Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, Manitoba R3E 0J9, Canada.
J Antimicrob Chemother. 2014 Jan;69(1):59-66. doi: 10.1093/jac/dkt332. Epub 2013 Aug 22.
Studies were performed to assess resistance mechanisms, multidrug resistance (MDR), genetic relatedness, serotype distribution, heptavalent pneumococcal conjugate vaccine (PCV7) coverage and pili virulence factors among macrolide-resistant Streptococcus pneumoniae (MRSP) isolated from respiratory samples submitted to hospital laboratories across Canada from 1998 to 2008.
Isolates of MRSP (n = 1518) collected by the national surveillance studies CROSS (Canadian Respiratory Organism Susceptibility Study; 1998-2006) and CANWARD (Canadian Ward Surveillance Study; 2007-08) were tested using the CLSI broth microdilution method to establish antimicrobial susceptibilities. PCR was used to detect macrolide resistance genes [mef(A) and erm(B)] and pili virulence factors (type 1 pili and type 2 pili), the Quellung reaction was used to identify serotypes and PFGE was used to determine genetic relatedness.
The prevalence of MRSP increased from 8% in 1998 to 22% in 2008 (P = 0.0001). MRSP were 51% mef(A) positive, 36% erm(B) positive, 8% dual mef(A) and erm(B) positive and 5% mef(A) and erm(B) negative. Dual mef(A)- and erm(B)-positive isolates increased in prevalence from 3% in 1998 to 19% in 2008 (P = 0.001). The prevalence of PCV7 serotypes (4, 6B, 9V, 14, 18C, 19F and 23F) decreased from 67% in 1998 to 31% in 2008 (P = 0.0072). The prevalence of serotype 19A, a non-PCV7 serotype, increased by 15% from 1998 to 2008; isolates of serotype 19A were MDR, dual mef(A) and erm(B) positive, genetically related by PFGE and associated with the presence of pili virulence factors.
From 1998 to 2008, respiratory isolates of MRSP in Canada increased significantly due primarily to the emergence and spread of serotypes 6A, 19A and other non-PCV7 serotypes.
评估对 1998 年至 2008 年期间从加拿大各地医院实验室提交的呼吸道样本中分离的大环内酯类耐药肺炎链球菌(MRSP)的耐药机制、多重耐药(MDR)、遗传相关性、血清型分布、七价肺炎球菌结合疫苗(PCV7)覆盖率和菌毛毒力因子。
使用 CLSI 肉汤微量稀释法检测通过全国监测研究 CROSS(加拿大呼吸道生物体易感性研究;1998-2006 年)和 CANWARD(加拿大病房监测研究;2007-08 年)收集的 MRSP(n=1518)分离株的抗生素药敏性。PCR 用于检测大环内酯类耐药基因 [mef(A)和 erm(B)]和菌毛毒力因子(1 型菌毛和 2 型菌毛),Quellung 反应用于鉴定血清型,PFGE 用于确定遗传相关性。
MRSP 的患病率从 1998 年的 8%上升至 2008 年的 22%(P=0.0001)。MRSP 中 51% mef(A)阳性,36% erm(B)阳性,8% dual mef(A)和 erm(B)阳性,5% mef(A)和 erm(B)阴性。1998 年,dual mef(A)-和 erm(B)-阳性分离株的患病率从 3%上升至 2008 年的 19%(P=0.001)。PCV7 血清型(4、6B、9V、14、18C、19F 和 23F)的患病率从 1998 年的 67%下降至 2008 年的 31%(P=0.0072)。非 PCV7 血清型 19A 的患病率从 1998 年至 2008 年上升了 15%;19A 血清型分离株为 MDR,dual mef(A)和 erm(B)阳性,PFGE 遗传相关,并与菌毛毒力因子的存在有关。
1998 年至 2008 年期间,加拿大呼吸道 MRSP 分离株显著增加,主要是由于血清型 6A、19A 和其他非 PCV7 血清型的出现和传播所致。