Grishin Anatoly, Papillon Stephanie, Bell Brandon, Wang Jin, Ford Henri R
Department of Surgery, University of Southern California, and Division of Pediatric Surgery, Childrens Hospital Los Angeles, 4650 Sunset Blvd, Mailstop 72, Los Angeles, California 90027, USA.
Semin Pediatr Surg. 2013 May;22(2):69-75. doi: 10.1053/j.sempedsurg.2013.01.002.
Development of necrotizing enterocolitis (NEC) requires a susceptible host, typically a premature infant or an infant with congenital heart disease, enteral feedings and bacterial colonization. Although there is little doubt that microbes are critically involved in the pathogenesis of NEC, the identity of specific causative pathogens remains elusive. Unlike established normal adult gut microbiota, which is quite complex, uniform, and stable, early postnatal bacterial populations are simple, diverse, and fluid. These properties complicate studies aimed at elucidating characteristics of the gut microbiome that may play a role in the pathogenesis of NEC. A broad variety of bacterial, viral, and fungal species have been implicated in both clinical and experimental NEC. Frequently, however, the same species have also been found in physiologically matched healthy individuals. Clustered outbreaks of NEC, in which the same strain of a suspected pathogen is detected in several patients suggest, but do not prove, a causative relationship between the specific pathogen and the disease. Studies in Cronobacter sakazakii, the best characterized NEC pathogen, have demonstrated that virulence is not a property of a bacterial species as a whole, but rather a characteristic of certain strains, which may explain why the same species can be pathogenic or non-pathogenic. The fact that a given microbe may be innocuous in a full-term, yet pathogenic in a pre-term infant has led to the idea of opportunistic pathogens in NEC. Progress in understanding the infectious nature of NEC may require identifying specific pathogenic strains and unambiguously establishing their virulence in animal models.
坏死性小肠结肠炎(NEC)的发生需要一个易感宿主,通常是早产儿或患有先天性心脏病的婴儿、肠内喂养和细菌定植。尽管毫无疑问微生物在NEC的发病机制中起着关键作用,但具体致病病原体的身份仍然难以捉摸。与已确立的正常成人肠道微生物群不同,后者相当复杂、统一且稳定,出生后早期的细菌种群则简单、多样且不稳定。这些特性使旨在阐明可能在NEC发病机制中起作用的肠道微生物组特征的研究变得复杂。多种细菌、病毒和真菌物种都与临床和实验性NEC有关。然而,通常在生理状况匹配的健康个体中也发现了相同的物种。NEC的聚集性暴发,即在几名患者中检测到同一株疑似病原体,提示但不能证明特定病原体与疾病之间存在因果关系。对阪崎克罗诺杆菌(Cronobacter sakazakii)这一特征最明确的NEC病原体的研究表明,毒力并非整个细菌物种的属性,而是某些菌株的特征,这可能解释了为什么同一物种可能致病或不致病。一种特定微生物在足月儿中可能无害,但在早产儿中可能致病,这一事实引发了NEC中机会致病菌的概念。了解NEC感染性质的进展可能需要识别特定的致病菌株,并在动物模型中明确确定它们的毒力。