首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Pre- and Postvaccination Clonal Compositions of Invasive Pneumococcal Serotypes for Isolates Collected in the United States in 1999 2001 and 2002
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Pre- and Postvaccination Clonal Compositions of Invasive Pneumococcal Serotypes for Isolates Collected in the United States in 1999 2001 and 2002

机译:分别于1999年2001年和2002年在美国收集的有侵袭性肺炎球菌血清型的疫苗接种前后的克隆成分

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摘要

Monitoring of serotypes and their clonal associations is critical as pneumococci adapt to the selective pressures exerted by the pneumococcal seven-valent conjugate vaccine (PCV7). We genotyped 1,476 invasive isolates from the Active Bacterial Core surveillance (705 [89.8%] of the isolates were obtained from children <5 years of age, and 771 [18.4%] of the isolates were obtained from individuals >5 years of age) in 2001 and 2002 (after the introduction of PCV7). The data were compared to the results for 1,168 invasive isolates (855 [83.9%] of the isolates were from children <5 years of age) collected in 1999. Among children <5 years of age, the incidence of invasive disease due to non-PCV7 serogroups together with serogroup 19A increased (P < 0.001). Eighty-three clonal sets, representing 177 multilocus sequence types (STs), were compiled from the 3-year isolate set. Among the non-PCV7 serogroups, newly emerging clones were uncommon; and a significant expansion of already established clones occurred for serotypes 3 (ST180), 7F (ST191), 15BCF (ST199), 19A (ST199), 22F (ST433), 33F (ST662), and 38 (ST393). However, additional minor clonal types within serotypes 1, 6A, 6B, 7C, 9N, 10A, 12F, 14, 15B/C, 17F, 19A, 19F, 20, 22F, and 33F that were absent in 1999 were found during 2001 and 2002. Although 23 clonal sets exhibited multiple serotypes, for most serotypes there were either no changes or modest changes in clonal compositions since the introduction of PCV7. The only example of an identical ST shared between non-PCV7 and PCV7 or PCV7-related serotypes was ST199; however, ST199 was prevalent within serotypes 15B/C and 19A before and after PCV7 introduction. Continued genotypic surveillance is warranted, since certain clones not targeted by PCV7 are expanding, and their emergence as significant pathogens could occur with maintained vaccine pressure.
机译:血清型及其克隆关联的监测至关重要,因为肺炎球菌可适应肺炎球菌七价结合疫苗(PCV7)施加的选择性压力。我们对来自主动细菌核心监测的1476例侵入菌进行了基因分型(705株[89.8%]的分离株来自5岁以下的儿童,而771株[18.4%]的分离株则来自5岁以上的个体)。 2001年和2002年(引入PCV7之后)。将数据与1999年收集的1168例侵袭性隔离株的结果进行比较(其中855株[83.9%]来自5岁以下的儿童)。在5岁以下的儿童中,非PCV7血清群与19A血清群一起增加(P <0.001)。从3年分离株中收集了代表177个多位点序列类型(ST)的83个克隆集。在非PCV7血清群中,新出现的克隆并不常见。对于血清型3(ST180),7F(ST191),15BCF(ST199),19A(ST199),22F(ST433),33F(ST662)和38(ST393),已经建立的克隆发生了显着扩增。但是,在2001年和2001年之间发现了血清型1、6A,6B,7C,9N,10A,12F,14、15B / C,17F,19A,19F,20、22F和33F内的其他次要克隆类型。 2002年。尽管23个克隆集表现出多种血清型,但自引入PCV7以来,对于大多数血清型,克隆成分没有变化或没有适度变化。非PCV7与PCV7或与PCV7相关的血清型之间共享的相同ST的唯一示例是ST199;而在非PCV7和PCV7相关血清型之间共享相同的ST。然而,在引入PCV7前后,ST199在15B / C和19A血清型中普遍存在。有必要继续进行基因型监测,因为某些不受PCV7靶向的克隆正在扩大,在维持疫苗压力的情况下,它们可能会作为重要病原体出现。

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