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Profiling bacterial community in upper respiratory tracts
  • 작성일2018-02-05
  • 최종수정일2018-02-05
  • 담당부서연구기획과
  • 연락처043-719-8033
  • 1,795
BMC Infectious Diseases, 2014, 01, 583─596

Profiling bacterial community in upper respiratory tracts

Hanan Yi, D Yong, K Lee, Y Cho and J Chun

Abstract

    Background
    Infection by pathogenic viruses results in rapid epithelial damage and significantly impacts on the condition of the upper respiratory tract, thus the effects of viral infection may induce changes in microbiota. Thus, we aimed to define the healthy microbiota and the viral pathogen-affected microbiota in the upper respiratory tract. In addition, any association between the type of viral agent and the resultant microbiota profile was assessed.
    Methods
    We analyzed the upper respiratory tract bacterial content of 57 healthy asymptomatic people (17 health-care workers and 40 community people) and 59 patients acutely infected with influenza, parainfluenza, rhino, respiratory syncytial, corona, adeno, or metapneumo viruses using culture-independent pyrosequencing.
    Results
    The healthy subjects harbored primarily Streptococcus, whereas the patients showed an enrichment of Haemophilus or Moraxella. Quantifying the similarities between bacterial populations by using Fast UniFrac analysis indicated that bacterial profiles were apparently divisible into 6 oropharyngeal types in the tested subjects. The oropharyngeal types were not associated with the type of viruses, but were rather linked to the age of the subjects.
    Moraxella nonliquefaciens exhibited unprecedentedly high abundance in young subjects aged <6 years. The genome of M. nonliquefaciens was found to encode various proteins that may play roles in pathogenesis.
    Conclusions
    This study identified 6 oropharyngeal microbiome types. No virus-specific bacterial profile was discovered, but comparative analysis of healthy adults and patients identified a bacterium specific to young patients, M. nonliquefaciens.


  • ISBN or ISSN: 1471-2334

  • 본 연구는 질병관리본부 연구개발과제(과제번호 2012-E43001-00) 연구비를 지원받아 수행되었습니다.
  • This research was supported by a fund(code 2012-E43001-00) by Research of Korea Centers for Disease Control and Prevention.


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