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High Nasopharyngeal Carriage of Non-Vaccine Serotypes in Western Australian Aboriginal People Following 10 Years of Pneumococcal Conjugate Vaccination

机译:肺炎球菌共轭疫苗接种10年后,西澳大利亚州原住民的非疫苗血清型高鼻咽携带力。

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摘要

BackgroundInvasive pneumococcal disease (IPD) continues to occur at high rates among Australian Aboriginal people. The seven-valent pneumococcal conjugate vaccine (7vPCV) was given in a 2-4-6-month schedule from 2001, with a 23-valent pneumococcal polysaccharide vaccine (23vPPV) booster at 18 months, and replaced with 13vPCV in July 2011. Since carriage surveillance can supplement IPD surveillance, we have monitored pneumococcal carriage in western Australia (WA) since 2008 to assess the impact of the 10-year 7vPCV program. MethodsWe collected 1,500 nasopharyngeal specimens from Aboriginal people living in varied regions of WA from August 2008 until June 2011. Specimens were cultured on selective media. Pneumococcal isolates were serotyped by the quellung reaction. ResultsStreptococcus pneumoniae, Haemophilus influenzae and Moraxella catarrhalis were carried by 71.9%, 63.2% and 63.3% respectively of children 5 years of age, and 34.6%, 22.4% and 27.2% of people ≥5 years. Of 43 pneumococcal serotypes identified, the most common were 19A, 16F and 6C in children 5 years, and 15B, 34 and 22F in older people. 7vPCV serotypes accounted for 14.5% of all serotypeable isolates, 13vPCV for 32.4% and 23vPPV for 49.9%, with little variation across all age groups. Serotypes 1 and 12F were rarely identified, despite causing recent IPD outbreaks in WA. Complete penicillin resistance (MIC ≥2µg/ml) was found in 1.6% of serotype 19A (5.2%), 19F (4.9%) and 16F (3.2%) isolates and reduced penicillin susceptibility (MIC ≥0.125µg/ml) in 24.9% of isolates, particularly 19F (92.7%), 19A (41.3%), 16F (29.0%). Multi-resistance to cotrimoxazole, tetracycline and erythromycin was found in 83.0% of 23F isolates. Among non-serotypeable isolates 76.0% had reduced susceptibility and 4.0% showed complete resistance to penicillin.ConclusionsTen years after introduction of 7vPCV for Aboriginal Australian children, 7vPCV serotypes account for a small proportion of carried pneumococci. A large proportion of circulating serotypes are not covered by any currently licensed vaccine.
机译:背景侵袭性肺炎球菌疾病(IPD)继续在澳大利亚原住民中以高发病率发生。从2001年开始,在2-4-6个月内接种7价肺炎球菌结合疫苗(7vPCV),在18个月时加强接种23价肺炎球菌多糖疫苗(23vPPV),并于2011年7月更换为13vPCV。运输监视可以补充IPD监视,自2008年以来,我们已经在澳大利亚西部(WA)进行了肺炎球菌运输监视,以评估10年7vPCV计划的影响。方法从2008年8月至2011年6月,我们从西澳州不同地区的原住民那里收集了1500份鼻咽标本。在选择性培养基上培养标本。肺炎球菌分离株通过质联反应进行血清分型。结果5岁以下儿童携带肺炎链球菌,流感嗜血杆菌和卡他莫拉菌分别占71.9%,63.2%和63.3%,≥5岁的儿童分别占34.6%,22.4%和27.2%。在确定的43种肺炎球菌血清型中,最常见的是5岁以下儿童为19A,16F和6C,老年人为15B,34和22F。 7vPCV血清型占所有可血清分型分离株的14.5%,13vPCV占32.4%,23vPPV占49.9%,在所有年龄组中差异很小。尽管引起西澳州近期爆发IPD,但很少鉴定出血清型1和12F。在血清型19A(5.2%),19F(4.9%)和16F(3.2%)分离株中,有1.6%的菌株对青霉素具有完全耐药性,在24.9%的菌株中,青霉素敏感性降低(MIC ≥0.125µg / ml)分离株,特别是19F(92.7%),19A(41.3%),16F(29.0%)。在23F分离株中有83.0%发现对考特莫唑,四环素和红霉素具有多重耐药性。在非血清型分离株中,76.0%的药敏性降低,4.0%表现出对青霉素的完全耐药性。结论在澳大利亚土著儿童中引入7vPCV十年后,7vPCV血清型占携带的肺炎球菌的一小部分。当前许可的疫苗未涵盖很大一部分循环血清型。

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