Alhhazmi Areej, Hurteau Donna, Tyrrell Gregory J
Division of Diagnostic and Applied Microbiology, Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
Provincial Laboratory for Public Health (Microbiology), Edmonton, Alberta, Canada.
J Clin Microbiol. 2016 Jul;54(7):1774-1781. doi: 10.1128/JCM.00355-16. Epub 2016 Apr 20.
Group B streptococci (GBS) cause severe invasive disease in both neonates and adults. Understanding the epidemiology of GBS provides information that can include determining disease prevalence rates in defined populations and geographic regions, documenting the success of GBS screening programs, and understanding antimicrobial susceptibility patterns. In Alberta, only neonatal invasive GBS (iGBS) disease is notifiable to health authorities. We performed a surveillance study of iGBS in Alberta, Canada, from 2003 to 2013. Over the 11-year period, the disease incidence rate increased from a low of 3.92 cases/100,000 population to a high of 5.99 cases/100,000 population. The capsular polysaccharide serotypes (CPSs) found were CPS III (20.3%), CPS V (19.1%), CPS Ia (18.9%), CPS Ib (12.7%), CPS II (11.1%), CPS IV (6.3%), and nontypeable GBS (9.4%). Rates of early-onset disease (0 to 7 days) increased from 0.15 cases/1,000 live births (in 2003) to 0.34 cases/1,000 live births (in 2013). Rates of late-onset disease (>7 to 90 days) also rose, from 0.15 cases/1,000 live births (in 2003) to 0.39 cases/1,000 live births (in 2013). Alberta also experienced an increase in CPS IV isolates, from 2 cases (in 2003) to 24 cases (in 2013), of which the majority were hvgA negative (93.4%) [corrected]. The predominant sequence type (ST) in 2013 was ST459. Erythromycin resistance rose from 23.6% to 43.9% (in 2013). Clindamycin resistance also increased, from 12.2% to 32.5%. In summary, Alberta, Canada, has experienced an increase in GBS disease; the increase includes both neonatal and adult disease. CPS IV cases also notably increased during the surveillance period, as did resistance to erythromycin and clindamycin.
B族链球菌(GBS)可在新生儿和成人中引发严重的侵袭性疾病。了解GBS的流行病学情况能提供诸多信息,包括确定特定人群和地理区域的疾病患病率、记录GBS筛查项目的成效以及了解抗菌药物敏感性模式。在艾伯塔省,只有新生儿侵袭性GBS(iGBS)疾病需向卫生当局报告。我们对2003年至2013年加拿大艾伯塔省的iGBS进行了一项监测研究。在这11年期间,该疾病的发病率从每10万人口中3.92例的低点升至每10万人口中5.99例的高点。所发现的荚膜多糖血清型(CPS)有CPS III(20.3%)、CPS V(19.1%)、CPS Ia(18.9%)、CPS Ib(12.7%)、CPS II(11.1%)、CPS IV(6.3%)以及不可分型GBS(9.4%)。早发型疾病(0至7天)的发病率从2003年每1000例活产中0.15例增至2013年每1000例活产中0.34例。晚发型疾病(>7至90天)的发病率也有所上升,从2003年每1000例活产中0.15例升至2013年每1000例活产中0.39例。艾伯塔省CPS IV分离株也有所增加,从2003年的2例增至2013年的24例,其中大多数为hvgA阴性(93.4%)[已修正]。2013年的主要序列型(ST)为ST459。红霉素耐药率从23.6%升至43.9%(2013年)。克林霉素耐药率也有所增加,从12.2%升至32.5%。总之,加拿大艾伯塔省的GBS疾病有所增加;这种增加包括新生儿和成人疾病。在监测期间,CPS IV病例也显著增加,对红霉素和克林霉素的耐药性亦是如此。