Gonzalez Blanca E, Martinez-Aguilar Gerardo, Hulten Kristina G, Hammerman Wendy A, Coss-Bu Jorge, Avalos-Mishaan Anna, Mason Edward O, Kaplan Sheldon L
Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Pediatrics. 2005 Mar;115(3):642-8. doi: 10.1542/peds.2004-2300.
More than 70% of the community-acquired (CA) staphylococcal infections treated at Texas Children's Hospital are caused by methicillin-resistant Staphylococcus aureus (MRSA). Since September 2002, an increase in the number of severely ill patients with S aureus infections has occurred. This study provides a clinical description of severely ill adolescent patients and an analysis of their isolates using molecular methods.
We identified adolescent patients meeting criteria for severe sepsis requiring admission to the PICU. Patient records were reviewed, and isolates were obtained for susceptibility testing and DNA extraction. Isolates were tested for the presence of virulence genes (cna, tst, lukS-PV, and lukF-PV) and enterotoxin genes (sea, seb, sec, sed, seh, and sej) by polymerase chain reaction. Genomic fingerprints were determined by repetitive-element polymorphism polymerase chain reaction and pulse-field gel electrophoresis. SCCmec cassette type was determined.
Fourteen adolescents with severe CA S aureus infections were identified between August 2002 and January 2004. All were admitted to the PICU with sepsis and coagulopathy. Twelve patients had CA-MRSA infections; 2 had CA methicillin-susceptible Staphylococcus aureus (MSSA) infections. The mean age was 12.9 years (range: 10-15 years). Thirteen patients had pulmonary involvement and/or bone and joint infection; 10 patients had > or =2 bones or joints infected (range: 2-10); 4 patients developed vascular complications (deep venous thrombosis); and 3 patients died. All isolates were identical or closely related to the previously reported predominant clone in Houston, Texas (multilocus sequence type 8, USA300), and carried lukS-PV and lukF-PV genes as well as the SCCmec type IVa cassette (12 MRSA isolates) but did not contain cna or tst. Only 1 strain carried enterotoxin genes (sed and sej).
Severe staphylococcal infections in previously healthy adolescents without predisposing risk factors have presented more frequently at Texas Children's Hospital since September 2002. CA MRSA and clonally related CA MSSA characterized as USA300 and sequence type 8 have been isolated from these patients.
在德克萨斯儿童医院接受治疗的70%以上的社区获得性(CA)葡萄球菌感染由耐甲氧西林金黄色葡萄球菌(MRSA)引起。自2002年9月以来,患有金黄色葡萄球菌感染的重症患者数量有所增加。本研究提供了重症青少年患者的临床描述,并使用分子方法对其分离株进行了分析。
我们确定了符合严重脓毒症标准、需要入住儿科重症监护病房(PICU)的青少年患者。查阅患者记录,并获取分离株进行药敏试验和DNA提取。通过聚合酶链反应检测分离株中是否存在毒力基因(cna、tst、lukS-PV和lukF-PV)和肠毒素基因(sea、seb、sec、sed、seh和sej)。通过重复元件多态性聚合酶链反应和脉冲场凝胶电泳确定基因组指纹图谱。确定SCCmec盒式类型。
2002年8月至2004年1月期间,确定了14例患有严重社区获得性金黄色葡萄球菌感染的青少年。所有患者均因脓毒症和凝血病入住PICU。12例患者为社区获得性MRSA感染;2例为社区获得性甲氧西林敏感金黄色葡萄球菌(MSSA)感染。平均年龄为12.9岁(范围:10 - 15岁)。13例患者有肺部受累和/或骨与关节感染;10例患者有≥2处骨骼或关节感染(范围:2 - 10处);4例患者出现血管并发症(深静脉血栓形成);3例患者死亡。所有分离株均与德克萨斯州休斯顿先前报道的主要克隆株相同或密切相关(多位点序列类型8,USA300),并携带lukS-PV和lukF-PV基因以及IVa型SCCmec盒(12株MRSA分离株),但不包含cna或tst。只有1株携带肠毒素基因(sed和sej)。
自2002年9月以来,在德克萨斯儿童医院,先前健康且无易感危险因素的青少年中严重葡萄球菌感染的病例更为常见。已从这些患者中分离出特征为USA300和序列类型8的社区获得性MRSA和克隆相关的社区获得性MSSA。