链球菌坏死性筋膜炎:研究其发病机制的动物模型的建立。

D V Seal, D Kingston
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摘要

坏死性筋膜炎是一种严重且日益常见的人类疾病,可由兰斯菲尔德a、C或G群β -溶血性链球菌(BHS)感染引起,在肌肉筋膜上的松散结缔组织中迅速传播。为了促进其发病机制的研究,我们建立了一种动物模型,用于在新西兰白兔皮肤肌肉层上的松散结缔组织中产生BHS扩散感染。单独皮下注射A组BHS到侧腹是不令人满意的,只有12%的情况下发生了扩散病变。当A组BHS与金黄色葡萄球菌培养物共同注射时,结果取决于所使用的金黄色葡萄球菌菌株:从猪身上分离出的产生脓肿的菌株在50%的情况下引起了扩散性病变。当BHS以一定滴度注射金黄色葡萄球菌的α -溶素时,产生炎症但没有坏死,75%的情况下发生扩散性病变。然而,接种和未接种的肉汤都与α -溶酶协同作用,增强链球菌的传播。这种BHS和金黄色葡萄球菌α -溶素之间协同作用的证明可能反映了人类的临床情况,因为发现这两种生物在传播链球菌感染起源的地方同时发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Streptococcal necrotizing fasciitis: development of an animal model to study its pathogenesis.

Necrotizing fasciitis is a serious and increasingly common human disease which can be caused by an infection with beta-haemolytic streptococci (BHS) of Lancefield groups A, C or G, spreading rapidly in the loose connective tissue over the muscle fascia. To facilitate study of its pathogenesis, we have developed an animal model for the production of a spreading infection with BHS in the loose connective tissue over the muscle layer in the skin of New Zealand White rabbits. Intradermal injection of group A BHS alone into the flank was unsatisfactory in that a spreading lesion occurred on only 12% of occasions. When the group A BHS were co-injected with cultures of Staphylococcus aureus, the results depended on the strain of S. aureus used: an abscess-producing strain isolated from pigs gave rise to a spreading lesion on 50% of occasions. When BHS were injected with the alpha-lysin of S. aureus at a titre which produced inflammation without necrosis, spreading lesions occurred on 75% of occasions. However, both inoculated and uninoculated broth acted synergistically with the alpha-lysin in potentiating the spread of the streptococci. This demonstration of synergy between BHS and alpha-lysin of S. aureus may reflect the clinical situation in the human, as both organisms have been found to occur together at sites where spreading streptococcal infections have originated.

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