Centre National de Référence des Pneumocoques, Laboratoire de Microbiologie, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges-Pompidou; EA 4043, Unité Bactéries Pathogènes et Santé, Université Paris-Saclay, Université Paris-Sud, Châtenay-Malabry.
Institut de Veille Sanitaire , St. Maurice , France.
Open Forum Infect Dis. 2016 Feb 2;3(1):ofw020. doi: 10.1093/ofid/ofw020. eCollection 2016 Jan.
Background. In 2010, the pneumococcal 13-valent conjugate vaccine (PCV13), containing 6 additional serotypes including the multidrug-resistant 19A, replaced the PCV7 in France. This study aimed at analyzing trends in antibiotic resistance in invasive pneumococcal disease (IPD) isolates in France after PCV13 introduction. Methods. A total of 5243 pneumococci isolated from IPD in 2008-2009 (late PCV7 era) and 2011-2012 (PCV13 era) were studied according to their serotype and antibiotic resistance profile. Multilocus sequence typing analysis was performed on strains of the predominant serotypes (12F and 24F) isolated from young children. Results. Overall, the prevalence of antibiotic resistance decreased in France (-21.5% for penicillin from 2008-2009 to 2011-2012), mainly driven by the decline of the 19A serotype. Among non-PCV13 serotypes that concomitantly emerged, serotypes 12F, 24F, 15A, and 35B were consistently associated with resistance to 1 or more antibiotics. In children under 2 years, serotypes 15A, 35B, and 24F accounted together for 37.8% and 31.9% of penicillin-nonsusceptible and erythromycin-resistant isolates, respectively. Chloramphenicol and cotrimoxazole resistance were mainly associated with serotypes 12F and 24F, respectively. Genetic analysis showed that although emergence of serotype 12F pneumococci resulted from the expansion of various pre-existing lineages, increase in serotype 24F was related to the clonal expansion of the ST162 penicillin-susceptible cotrimoxazole-resistant lineage. Conclusions. We showed that decline of PCV13-related IPD was associated with a decline in antibiotic resistance in France, but that it likely favored the spread of several resistant nonvaccine serotypes. However, antibiotic resistance does not seem to be the only element that may drive this phenomenon.
2010 年,含有 6 种额外血清型(包括多药耐药性 19A)的肺炎球菌 13 价结合疫苗(PCV13)取代了法国的 PCV7。本研究旨在分析 PCV13 引入后法国侵袭性肺炎球菌病(IPD)分离株抗生素耐药趋势。
根据血清型和抗生素耐药谱,对 2008-2009 年(晚期 PCV7 时代)和 2011-2012 年(PCV13 时代)5243 株 IPD 分离株进行了研究。对从小儿分离的主要血清型(12F 和 24F)菌株进行多位点序列分型分析。
总体而言,法国的抗生素耐药性有所下降(2008-2009 年至 2011-2012 年,青霉素的耐药率下降了 21.5%),主要是由 19A 血清型的下降所致。在同时出现的非 PCV13 血清型中,血清型 12F、24F、15A 和 35B 始终与 1 种或多种抗生素耐药相关。在 2 岁以下儿童中,血清型 15A、35B 和 24F 分别占青霉素耐药和红霉素耐药分离株的 37.8%和 31.9%。氯霉素和复方磺胺甲噁唑耐药主要与血清型 12F 和 24F 相关。遗传分析表明,虽然血清型 12F 肺炎球菌的出现是由于各种先前存在的谱系的扩展,但血清型 24F 的增加与青霉素敏感复方磺胺甲噁唑耐药 ST162 谱系的克隆扩展有关。
我们表明,PCV13 相关 IPD 的下降与法国抗生素耐药性的下降有关,但这可能有利于几种耐药非疫苗血清型的传播。然而,抗生素耐药性似乎不是唯一可能推动这一现象的因素。