Phongsamart Wanatpreeya, Srifeungfung Somporn, Chatsuwan Tanittha, Nunthapisud Pongpun, Treerauthaweeraphong Vipa, Rungnobhakhun Pimpha, Sricharoenchai Sirintip, Chokephaibulkit Kulkanya
a Department of Pediatrics; Faculty of Medicine Siriraj Hospital; Mahidol University; Bangkok, Thailand.
Hum Vaccin Immunother. 2014;10(7):1866-73. doi: 10.4161/hv.28675.
To describe the trends in serotype distribution and antimicrobial susceptibility of S. pneumoniae causing invasive pneumococcal diseases (IPD) we tested 238 pneumococci isolates from normally sterile sites between 2009 and 2012 and compared these findings with previous data collected within our network. Serotyping was performed for 15 serotypes contained in the 7-,10-, 13-, and experimental 15-valent pneumococcal conjugate vaccines (PCV). The most common serotypes found were 6B (13.9%), 19A (12.6%), 14 (8.0%), 18C (5.9%), and 6A (3.8%); and 39.9% were non-PCV15 serotypes. One of 81 patients with available data had breakthrough infection with vaccine serotype (19F). There was a significant increase of serotype 19A among children ≤5 years (5.6% in 2000-2009 vs 18.3% in 2009-2012, P = 0.003). The all-age serotype coverage was 36.4%, 41.5%, 59.3%, and 59.7% for PCV7, PCV10, PCV13, and PCV 15, respectively. The corresponding coverage in children ≤5 years were 46.4%, 48.8%, 73.2%, and 73.2% respectively. High susceptibilities to penicillin (89.7%), cefotaxime (95.7%), cefditoren (90.2% by Spanish breakpoints), ofloxacin (97.9%), and levofloxacin (100%), but low to cefdinir (50.0%), cefditoren (45.1% by US-FDA breakpoints), macrolides (<50%), clindamycin (67.7%), tetracycline (41.4%), and trimethoprim-sulfamethoxazole (32.4%) were observed. Serotype 19A was less susceptible to penicillin (80.0 vs 91.2%, P = 0.046), cefditoren (66.7 vs 95.5% by Spanish breakpoints, P = 0.004), and tetracycline (9.1 vs 45.5%, P = 0.024) than non-19A isolates. These data emphasize the need for continued surveillance to monitor changes in serotypes as well as antimicrobial susceptibilities in order to guide strategies for prevention and treatment.
为描述引起侵袭性肺炎球菌疾病(IPD)的肺炎链球菌血清型分布和抗菌药物敏感性趋势,我们检测了2009年至2012年间从通常无菌部位分离出的238株肺炎球菌,并将这些结果与我们网络中之前收集的数据进行比较。对7价、10价、13价和实验性15价肺炎球菌结合疫苗(PCV)中包含的15种血清型进行了血清分型。最常见的血清型为6B(13.9%)、19A(12.6%)、14(8.0%)、18C(5.9%)和6A(3.8%);39.9%为非PCV15血清型。81例有可用数据的患者中有1例发生了疫苗血清型(19F)突破性感染。在≤5岁儿童中,19A血清型显著增加(2000 - 2009年为5.6%,2009 - 2012年为18.3%,P = 0.003)。PCV7、PCV10、PCV13和PCV15的全年龄血清型覆盖率分别为36.4%、41.5%、59.3%和59.7%。≤5岁儿童的相应覆盖率分别为46.4%、48.8%、73.2%和73.2%。对青霉素(89.7%)、头孢噻肟(95.7%)、头孢地尼(根据西班牙标准为90.2%)、氧氟沙星(97.9%)和左氧氟沙星(100%)的敏感性较高,但对头孢地尼(50.0%)、头孢地尼(根据美国食品药品监督管理局标准为45.1%)、大环内酯类(<50%)、克林霉素(67.7%)、四环素(41.4%)和复方磺胺甲恶唑(32.4%)敏感性较低。与非19A分离株相比,19A血清型对青霉素(80.0%对91.2%,P = 0.046)、头孢地尼(根据西班牙标准为66.7%对95.5%,P = 0.004)和四环素(9.1%对45.5%,P = 0.024)的敏感性较低。这些数据强调需要持续监测,以监测血清型以及抗菌药物敏感性的变化,从而指导预防和治疗策略。