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嗜水气单胞菌气溶素决定簇的标记交换诱变证明了气溶素在嗜水气单胞菌相关全身感染中的作用。

Marker exchange mutagenesis of the aerolysin determinant in Aeromonas hydrophila demonstrates the role of aerolysin in A. hydrophila-associated systemic infections.

作者信息

Chakraborty T, Huhle B, Hof H, Bergbauer H, Goebel W

出版信息

Infect Immun. 1987 Sep;55(9):2274-80. doi: 10.1128/iai.55.9.2274-2280.1987.

Abstract

We report here on the isolation of isogenic strains of Aeromonas hydrophila AB3 deleted for a segment of the aerolysin gene. All aer mutants obtained lacked the 49-kilodalton aerolysin gene product and were neither hemolytic for blood erythrocytes nor cytotoxic for Chinese hamster ovary tissue culture cells. One such mutant, AB3-5, was used in a mouse toxicity model to evaluate the role of aerolysin in the pathogenesis of A. hydrophila infections. The strain had a 50% lethal dose (LD50) of greater than 10(9) as compared with the parental strain which had an LD50 of 5 X 10(7). Reintegration of the deleted segment into AB3-5 resulted in an LD50 of 6 X 10(7) cells for this revertant. Furthermore, all mice injected with a sublethal dose of the parental strains developed necrotic lesions; this was never obtained with the aerolysin-deficient strain AB3-5. More importantly, specific neutralizing antibody to aerolysin was detected in mice surviving A. hydrophila infection, demonstrating that aerolysin is produced during the course of systemic A. hydrophila infections.

摘要

我们在此报告嗜水气单胞菌AB3同基因菌株的分离情况,这些菌株缺失了一段气溶素基因。所有获得的气溶素突变体均缺乏49千道尔顿的气溶素基因产物,对血红细胞无溶血作用,对中国仓鼠卵巢组织培养细胞也无细胞毒性。其中一个这样的突变体AB3 - 5被用于小鼠毒性模型,以评估气溶素在嗜水气单胞菌感染发病机制中的作用。与亲本菌株的半数致死剂量(LD50)为5×10⁷相比,该菌株的LD50大于10⁹。将缺失片段重新整合到AB3 - 5中,该回复菌株的LD50为6×10⁷个细胞。此外,所有注射亚致死剂量亲本菌株的小鼠都出现了坏死性病变;而气溶素缺陷菌株AB3 - 5从未出现这种情况。更重要的是,在嗜水气单胞菌感染存活的小鼠中检测到了针对气溶素的特异性中和抗体,这表明在全身性嗜水气单胞菌感染过程中会产生气溶素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad91/260690/1385009e0d6e/iai00093-0337-a.jpg

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