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2010 - 2014年挪威侵袭性A组链球菌感染的流行病学:一项回顾性队列研究。

Epidemiology of invasive group A streptococcal infections in Norway 2010-2014: A retrospective cohort study.

作者信息

Naseer U, Steinbakk M, Blystad H, Caugant D A

机构信息

Domain for Environmental Health and Infectious Disease Control, Norwegian Institute of Public Health, P. O. Box 4404, Nydalen, 0403, Oslo, Norway.

European Programme for Public Health Microbiology Training (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden.

出版信息

Eur J Clin Microbiol Infect Dis. 2016 Oct;35(10):1639-48. doi: 10.1007/s10096-016-2704-y. Epub 2016 Jun 16.

Abstract

Streptococcus pyogenes or group A streptococcus (GAS) causes mild to severe infections in humans. GAS genotype emm1 is the leading cause of invasive disease worldwide. In the Nordic countries emm28 has been the dominant type since the 1980s. Recently, a resurgence of genotype emm1 was reported from Sweden. Here we present the epidemiology of invasive GAS (iGAS) infections and their association with emm-types in Norway from 2010-2014. We retrospectively collected surveillance data on antimicrobial susceptibility, multilocus sequence type and emm-type, and linked them with demographic and clinical manifestation data to calculate age and sex distributions, major emm- and sequence types and prevalence ratios (PR) on associations between emm-types and clinical manifestations. We analysed 756 iGAS cases and corresponding isolates, with overall incidence of 3.0 per 100000, median age of 59 years (range, 0-102), and male 56 %. Most frequent clinical manifestation was sepsis (49 %) followed by necrotizing fasciitis (9 %). Fifty-two different emm-types and 67 sequence types were identified, distributed into five evolutionary clusters. The most prevalent genotype was emm1 (ST28) in all years (range, 20-33 %) followed by 15 % emm28 in 2014. All isolates were susceptible to penicillin, 15 % resistant to tetracycline and <4 % resistant to erythromycin. A PR of 4.5 (95 % CI, 2.3-8.9) was calculated for emm2 and necrotizing fasciitis. All emm22 isolates were resistant to tetracycline PR 7.5 (95 % CI, 5.8-9.9). This study documented the dominance of emm1, emergence of emm89 and probable import of tetracycline resistant emm112.2 into Norway (2010-2014). Genotype fluctuations between years suggested a mutual exclusive dominance of evolutionary clades.

摘要

化脓性链球菌或A组链球菌(GAS)可引起人类从轻度到重度的感染。GAS基因型emm1是全球侵袭性疾病的主要病因。自20世纪80年代以来,emm28在北欧国家一直是主要类型。最近,瑞典报告了基因型emm1的再次流行。在此,我们展示了2010年至2014年挪威侵袭性GAS(iGAS)感染的流行病学及其与emm型的关联。我们回顾性收集了关于抗菌药物敏感性、多位点序列类型和emm型的监测数据,并将它们与人口统计学和临床表现数据相关联,以计算年龄和性别分布、主要的emm和序列类型以及emm型与临床表现之间关联的患病率比(PR)。我们分析了756例iGAS病例及相应分离株,总体发病率为每10万人3.0例,中位年龄为59岁(范围0 - 102岁),男性占56%。最常见的临床表现是败血症(49%),其次是坏死性筋膜炎(9%)。鉴定出52种不同的emm型和67种序列类型,分为五个进化簇。所有年份中最常见的基因型是emm1(ST28)(范围20% - 33%),2014年其次是15%的emm28。所有分离株对青霉素敏感,15%对四环素耐药,对红霉素耐药的<4%。计算出emm2与坏死性筋膜炎的PR为4.5(95%CI,2.3 - 8.9)。所有emm22分离株对四环素耐药,PR为7.5(95%CI,5.8 - 9.9)。本研究记录了emm1的主导地位、emm89的出现以及四环素耐药的emm112.2可能传入挪威(2010 - 2014年)。年份之间的基因型波动表明进化分支存在相互排斥的主导地位。

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