• Asian-Australasian Journal of Animal Sciences
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• 제22권7호
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• pp.1043-1047
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• 2009

Three experiments were conducted to determine the conversion rate of formic and acetic acids into methane in the gastrointestinal tracts of geese. In experiment I, two sets of two 4-month-old male White Roman geese were allocated to one of two treatment groups. Each set of geese was inoculated either with formic acid or with phosphate buffer solution (PBS). After the acid or the PBS was inoculated into the esophagi of the geese, two birds from each treatment were placed in a respiratory chamber as a measurement unit for 4 h in order to determine methane production rate. In experiment II and III, 6- and 7-wk-old male White Roman goslings were used, respectively. Birds were allocated to receive either formic acid or PBS solution injected into the ceca in experiment II. Acetic acid or PBS solution injected into the cecum were used for experiment III. After either the acids or the PBS solution were injected into the cecum, two birds from each treatment were placed in a respiratory chamber as a measurement unit for 3 h; each treatment was repeated 3 times. The results indicated that formic acid inoculated into the oesophagi of geese was quickly converted into methane. Compared with the PBS-injected group, methane production increased by 5.02 times in the formic acid injected group (4.32 vs. 0.86 mg/kg BW/d; p<0.05). Acetic acid injected into the ceca did not increase methane production; conversely, it tended to decrease methane production. The present study suggests that formic acid may be converted to methane in the ceca, and that acetic acid may not be a precursor of methane in the ceca of geese.

• Genes and Genomics
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• 제40권12호
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• pp.1383-1388
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• 2018

The development of therapeutic bacteriophages will provide several benefits based on an understanding the basic physiological dynamics of phage and bacteria interactions for therapeutic use in light of the results of antibiotic abuse. However, studies on bacteriophage therapeutics against microbes are very limited, because of lack of phage stability and an incomplete understanding of the physiological intracellular mechanisms of phage. The major objective of this investigation was to provide opportunity for development of a novel therapeutic treatment to control respiratory diseases in swine. The cytokine array system was used to identify the secreted cytokines/chemokines after Bordetella bronchiseptica infection into swine nasal turbinate cells (PT-K75). We also performed the real-time quantitative PCR method to investigate the gene expression regulated by B. bronchiseptica infection or bacteriophage treatment. We found that B. bronchiseptica infection of PT-K75 induces secretion of many cytokines/chemokines to regulate airway inflammation. Of them, secretion and expression of IL-$1{\beta}$ and IL-6 are increased in a dose-dependent manner. Interestingly, membrane-bound mucin production via expression of the Muc1 gene is increased in B. bronchiseptica-infected PT-K75 cells. However, cytokine production and Muc1 gene expression are dramatically inhibited by treatment with a specific B. bronchiseptica bacteriophage (Bor-BRP-1). The regulation of cytokine profiles in B. bronchiseptica-induced inflammation by B. bronchiseptica bacteriophage is essential for avoiding inappropriate inflammatory responses. The ability of bacteriophages to downregulate the immune response by inhibiting bacterial infection emphasizes the possibility of bacteriophage-based therapies as a novel anti-inflammatory therapeutic strategy in swine respiratory tracts.

• IMMUNE NETWORK
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• 제22권6호
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• pp.48.1-48.13
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• 2022

With the spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, which are randomly mutated, the dominant strains in regions are changing globally. The development of preclinical animal models is imperative to validate vaccines and therapeutics against SARS-CoV-2 variants. The objective of this study was to develop a non-human primate (NHP) model for SARS-CoV-2 Delta variant infection. Cynomolgus macaques infected with Delta variants showed infectious viruses and viral RNA in the upper (nasal and throat) and lower respiratory (lung) tracts during the acute phase of infection. After 3 days of infection, lesions consistent with diffuse alveolar damage were observed in the lungs. For cellular immune responses, all macaques displayed transient lymphopenia and neutrophilia in the early stages of infection. SARS-CoV-2 Delta variant spike protein-specific IgM, IgG, and IgA levels were significantly increased in the plasma of these animals 14 days after infection. This new NHP Delta variant infection model can be used for comparative analysis of the difference in severity between SARS-CoV-2 variants of concern and may be useful in the efficacy evaluation of vaccines and universal therapeutic drugs for mutations.

• Clinical and Experimental Pediatrics
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• 제50권5호
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• pp.416-421
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• 2007

Many previous studies have proved that human allergic disease resulted from the formation of antibodies belonging to a unique immunoglobulin isotype termed immunoglobulin E (IgE). Most of IgE-producing plasma cells are found in the lymphoid tissue associated with the gastrointestinal and respiratory tracts. IgE may be found free in the mucosal secretions of these tissues, bound to local mast cells, or distributed by the systemic circulation to mast cells and basophils throughout the body. Total serum IgE concentrations tend to be higher in allergic adults and children compared with non-allergic individuals, but the value of total serum IgE as a screening test for allergic disease is limited. Total serum IgE levels are related to the probability of an individual having detectable allergen-specific IgE. Allergen-specific IgE concentrations vary with a person's age, the degree and duration of the recent allergen or cross-reactive allergen exposure. The value of quantitative assays for allergen-specific IgE has been suggested in recent studies. Serum IgE increases in many non-allergic diseases, including infectious and parasitic diseases. The IgE changes appear to be specific to the infectious agents, whereas non-specific in other diseases. The increased serum IgE in some of these conditions probably results from alterations in immune function. This review summarizes the clinical significance of total and allergen-specific IgE examinations in allergic diseases.

• 대한기관식도과학회:학술대회논문집
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• 대한기관식도과학회 1981년도 제15차 학술대회연제순서 및 초록
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• pp.13.5-14
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• 1981

Wegener써 육아종증은 1939년 Wegener가 \circled1 상하호흡기의 혈관염 및 괴사성 육아종, \circled2 전신적인 혈관염, \circled3 국한된 괴사성 사구체신염을 특징으로하는 질병을 Rhinogenic Granulomatosis라고 명명한데서 유래되었다. 초기에 이 질환은 몇달내에 사망하는 것으로 알고 있다. 그러나 최근 이 질환의 한정된 형(limited form)은 전형적인 형(classic form)에 비해 일반적으로 양성인 경과를 한다고 인지 되였다. 병리학적으로 이 질환은 한번의 조직생검으로 진단하기 힘들며 간혹 부검에서 확진되는 경우도 많다고 한다. 본교실에서는 최근 심한 시력장애, 청력장애를 일으킨 Wegener씨 육아종증 1례를 경험하였기에 이에 문헌고찰과 더불어 보고하는 바이다.

• Clinical and Experimental Pediatrics
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• 제48권3호
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• pp.266-275
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• 2005

목 적 : 바이러스는 소아 하기도 감염증의 가장 흔한 원인으로 소아에서 흔히 이환되어 모세기관지염, 폐렴, 크룹, 기관 기관지염 등의 하기도 감염을 일으키는 원인 바이러스들로서 이들의 유행 시기 및 임상 양상을 조사하여 각 질환의 특성을 알아 보고자 하였다. 방 법 : 1998년 9월부터 2003년 5월까지 한림대학교 한강성심병원과 강남성심병원 소아과에 급성 호흡기 감염증으로 입원했던 환아 10,630명 중 총 4,554례에서 비인두 흡인물을 채취하여 바이러스 배양 및 단일 클론 항체를 이용한 면역 형광 검사법으로 881례(19%)에서 호흡기바이러스가 분리되었다. 그 중 모세기관지염, 폐렴, 크룹, 기관 기관지염 등의 급성 하기도 감염증으로 진단 받은 837례의 의무기록을 후향적으로 고찰하였다. 결 과 : 1) RSV가 485례(55%)로 가장 많았고, PIV 152례(17%), FluA 114례(13%), ADV 79례(9%), FluB 51례(6%) 순이었다. 2) 발생시기는 RSV의 경우 연중 발생하였고, 주로 11-12월에 많았다. PIV 매년 4-6월에 최고치를 이루었고, FluA는 매년 11-12월부터 다음해 1월까지 발생하였으나, 2002년 1월과 11월에 가장 많았다. FluB는 매년 3-4월에 유행하였고, 그 중 2002년 4월에 최고치를 이루었다. ADV는 연중 비슷하게 발생하였다. 3) 남녀 성별 비는 3 : 2로 남아가 더 많았고, 중앙연령은 9개월이었다. 4) 임상적 진단에는 세기관지염 395례(47%), 폐렴 305례(36%), 크룹73례(9%), 기관 기관지염 64례(8%)의 순이었고, RSV의 경우 세기관지염이 280례(60%)였다. 5) 임상증상 및 징후에는 각 바이러스 모두 기침(96%), 가래(83%), 비루(65%), 발열(61%)이 많았고, ADV는 설사(23%)가 다른 바이러스에 비해 많았다. 6) 청진 소견으로 천명음이 들렸던 경우는 RSV가 55%로 많았고, 수포음은RSV(47%), ADV(43%), FluA(40%) 순이었다. 건성수포음은 FluB가 49%로 많았으며, 협착음은 PIV가 27%로 높았다. 7) 말초 혈액 백혈구 수는 전체 62%에서 정상이었고, 36%에서 증가하였다. 적혈구 침강 속도는 30%에서 증가하였고, C 반응 단백은 20%에서 양성이었다. 8) 방사선 소견은 고찰이 가능하였던 803례 중 각 바이러스 모두 정상 소견이 557례(69%)로 가장 많았고, 특징적으로 하인두 확장은 PIV에서 31례(21%)로 현저하게 많았다. 결 론 : 소아에서 급성 하기도 감염증의 중요한 원인을 차지하는 호흡기 바이러스는 각각 발생시기 및 유행 양상에서 차이를 보였으나, 임상 양상은 서로 비슷하였고, 배양검사 결과가 확인되기 이전에 정확한 원인 바이러스를 예측하고 규명하기에는 어려운 점이 있었다. 이에 질병을 예측할 수 있는 신속한 진단법들이 개발되어 항바이러스제제를 적절한 시기에 선택하고 또한 예방접종시기를 예측하는데 도움이 되어야겠다.

• Pediatric Infection and Vaccine
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• 제10권1호
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• pp.102-113
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• 2003

목 적 : 바이러스는 소아 하기도 감염증의 가장 흔한 원인으로 소아에서 흔히 이환되어 모세기관지염, 폐렴, 크룹, 기관 기관지염 등의 하기도 감염을 일으키는 원인 바이러스들의 유행 및 임상 양상을 조사하기 위해 본 연구를 시작하였다. 방 법 : 1998년 9월부터 2002년 8월까지 한림대학교 한강성심병원 소아과에 급성 호흡기 감염증으로 입원했던 환아 중 총 913례에서 비인두 흡인물을 채취하여 바이러스 배양 및 단일 클론 항체를 이용한 면역 형광 검사법으로 251례(27%)에서 호흡기바이러스가 분리되었다. 그 중 모세기관지염, 폐렴, 크룹, 기관 기관지염 등의 급성 하기도 감염증으로 진단 받은 208례의 의무기록을 후향적으로 고찰하였다. 결 과 : 1) RSV가 122례(58%)로 가장 많았고, PIV 30례(14%), INFB 21례(11%), INFA 20례(10%), ADV 15례(7%) 순이었다. 2) 발생시기는 RSV의 경우 1998년 12월과 1999년 11월에 많이 발생하였다. PIV는 연중 비슷하였고, INFA는 1999년 3월과 2000년 1월에 많이 검출되었다. INFB는 2002년 4월에 많이 발생하였고, ADV는 2000년을 제외하고는 연중 비슷하게 검출되었다. 3) 남녀 성별비는 1.8 : 1로 남아가 더 많았고, 중앙연령은 10개월이었다. 4) 임상적 진단에는 세기관지염 88례(43%), 폐렴 87례(42%), 크룹19례(9%), 기관 기관지염 14례(6%)의 순이었고, RSV의 경우 세기관지염이 70례(58%)였다. 5) 임상증상 및 징후에는 각 바이러스 모두 기침(93%), 비루(83%), 가래(74%), 발열(56%)이 많았고, ADV의 경우 발열(89%), 호흡곤란(56%)이 다른 바이러스에 비해서 높았다. 6) 청진 소견으로 천명음이 들렸던 경우는 RSV가 69%, INFA가 45%로 많았고, 건성수포음은 PIV가 52%, INFB가 38%로 많았으며 수포음은 ADV에서 89%로 높았다. 7) 말초 혈액 백혈구 수는 전체 59%에서 정상이었고, 39%에서 증가하였다. 적혈구 침강 속도는 73%에서 증가하였고, C 반응 단백은 21%에서 양성이었다. 8) 방사선 소견은 고찰이 가능하였던 206례 중 각 바이러스 모두 정상 소견이 가장 많았고, 과팽창은 RSV에서 많았다. 폐문 부위 기관지 침윤과 폐경화는 ADV에서 많았고, 하인두 확장은 PIV에서 현저하게 많았으며, 그 외 무기폐 소견도 있었다. 결 론 : 소아에서 급성 하기도 감염증의 중요한 원인을 차지하는 호흡기 바이러스는 각각 발생시기 및 유행양상이 다르고 임상 양상에서도 차이를 보였으나, 이에 더욱 많은 보고와 연구가 진행되어야 할 것으로 본다.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제34권3호
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• pp.220-225
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• 2012

Wegener's granulomatosis (WG) is an autoimmune disease of unknown etiology characterized by the triad of necrotizing granulomatous lesion in the upper and lower respiratory tracts or both, disseminated vasculitis involving both small arteries and veins, and necrotizing glomerulonephritis. The most common oral lesions associated with WG are ulceration and strawberry gingivitis. A 47-years old man in medical care associated WG was consulted our Division of Oral and Maxillofacial Surgery for the chief complaint of toothaches. Pre-operative panorama showed the alveolar radiolucency and the loss of lamina dura regarding the left upper teeth. An oropharyngeal magnetic resonance imaging also revealed the increased bone marrow signal intensity on the left maxilla. Under the impression of maxillary osteonecrosis due to WG, maxillary saucerization with removal of involved teeth was performed. We obtained good results and report the first case of WG in Korea, with the review of literatures regarding oral and general systemic features.

• 대한수의학회지
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• 제52권4호
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• pp.223-230
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• 2012

The worldwide distribution and continuing genetic mutation of avian influenza virus (AIV) has been posed a great threat to human and animal health. A comparison of 3 isolates of AIV H9N2, A/chicken/Korea/KBNP-0028/00 (H9N2) (KBNP-0028), A/chicken/Korea/SNU8011/08 (H9N2) (SNU 8011) and an inactivated oil vaccine strain A/chicken/Korea/01310/01 (H9N2) (01310), was performed. The former 2 AIVs were isolated from field cases before and after the application of an inactivated H9N2 vaccine in 2007, respectively. The antigenic relationship, viral shedding, tissue tropism and genetic analysis were examined. The comparison of virus shedding from the cloaca and the oropharynx revealed that both isolates were more frequently isolated from the upper respiratory tract (90~100%) 1 day post inoculation (DPI) compared with isolation 5 DPI from gastrointestinal tracts (10~60%). Moreover, the isolate KBNP-0028 were recovered from all organs including bone marrow, brain and kidneys, indicating higher ability for broad tissue dissemination than that of SNU 8011. KBNP-0028 replicated earlier than other strains and with a higher titer than SNU 8011. In full-length nucleotide sequences of the NA gene and a partial sequence of the HA gene of SNU 8011, we found that there might be significant changes in tissue tropism, virus replication and genetic mutation in AIV H9N2 isolates.

• 한국가금학회:학술대회논문집
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• 한국가금학회 2006년도 제23차 정기총회 및 학술발표회
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• pp.7-16
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• 2006

Poultry products including meat and eggs constitute a major protein source in the American diet and disease - causing pathogens represent major challenges to the poultry industry. More than 95 % of pathogens enter the host through the mucosal surfaces of the respiratory, digestive and reproductive tracts and over the past few decades, the two main mechanisms used to control diseases have been the use of vaccines and antibiotics. However, in the poultry industry, there are mounting concerns over the ability of current vaccines to adequately protect against emerging hyper - virulent strains of pathogens and a lack of suitable, cost effective adjuvants. Thorough investigation of the immunogenetic responses involved in host-pathogen interactions will lead to the development of new and effective strategies for improving poultry health, food safety and the economic viability of the US poultry industry. In this paper, I describe the development of immunogenomic and proteomic tools to fundamentally determine and characterize the immunological mechanisms of the avian host to economically significant mucosal pathogens such as Eimeria. Recent completion of poultry genome sequencing and the development of several tissue-specific cDNA libraries in chickens are facilitating the rapid application of functional immunogenomics in the poultry disease research. Furthermore, research involving functional genomics, immunology and bioinformatics is providing novel insights into the processes of disease and immunity to microbial pathogens at mucosal surfaces. In this presentation, a new strategy of global gene expression using avian macrophage (AMM) to characterize the multiple pathways related to the variable immune responses of the host to Eimeria is described. This functional immunogenomics approach will increase current understanding of how mucosal immunity to infectious agents operates, and how it may be enhanced to enable the rational development of new and effective strategies against coccidiosis and other mucosal pathogens.