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铜绿假单胞菌慢性肺部感染模型的建立及评价 被引量:4

Establishment and evaluation of a chronic pulmonary infection model due to Pseudomonas aeruginosa
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摘要 目的建立大鼠铜绿假单胞菌(PA)慢性肺部感染模型。方法健康Sprague-Dawley大鼠分为铜绿假单胞菌感染组与对照组。将铜绿假单胞菌包被的硅胶管(3Fr,直径1.0mm,长3.0mm)置入感染组大鼠的一侧主支气管处;对照组置入生理盐水浸泡的无菌硅胶管。接种后28d处死大鼠,分离肺组织,进行病理学检查和肺组织匀浆菌落计数。结果硅胶管置入后28d,感染组肺组织培养出野生型铜绿假单胞菌,匀浆菌落计数超过103cfu/g;大体病理表现为纤维增生、肉芽肿形成,镜下表现为淋巴细胞浸润为主的炎症反应;对照组大鼠肺组织未培养出铜绿假单胞菌,病理上未见明显改变。结论铜绿假单胞菌包被的硅胶管置入大鼠一侧主支气管,可成功建立慢性肺部感染模型。该方法造价低廉、可操作性较强,易于推广,为PA肺部感染药物治疗提供了依据。 Objective To establish a rat model of chronic pulmonary infection by inoculating Pseudomonas aeruginosa to Sprague-Dawley (SD) rats. Methods Sixty SD rats were divided into 2 groups, ie. the P. aeruginosa group and the control group. Silicone tube precoatod with P. aeruginosa was placed into the main bronchus. For the control group, sterile silicon tube was intubated. Results P. aeruginosa was detected from lung tissue of rats in infected groups. Bacterial number was higher than 10^3cfu/g 28 days after inoculation. The pathological study showed fibrinous proliferation and granulomas formation in the lungs of infected rats 28 days after inoculation. Microscopy examination showed a inflammation predominantly with lymphocyte infiltration. In control group, no bacterial and pathological changes could be detected. Condusion The animal model with P. aeruginosa chronic pulmonary infection can be established successfully by silicone tubes precoated with P. aeruginosa intubated into the main bronchus.
出处 《中国呼吸与危重监护杂志》 CAS 2008年第1期40-42,56,80,共5页 Chinese Journal of Respiratory and Critical Care Medicine
关键词 铜绿假单胞菌 慢性肺部感染模型 硅胶管 Pseudomonas aeruginosa Chronic pulmonary infection model Silicone tube
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参考文献14

  • 1Knapp B, Hundt E, Lens U, et al. A recombinant hybrid outer membrarne protein for vaccination against Pseudmnmms aeruginosa. Vacine, 1999,17 : 1663-1666.
  • 2Katsunori Y, Kazunori T, Yukihiro K, et al. Role of elastase in a mouse model of chronic respiratory Pseudomonas aeruginosa infection that mimics diffuse panbronchiolitis. J Medl Microbiol,2003 ,52 :531-535.
  • 3小林宏行,雷雨.细菌菌膜的基础与临床[J].中国临床药理学杂志,1999,15(4):299-307. 被引量:108
  • 4刘晓岚,宋志军,王立赞,刘海静,王恒壮,陈一强,孔晋亮,陈海荣,蔡双启.铜绿假单胞菌QS系统缺陷对生物膜形成及大鼠肺部慢性感染的影响[J].济宁医学院学报,2007,30(2):100-103. 被引量:2
  • 5Yanagihara K,Tomono K,Sawal T,et al. Effect of clarithromycin on lymphocytes in chronic respiratory Pseudomonas aeruginosa infection. Am J Respir Crit Care, 1997, 155: 337-342.
  • 6Jun-ichi K,Takayoshi T, Shigeru K. Combination therapy for chronic Pseudomonas aeruginosa respiratory infection associated with biofilm formation. J Antim Chem,2000 ,46 :69-72.
  • 7Gilleland HE, Gilleland JR, Matthews-Greer JM. Outer Membrane Protein F Preparation of Pseudomonas aeruginosa as a Vaccine against Chronic Pulmonary Infection with Heterologous Immunotype Strains in a Rat Model. Infect Immun, 1988,56 : 1017-1022.
  • 8陆淼泉,王复甦,尹秀.铜绿假单胞菌胞外粘液多糖结合菌苗的实验研究[J].中国人兽共患病杂志,2001,17(3):19-21. 被引量:6
  • 9Yu H,Hanes M ,Chrisp CE,et al. Microbial pathogenesis in cystic fibrosis:pulmonary clearance of mucoid Pseudomonas aeruginosa and inflammation in a mouse model of repeated repiratory challenge. Infect Immun, 1998,66:280-288.
  • 10Imamura Y, Yanagihara K, Tomono K, et al. Role of Pseudomonas aeruginosa quorum-sensing systems in a mouse model of chronic respiratory infection. J Med Microbiol,2005, 54:515-518.

二级参考文献31

  • 1方向群,刘又宁.藻酸盐在铜绿假单胞菌肺部感染中的致病作用及与细胞因子的关系[J].中华医院感染学杂志,2004,14(2):126-129. 被引量:27
  • 2[1]Roilides E,Butler KM,Husson RN,et al.Pseudomonas infection in children with human immunodeficiency virus infection[J].Pediatr Infect Dis,1992,11(7):547.
  • 3[2]Marty N,Dournes JL,Chabanon G,et al.Influence of nutrient media on the chemical composition of the exopolysaccharide from mucoid and non-mucoid Pseudomonas aeruginosa[J].FEMS Microbiol lett,1992,77 (1-3):35.
  • 4[3]Marty N,Pasquier C,Dournes JL,et al.Effects of characterized Pseudomonas aeruginosa exopolysacharides on adherence to human tracheal cells[J].J Med Microbiol,1998,47(2):129.
  • 5[4]Meluleni GJ,Grout M,Evans DJ,et al.Mucoid Pseudomonas aeruginosa growing in a biofilm in vitro are killed by antibodies produced during chronic lung infection in cystic fibrosis[J].J Immunol,1995,155(4):2029.
  • 6[5]Feavers IM,Suker J,Mckenna AJ,et al.Molecular analysis of the serotyping antigen of Neisseria Meningitidis[J].Infect Immun,1992,60 (9):3620.
  • 7[6]Hatano K,Boisot S,DesJardins D,et al.Immunogenic and antigenic properties of a hepavalent high-molecular-weight o-polysaccharide vaccine derived from Pseudomonas aeruginosa[J].Infect Immun,1994,62 (9):3608.
  • 8[7]Staczek J,Gilleland HE Jr,Gilleland LB,et al.A chimeric influenza virus expressing an epitope of outermembrane protein F of Pseudomonas aeruginosa affords protection against challenge with P.aeruginosa in a murine model of chronic pulmonary infection[J].Infect Immun,1998,66(8):3990.
  • 9[8]Matsumoto T,Tateda K,Furuya N,et al.Efficacies of alkaline protease、elastase and exotoxin A toxoid vaccine against gut-derived Pseudomonas aeruginosa sepsis in mice[J].J Med Microbiol,1998,47(4):303.
  • 10[9]Pier GB,Small GJ,Warren HB.Protection against mucoid Pseudomonas aeruginosa in rodent model of endobronchial infection[J].Science,1990,249(4968):537.

共引文献142

同被引文献41

  • 1董培红,李骥,张慧芳,张友才,王邦松.铜绿假单胞菌的临床分布和耐药性变迁[J].中国微生态学杂志,2007,19(5):452-454. 被引量:26
  • 2Sakaguchi S, Sakaguchi N, Asano M, et al. hnmunologic self-tolerance maintained by activated T cells expressing IL- 2 receptor alpha-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases. J Immunol, 1995,155 : 1151-1164.
  • 3Wickelgren I. Immunology. Policing the immune system. Science, 2004,306 : 596-599.
  • 4Kelsen J,Hvas CL,Agnhoh J,et al. CD4 + CD25 + regu-latory T cells and their importance to human illnesses. Ugeskr Laeger,2006,168:32-37.
  • 5Moberg M, Gustavsson I, Gyllensten U. Type-specific associations of human papillomavirus load with risk of developing cervical carcinoma in situ. Int J Cancer,2004, 112: 854-859.
  • 6Belkaid Y, Rouse BT. Natural regulatory T cells in infectious disease. Nat Immunol,2005,6:353-360.
  • 7Hisaeda H, Maekawa Y, Iwakawa D, et al. Escape of malaria parasites from host immunity requires CD4 + CD 25 + regulatory T cells. Nat Med ,2004,10:29-30.
  • 8Dittmer U, He H, Messer R J, et al. Functional impairment of CD8 ( + ) T cells by regulatory T cells during persistent retroviral infection. Immunity ,2004,20:293-303.
  • 9Bantel H,Lugering A, Heidemann J, et al. Detection of apoptotic caspase activation in sera from patients with chronic HCV infection is associated with fibrotic liver injury. Hepatology, 2004,40 : 1078 - 1087.
  • 10Raghavan S, Fredriksson M, Svennerholm AM, et al. Absence of CD4 + CD25 + regulatory T cells is associated with a loss of regulation leading to increased pathology in Helicobacter pylori-infected mice. Clin Exp Immunol, 2003, 132:393-400.

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