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在引入7价结合疫苗之前,美国儿童和部分成人侵袭性肺炎球菌分离株的克隆分布情况。

Clonal distribution of invasive pneumococcal isolates from children and selected adults in the United States prior to 7-valent conjugate vaccine introduction.

作者信息

Gertz Robert E, McEllistrem M Catherine, Boxrud David J, Li Zhongya, Sakota Varja, Thompson Terry A, Facklam Richard R, Besser John M, Harrison Lee H, Whitney Cynthia G, Beall Bernard

机构信息

Division of Bacterial and Mycotic Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

J Clin Microbiol. 2003 Sep;41(9):4194-216. doi: 10.1128/JCM.41.9.4194-4216.2003.

Abstract

Theseven-valent pneumococcal conjugated polysaccharide vaccine PC7V was licensed for use among children in 2000. Since 90 serotypes of pneumococci exist, an increase in nonvaccine serotypes could occur through immune selection for capsular type switching. Eleven hundred sixty-eight invasive isolates (24 serotypes), recovered primarily from pediatric patients (855 isolates = 73%) and 22 reference strains of known multilocus sequence types (STs) were subjected to macrorestriction profiling (pulsed-field gel electrophoresis [PFGE]). The correlation of 187 ST results (including 49 newly discovered STs) with the PFGE data assigned 1,042 (89.2%) study isolates to 46 defined clonal complexes or genetic lineages based on related multilocus STs (BURST). Seventeen clonal complexes were represented by 2 to 10 related allelic profiles (STs), while 33 lineages (including reference strains) consisted of single STs with 4 or fewer allelic identities to other STs found in the study. Expansion of the BURST analysis to a global analysis of all known pneumococcal STs (as of 27 November 2002) reduced the number of single ST lineages from 33 to 8, and the number of multi-ST clonal complexes was reduced from 17 to 13. In this work, we established the basic genetic structure within individual serotypes prior to PC7V use. The resultant database will be useful for detecting potential selective effects of this vaccine in postvaccine surveillance.

摘要

七价肺炎球菌结合多糖疫苗PC7V于2000年获得许可用于儿童。由于存在90种肺炎球菌血清型,通过对荚膜类型转换的免疫选择,非疫苗血清型可能会增加。对主要从儿科患者中分离出的1168株侵袭性菌株(24种血清型)(855株=73%)以及22株已知多位点序列类型(STs)的参考菌株进行了宏观限制性分析(脉冲场凝胶电泳[PFGE])。187个ST结果(包括49个新发现的STs)与PFGE数据的相关性,根据相关的多位点STs(BURST)将1042株(89.2%)研究菌株归为46个定义的克隆复合体或遗传谱系。17个克隆复合体由2至10个相关的等位基因谱(STs)代表,而33个谱系(包括参考菌株)由单个ST组成,与研究中发现的其他STs的等位基因同一性为4个或更少。将BURST分析扩展到对所有已知肺炎球菌STs的全球分析(截至2002年11月27日),单ST谱系的数量从33个减少到8个,多ST克隆复合体的数量从17个减少到13个。在这项工作中,我们在PC7V使用之前建立了各血清型内的基本遗传结构。所得数据库将有助于在疫苗接种后监测中检测该疫苗的潜在选择效应。

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