志贺氏效应蛋白的分子机制:腹泻儿童人群中的常见病原体。

IF 2.4 Q1 PEDIATRICS Molecular and cellular pediatrics Pub Date : 2022-06-19 DOI:10.1186/s40348-022-00145-z
Ahmad Nasser, Mehrdad Mosadegh, Taher Azimi, Aref Shariati
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引用次数: 12

摘要

不同的胃肠道病原体引起腹泻,这是5岁以下儿童非常常见的问题。在细菌性病原体中,志贺氏菌是导致儿童腹泻的主要原因之一,约占5岁以下儿童死亡总数的11%。1至4岁婴儿和儿童的志贺氏菌病死率分别为13.9%和9.4%。志贺氏菌使用独特的效应蛋白来调节细胞内通路。志贺氏菌不能侵袭根尖部位的上皮细胞;因此,它需要通过其他细胞而不是上皮细胞通过上皮细胞。通过上皮后,巨噬细胞吞噬志贺氏菌,志贺氏菌应准备好表现出至少两种类型的反应:(I)逃离吞噬细胞和(II)介导对复发PMN的侵袭和损伤。PMN的存在和邀约在更大程度上导致肠膜损伤和更大的细菌渗透。志贺氏菌向基底外侧间隙浸润介导(A)细胞附着,(B)细胞进入,(C)逃避自噬识别,(D)液泡形成和液泡破裂,(E)细胞内生命,(F)志贺氏菌毒素和(G)免疫应答。在这篇综述中,试图解释每个因素在志贺氏菌感染中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Molecular mechanisms of Shigella effector proteins: a common pathogen among diarrheic pediatric population.

Different gastrointestinal pathogens cause diarrhea which is a very common problem in children aged under 5 years. Among bacterial pathogens, Shigella is one of the main causes of diarrhea among children, and it accounts for approximately 11% of all deaths among children aged under 5 years. The case-fatality rates for Shigella among the infants and children aged 1 to 4 years are 13.9% and 9.4%, respectively. Shigella uses unique effector proteins to modulate intracellular pathways. Shigella cannot invade epithelial cells on the apical site; therefore, it needs to pass epithelium through other cells rather than the epithelial cell. After passing epithelium, macrophage swallows Shigella, and the latter should prepare itself to exhibit at least two types of responses: (I) escaping phagocyte and (II) mediating invasion of and injury to the recurrent PMN. The presence of PMN and invitation to a greater degree resulted in gut membrane injuries and greater bacterial penetration. Infiltration of Shigella to the basolateral space mediates (A) cell attachment, (B) cell entry, (C) evasion of autophagy recognition, (D) vacuole formation and and vacuole rapture, (E) intracellular life, (F) Shiga toxin, and (G) immune response. In this review, an attempt is made to explain the role of each factor in Shigella infection.

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