• 제목/요약/키워드: host-specificity

검색결과 155건 처리시간 0.021초

Diagnosis of Graft-Versus-Host Disease after Bone Marrow Transplantation by in vivo Proton MR Spectroscopy of the Liver: Correlation with Pathologic Results

  • Cho, Soon-Gu;Lee, Moon-Hee;Suh, Chang-Hae
    • 대한자기공명의과학회:학술대회논문집
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    • 대한자기공명의과학회 2001년도 제6차 학술대회 초록집
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    • pp.135-135
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    • 2001
  • Purpose: To know the differences of the proton MR spectroscopic features of the liver between th patients with graft-versus-host disease (GVHD) and without GVHD (non-GVHD) after to marrow transplantation (BMT), and to evaluate the possibility to discriminate GVHD fro non-GVHD by analysis of the in vivo proton MR spectra. Method: We evaluated the in vivo proton MR spectra from the livers of 37 patients wh underwent BMT. Our series included 14 cases with GVHD and 23 without GVHD in the liver. Nineteen men and 18 women were included in our series. All cases of GVHD and 2 o non-GVHD were confirmed by liver biopsy and remaining of non-GVHD by evaluation clinical follow up. Proton MR spectroscopy (1H-MRS) was performed at 1.5T GE Sign Horizon (GE Medical System, Milwaukee, USA) system using localized proton STEAM sequence and body coil in all cases with subjects were located in supine position. N respiratory interruption was required during the spectroscopic signal acquisition. Paramete using in MRS were: TR = over 3000ms, TE = 30ms, number of scans = 128, voxel size = ($2{\times}2{\times}2$)$cm^3$, and one NEX. We evaluated the spectra with an attention to the differences o patterns of the peaks between GVHD and non-GVHD groups. The ratio of peak area of peaks at 1.6-4.1ppm to lipid (0.9-1.6ppm) [P(1.6-4.1ppm)/P(0.9-1.6ppm)] was calculated in GVHD and non-GVHD group, and compared the results between these groups. We als evaluated the sensitivity and specificity for discriminating GVHD from non-GVHD by anal of 1H-MRS.

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Genomic Approaches for Understanding the Characteristics of Salmonella enterica subsp. enterica Serovar Typhimurium ST1120, Isolated from Swine Feces in Korea

  • Kim, Seongok;Kim, Eunsuk;Park, Soyeon;Hahn, Tae-Wook;Yoon, Hyunjin
    • Journal of Microbiology and Biotechnology
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    • 제27권11호
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    • pp.1983-1993
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    • 2017
  • Salmonella enterica subsp. enterica serovar Typhimurium, one of the most common foodborne pathogens, is transmitted mainly through contaminated food derived from infected animals. In this study, S. Typhimurium ST1120, an isolate from pig feces in Korea, was subjected to whole-genome analysis to understand its genomic features associated with virulence. The genome of ST1120 was found to have a circular chromosome of 4,855,001 bp (GC content 52.2%) and a plasmid of 6,863 bp (GC content 46.0%). This chromosome was predicted to have 4,558 open reading frames (ORFs), 17 pseudogenes, 22 rRNA genes, and 86 tRNA genes. Its plasmid was predicted to have three ORFs. Comparative genome analysis revealed that ST1120 was phylogenetically close to S. Typhimurium U288, a critical isolate in piggery farms and food chains in Europe. In silico functional analysis predicted that the ST1120 genome harbored multiple genes associated with virulence and stress resistance, including Salmonella pathogenicity islands (SPIs containing SPI-1 to SPI-5, SPI-13, and SPI-14), C63PI locus, ST104 prophage locus, and various antibiotic resistance genes. In accordance with these analysis results, ST1120 showed competence in invasion and survival abilities when it was added to host cells. It also exhibited robust resistance against antibiotics in comparison with other S. Typhimurium strains. This is the first report of the complete genome sequence of S. Typhimurium isolated from swine in Korea. Comparative genome analysis between ST1120 and other Salmonella strains would provide fruitful information toward understanding Salmonella host specificity and developing control measures against S. Typhimurium infection.

Flavonoids와 근류균의 상호작용 (Interactions between Rhizobia and Flavonoids)

  • 강상재;박우철;서상현
    • Applied Biological Chemistry
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    • 제40권6호
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    • pp.551-555
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    • 1997
  • 본 연구는 숙주특이적인 근류형성에 두과작물의 뿌리분비물에 포함된 기주특이적인 flavonoids와 근류균의 상호작용에 대해 실험하였다. Flavonoid 화합물에 대한 근류균의 생물학적 활성은 B. japonocum의 경우 대두의 뿌리분비물에 포함된 flavonoid화합물인 daidzein과 genistein에서는 생장 증진 효과가 나타났으며, alfalfa의 뿌리분비물에 포함된 flavonoid인 luteolin에서는 생장 저해 효과가 나타났으며, R. meliloti의 경우 luteolin의 경우 생장증진 효과가 나타났으며, daidzein과 genistein의 경우 생장저해효과가 나타났다. 각 근류균의 흡수 특이성은 B. japonicum에서 daidzein과 genistein이 각각 $14.95\;{\mu}g/g$$14.20\;{\mu}g/g$로 가장 높고 luteolin이 가장 낮게 나타났으며, R. meliloti의 경우 luteolin이 $18.31\;{\mu}g/g$으로 가장 높고 daidzein과 genistein이 가장 낮게 나타났다. 이와 같은 사실로 숙주특이적인 flavonoids가 근류균의 숙주특이성에 깊은 관련이 있을 것으로 사료된다.

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식이성 윤충류질환의 관리전략 수립을 위한 감염원의 역학 및 병원체의 생물학적 특성에 관한 조사연구 - 한국산 민물어류에 기생하는 Metagonimus속 피낭유충의 숙주특이성과 감염실험을 통한 성충의 분류 (Classification and host specificity of Metagonimus spp. from Korean freshwater fish)

  • 임한종;김기홍;주경환
    • Parasites, Hosts and Diseases
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    • 제34권1호
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    • pp.7-14
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    • 1996
  • 한국인에 널리 유행하는 Metagonimus속 흡충류의 분류학적 문제점들을 해결하기 위해 다양한 지역에서 채집한 여러 종의 민물어류로부터 Metugonim속 피낭유충을 검출하여 햄스터에 감염 실험을 하였다. 감염실험 결과 은어는 기존에 알려져 있던 M. yokogawnia 피낭유충 외에 M. tokqhashii의 피낭유충에도 감염되어 있는 것이 밝혀졌으며 붕어에는 M. takohoshii의 피낭유충만 이 감염되어 있었다 피라미, 끄리, 갈겨니등에서 검출된 Metqgonim속 피낭유충의 감염실험 결과, 이들 어종은 모두가 Metosonim Miyata type의 피낭유충에만 감염되어 있는 것으로 나타났다. Metagonimus Miyata type의 성충은 여러 가지 특징 및 숙주특이성 등에 의해서 다른 두 종과 구별되었으며. 그 분류학적 위치에 대해서 몇 가지 가능성을 고찰하였다.

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그물버섯속(屬)의 검색표(檢索表) (Key to the Species of Boletus)

  • 구창덕
    • 한국균학회지
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    • 제21권2호
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    • pp.146-156
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    • 1993
  • 그물버섯속(屬)(Boletus)의 버섯은 대부분이 소나무과(科), 참나무과(科), 자작나무과(科) 수목과 공생하는 것으로서 기주선택성이 강한 것이 있으면서 기주식물의 생장을 촉진하기도 한다. 또한 맛과 향기가 특이하여 기호식품으로 즐겨 채집되는 것도 있지만 국내에서는 이런 면에서 전혀 인기가 없으며 그물버섯(B.edulis)는 국내에서는 아직 채집된 바가 없다. 현재 우리나라에서는 그물버섯속(屬)에서 26종(種)이 보고되어 있으나 새로운 종(種)이 계속 보고되고 있다 . 여기서는 국내외에서 발표된 기존 논문을 참고로 하여 귀신그물버섯과(科)와 그물버섯과(科)에 이르는 검색표(檢索表), 그물버섯과(科)의 속(屬)에 대한 검색표(檢索表) 그리고 국내 분포 종(種)을 포함하는 111종(種)의 그물버섯속(屬)의 종(種)에 대한 검색표(檢索表)를 제시하였다.

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병원균 Klebsiella pneumoniae를 감염시키는 용균 박테리오파지 KP1의 유전체 염기서열 초안 (Draft genome sequence of lytic bacteriophage KP1 infecting bacterial pathogen Klebsiella pneumoniae)

  • 김영주;방인아;연영은;박준영;한범구;김현일;김동혁
    • 미생물학회지
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    • 제54권2호
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    • pp.152-154
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    • 2018
  • Klebsiella pneumoniae는 그람 음성균에 속하고 막대 형태를 가지며 인간이나 동물의 폐에 감염하여 병을 일으키는 균이다. K. pneumoniae는 흔히 항생제 내성을 나타내는데 이로 인해 항생제를 통한 치료가 어려워지게 된다. 이런 상황에서 숙주 균에 특이적이고 민감하게 반응하는 박테리오파지는 항생제 내성균의 치료에 대한 대체적인 접근법으로 제안될 수 있다. 박테리오파지 KP1은 하수처리장에서 분리되었으며 K. pneumoniae에 대해 특정적인 감염성이 있다. 본 연구에서는 Klebsiella pneumoniae 박테리오파지 KP1의 유전체 초안 분석을 수행하였다. KP1의 유전체 초안은 167,989 bp의 길이, 39.6%의 G + C 비율로 구성되어있다. 295개의 예측된 ORF들과 14개의 tRNA 유전자를 가지고 있다. 또한 이들은 lysozyme, 그리고 holin과 같은 다양한 세포 용해 관련 효소들을 포함하고 있다.

돼지풀잎벌레의 섭식에 의한 생태계교란 식물인 단풍잎돼지풀의 제어 가능성 연구 ( A Study on Control Possibility of Ambrosia trifida L., an Invasive Alien Plant by the Feeding of Ophraella communa LeSage)

  • 이수인;박재훈;김의주;박지원;이정민;김윤서;김세희;박여빈;이응필
    • 한국습지학회지
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    • 제25권3호
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    • pp.184-195
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    • 2023
  • 한국에서 생태계교란 식물인 단풍잎돼지풀의 효과적인 관리방안을 마련하고자, 초식자인 돼지풀잎벌레의 기주특이성, 연간 이동거리를 조사하여 생물학적 방제 수단으로의 활용 가능성과 이 곤충의 섭식이 단풍잎돼지풀의 활력에 미치는 영향을 연구하였다. 이를 위해서 돼지풀잎벌레의 기주선호도를 조사하였고, 돼지풀잎벌레가 확인된 지점을 기준으로 거리가 10m, 20m, 30m, 100m 떨어진 지점에 돼지풀잎벌레가 없는 단풍잎돼지풀군락을 선정하여 돼지풀잎벌레의 출현 여부 파악을 통해 이들의 이동 거리를 확인하였다. 그리고 돼지풀잎벌레의 섭식에 따른 단풍잎돼지풀의 생육, 번식 그리고 생리반응을 측정하였다. 그 결과 돼지풀잎벌레는 국화과의 3분류군만을 섭식하였고, 숙주로부터 반경 30m/yr 이내로 단거리 이동하였다. 초식자의 섭식은 단풍잎돼지풀의 생육, 번식 그리고 생리반응에 부정적인 영향을 주었고, 초식자가 있는 곳으로부터 거리가 멀어질수록 생육 및 번식이 양호하였다. 또한, 단풍잎돼지풀의 식피율이 50% 이하일 때 초식자를 도입하면 90% 이상의 단풍잎돼지풀을 제어할 수 있었지만, 식피율이 90% 이상에서는 제거의 효과가 감소했다. 결과적으로 돼지풀잎벌레는 단풍잎돼지풀의 생태학적 제어자로서 활용 가능성이 있고, 제어의 효과를 높이기 위해서는 단풍잎돼지풀의 식피율이 낮은 봄(5월)에 이 곤충을 도입하는 것이 유리하다.

Expression of Hepatitis B Virus S Gene in Pichia pastoris and Application of the Product for Detection of Anti-HBs Antibody

  • Hu, Bo;Liang, Minjian;Hong, Guoqiang;Li, Zhaoxia;Zhu, Zhenyu;Li, Lin
    • BMB Reports
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    • 제38권6호
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    • pp.683-689
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    • 2005
  • Antibody to hepatitis B surface antigen (HBsAb) is the important serological marker of the hepatitis B virus (HBV) infection. Conventionally, the hepatitis B surface antigen (HBsAg) obtained from the plasma of HBV carriers is used as the diagnostic antigen for detection of HBsAb. This blood-origin antigen has some disadvantages involved in high cost, over-elaborate preparation, risk of infection, et al. In an attempt to explore the suitable recombinant HBsAg for the diagnostic purpose, the HBV S gene was expressed in Pichia pastoris and the product was applied for detection of HBsAb. Hepatitis B virus S gene was inserted into the yeast vector and the expressed product was analyzed by sodium dodecyl sulphate polyacrolamide gel electrophoresis (SDS-PAGE), immunoblot, electronic microscope and enzyme linked immunosorbent assay (ELISA). The preparations of synthesized S protein were applied to detect HBsAb by sandwich ELISA. The S gene encoding the 226 amino acid of HBsAg carrying ahexa-histidine tag at C terminus was successfully expressed in Pichia pastoris. The His-Tagged S protein in this strain was expressed at a level of about 14.5% of total cell protein. Immunoblot showed the recombinant HBsAg recognized by monoclonal HBsAb and there was no cross reaction between all proteins from the host and normal sera. HBsAb detection indicated that the sensitivity reached 10 mIu (micro international unit)/ml and the specificity was 100% with HBsAb standard of National Center for Clinical Laboratories. A total of 293 random sera were assayed using recombinant S protein and a commercial HBsAb ELISA kit (produced by blood-origin HBsAg), 35 HBsAb positive sera and 258 HBsAb negative sera were examined. The same results were obtained with two different reagents and there was no significant difference in the value of S/CO between the two reagents. The recombinant HBV S protein with good immunoreactivity and specificity was successfully expressed in Pichia pastoris. The reagent for HBsAb detection prepared by Pichia pastoris-derived S protein showed high sensitivity and specificity for detection of HBsAb standard. And a good correlation was obtained between the reagent produced by recombinant S protein and commercial kit produced by blood-origin HBsAg in random samples.

Opportunities and Challenges in Nutrigenomics and Health Promotion

  • Milner John A.
    • 한국식품영양과학회:학술대회논문집
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    • 한국식품영양과학회 2004년도 Annual Meeting and International Symposium
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    • pp.17-23
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    • 2004
  • Not all individuals respond identically, or at times in the same direction, to dietary interventions. These inconsistencies likely arise because of diet and genomic interactions (nutrigenomics effects). A host of factors may influence the response to bioactive food components including specific polymorphisms (nutrigenetic effect), DNA methylation patterns and other epigenomic factors (nutritional epigenomic effects), capacity to induce anuo. suppress specific mRNA expression and patterns (nutritional transcriptomics), the occurrence and activity of proteins (proteomic effects), and/or the dose and temporal changes in cellular small molecular weight compounds will not only provide clues about specificity in response to food components, but assist in the identification of surrogate tissues and biomarkers that can predict a response. While this 'discovery' phase is critical for defining mechanisms and targets, and thus those who will benefit most from intervention, its true usefulness depends on moving this understanding into 'development' (interventions for better prevention, detection, diagnosis, and treatment) and a 'delivery' phase where information is provided to those most in need. It is incumbent on those involved with food and nutrition to embrace the 'omics' that relate to nutrition when considering not only the nutritional value of foods and their food components, but also when addressing acceptability and safety. The future of 'Nutrigenomics and Health Promotion' depends on the ability of the scientific community to identity appropriate biomarkers and susceptibility variants, effective communications about the merits of such undertakings with the health care community and with consumers, and doing all of this within a responsible bioethical framework.

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Identification of a host range determinant from Ralstonia solancearum race 3

  • Yeonhwa Jeong;Lee, Seungdon;Ingyu Hwang
    • 한국식물병리학회:학술대회논문집
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    • 한국식물병리학회 2003년도 정기총회 및 추계학술발표회
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    • pp.71.2-71
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    • 2003
  • Ralstonia solancearum infects many solanaceous plants, however race 3 infects only potato and tomato weakly. To identify genes responsible for race specificity of R. solanacearum, we mobilized genomic library of LSD2029 (race 3) into LSD341 (race 1) and inoculated 1,000 transconjugants into hot pepper. One transconjugant that did not induce wilt symptom in hot pepper was isolated. We found that a cosmid clone, pRSl, conferred avirulence to LSD341. By deletion and mutational analyses of pRSl, we found the 0.9-kb PstI/Hindlll fragment carries avirulence functions. We sequenced the fragment and identified one possible open reading frame, a rsal gene, possibly encoding 110 amino acids. The rsal was preceded with a plant-inducible promoter (PIP) box, indicating that the gene might be regulated by HrpB. Interestingly, the promoter region of the rsal homolog in the strain GM11000 (race 1) did not have the PIP box. Rsal did not show any significant homologies with proteins in the database, indicating th e protein is different from the previously reported avirulence proteins. When we mutated the rsal gene by marker-exchange in LSD2029, the mutant was less virulent in potato.

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