• 제목/요약/키워드: tef1

검색결과 124건 처리시간 0.021초

Specific PCR Detection of Four Quarantine Fusarium Species in Korea

  • Hong, Sae-Yeon;Kang, Mi-Ran;Cho, Eun-Ji;Kim, Hee-Kyoung;Yun, Sung-Hwan
    • The Plant Pathology Journal
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    • 제26권4호
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    • pp.409-416
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    • 2010
  • Fusarium species, a large group of plant pathogens, potentially pose quarantine concerns worldwide. Here, we focus on the development of a method for detecting four Fusarium species in quarantined plants in Korea: F. solani f. sp. cucurbitae, F. stilboides, F. redolens, and F. semitectum var. majus. Species-specific primers were designed from the nucleotide sequences of either the translation elongation factor-1 alpha (TEF1) gene or RNA polymerase II subunit (RPB2) gene. Two different primer sets derived from TEF1, all specific to F. solani f. sp. cucurbitae, were able to differentiate the two races (1 and 2) of this species. A set of nested primers for each race was designed to confirm the PCR results. Similarly, two primer sets derived from RPB2 successfully amplified specific fragments from five F. stilboides isolates grouped within a single phylogenetic clade. A specific TEF1 primer set amplified a DNA fragment from only four of the 12 F. redolens strains examined, which were grouped within a single phylogenetic clade. All of the F. semitectum var. majus isolates could be specifically detected with a single RPB2 primer set. The specificity of the primer sets developed here was confirmed using a total of 130 Fusarium isolates.

Congenital Esophageal Atresia Associated with a Tracheobronchial Remnant

  • Wu, Yuhao;Wu, Chun
    • Journal of Chest Surgery
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    • 제52권3호
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    • pp.170-173
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    • 2019
  • A rare case of esophageal atresia/tracheo-esophageal fistula (EA-TEF) with an associated tracheobronchial remnant (TBR) is reported and discussed herein. A 13-month-old patient was seen with a complaint of vomiting of solid food 1 year after EA-TEF repair. An esophagogram showed a tapered narrowing in the lower segment of the esophagus. A re-operation was carried out and a pathologic examination of the resected stenotic segment revealed the presence of a TBR.

후천성 기관식도루의 임상적 고찰 (Clinical Analysis of Acquired Tracheoesophageal Fistula)

  • 백효채;김도형;조현민;이두연
    • 대한기관식도과학회지
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    • 제8권1호
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    • pp.61-65
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    • 2002
  • Background : Acquired tracheoesophageal fistula(TEF) results mostly from Prolonged tracheal intubation and insertion of nasogastric tube. Although the incidence has decreased since the usage of low pressure, high volume cuff of endotracheal tube, it is seldom cured spontaneously and needs surgical treatment. Material and Methods : We have retrospectively reviewed five cases of TEF who underwent surgical treatment for cure from March, 1990 to September, 2001 and analyzed the cause, treatment, postoperative complications and prognostic factors. Results : Majority were men(80% : 4 of 5 patients) and the mean age was 29.4 years old(range, 11-58). The most predominant etiology was prolonged intubation or tracheostomy(80% : 4 of 5 patients) and 3 of 5 patients were treated by tracheal resection and end to end anastomosis with primary closure of esophagus. Postoperative complications occurred in 4 patients the most common complications were wound infection(4 cases) and esophageal leakage(2 cases). Extubation was done on postoperative day 11.5(range, 1-33) days, and factors causing delayed extubation were status esophagus. epilepticus, edema, and tracheal stenosis. Conclusion : Spontaneous closure of TEF is seldom possible and the surgical treatment of choice is tracheal resection and end to end anastomosis with primary repair of the esophagus. preoperative pulmonary rehabilitation and early extubation postoperatively are important factors for success.

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선천성 식도무공증의 임상적 고찰 (Clinical Experience of Esophageal Atresia)

  • 김성철;김대연;김애란;김기수;피수영;김인구
    • Advances in pediatric surgery
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    • 제9권1호
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    • pp.6-11
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    • 2003
  • This study reviews 14 years' experience treating esophageal atresia with special emphasis on the clinical profile and outcome. From May 1989 to February 2003, 65 cases of esophageal atresia (EA) were treated at Asan Medical Center. Boys outnumbered girls 2.4 to 1. Prematutity and low birth weight were 27.7% and 38.5%. Esophageal atresia with distal tracheoesophageal fistula (TEF) was the most common type (87.7%), followed by pure EA and H type fistula. Forty-six patients (70.8%) had one or more associated anomalies, cardiac malformations were the most common. Duodenal atresia was found in 7 cases. There were 6 patients (9.2 %) with VATER cluster. VACTERL cluster was present in 18 patients (27.7%), one of who fulfilled the complete syndrome. Waterston group A, B and C made up 21.5%, 40.0% and 38.5% of the total group. Surgical treatment was attempted in 63 patients and deferred in 2 who had severe associated malformations. For EA with distal TEF, primary esophago esophagostomy was carried out in 51 cases, and division of TEF and gastrostomy in 4 cases and no operation in 2 cases. For pure EA, colonic graft was done in 2 after gastrostomy and esophagostomy, and esophago esophagostomy was performed in 2 after gastrostomy. Two patients with pure EA are waiting for the second operation after gastrostomy. Division of TEF was carried out in 2 cases with H type TEF. The overall survival rate was 76.9%, and survival by Waterston classification was 100% in group A, 80.8% in B and 60.0% in C. Thorough workup for associated anomalies, interdepartmental approach and more careful surgical decision and technique are required to improve the outcome of EA.

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Construction of High Sensitive Detection System for Endocrine Disruptors with Yeast n-Alkane-assimilating Yarrowia lipolytica

  • Cho, Eun-Min;Lee, Haeng-Seog;Eom, Chi-Yong;Ohta, Akinori
    • Journal of Microbiology and Biotechnology
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    • 제20권11호
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    • pp.1563-1570
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    • 2010
  • To construct a highly sensitive detection system for endocrine disruptors (EDs), we have compared the activity of promoters with the n-alkane-inducible cytochrome P450 gene (ALK1), isocitrate lyase gene (ICL1), ribosomal protein S7 gene (RPS7), and the translation elongation factor-1${\alpha}$ gene (TEF1) for the heterologous gene in Yarrowia lipolytica. The promoters were introduced into the upstream of the lacZ or hERa reporter genes, respectively, and the activity was evaluated by ${\beta}$-galactosidase assay for lacZ and Western blot analysis for hER${\alpha}$. The expression analysis revealed that the ALK1 and ICL1 promoters were induced by n-decane and by EtOH, respectively. The constitutive promoter of RPS7 and TEF1 showed mostly a high level of expression in the presence of glucose and glycerol, respectively. In particular, the TEF1 promoter showed the highest ${\beta}$-galactosidase activity and a significant signal by Western blotting with the anti-estrogen receptor, compared with the other promoters. Moreover, the detection system was constructed with promoters linked to the upstream of the expression vector for the hER${\alpha}$ gene transformed into the Y. lipolytica with a chromosome-integrated lacZ reporter gene under the control of estrogen response elements (EREs). It was indicated that a combination of pTEF1p-hER${\alpha}$ and CXAU1-2XERE was the most effective system for the $E_2$-dependent induction of the ${\beta}$-galactosidase activity. This system showed the highest ${\beta}$-galactosidase activity at $10^{-6}\;M\;E_2$, and the activity could be detected at even the concentration of $10^{-10}\;M\;E_2$. As a result, we have constructed a strongly sensitive detection system with Y. lipolitica to evaluate recognized/suspected ED chemicals, such as natural/synthetic hormones, pesticides, and commercial chemicals. The results demonstrate the utility, sensitivity, and reproducibility of the system for identifying and characterizing environmental estrogens.

십이지장 폐쇄를 동반한 선천성 식도 폐쇄에 대한 고찰 (Clinical Experience with Esophageal Atresia Combined with Duodenal Atresia)

  • 이유미;남소현;김대연;김성철;김인구
    • Advances in pediatric surgery
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    • 제14권1호
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    • pp.21-26
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    • 2008
  • There is significant morbidity and mortality associated with the combination of esophageal atresia (EA) and duodenal atresia (DA). Nevertheless, the management protocol for the combined anomalies is not well defined. The aim of this study is to review our experience with the combined anomalies of EA and DA. From May 1989 to August 2006, seven neonates were diagnosed as EA with DA at Asan Medical Center. In all cases, the type of EA was proximal EA and distal tracheoesophageal fistula (TEF). The diagnosis of DA was made in theprenatal period in 1, at birth in 4, 4 days after birth in 1 (2 days after EA repair) and at postmortem autopsy in 1. Except the one case where DA was missed initially, primary simultaneous repair was attempted. DA repair with gastrostomy followed by EA repair in 2, EA repair followed by DA repair without gastrostomy in 2, and TEF ligation followed by DA repair with gastrostomy in 1. There were two deaths. One baby had a large posterolateral diaphragmatic hernia, and operative repair was not attempted. The other infant who had a TEF ligation and DA repair with gastrostomy expired from cardiac failure due to a large patent ductus arteriosus. Simultaneous repair of EA and DA appears to be an acceptable management approach for the combined anomalies, but more experience would be required for the selection of the primary repair of both anomalies.

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식품을 통한 다이옥신류의 노출 평가 (Exposure assessment of dioxins through foods)

  • 오금순;서정혁;백옥진;김미혜;이광호
    • 분석과학
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    • 제23권6호
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    • pp.595-606
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    • 2010
  • 4년 동안(2004-2007) 국내 유통중인 식품 총 221건을 구입하여 다이옥신류(PCDD/DF + 다이옥신유사 PCBs)를 동위원소희석법을 이용하여 분석하였고, 한국인의 다이옥신 1일 노출량을 산출하였다. 식품 중 다이옥신류의 검출량은 2004년과 2005년은 오염도 자료에 1998 WHO TEF값을, 2006년부터는 오염도 자료에 2005 WHO TEF값을 사용하여 다이옥신류 함량을 산출하였으며, 평균 검출량은 백미는 < 0.01 pg TEQ/g, 소고기 0.13 pg TEQ/g, 돼지고기 0.07 pg TEQ/g, 닭고기 0.04 pg TEQ/g, 우유 0.04 pg TEQ/g, 치즈 0.05 pg TEQ/g, 계란(노른자)는 0.13 pg TEQ/g, 수산물 중 고등어는 1.35 pg TEQ/g, 삼치 1.03 pg TEQ/g, 갈치 1.00 pg TEQ/g, 조기 0.16 pg TEQ/g, 명태 0.11 pg TEQ/g, 장어 0.52 pg TEQ/g, 굴 0.32 pg TEQ/g, 꽃게 0.14 pg TEQ/g 수준으로 조사되었다. 식품을 통한 한국인의 다이옥신류의 노출량은 체중 1 kg 당 1일 0.47 pg TEQ로 다이옥신류의 TDI (4 pg TEQ/kg bw/day) 대비 약 11%수준으로 조사되었으며, 이 수준은 건강상 위해가 없는 것으로 평가되었다.

꽃도라지 뿌리썩음병을 일으키는 Fusarium solani 의 특성 (Characterization of Fusarium solani Causing Fusarium Root Rot of Lisianthus in Korea)

  • 최효원;홍성기;이영기;김점순;이재금;김효원;강은혜;이은형
    • 한국균학회지
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    • 제45권1호
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    • pp.74-82
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    • 2017
  • 꽃도라지(Eustoma grandiflorum)는 국내에서 장식용 화훼류로 널리 이용되는 절화류이다. 2015년 경기도 여주와 경남 김해 지역에서 꽃도라지가 시들고, 지제부가 잘록해지면서 위축되고, 뿌리가 썩는 증상이 나타났다. 병든 식물체는 포장이나 육묘상자에서 황화되고, 뿌리 발육이 저해되었고, 진전되면 전체적으로 황화되면서 시들고, 위축되며, 결국 2~3개월 안에 완전히 말라 죽는다. 병든 식물체 지제부에서 Fusarium균이 분리되었고, 9개 균주를 단포자 분리하여 형태적 특성을 조사한 결과, Fusarium solani로 동정되었다. 대형포자는 통통하고, 직선형이거나 약간 굽은 초승달 모양이고, 소형분생포자는 긴mono형태의 분생포자원세포에서 false head상으로 형성되었다. 후벽포자는 균사 중간 혹은 끝부분에 풍부하게 형성되었다. 이와 같은 동정 결과는 translation elongation factor 1 alpha (TEF)와 RNA polymerase II subunit (RPB2) 유전자의 염기서열 분석으로 재확인되었다. 그 결과, 분리 균주는 NCBI GenBank에 등록된 F. solani와 TEF 유전자는 99.2~99.9%, RPB2 유전자는 98.0~98.1%의 상동성을 나타내었다. 건전한 꽃도라지 유묘의 뿌리를 포자현탁액에 침지 접종하여 병원성 검정을 수행한 결과, 접종 7일 이내에 접종한 식물체에서만 병징이 관찰되었다. 따라서 이 병을 F. solani에 의한 꽃도라지 뿌리썩음병으로 명명하며, 병의 발생을 국내에서 처음으로 보고한다.

클로탈라리아 시들음병을 일으키는 Fusarium udum의 특성 (Characterization of Fusarium udum Causing Fusarium Wilt of Sunn Hemp in Korea)

  • 최효원;홍성준;홍성기;이영기;김점순
    • 한국균학회지
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    • 제46권1호
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    • pp.58-68
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    • 2018
  • 클로탈라리아는 국내에서 토양개량을 위한 질소고정, 토양침식 감소, 잡초 및 선충 억제를 위해 풋거름작물로 이용하고 있다. 2014년, 클로탈라리아를 풋거름작물로 재배하는 완주 지역의 포장에서 시들음 증상이 관찰되었다. 감염된 식물체의 잎은 아래잎부터 황화 되면서 시들기 시작하였고, 위쪽 잎도 황화 되었으며, 결국 식물체는 완전히 고사하였다. 감염된 식물체 줄기에서 어두운 색의 자낭각이 다수 관찰되었고, 이 자낭각으로부터 자낭포자를 단포자 분리하여 6개 균주를 분리하였다. 균학적 특성에 의해 분리균은 Fusarium udum(완전세대: Gibberella indica)로 동정되었다. 대형포자의 정단세포는 대부분 갈고리 모양으로 굽어 있고, 소형포자는 단경자에서 false head 상으로 형성되었다. 후벽포자는 균사에서 단일 혹은 무리지어 풍부하게 형성되었다. 이와 같은 동정 결과는 translation elongation factor 1 alpha(TEF), calmodulin (CAL), histone 3 (HIS3) 유전자 염기서열 분석으로 재확인되었다. 그 결과, 분리 균주는 NCBI GanBank에 등록된 F. udum과 TEF 유전자는 94.4~96.2%, CAL 유전자는 99.7%, HIS3 유전자는 99.6~99.8%의 상동성을 보였다. 클로탈라리아와 두 품종의 콩을 대상으로 포자현탁액을 토양에 관주 접종하여 병원성 검정을 수행한 결과, 접종 14~21일 이내에 접종한 클로탈라리아와 태광콩에서 병징이 관찰되었다. 따라서 이 병을 F. udum에 의한 클로탈라리아 시들음병으로 명명하고자 제안하며, 국내에서 처음으로 보고한다.

Genetic Diversity of the Pear Scab Fungus Venturia nashicola in Korea

  • Choi, Eu Ddeum;Kim, Gyoung Hee;Park, Sook-Young;Song, Jang Hoon;Lee, Young Sun;Jung, Jae Sung;Koh, Young Jin
    • Mycobiology
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    • 제47권1호
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    • pp.76-86
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    • 2019
  • Scab disease caused by Venturia nashicola is of agroeconomic importance in cultivation of Asian pear. However, little is known about the degree of genetic diversity in the populations of this pathogen. In this study, we collected 55 isolates from pear scab lesions in 13 major cultivation areas in Korea and examined the diversity using sequences of internal transcribed spacer (ITS) region, ${\beta}$-tubulin (TUB2), and translation elongation factor-$1{\alpha}$ ($TEF-1{\alpha}$) genes as molecular markers. Despite a low level of overall sequence variation, we found three distinctive subgroups from phylogenetic analysis of combined ITS, TUB2, and $TEF-1{\alpha}$ sequences. Among the three subgroups, subgroup 1 (60% of isolates collected) was predominant compared to subgroup 2 (23.6%) or subgroup 3 (16.4%) and was distributed throughout Korea. To understand the genetic diversity among the subgroups, RAPD analysis was performed. The isolates yielded highly diverse amplicon patterns and none of the defined subgroups within the dendrogram were supported by bootstrap values greater than 30%. Moreover, there is no significant correlation between the geographical distribution and the subgroups defined by molecular phylogeny. Our data suggest a low level of genetic diversification among the populations of V. nashicola in Korea.