• Journal of Animal Science and Technology
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• 제51권4호
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• pp.265-272
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• 2009

본 연구는 임실군 관내 16농가를 선정하여 총 486두에 대한 비유기록을 수집하였으며, 얻어진 결과는 다음과 같다. 평균 비유개시 3분이내 유량(3MG)은 7.44 kg으로 총 유량의 55%가 3분이내에 비유되는 것으로 나타났고 평균 우유속 거품함량(SPL)은 33.93%였으며, 평균 후착유 유량은(MNG)은 0.14 kg으로 총 유량의 1%에 불과하였다. 순간최고유속(HMF), 분당최고유속(HMG)과 주착유시평균유속(DMHG)에 대한 평균치는 각각 3.03 kg/min, 2.94 kg/min과 2.05 kg/min으로 임실군 젖소군의 비유속도는 대체적으로 느린 것으로 조사되었다. 비유개시부터 유속 500 g/min 도달시간(tS500)은 평균 0.23분(약 14초) 이었으며, 총비유 시간(tMGG)의 평균은 7.75분이었다. 평균 과착유소요시간(tMBG)은 0.58분(35초) 이었으며, 후착유소요시간(tMNG)은 평균 0.42분(14초) 걸리는 것으로 조사되었다. 최고유속시 전기전도도(ELHMF)와 비유개시시 최고전기전도도(ELAP)의 평균은 각각 6.81 mS/cm와 7.58 mS/cm로 조사되었고 최고유속이후 최고전기전도도(ELMAX)는 평균 7.48 mS/cm로 나타났으며, 비유초기와 최고유속의 전기전도도 차이(ELAD)는 평균 0.61 mS/cm로 나타났다. 총비유량은 주착유시 평균유속(DMHG), 주착유시간(tMHG), Plateau 비유 소요시간(tPL), 비유하강기 소요시간(tAB)과 총착유 시간(tMGG)에 대하여 0.35~0.54 범위의 정(+)의 상관관계를 나타낸 반면, 과착유시간(tMBG)과 우유속 거품함량(SPL)과는 각각 -0.11과 -0.27의 부(-)의 상관을 나타내었다. 주착유시 평균유속(DMHG)이 증가하면 총비유시간(tMHG), Plateau 비유 소요시간(tPL), 비유하강기 소요시간(tAB), 총비유시간(tMGG)과 우유속 거품함량(SPL)은 감소하는 것으로 나타났다. 비유개시시 전기전도도가 높은 개체의 우유는 체세포 수가 적은 반면 최고 비유기 이후 최고전도도가 높은 개체의 우유는 체세포 수가 높은 것으로 나타났다. 따라서 비유상태를 정기적으로 점검하고 착유 및 비유에 대한 표준안을 바탕으로 착유를 실시하면 유량과 유질의 향상을 기대할 수 있다고 판단되었다.

• Parasites, Hosts and Diseases
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• 제54권2호
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• pp.191-195
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• 2016

The aim of this study was to evaluate different methods for Trichomonas vaginalis diagnosis during pregnancy in order to prevent maternal and perinatal complications. A total of 386 vaginal exudates from pregnant women were analyzed. T. vaginalis was investigated by 3 types of microscopic examinations direct wet mount with physiologic saline solution, prolonged May-Grunwald Giemsa (MGG) staining, and wet mount with sodium-acetate-formalin (SAF)/methylene blue method. PCR for 18S rRNA gene as well as culture in liquid medium were performed. The sensitivity and specificity of the microscopic examinations were evaluated considering the culture media positivity or the PCR techniques as gold standard. The frequency of T. vaginalis infection was 6.2% by culture and/or PCR, 5.2% by PCR, 4.7% by culture, 3.1% by SAF/methylene blue method and 2.8% by direct wet smear and prolonged MGG staining. The sensitivities were 83.3%, 75.0%, 50.0%, and 45.8% for PCR, culture, SAF/methylene blue method, and direct wet smear-prolonged MGG staining, respectively. The specificity was 100% for all the assessed methods. Microscopic examinations showed low sensitivity, mainly in asymptomatic pregnant patients. It is necessary to improve the detection of T. vaginalis using combined methods providing higher sensitivity, such as culture and PCR, mainly in asymptomatic pregnant patients, in order to prevent maternal and perinatal complications.

• The Plant Pathology Journal
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• 제26권1호
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• pp.8-16
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• 2010

The phytopathogenic fungus Magnaporthe oryzae is a major limiting factor in rice production. To understand the genetic basis of M. oryzae pathogenic development, we previously analyzed a library of T-DNA insertional mutants of M. oryzae, and identified ATMT0879A1 as one of the pathogenicity-defective mutants. Molecular analyses and database searches revealed that a single TDNA insertion in ATMT0879A1 resulted in functional interference with an annotated gene, MGG00056, which encodes a short-chain dehydrogenase/reductase (SDR). The mutant and annotated gene were designated as $MoSDR1^{T-DNA}$ and MoSDR1, respectively. Like other SDR family members, MoSDR1 possesses both a cofactor-binding motif and a catalytic site. The expression pattern of MoSDR1 suggests that the gene is associated with pathogenicity and plays an important role in M. oryzae development. To understand the roles of MoSDR1, the deletion mutant ${\Delta}Mosdr1$ for the gene was obtained via homology-dependent gene replacement. As expected, ${\Delta}Mosdr1$ was nonpathogenic; moreover, the mutant displayed pleiotropic defects in conidiation, conidial germination, appressorium formation, penetration, and growth inside host tissues. These results suggest that MoSDR1 functions as a key metabolic enzyme in the regulation of development and pathogenicity in M. oryzae.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 1994년도 춘계학술대회 and 제3회 신약개발 연구발표회
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• pp.131-136
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• 1994

In the present study, in order to make an in vitro model of gastric mucosa for physiological and pharmacological studies, we established two immortalized gastric surface mucous cell lines (GSM06 and GSM10), which produce periodic acid-Schiff (PAS)-and concanavalin A (Con A)-positive glycoproteins, from a primary culture of gastric fundic mucosal cells of adult transgenic mice harboring a temperature-sensitive simian virus 40 large T-antigen gene 〔1]. Gastric fundic mucosal cells were isolated as a modification of a previously described method for rats by Schepp et al. (2). The isolated gastric fundic mucosal cells were cultured in DME/F12 medium supplemented with 2% fetal bovine serum (FBS), 1% ITES (consisting of 2 mg/1 insulin, 2 mgg/1 transferrin, 0.122 mg/1 ethanolamine and 0.00914 mg/1 sodium selenite) and 10 ng/ml recombinant epidermal growth factor (EGF) in a collagen-coated culture dish. To remove fibroblastic cells from the culture, gastric mucosal cells were incubated in the culture medium containing dispase (25 U/ml) for 24 h. The cells, uncontaminated with fibroblastic cells, were then cloned by colony formation. In our series of three attempts, two cell lines (GSM06 and GSM10) have been established at last. The cells proliferated, attached to the dish ana grew until confluent monolayers were formed, and maintained tight contact with neighboring cells. Both GSM06 and GSM10 cells have now been in culture for more than 9 months with regular passaging. The either cell produced