Waligora-Dupriet Anne-Judith, Dugay Annabelle, Auzeil Nicolas, Huerre Michel, Butel Marie-José
Laboratoire de Microbiologie, Faculté des Sciences Pharmaceutiques et Biologiques, Université René Descartes, Paris, France.
Pediatr Res. 2005 Oct;58(4):629-35. doi: 10.1203/01.PDR.0000180538.13142.84.
Despite extensive research, the pathogenesis of neonatal necrotizing enterocolitis (NEC) remains elusive. The aim of our work was to investigate the role of bacterial strains involved in NEC in gnotobiotic quails as experimental model. Six groups of germ-free quails that were fed a lactose diet were associated with Klebsiella pneumoniae, Clostridium perfringens, C. difficile, C. paraputrificum, or C. butyricum (two strains). Implantation level, incidence of cecal lesions, production of short-chain fatty acids, and histologic lesions of the cecal wall were investigated. Whatever the strain, the implantation level was high (10(9) UFC/g). Neither K. pneumoniae nor C. difficile induced any cecal lesions. In contrast, the four other clostridial strains led to cecal NEC-like lesions with a variable occurrence: four of 12 quails for C. perfringens, eight of 12 quails for C. paraputrificum, and the same highest value, nine of 12 quails and eight of 10 quails for both C. butyricum strains. Gross aspects of the lesions may be linked to the short-chain fatty acid profiles and/or concentrations: thickening of the cecal wall (C. butyricum and C. perfringens) with high proportion of butyric acid, hemorrhages (C. paraputrificum) with high proportion of iso-butyric acid, and presence of other iso-acids. In addition, C. butyricum was characterized by pneumatosis, linked to a high gas production. Microscopic aspects confirmed the presence of edemas and intramucosa hemorrhages. Clostridia species, whose role is controversial, seem to be strongly implicated in NEC through excessive production of butyric acid as a result of colonic lactose fermentation. These results call for anaerobe detection in feces of infants who have NEC.
尽管进行了广泛研究,但新生儿坏死性小肠结肠炎(NEC)的发病机制仍不清楚。我们研究的目的是在无菌鹌鹑这一实验模型中研究参与NEC的细菌菌株的作用。六组喂食乳糖饮食的无菌鹌鹑分别与肺炎克雷伯菌、产气荚膜梭菌、艰难梭菌、副腐败梭菌或丁酸梭菌(两种菌株)建立联系。研究了植入水平、盲肠病变发生率、短链脂肪酸的产生以及盲肠壁的组织学病变。无论何种菌株,植入水平都很高(10⁹CFU/g)。肺炎克雷伯菌和艰难梭菌均未诱发任何盲肠病变。相反,其他四种梭菌菌株导致了不同发生率的盲肠NEC样病变:产气荚膜梭菌组12只鹌鹑中有4只出现病变,副腐败梭菌组12只鹌鹑中有8只出现病变,丁酸梭菌的两组分别为12只鹌鹑中有9只、10只鹌鹑中有8只出现病变,病变发生率最高。病变的大体表现可能与短链脂肪酸的谱和/或浓度有关:盲肠壁增厚(丁酸梭菌和气荚膜梭菌)且丁酸比例高,出血(副腐败梭菌)且异丁酸比例高,还有其他异酸的存在。此外,丁酸梭菌的特征是有气肿,与产气过多有关。显微镜下表现证实存在水肿和黏膜内出血。梭菌属的作用存在争议,但其似乎通过结肠乳糖发酵过度产生丁酸而与NEC密切相关。这些结果呼吁对患有NEC的婴儿粪便进行厌氧菌检测。