Immune response and pathophysiological features of Klebsiella pneumoniae liver abscesses in an animal model

被引:44
作者
Fung, Chang-Phone [1 ,2 ]
Chang, Feng-Yee [3 ]
Lin, Jung-Chung [3 ]
Ho, Donald Ming-Tak [2 ,4 ]
Chen, Chiung-Tong [5 ]
Chen, Jiun-Han [6 ]
Yeh, Kuo-Ming [3 ]
Chen, Te-Li [1 ,2 ]
Lin, Yi-Tsung [1 ,2 ]
Siu, L. Kristopher [7 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med, Div Infect Dis, Taipei 11217, Taiwan
[2] Natl Yang Ming Univ, Taipei 112, Taiwan
[3] Triserv Gen Hosp, Natl Def Med Ctr, Dept Internal Med, Taipei, Taiwan
[4] Taipei Vet Gen Hosp, Dept Pathol & Lab Med, Taipei 11217, Taiwan
[5] Natl Hlth Res Inst, Div Biotechnol & Pharmaceut Res, Zhunan, Taiwan
[6] Yuanpei Univ, Dept Med Lab Sci & Biotechnol, Hsinchu, Taiwan
[7] Natl Hlth Res Inst, Div Infect Dis, Zhunan, Taiwan
关键词
aerobactin; capsular serotypes; cytokine production; Klebsiella pneumoniae; pyogenic liver abscess; rmpA gene; TUMOR-NECROSIS-FACTOR; SEROTYPE K1; VIRULENCE DETERMINANT; EMERGING DISEASE; MICE; MAGA; K2; ENDOPHTHALMITIS; PREVALENCE; PIGLETS;
D O I
10.1038/labinvest.2011.52
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Capsular serotypes K1 and K2, the rmpA gene (a regulator of the mucoid phenotype) and aerobactin from Klebsiella pneumoniae have been identified as the major virulence factors for pyogenic liver abscesses with high morbidity, mortality and severe complications. The pathological mechanisms remain unclear. In this study, we compared liver immune responses and pathological changes in response to different serotypes of K. pneumoniae infections. A mouse model was used to investigate cytokine and chemokine production, histopathology findings, phagocytic uptake and mortality induced by serotypes K1 (magA(+), rmpA(+), aerobactin(+)), K2 (magA(-), rmpA(+), aerobactin(+)), K62 (magA(-), rmpA(-), aerobactin(-)) and an acapsulated isogenic K1 mutant (Delta K1, magA(+), rmpA(+), aerobactin(+)). K. pneumoniae serotypes K1 and K2 showed lower 50% lethal dose values and more phagocytic resistance to neutrophils than K62 and the DK1 mutant. In sequential liver samples, viable bacteria counts increased 3 h to 3 days after low-dose inoculation (<10(1) colony-forming unit (cfu)) with K1 and K2, while K62 and Delta K1 cleared rapidly and became undetectable even with high-dose inoculation (similar to 2.9 x 10(5) cfu). Time-dependent increases in cytokines and chemokines, including tumor necrosis factor-alpha, interleukin (IL)-1 beta, IL-6, IL-10, keratinocyte-derived chemokines and macrophage inflammatory protein-2, were observed in the serum and liver tissue of K1- and K2-infected mice, and severe disease progression manifesting as microabscesses was also identified. K62 and Delta K1 inoculation did not result in similar immune responses and histological changes. These findings illustrate the critical role of phagocytic resistance against innate immunological defense mechanisms as well as its contribution to the development of liver abscesses. Laboratory Investigation (2011) 91, 1029-1039; doi:10.1038/labinvest.2011.52; published online 4 April 2011
引用
收藏
页码:1029 / 1039
页数:11
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