• 한국미생물·생명공학회지
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• 제25권2호
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• pp.129-136
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• 1997

Helicobacter pylori is a spiral-shaped, microaerophilic human gastric pathogen causing chronic-active gastritis in association with duodenal ulcer and gastric cancer. To investigate the possibility of H. pylori outer membrane proteins (OMPS) as the oral vaccine antigens, sarcosine-insoluble outer membrane fraction has been prepared from H. pylori NCTC 11637. The major OMPs having apparent molecular masses of 62 kDa, 54 kDa and 33 kDa were detected by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), which were identified as urease B subunit (UreB), heat shock protein (Hsp54 kDa) and urease A subunit (UreA), respectively. Minor protein bands of 57 kDa, 52 kDa, 40 kDa, 36 kDa and 31 kDa were also observed. The antigenicity of H. pylori OMPs and antigenic cross-reactivity among the strains were determined by immunoblot analysis using anti-H. pylori OMPs antisera or intestinal lavage solutions. The results showed that UreB, Hsp54 kDa, UreA and 40 kDa proteins vigorously stimulated mucosal immune response rather than systemic immunity. From this results, these proteins seemed to be useful as the antigen candidates for the oral vaccine. The immunoblotting results with surface proteins from eight isolated H. pylori strains were similar to that of H. pylori NCTC 11637. The IgA which had been arised from oral administration of H. pylori OMPs, was able to bind H. pylori whole-cells.

• Journal of Microbiology and Biotechnology
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• 제16권2호
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• pp.318-324
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• 2006

In order to develop an oral vaccine to prevent H. pylori infection, we have expressed the hpaA gene of H. pylori K51 isolated from Korean patients, encoding 29-kDa HpaA that is known to be localized on the cell surface and flagella sheath, in a live delivery vector system, Lactococcus lactis. The hpaA gene, amplified by PCR using the genomic DNA of H. pylori K51, was cloned in the pGEX-2T vector, and the DNA sequence analysis revealed that the hpaA gene of H. pylori K51 had 99.7% and 94.8% identity with individual hpaA genes of the H. pylori 26695 strain (U.K) and the J99 strain (U.S.A). A polyclonal anti-HpaA antibody was raised in rats using GST-HpaA fusion protein as the antigen. The hpaA gene was inserted in an E. coli-L. lactis-shuttle vector (pMG36e) to express in L. lactis. Western blot analysis showed that the expression level of HpaA in the L. lactis transformant remained constant from the exponential phase to the stationary phase, without extracelluar secretion. These results indicate that the HpaA of H. pylori K51 was successfully expressed in L. lactis, and suggest that the recombinant L. lactis expressing HpaA may be applicable as an oral vaccine to induce a protective immune response against H. pylori.

• 한국식품영양과학회지
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• 제34권4호
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• pp.484-488
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• 2005

본 연구는 위염, 위궤양, 위림프종 및 위암과 같은 소화기 질환의 원인균으로 알려진 Helicobacter pylori균을 항원으로 하여 젖소에 면역시킨 후 생산된 우유의 anti-H. pylori 항체 생성능을 검토하고, 백신 투여량과 항체 생성과의 관계, 비유시기에 따른 항체생성과의 관계 그리고 백신투여가 젖소에 미치는 영향을 알아보았다. 백신 투여량에 따른 혈청과 유청내의 anti-H. pylori항체의 함량은 10 mL, 20 mL, 30 mL 백신투여 모든 군에서 대조구에 비해서 높은 항체 생성량을 확인하였으며, 그 중 20 mL 투여가 항체 생성에 가장 큰 영향을 미친 것으로 조사되었다. 백신 투여량에 따른 유청내의 antl-H. pylori항체 생성량은 혈청에서 나타난 결과와 유사한 결과를 나타내었다. 백신투여에 따른 비유시기별 항체함량은 혈액내에서는 $2\~4$주까지 증가하는 경향을 보이다가 $6\~12$주 사이에는 대조구와 유의성 있는 차이를 보였고, 처리구간 항체생성량은 비유초기>비유중기>비유 후기 순으로 유의성있는 차이를 나타내었다(p<0.05). 그리고 유청내 항체 함량은 혈액과 유사한 경향을 나타내며 항체함량이 증가하였으나, 처리구간의 유의적인 차이는 나타나지 않았다. 백신투여로 인하여 백신투여 1일째의 산유량은 $12\%$ 감소하는 경향을 나타냈고, 최장 1주일 정도 지나면서 회복되었다. 백신투여 후 젖소의 체온을 측정한 결과 정상적인 범위 내에서 체온이 상승하여 백신투여가 젖소의 생리적 변화에 큰 영향을 미치지 않는 것으로 나타났다.

• Journal of Microbiology and Biotechnology
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• 제10권6호
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• pp.865-872
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• 2000

Helocobacter phylori is the major cause of gastritis, peptic ulcer, and a principal risk factor for gastric cancer. As the firs step towards a vaccine against H. pylori infection, Hy.pylori urease was expressed and purified as a recombinant apoenzyme (rUrease) in E. coli. In order to develop an effective immunization protocol using rUrease, the host immune responses were evaluated after the oral immunization of mice with rUrease preparations plus cholera toxin relative to various conditions, such as the physical nature of the antigen, the frequency of the booster immunization, the dose of the antigen, and the route of administration. The protective efficacy was assessed using a quantitative culture following an H. pylori SS1 challenge. It was demonstrated that rUrease, due to its particulated nature, was more superior than the UreB subunit as a vaccine antigen. The oral immunization of rUrease elicited significant systemic and secretory antibody responses, and activated predominantly Th2-type cellular responses. The bacterial colonization was significantly reduced (~100-fold) in those mice immunized with three or four weekly oran doses of rUrease plus cholera toxin (p<0.05), when compared to the non-immunized/challenged controls. The protection correlated well with the elicited secretory IgA level against rUrease, and these secretory antibody responses were highly dependent on the frequency of the booster immunization, yet unaffected by the dose of the antigen (25-200$\mu\textrm{g}$). These results demonstrate the remarkable potential of rUrease as a vaccine antigen, thereby strengthening the possibility of developing an H. pylori vaccine for humans.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2003년도 생물공학의 동향(XIII)
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• pp.186-189
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• 2003

Helicobacter pylori is the etiologic agent of human gastritis and peptic ulceration and produces urease as the major protein component on its surface. H. pylori urease is known to serve as a potent immunogen as well as major virulence factor. In order to express the recombinant urease in tobacco plants, a DNA fragment containing the minimal H. pylori urease gene cluster was subcloned into a plant expression vector. The recombinant vector was transformed to tobacco plants. The integration of the recombinant plasmids into tobacco chromosomal genome was verified by genomic PCR. Expression to mRNA was confirmed by Northern blot analysis, and expression to recombinant urease protein was observed by Western blot analysis. These results showed that the recombinant urease can be produced in tobacco plants and will be tested for immune response to use as an edible vaccine.

• 식물조직배양학회지
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• 제27권3호
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• pp.239-243
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• 2000

위염과 위궤양을 일으키는 Helicobacter pylori는 그 감염 환자에서 강한 항체형성을 유도하는 urease를 생산한다. 식물체를 이용하여 H. pylori에 대한 식용백신 모델을 제조하기 위하여 H. pylori의 urease 유전자를 지니고 있는 pH808 plasmid로부터 750bp의 ureA DNA를 PCR에 의해서 증폭한 후 이를 담배식물에서 발현이 되도록 조작하였다. 재분화된 형질전환 식물체로부터 ureA 유전자의 도입과 mRNA발현 및 단백질합성을 분석하였다. CaMV 35S promoter에 의한 ureA 유전자의 발현은 SDS polyacrylamide 전기영동 및 immunoblot실험에서 박테리아로부터의 재조합 단백질과 같은 크기의 30 kDA UreA 단백질이 생산되었음을 확인할 수 있었다.

• Journal of the Korean Society for Industrial and Applied Mathematics
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• 제13권1호
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• pp.1-11
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• 2009

Current therapies against ulcers caused by H. pylori infection consist of antibiotics, an acid reducer, and some clinical trials underway to develop a H. pylori vaccine. We develop a structured model with age-dependent mortality of peptic ulcers and H. pylori infection. Our main goal is to analyze our structured model mathematically and to compare it to our previously unstructured model to examine the disease transmission dynamics in terms of annual prevalence and annual incidence of the disease.

• 대한수의학회지
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• 제46권4호
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• pp.327-335
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• 2006

A stable and reliable Helicobacter pylori (H. pylori) infection animal model would be necessary for evaluating vaccine efficacy and helpful for understanding the pathological mechanism of the organism. The aim of the present study is to investigate the effect of ethanol treatment prior to H. pylori inoculation on associated gastric mucosal injury and to establish ethanol-pretreating animal model to study H. pylori infection. Male Mongolian gerbils were used for the study. H. pylori was orally inoculated after 12 h fasting. 3 h prior to H. pylori inoculation, a group of gerbils was orally treated with absolute ethanol, 60% and 40% ethanol respectively. Another group of animals was treated either with H. pylori culture media alone or with different concentrations of ethanol plus culture media. Gerbils were killed 4 or 8 weeks after H. pylori inoculation. The colonization of H. pylori was confirmed by both histological examination and rapid urease test. Mucosal damage was evaluated grossly and histologically according to the criteria. The colonization of H. pylori and pathological changes in gastric mucosa of the animals were also observed. Although no significant change to the gastric mucose was observed in the animals treated either with H. pylori culture media alone or with different concentrations of ethanol plus culture media, persistent H. pylori infection was seen in the mucosa and mucosal leucocyte infiltration and severe epithelial damage was observed in the Helicobacter and ethanol + Helicobacter groups after 4 weeks. The gross and histological scores were higher in the ethanol + Helicobacter than in the Helicobacter alone group. As the results, ethanol-pretreatment with 60% concentration induced severe pathogenic changes by H. pylori infection in 5 weeks-old Mongolian gerbils. These results suggested that ethanol-pretreatment before H. pylori inoculation could increase the severity of gastric mucosal inflammation and enhance the colonization of H. pylori. The established ethanol-pretreating animal model would contribute to screen new drugs against H. pylori and be used as an useful tool for various animal experiments with H. pylori strains.

• Journal of Microbiology
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• 제45권1호
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• pp.21-28
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• 2007

In order to search for specific genotypes related to this unique phenotype, we used whole genomic DNA microarray to characterize the genomic diversity of Helicobacter pylori (H. pylori) strains isolated from clinical patients in China. The open reading frame (ORF) fragments on our microarray were generated by PCR using gene-specific primers. Genomic DNA of H. pylori 26695 and J99 were used as templates. Thirty-four H. pylori isolates were obtained from patients in Shanghai. Results were judged based on In(x) transformed and normalized Cy3/Cy5 ratios. Our microarray included 1882 DNA fragments corresponding to 1636 ORFs of both sequenced H. pylori strains. Cluster analysis, revealed two diverse regions in the H. pylori genome that were not present in other isolates. Among the 1636 genes, 1091 (66.7%) were common to all H. pylori strains, representing the functional core of the genome. Most of the genes found in the H. pylori functional core were responsible for metabolism, cellular processes, transcription and biosynthesis of amino acids, functions that are essential to H. pylori's growth and colonization in its host. In contrast, 522 (31.9%) genes were strain-specific genes that were missing from at least one strain of H. pylori. Strain-specific genes primarily included restriction modification system components, transposase genes, hypothetical proteins and outer membrane proteins. These strain-specific genes may aid the bacteria under specific circumstances during their long-term infection in genetically diverse hosts. Our results suggest 34 H. pylori clinical strains have extensive genomic diversity. Core genes and strain-specific genes both play essential roles in H. pylori propagation and pathogenesis. Our microarray experiment may help select relatively significant genes for further research on the pathogenicity of H. pylori and development of a vaccine for H. pylori.

• Pediatric Infection and Vaccine
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• 제14권1호
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• pp.97-103
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• 2007

목 적 : Lewis b($Le^b$) 항원과 BabA 단백은 H. pylori가 위점막에 부착하는 것과 연관이 있는 것으로 알려져 있다. 소아에서 H pylori 감염에 대한 위점막의 면역 반응은 성인에서의 반응과 차이가 있을 것으로 추정되지만 Le 항원의 발현에 관한 연구는 매우 드물다. 이에 저자들은 국내 소아 H. pylori 양성 환자의 위점막에서 Le 항원의 발현 양상을 알아보기 위하여 본 연구를 시행하였다. 방 법 : 2002년 1월부터 2004년 1월까지 상부 위장관 증상 때문에 소아과를 방문하여 내시경 검사를 시행받은 소아 환자를 대상으로 하였다. 위전정부에서 최소한 2개 이상의 조직 검체를 생검하여 CLO 검사와 조직 특수 염색(Warthin-starry) 검사를 각각 시행하여 모두 양성인 경우에 H. pylori에 감염된 것으로 판정하였다. H. pylori 양성 35명과 H. pylori 음성 19명의 위점막 파라핀 조직에서 DNA를 추출하여 cagA, babA2 특이 시발체를 이용하여 PCR을 시행하였다. 위점막 생검 조직을 대상으로 $Le^a$, $Le^b$, $Le^x$와 $Le^y$ 항체를 사용하여 면역조직화학적 염색을 시행한 다음 각각의 Le 항원의 발현 정도를 평가하였다. 결 과 : H. pylori 양성 환자에서 $Le^a$ 항원은 60%(21명/35명), $Le^b$ 항원 97%(34명/35명), $Le^x$ 항원 88%, $Le^y$ 항원은 100%에서 발현이 확인되었다. H. pylori 음성 환아군에서는 $Le^a$, $Le^b$, $Le^x$ 및 $Le^y$ 항원이 각각 52%, 100%, 89%, 100%에서 발현되었다. H. pylori 양성 유무에 따른 $Le^b$ 항원 발현의 차이는 없었다. CagA 및 babA2 유전자는 H. pylori 양성 환자군 중 각각 65.7%(23명/35명), 25.6%(8명/35명)에서 확인되었다. Lewis 항원들의 발현에 따른 H. pylori 감염, cagA 양성 및 babA2 양성율의 차이는 없었다. 결 론 : 국내 소아의 위점막에서 높은 $Le^x$와 $Le^y$ 항원의 발현율을 확인할 수 있었으나 H. pylori 감염 및 babA2의 양성 여부와는 관련이 없었다. Lewis 항원 이외의 다른 점막 수용체들과 세균 독소들에 대한 지속적 연구가 필요할 것으로 생각된다.