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20世纪80年代严重化脓性链球菌疾病复发的克隆基础。

Clonal basis for resurgence of serious Streptococcus pyogenes disease in the 1980s.

作者信息

Cleary P P, Kaplan E L, Handley J P, Wlazlo A, Kim M H, Hauser A R, Schlievert P M

机构信息

Department of Microbiology, UMHC, University of Minnesota, Minneapolis 55455.

出版信息

Lancet. 1992 Feb 29;339(8792):518-21. doi: 10.1016/0140-6736(92)90339-5.

Abstract

During the 1980s there was a resurgence of serious Streptococcus pyogenes infections with complications, including rheumatic fever, sepsis, severe soft-tissue invasion, and toxic-shock-like syndrome (TSLS). We have investigated the suggested association between expression of a scarlet fever toxin, SPE A, and systemic toxicity, and the possibility that a new highly virulent clone of S pyogenes has emerged and spread world wide. We studied serotype M1 strains, the serotype most commonly associated with serious complications. 19 isolates from patients with sepsis, with or without TSLS, and 48 from patients with uncomplicated pharyngitis or superficial skin infection were subjected to restriction-enzyme digestion and electrophoresis; 56 isolates (19 serious, 37 uncomplicated disease) were then examined by hybridisation to an speA gene probe. 17 (90%) of the 19 serious-disease isolates had a characteristic ("invasive", I) restriction-fragment profile and were positive for the speA gene. Significantly lower proportions of the isolates from patients with uncomplicated disease had the I profile (21/48 [44%]; p = 0.0035) and speA (20/37 [54%]; p less than 0.001). These findings suggest that the strains from patients with serious disease are a unique clone, which became the predominant cause of severe streptococcal infections in the United States and elsewhere in the late 1980s.

摘要

20世纪80年代,严重的化脓性链球菌感染及其并发症再度出现,包括风湿热、败血症、严重的软组织感染以及中毒性休克样综合征(TSLS)。我们研究了猩红热毒素SPE A的表达与全身毒性之间的假定关联,以及化脓性链球菌新的高毒力克隆株出现并在全球传播的可能性。我们研究了M1血清型菌株,该血清型最常与严重并发症相关。对19例败血症患者(有或无TSLS)的分离株以及48例无并发症咽炎或浅表皮肤感染患者的分离株进行限制性酶切消化和电泳;然后对56株分离株(19例严重疾病,37例无并发症疾病)进行speA基因探针杂交检测。19例严重疾病分离株中有17株(90%)具有特征性(“侵袭性”,I)限制性片段图谱,且speA基因呈阳性。无并发症疾病患者的分离株中具有I图谱(21/48 [44%];p = 0.0035)和speA(20/37 [54%];p<0.001)的比例明显较低。这些发现表明,严重疾病患者的菌株是一个独特的克隆株,它在20世纪80年代后期成为美国和其他地区严重链球菌感染的主要原因。

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