首页> 外文期刊>Journal of Clinical Microbiology >Analysis of Invasiveness of Pneumococcal Serotypes and Clones Circulating in Portugal before Widespread Use of Conjugate Vaccines Reveals Heterogeneous Behavior of Clones Expressing the Same Serotype
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Analysis of Invasiveness of Pneumococcal Serotypes and Clones Circulating in Portugal before Widespread Use of Conjugate Vaccines Reveals Heterogeneous Behavior of Clones Expressing the Same Serotype

机译:广泛使用共轭疫苗之前在葡萄牙流通的肺炎球菌血清型和克隆的侵袭性分析揭示了表达相同血清型的克隆的异质行为

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To estimate the invasive disease potential of serotypes and clones circulating in Portugal before extensive use of the seven-valent pneumococcal conjugate vaccine, we analyzed 475 invasive isolates recovered from children and adults and 769 carriage isolates recovered from children between 2001 and 2003. Isolates were serotyped and genotyped by pulsed-field gel electrophoresis, and a selection of isolates were also characterized by multilocus sequence typing. We found that the diversities of serotypes and genotypes of pneumococci responsible for invasive infections and carriage were identical and that most carried clones could also be detected as causes of invasive disease. Their ability to do so, however, varied substantially. Serotypes 1, 3, 4, 5, 7F, 8, 9N, 9L, 12B, 14, 18C, and 20 were found to have an enhanced propensity to cause invasive disease, while serotypes 6A, 6B, 11A, 15B/C, 16F, 19F, 23F, 34, 35F, and 37 were associated with carriage. In addition, significant differences in invasive disease potential between clones sharing the same serotype were found among several serotypes, namely, 3, 6A, 6B, 11A, 14, 19A, 19F, 22F, 23F, 34, and NT. This heterogeneous behavior of the clones was found irrespective of the serotype's overall invasive disease potential. Our results highlight the importance of the genetic background when analyzing the invasive disease potential of certain serotypes and provide an important baseline for its monitoring following conjugate vaccine use. Continuous surveillance should be maintained, and current research should focus on uncovering the genetic determinants that contribute to the heterogeneity of invasive disease potential of clones sharing the same serotype.
机译:为了评估在葡萄牙广泛使用七价肺炎球菌结合疫苗之前在葡萄牙传播的血清型和克隆的侵袭性疾病潜力,我们分析了从2001年至2003年从儿童和成人中回收的475株侵袭性分离株和从儿童中回收的769株携带型分离株。通过脉冲场凝胶电泳进行基因分型,并通过多基因座序列分型对分离株进行选择。我们发现,负责侵袭性感染和携带的肺炎球菌血清型和基因型的多样性是相同的,而且大多数携带的克隆也可以被检测为侵袭性疾病的原因。但是,他们这样做的能力差异很大。发现血清型1、3、4、5、7F,8、9N,9L,12B,14、18C和20具有增加的引起侵袭性疾病的倾向,而血清型6A,6B,11A,15B / C,16F ,19F,23F,34、35F和37与运输相关联。另外,在几种血清型中发现具有相同血清型的克隆之间在侵袭性疾病潜能上的显着差异,即3、6A,6B,11A,14、19A,19F,22F,23F,34和NT。无论血清型的总体侵袭性疾病潜力如何,都可以发现克隆的这种异质性行为。我们的结果突出了分析某些血清型的侵袭性疾病潜力时遗传背景的重要性,并为使用联合疫苗进行监测提供了重要的基线。应该保持连续的监测,并且当前的研究应该集中在揭示有助于共享相同血清型的克隆的侵袭性疾病潜力异质性的遗传决定因素上。

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