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A Possible Murine Model for Investigation of Pathogenesis of Sudden Infant Death Syndrome

机译:婴儿猝死综合症发病机制研究的可能小鼠模型

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Several studies have indicated a possible causative role of toxigenic bacteria in sudden infant death syndrome (SIDS). This study examined the effect of toxigenic E. coli on pregnant and infant mice to determine if these animals could be used as a model for SIDS pathogenesis. Strains of E. coli from the intestinal contents of infants who have died of SIDS or other causes and from the faeces of healthy infants were collected over a broad time scale. The isolates were tested for their ability to produce then known toxins of E. coli and were serotyped (O and H antigens). Certain serotypes (e.g. O1:H- and O25:H1) emerged significantly more frequently from cases of SIDS than from healthy infants and isolates of these types were generally toxigenic in Vero-cell cultures but whose verotoxicity was not related to classical Shiga or other known toxins. This mouse model was developed to test the effects of these toxigenic and also non-toxigenic strains. Four apparently healthy pups aged between 17 and 21 days died unobserved overnight but no pups of the 54 control mice died suddenly (P = 0.0247, Fisher's exact test). These were considered to represent sudden unexpected deaths. Pathological effects compatible with those in SIDS were observed in mouse pups exposed to toxigenic strains indicating this model may be suitable for further study into the pathogenesis of unexpected deaths in infancy. Providing an animal model of SIDS would promote a much better avenue for studying the pathogenesis of this enigmatic condition.
机译:几项研究表明,产毒细菌在婴儿猝死综合症(SIDS)中可能起了致病作用。这项研究检查了有毒的大肠杆菌对孕妇和婴儿小鼠的影响,以确定这些动物是否可以用作SIDS发病机制的模型。在较宽的时间范围内,收集了死于小岛屿发展中国家或其他原因的婴儿肠中的大肠杆菌和健康婴儿的粪便。测试分离物产生当时已知的大肠杆菌毒素的能力,并进行血清分型(O和H抗原)。在小岛屿发展中国家,某些血清型(例如O1:H-和O25:H1)的出现频率要比健康婴儿高得多,这些类型的分离株在Vero细胞培养物中通常具有毒性,但其毒性与经典志贺氏菌或其他已知志贺氏菌无关毒素。开发该小鼠模型以测试这些产毒菌株以及非产毒菌株的作用。未观察到四只年龄在17至21天之间的显然健康的幼仔过夜死亡,但54只对照小鼠中没有一只幼仔突然死亡(P = 0.0247,Fisher精确检验)。这些被认为代表突然的意外死亡。在暴露于产毒株的小鼠幼崽中观察到与SIDS相容的病理效应,表明该模型可能适合进一步研究婴儿意外死亡的发病机理。提供小岛屿发展中国家的动物模型将为研究这种神秘病的发病机理提供更好的途径。

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