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Chemotherapy-Associated Changes of Histopathological Features of Mycobacterium ulcerans Lesions in a Buruli Ulcer Mouse Model

机译:在布鲁氏溃疡小鼠模型中化学治疗相关的溃疡分枝杆菌病变组织病理学特征的变化

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摘要

Combination chemotherapy with rifampin and streptomycin (RIF-STR) for 8 weeks is currently recommended by the WHO as the first-line treatment for Mycobacterium ulcerans infection (Buruli ulcer). To gain better insight into the mode of action of these antibiotics against established M. ulcerans infection foci and to characterize recovery of local immune responses during chemotherapy, we conducted a detailed histopathological study of M. ulcerans-infected and RIF-STR-treated mice. Mice were inoculated with M. ulcerans in the footpad and 11 weeks later treated with RIF-STR. Development of lesions during the first 11 weeks after infection and subsequent differences in disease progression between RIF-STR-treated and untreated mice were studied. Changes in histopathological features, footpad swelling, and number of CFU were analyzed. After inoculation with M. ulcerans, massive infiltrates dominated by polymorphonuclear leukocytes developed at the inoculation site but did not prevent bacterial multiplication. Huge clusters of extracellular bacteria located in large necrotic areas and surrounded by dead leukocytes developed in the untreated mice. Chemotherapy with RIF-STR led to a rapid drop in CFU associated with loss of solid Ziehl-Neelsen staining of acid-fast bacilli. Development of B-lymphocyte clusters and of macrophage accumulations surrounding the mycobacteria demonstrated the resolution of local immune suppression. Results demonstrate that the experimental M. ulcerans mouse infection model will be a valuable tool to investigate efficacy of new treatment regimens and of candidate vaccines.
机译:世界卫生组织目前建议将利福平和链霉素(RIF-STR)联合化疗8周,作为溃疡分枝杆菌感染(布鲁里溃疡)的一线治疗。为了更好地了解这些抗生素对已确定的溃疡分枝杆菌感染灶的作用方式并表征化疗期间局部免疫反应的恢复,我们对感染了溃疡分枝杆菌的小鼠和RIF-STR治疗的小鼠进行了详细的组织病理学研究。在足垫中用溃疡分支杆菌接种小鼠,并在11周后用RIF-STR治疗。研究了感染后前11周内病变的发展以及RIF-STR治疗和未治疗小鼠之间疾病进展的差异。分析组织病理学特征,足垫肿胀和CFU数量的变化。接种溃疡分枝杆菌后,在接种部位形成了由多形核白细胞为主的大量浸润,但并未阻止细菌繁殖。在未治疗的小鼠中,巨大的胞外细菌簇位于大的坏死区域,并被死白细胞包围。使用RIF-STR进行化学疗法可导致CFU迅速下降,并导致耐酸杆菌的固体Ziehl-Neelsen染色消失。 B淋巴细胞簇和分枝杆菌周围巨噬细胞积累的发展证明了局部免疫抑制的解决。结果表明,实验性溃疡分枝杆菌小鼠感染模型将是研究新治疗方案和候选疫苗功效的有价值的工具。

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