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Pneumococcal otitis media: A polyfactorial disease in a complex microbial community.

机译:肺炎球菌中耳炎:复杂微生物群落中的多因素疾病。

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摘要

Introduction: Streptococcus pneumoniae asymptomatically colonizes the upper respiratory tract of children and is a major childhood pathogen worldwide. S. pneumoniae are genetically heterogeneous and strains differ in their propensity for colonization and disease. Although the heptavalent pneumococcal conjugate vaccine is effective in preventing invasive pneumococcal disease, it has not provided the same level of protection against pneumococcal otitis media (OM). Most studies of children's upper respiratory tract are culture-based and focus on culture of bacterial OM pathogens. However, in our bodies, bacterial cells outnumber human cells. Therefore, it is likely that other taxa not routinely studied influence OM susceptibility. Methods: In the first project (Chapter 2), clinical isolates of the same genetic background (sequence type (ST199)) but different serotypes (15B/C, 19A) were compared in vitro and for pathogenic potential in a chinchilla model of middle ear disease. A qPCR assay was developed to quantitatively assess each isolate, circumventing the need for selectable markers. The second and third studies (Chapters 3 and 4) used nasal swabs and clinical and demographic data collected in a cross sectional study of Philadelphia children during two winter respiratory virus seasons. Advanced pyrosequencing technology was used to characterize the microbial communities residing in children's anterior nares. URI is a major risk factor for OM. Chapter 3 characterized children experiencing URI with and without concurrent OM. Results were used to direct analyses in Chapter 4, which included healthy children as well as children experiencing URI with and without concurrent acute OM. Swabs were cultured for S. pneumoniae . Microbial communities were described using Shannon diversity and Evenness indices. Principal component analysis (PCA), which identifies a small number of variables that account for the majority of variance within a population, was used in a novel application to highlight influential microbial community taxa and group correlated taxa into factors. In Chapter 4, a qPCR assay was also included to identify the presence of OM pathogens: S. pneumoniae, H. influenzae, and M. catorrhalis. Results/Discussion: In Chapter 2 serotype 19A grew faster in vitro, however both 19A and 15B/C were equally capable of colonization and middle ear infection in the chinchilla model. Serotype 19A is included in the new conjugate vaccines while 15B/C is not. Serotype 15B/C should be considered for future capsule vaccine development. Interestingly, Chapters 3 and 4 demonstrated that, regardless of health status, S. pneumoniae is associated with decreased levels of diversity. In Chapter 3, PCA identified taxa that may be important in OM susceptibility and/or OM pathogen colonization. These results were applied to the Chapter 4 analysis with equivalent results. Potentially protective taxa included: Corynebacterium, Dolosigranulum, and Lactococcus. Taxa that may contribute to the causal pathway of OM include Actinomyces, Neisseria, Rothia, and Veillonella . An increased understanding of upper respiratory tract microbial communities may contribute to the development of prevention strategies, such as multispecies probiotics.
机译:简介:肺炎链球菌无症状地定植于儿童的上呼吸道,并且是全世界主要的儿童期病原体。肺炎链球菌在遗传上是异质的,并且菌株在定植和疾病方面的倾向也不同。尽管七价肺炎球菌结合疫苗可有效预防侵袭性肺炎球菌疾病,但并未提供相同水平的针对肺炎球菌性中耳炎(OM)的保护。对儿童上呼吸道的大多数研究都是基于培养的,并且侧重于细菌性OM病原体的培养。但是,在我们体内,细菌细胞的数量超过了人类细胞。因此,很可能没有常规研究的其他分类单元会影响OM敏感性。方法:在第一个项目(第2章)中,对具有相同遗传背景(序列类型(ST199))但具有不同血清型(15B / C,19A)的临床分离株进行了体外比较,并比较了中耳黄鼠模型的致病性疾病。开发了qPCR测定法以定量评估每种分离物,从而避免了对选择性标记的需求。第二和第三项研究(第3章和第4章)使用了鼻拭子以及费城儿童在两个冬季呼吸道病毒季节进行的横断面研究中收集的临床和人口统计学数据。先进的焦磷酸测序技术被用来表征儿童前鼻孔中的微生物群落。 URI是OM的主要风险因素。第3章介绍了在有和没有并发OM的情况下经历URI的孩子。将结果用于第4章中的直接分析,其中包括健康的儿童以及患有URI的儿童(有或没有并发急性OM)。培养拭子用于肺炎链球菌。使用香农多样性和均匀度指数描述了微生物群落。主成分分析(PCA)可识别少数变量,这些变量占总体变异的大部分,该变量被用于一种新颖的应用程序中,以强调有影响力的微生物群落分类群和将相关的分类群归为因素。在第4章中,还包括了qPCR测定法以鉴定OM病原体的存在:肺炎链球菌,流感嗜血杆菌和卡托莫拉菌。结果/讨论:在第2章中,血清型19A在体外生长较快,但是在黄鼠模型中19A和15B / C均具有相同的定殖能力和中耳感染能力。新结合疫苗中包括血清型19A,而15B / C没有。未来的胶囊疫苗开发应考虑血清型15B / C。有趣的是,第3章和第4章表明,无论健康状况如何,肺炎链球菌都与多样性水平下降有关。在第3章中,PCA确定了可能对OM易感性和/或OM病原菌定植重要的分类单元。这些结果以等效的结果应用于第四章分析。潜在的保护类群包括:棒杆菌,Dolosigranulum和乳球菌。可能导致OM因果关系的类群包括放线菌,奈瑟氏菌,Rothia和Veillonella。对上呼吸道微生物群落的更多了解可能有助于制定预防策略,例如多物种益生菌。

著录项

  • 作者

    Laufer, Alison Sheehan.;

  • 作者单位

    Yale University.;

  • 授予单位 Yale University.;
  • 学科 Biology Microbiology.;Health Sciences Epidemiology.;Health Sciences Public Health.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 133 p.
  • 总页数 133
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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