Nasal Microbiome and Its Interaction with the Host in Childhood Asthma

Cells. 2022 Oct 7;11(19):3155. doi: 10.3390/cells11193155.

Abstract

Childhood asthma is a major chronic non-communicable disease in infants and children, often triggered by respiratory tract infections. The nasal cavity is a reservoir for a broad variety of commensal microbes and potential pathogens associated with respiratory illnesses including asthma. A healthy nasal microenvironment has protective effects against respiratory tract infections. The first microbial colonisation in the nasal region is initiated immediately after birth. Subsequently, colonisation by nasal microbiota during infancy plays important roles in rapidly establishing immune homeostasis and the development and maturation of the immune system. Dysbiosis of microbiota residing in the mucosal surfaces, such as the nasopharynx and guts, triggers immune modulation, severe infection, and exacerbation events. Nasal microbiome dysbiosis is related to the onset of symptomatic infections. Dynamic interactions between viral infections and the nasal microbiota in early life affect the later development of respiratory infections. In this review, we summarise the existing findings related to nasal microbiota colonisation, dynamic variations, and host-microbiome interactions in childhood health and respiratory illness with a particular examination of asthma. We also discuss our current understanding of biases produced by environmental factors and technical concerns, the importance of standardised research methods, and microbiome modification for the prevention or treatment of childhood asthma. This review lays the groundwork for paying attention to an essential but less emphasized topic and improves the understanding of the overall composition, dynamic changes, and influence of the nasal microbiome associated with childhood asthma.

Keywords: asthma; dysbiosis; host–microbiome interaction; metagenome sequencing; metagenomics; nasal microbiota; prevention; respiratory infection; treatment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asthma*
  • Child
  • Dysbiosis
  • Humans
  • Infant
  • Microbiota*
  • Respiratory System
  • Respiratory Tract Infections*

Grants and funding

This study was supported by a Direct Grant for Research (2019.047) from the Faculty of Medicine at The Chinese University of Hong Kong.