Myllymäki Henna, Bäuerlein Carina A, Rämet Mika
BioMediTech, University of Tampere , Tampere , Finland.
BioMediTech, University of Tampere, Tampere, Finland; Department of Pediatrics, Tampere University Hospital, Tampere, Finland; Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland; PEDEGO Research Unit, Medical Research Center Oulu, University of Oulu, Oulu, Finland.
Front Immunol. 2016 May 19;7:196. doi: 10.3389/fimmu.2016.00196. eCollection 2016.
Tuberculosis (TB) is a global health emergency. Up to one-third of the world's population is infected with Mycobacterium tuberculosis, and the pathogen continues to kill 1.5 million people annually. Currently, the means for preventing, diagnosing, and treating TB are unsatisfactory. One of the main reasons for the poor progress in TB research has been a lack of good animal models to study the latency, dormancy, and reactivation of the disease. Although sophisticated in vitro and in silico methods suitable for TB research are constantly being developed, they cannot reproduce the complete vertebrate immune system and its interplay with pathogens and vaccines. However, the zebrafish has recently emerged as a useful alternative to more traditional models, such as mice, rabbits, guinea pigs, and non-human primates, for studying the complex pathophysiology of a mycobacterial infection. The model is based on the similarity between Mycobacterium marinum - a natural fish pathogen - and M. tuberculosis. In both zebrafish larvae and adult fish, an infection with M. marinum leads to the formation of macrophage aggregates and granulomas, which resemble the M. tuberculosis infections in humans. In this review, we will summarize the current status of the zebrafish model in TB research and highlight the advantages of using zebrafish to dissect mycobacterial virulence strategies as well as the host immune responses elicited against them. In addition, we will discuss the possibilities of using the adult zebrafish model for studying latency, dormancy, and reactivation in a mycobacterial infection.
结核病是全球卫生紧急事件。全球多达三分之一的人口感染了结核分枝杆菌,该病原体每年仍导致150万人死亡。目前,结核病的预防、诊断和治疗手段并不理想。结核病研究进展不佳的主要原因之一是缺乏良好的动物模型来研究该疾病的潜伏期、休眠期和再激活情况。尽管适合结核病研究的先进体外和计算机模拟方法不断涌现,但它们无法重现完整的脊椎动物免疫系统及其与病原体和疫苗的相互作用。然而,最近斑马鱼已成为一种有用的替代模型,可用于研究分枝杆菌感染的复杂病理生理学,而传统模型如小鼠、兔子、豚鼠和非人灵长类动物则不然。该模型基于海洋分枝杆菌(一种天然鱼类病原体)与结核分枝杆菌之间的相似性。在斑马鱼幼虫和成年鱼中,海洋分枝杆菌感染都会导致巨噬细胞聚集和肉芽肿形成,这与人类的结核分枝杆菌感染相似。在这篇综述中,我们将总结斑马鱼模型在结核病研究中的现状,并强调使用斑马鱼剖析分枝杆菌毒力策略以及针对这些策略引发的宿主免疫反应的优势。此外,我们将讨论使用成年斑马鱼模型研究分枝杆菌感染中的潜伏期、休眠期和再激活的可能性。