Puthucheary S D, Nathan S A
Department of Medical Microbiology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia.
Singapore Med J. 2006 Aug;47(8):697-703.
Burkholderia pseudomallei (B. pseudomallei) has been shown to persist intracellularly in patients with melioidosis, until reactivated by decreasing immunocompetence. We have previously demonstrated by transmission electron microscopy, the internalisation of B. pseudomallei by human macrophages and the occurrence of phagosome-lysosome fusion.
Phagocytosis and electron microscopy were used to compare the rate of phagosome-lysosome fusion and the intracellular survival of B. pseudomallei using monocytes obtained from five patients with melioidosis and five normal healthy adults.
Ingested bacilli were seen in various stages of degradation, with a few remaining viable within phagolysosomes, and the proliferation of these viable bacteria was observed. Phagocytosis of B. pseudomallei by normal macrophages was two-fold higher than uptake by the melioidosis macrophages (p-value is less than 0.001). Three times more phagolysosomes were present in the normal macrophages, indicating that fusion occurred slowly and inefficiently in the melioidosis macrophages (p-value is less than 0.001), resulting in higher number of organisms within the melioidosis macrophages (p-value is less than 0.001). Both variables were inversely related to each other.
Our observations suggest that phagolysosome fusion occurred slowly and inefficiently in monocytes of patients with melioidosis, leading to an increased number of intracellular organisms compared to monocytes obtained from healthy donors.
已证明类鼻疽杆菌(B. pseudomallei)在类鼻疽病患者细胞内持续存在,直至免疫能力下降时重新激活。我们之前通过透射电子显微镜证明了人巨噬细胞对类鼻疽杆菌的内化以及吞噬体 - 溶酶体融合的发生。
使用吞噬作用和电子显微镜,比较从五名类鼻疽病患者和五名正常健康成年人获取的单核细胞对类鼻疽杆菌的吞噬体 - 溶酶体融合率和细胞内存活情况。
观察到摄入的杆菌处于不同降解阶段,少数在吞噬溶酶体内仍存活,并观察到这些存活细菌的增殖。正常巨噬细胞对类鼻疽杆菌的吞噬作用比类鼻疽病巨噬细胞高两倍(p值小于0.001)。正常巨噬细胞中的吞噬溶酶体数量多三倍,表明类鼻疽病巨噬细胞中融合发生缓慢且效率低下(p值小于0.001),导致类鼻疽病巨噬细胞内的生物体数量更多(p值小于0.001)。这两个变量呈负相关。
我们的观察结果表明,类鼻疽病患者单核细胞中的吞噬溶酶体融合发生缓慢且效率低下,与从健康供体获取的单核细胞相比,导致细胞内生物体数量增加。