showed 100% larvicidal activity both two mosquitoes species at 1,000 ppm after treated 24 h. Purification of the biologically active constituents from the hexane extraction with larvicidal activity was done using silica gel column chromatography. H1 fraction gave 100% mortality to C. pipiens and A. albopictus at 100 ppm. H12 fraction was determined 100% and 87.8% larvicidal activity to C. pipiens and A. albopictus at 50 ppm, respectively. H12 fraction was analyzed as the sesquiterpene, ar-turmerone (C15H20O) and turmerone(C15H22O) by GC and GC-MS.

The detoxification enzymes activities were investigated to Tetranychus urticae Koch using five acaricide-resistant strains. Activities of detoxification enzymes which are glutathione S-transferase (GST), general esterases (α-naphthyl acetate and β-naphthyl acetate), and cytochrome C oxidase were determined to each resistant strain mite. Acequinocyl-resistant strain and bifenazate-resistant strain of T. urticae were showed 2.1 folds and 1.6 folds higher relative activity (RA) level of GST than susceptible strain. Other three resistant strain mites were not significant different to susceptible strain mite. General esterases and cytochrome C oxidase were not significant to all the strain of T. urticae. Acaricidal activities of acequinocylresistant strain and bifenazate-resistant strain of T. urticae showed cross-resistant both acequinocyl and bifenazate. However, other strain mites were showed susceptible acaricidal activities to two acaricides. In this result suggests that resistance of two acaricides (acequinocyl and bifenazate) might be influenced by glutathione S-tansferase activity.

The fumigant activity of phosphine (PH3) and ethyl formate (EF) was determined to all stage of Phthorimaea operculella (Zeller) under high oxygen concentration (50% and 80%). Oxygenated PH3 and EF were tested at two different temperatures (20°C and 4°C) during 7 days. Two oxygenated fumigants were treated with LC10, 30 and 50 values of single fumigant against each stage of P. operculella. At 10% inhibition of hatchability concentration value, inhibition of hatchability of P. operculella eggs was shown 20.3% and 9.2% with 50% and 80% oxygenated PH3 at 20°C at 1 day after treatment, respectively. The fumigant activity of oxygenated PH3 was increased at all stage of P. operculella except eggs both 20°C and 4°C. However, oxygenated EF was determined low fumigant efficacy to hatchability of eggs and emergence rate of pupae. The insecticidal activities of P. operculella larvae and adults were slightly increased mortality rather than single EF. In this result suggests that oxygenated phosphine is effective method for managing P. operculella. But, oxygenated EF is not effective.

In this study, we investigated the effects of X-ray irradiation to control six important insect pests of floriculture crops: Liriomyza trifolii, Spodoptera litura, Myzus persicae, Tetranychus urticae, Bemisia tabaci, and Frankliniella intonsa. We irradiated on six insect pests that were placed in different positions (top, middle, and bottom) of export flower boxes after filling the boxes with roses and chrysanthemums, respectively. When irradiated with X-ray of 150 Gy, the eggs of T. urticae, B. tabaci, F. intonsa, L. trifolii, and S. litura were prevented from hatching at every position in the boxes. The pupation and emergence of L. trifolii larvae and S. litura larvae and B. tabaci nymphs and F. intonsa nymphs were inhibited at every position in the boxes. However, the emergence of T. urticae and M. persicae nymphs was not inhibited, even at the top position in the boxes. When pupae were irradiated, the emergence of L. trifolii was inhibited at every position in the boxes, while S. litura was not inhibited completely, even at the top position in the boxes. When adult T. urticae, S. litura, and L. trifolii were irradiated, the hatching rate of the F1 generation was not completely inhibited at every position. The insect pests that were not inhibited completely at the dose of 150 Gy showed much higher inhibitory effects at the dose of 250 Gy. Therefore, the dose of X-ray irradiation required to inhibit may vary according to the types of flowers and insect pests and according to their positions within the boxes.

Three insect pest, Myzus persicae, Tetranychus urticae, and Liriomyza trifolii were irradiated with electron beam (50-250 Gy) or X-ray (10-150 Gy). Longevity, egg hatching, emergence and fecundity of the test insects were measured. When irradiated to the M. persicae, emergence of nymphs did not show any differences, but fecundity was inhibited at 100 Gy (electron beam) or 30 Gy (X-ray). When irradiated to the T. urticae, egg hatching was completely inhibited at 150 Gy (electron beam) or 50 Gy (X-ray) and egg hatching of F1 generation was decreased at 150 Gy of electron beam or 50 Gy of X-ray. When irradiated to the L. trifolii, egg hatching was completely inhibited at 30 Gy of X-ray, however, electron beam irradiation was not inhibited even at 200 Gy. Egg hatching from irradiated adults was completely inhibited at 150 Gy of electron beam and X-ray. These results indicate that electron beam and X-ray irradiation induced abnormal development and reproduction, however, the dose of irradiation required to inhibit may vary according to the types of insect pests.

Teratocytes (TCs) are the cells derived from the embryonic serosal membrane of some parasitic hymenopteran insects. As a parasitic factor, TCs are multifunctional in host regulation by inducing nutritional, immune, and developmental alterations. However, little is understood about their genetic constituents. This study reveals a comprehensive view of the genes expressed by TCs through a transcriptome analysis based on RNAseq technology. More than 6.29 Gb sequences were used to assemble 34,686 contigs (>200 bp) and annotated into different functional categories. The TC transcriptome profile was clearly distinct from those of hemocytes and the fat body. The TC transcriptome contained components of insulin signaling and biosynthesis of juvenile hormone and 20-hydroxyecdysone. TCs also expressed various groups of digestive enzymes, supporting its nutritional role for the growing parasitoid larvae in parasitism. Furthermore, this transcriptome analysis annotated two kinds of immunosuppressive serine protease inhibitors (serpins) and Rho GTPase-activating proteins (RhoGAPs). To determine the biological functions of these factors, we devised ex vivo RNA interference (RNAi) by conducting knockdown of gene expression in in vitro cultured TCs followed by injection of the treated TCs to test insects. Ex vivo RNAi revealed that some serpins and RhoGAPs expressed in TCs inhibited host cellular immunity. This study reports a transcriptome of the unique TC animal cell, and its immunosuppressive genetic factors using ex vivo RNAi technology.

Bean bug, Riptortus clavatus Thunberg (Heteroptera: Alydidae) causes serious damage to Leguminosae. Herein an entomopathogenic fungal virulence assay system against bean bugs was established to construct a fungal database which can be used in integrated pest management (IPM). First to obtain as many bean bugs as possible at the same stage, host plant-preference and developmental synchronization of bean bugs were investigated. In the preference assay, five pairs of adults were infested in a plastic cage, where a pot of green bean, pea or cowpea was previously placed. The highest fecundity and the fastest development of bean bug was observed in the green bean cage. Secondly, in the synchronization experiment, eggs were collected from the cage of adults in 1, 3, 5 and 7 days after oviposition and transferred to a fresh cage with green beans. From the every 4 days of survey, similar stages of bean bugs were found in the cages with the oviposition for 1 and 3 days, rather than the longer times of oviposition. A fungal bioassay against bean bugs was conducted using the bean bugs from the above insect rearing system. Ten Beauveria bassiana isolates were cultured on quarter-strength Sabouraud dextrose agar (¼SDA) for 7 days at 25°C. Ten 4th instar of nymphs were placed on a cultured plate for 1 hour and tranferred to a fresh moisturized plate with grains of green bean. ERL836 isolate treatment showed the highest virulence and fungal mycosis was observed on the bean bugs. In conclusion, these results can be useful to establish an entomopathogenic fungal database for IPM.

The effects of X-ray irradiation on development and reproduction of Spodoptera litura were examined. Eggs, larvae, pupae, and adults were irradiated at target doses of 10 - 250 Gy. When eggs were irradiated with 30 Gy, egg hatching was completely inhibited. When irradiated to the larvae, pupation was inhibited at 100 Gy and larval period was delayed. When irradiated to the pupae, emergence was inhibited at over 100 Gy. When irradiated to the adults, longevity and fecundity did not show any differences. However, egg hatching was significantly decreased at 70 Gy and above. Also, X-ray irradiation was not induced the rapid death of S. litura. Reciprocal crosses between irradiated and unirradiated moths demonstrated that males were more radiotolerant than females. The levels of DNA damage in S. litura adults were evaluated using the alkaline comet assay. Our results indicate that X-ray irradiation increased levels of DNA damage. The recovery of DNA damage in S. litura adults increased as time passed. But DNA damage hasn't recovered fully. These results indicate that X-ray irradiation induced abnormal development and reproduction by DNA damage in S. litura.

The effect of electron beam irradiation on development and reproduction of susceptible strain (S) and imidacloprid-resistance strain (IMI-R) of Aphis gossypii were compared. Nymphs and adults of S and IMI-R strain were irradiated at target doses of 50, 100, 150, and 200 Gy. When nymphs were irradiated, emergence rate was not affected at all target dose, but number of F1 nymphs was perfectly inhibited at 150 Gy in both strains when irradiated to the adults, longevity slightly decrease at 150 Gy and above. Fecundity was strongly decreased at 100 Gy, but was not completely inhibited even at 200 Gy. Emergence rate of F1 nymph was decreased at 100 Gy and completely inhibited at 200 Gy. However, there was no significant differences on development and reproduction of S and IMI-R strain. We also conducted the comet assay immediately after irradiation and over the following 7 day periods. In addition, we performed quantitative real-time PCR on several genes.

The effect of increased carbon dioxide concentration in atmosphere was examined on the pheromone system of Helicoverpa armigera reared from egg stage to adult in three room. Two of three room (2×2×2 m) were treated with carbon dioxide gas as 600 ppm and 1,000 ppm, respectively. Mean of carbon dioxide concentration was 429.1 ppm in the control, 603.3 ppm for 600 ppm, and 1011.5 ppm for 1,000 ppm during experiment. Electroantenograph (EAG) test was conducted on 3-d-old male adults with air, hexane, and a series of their sex pheromone component, Z11-16Al, from 0.01 to 100 ng. The result was that male EAG responses of 600 and 1,000 ppm were 30.3% lower than that of control room. Production of Z11-16:Al was examined on about twenty 2-d-old virgin females. Carbon dioxide increases did not show a statistically significant difference. However, higher amount of sex pheromone was produced in females of 600 and 1,000 ppm. So, This experiment was replicated with different population reared again. The amount of the sex pheromone per female was 108.9 and 118.1 ng in control room, 139.8 and 141.8 ng in 600 ppm room, and 124.6 and 125.8 ng in 1,000 ppm room.

Tingginya minat masyarakat Korea dalam pembelajaran bahasa Indonesia harus diimbangi dengan sistem pengajaran yang efektif dan efisien. Artikel ini menjelaskan masalah dan tantangan pengajaran Bahasa Indonesia untuk penutur asing dua dimensi sehingga dapat digunakan sebagai pedoman bagi guru dan peneliti. Metode yang digunakan adalah metode kualitatif. Subyek penelitian adalah masalah dan tantangan pengajaran Bahasa Indonesia untuk penutur asing dua dimensi. Obyek penelitian adalah semester pertama HUFS siswa kampus global dan karyawan Samsung yang telah mempelajari bahasa Indonesia selama 300 jam di HUFS kampus global. Kemudian, penelitian ini dijelaskan secara deskriptif. Dari hasil, diketahui bahwa kedua dimensi pengajaran menghasilkan produk yang berbeda. Secara teoritis dan praktis, keterampilan bahasa peserta kursus lebih baik dari mahasiswa semester pertama HUFS. Hal ini dipengaruhi oleh kemauan dan motivasi dalam belajar bahasa Indonesia. Selain itu, sistem pengajaran yang berbeda juga mempengaruhi itu. Namun, itu merupakan tantangan bagi guru untuk merancang metode pengajaran yang efektif dan efisien.

Brucellosis is an important bacterial zoonotic infection worldwide responsible for economic losses in livestock industries which represents a considerable and increasing public health burden. The disease is caused by Brucella which possess the ability to invade and replicate within phagocytes and may result to chronic infection, leading to difficulty in medical therapy of the disease. The treatment for brucellosis employs conventional principles that have been applied for a long time and a combination of antibiotics is currently used due to low efficacy of monotherapies. However, vital effects with respect to health and safety are neglected. Nevertheless, the preventive methods and treatments for brucellosis using traditional medicine have not yet been thoroughly studied, hence, alternative therapies such as the use of natural plant extracts as traditional medicine that are safe, efficient and economical should be explored in order to identify candidates that eliminate complications due to brucellosis. Coptis chinensis Franch (Huanglian) is a traditional Chinese medicinal herb and its extract has been known to possess strong antibacterial activity. In this study, the antibacterial effects of C. chinensis Franch extracts, and the major components of the herb namely berberine and palmatine, were investigated on B. abortus. The C. chinensis Franch ethanol extracts (CCFE) showed bactericidal effects at 1,000 μg/ml concentration and berberine at 100 μg/ml concentration. However, C. chinensis Franch and its components did not affect invasion and intracellular growth of B. abortus in RAW 264.7 cells. In conclusion, C. chinensis Franch ethanol extracts, water extract and its major components such as berberine and palmatine would be a beneficial antimicrobial agent without affecting phagocytic pathway within macrophages, and further study for the precise mechanisms of antibacterial effect would be necessary.

[6]-Gingerol, a major polyphenol of ginger(Zingiber officinale), exhibits a variety ofbiological properties including anti-oxidant, anti-inflammatory and anti-cancer activity. However,the radioprotective effect of [6]-gingerol is still unknown. The aim of this study was to investigatethe radioprotective effect of [6]-gingerol against radiation-induced cell cytotoxicity and oxidativestress in HepG2 cells. [6]-Gingerol pretreatment attenuated radiation-induced cell cytotoxicitycaused by 5Gy(half lethal dose, LD50of HepG2 cells). The measurements of superoxide dismutase(SOD) and catalase(CAT) activity were also performed. The results showed that [6]-gingerol pre-treatment reduced increasing SOD and CAT activity after exposure of IR, indicating that [6]-gin-gerol protected oxidative stress by regulating cellular antioxidant enzyme(SOD and CAT) activity.These findings suggest that [6]-gingerol acts as a radioprotector by attenuating cell cytotoxicityand oxidative stress.