Owen Jennifer L, Yang Tao, Mohamadzadeh Mansour
Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32610, USA.
Department of Infectious Diseases and Pathology, University of Florida, Gainesville, FL 32608, USA; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, University of Florida, Gainesville, FL 32610, USA.
Trends Mol Med. 2015 Mar;21(3):154-63. doi: 10.1016/j.molmed.2014.12.003. Epub 2014 Dec 19.
Bacterial infections are the primary cause of gastrointestinal (GI) disorders in both developing and developed countries, and are particularly dangerous for infants and children. Bacillus anthracis is the 'archetype zoonotic' pathogen; no other infectious disease affects such a broad range of species, including humans. Importantly, there are more case reports of GI anthrax infection in children than inhalational disease. Early diagnosis is difficult and widespread systemic disease develops rapidly. This review highlights new findings concerning the roles of the gut epithelia, commensal microbiota, and innate lymphoid cells (ILCs) in initiation of disease and systemic dissemination in animal models of GI anthrax, the understanding of which is crucial to designing alternative therapies that target the establishment of infection.
在发展中国家和发达国家,细菌感染都是胃肠道疾病的主要病因,对婴幼儿和儿童尤其危险。炭疽芽孢杆菌是“典型的人畜共患病”病原体;没有其他传染病能影响如此广泛的物种,包括人类。重要的是,儿童胃肠道炭疽感染的病例报告比吸入性疾病更多。早期诊断困难,且广泛的全身性疾病发展迅速。本综述重点介绍了关于肠道上皮、共生微生物群和固有淋巴细胞(ILCs)在胃肠道炭疽动物模型中疾病起始和全身播散作用的新发现,理解这些对于设计针对感染建立的替代疗法至关重要。