Porat Nurith, Benisty Rachel, Givon-Lavi Noga, Trefler Ronit, Dagan Ron
Pediatric Infectious Disease Unit, Soroka University Medical Center, Beer-Sheva, Israel; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Pediatric Infectious Disease Unit, Soroka University Medical Center, Beer-Sheva, Israel; Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Vaccine. 2016 May 27;34(25):2806-12. doi: 10.1016/j.vaccine.2016.04.043. Epub 2016 Apr 23.
The introduction of the 7-valent pneumococcal conjugate vaccine (PCV7) followed by PCV13 resulted in a dramatic reduction in carriage and disease rates of Streptococcus pneumoniae (Sp) serotype 6B (Sp6B) and Sp6A. The structural modifications of the capsule of Sp6A and Sp6B to become Sp6C and Sp6D, respectively, raised a concern that eradication of Sp6A/Sp6B by PCV could be accompanied by an increase in Sp6C/Sp6D. This study examines the dynamics and clonal distribution of Sp6C/Sp6D relative to Sp6A/Sp6B during 1999-2014, pre- and post-PCV implementation. Sp were cultured from Blood/CSF and MEF of children <2 years, and from conjunctiva and nasopharynx of children <5 years. PCR was applied for Sp6C and Sp6D identification. Clonality was determined by PFGE and MLST. PCV introduction resulted in decreased carriage rates and conjunctivitis caused by serogroup 6 serotypes. Incidence of Sp6A, Sp6B and Sp6D in otitis media dropped gradually along with PCV7/13 introduction, whereas Sp6C rates increased in the PCV7 period and then decreased following PCV13 implementation. In invasive pneumococcal disease, complete elimination of serogroup 6 was found in the PCV era. Similar clonal composition was found for Sp6C and Sp6D pre- and post-PCV. We conclude that Sp6C and Sp6D do not act as replacement serotypes for Sp6A and Sp6B following vaccination with PCV13. The major Sp6C and Sp6D clones present pre-PCV persisted also post-PCV implementation, suggesting that these clones possess an advantage retained post-vaccination.
7价肺炎球菌结合疫苗(PCV7)随后接种PCV13,导致肺炎链球菌(Sp)6B血清型(Sp6B)和6A血清型(Sp6A)的携带率和发病率大幅下降。Sp6A和Sp6B的荚膜结构分别发生改变成为Sp6C和Sp6D,这引发了人们对PCV根除Sp6A/Sp6B可能伴随着Sp6C/Sp6D增加的担忧。本研究考察了1999 - 2014年期间,即PCV实施前后,Sp6C/Sp6D相对于Sp6A/Sp6B的动态变化和克隆分布。从2岁以下儿童的血液/脑脊液和中耳积液中,以及5岁以下儿童的结膜和鼻咽部培养Sp。应用聚合酶链反应(PCR)鉴定Sp6C和Sp6D。通过脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)确定克隆性。引入PCV导致6血清型引起的携带率和结膜炎下降。随着PCV7/13的引入,中耳炎中Sp6A、Sp6B和Sp6D的发病率逐渐下降,而Sp6C的发病率在PCV7时期增加,随后在PCV13实施后下降。在侵袭性肺炎球菌疾病中,PCV时代发现6血清型被完全清除。PCV实施前后,Sp6C和Sp6D的克隆组成相似。我们得出结论,接种PCV13后,Sp6C和Sp6D不会作为Sp6A和Sp6B的替代血清型。PCV实施前存在的主要Sp6C和Sp6D克隆在PCV实施后也持续存在,这表明这些克隆具有疫苗接种后仍保留的优势。