Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/129965
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Type: Journal article
Title: A single nucleotide polymorphism in an IgA1 protease gene determines Streptococcus pneumoniae adaptation to the middle ear during otitis media
Author: Tikhomirova, A.
Trappetti, C.
Paton, J.C.
Watson-Haigh, N.
Wabnitz, D.
Jervis-Bardy, J.
Jardeleza, C.
Kidd, S.P.
Citation: Pathogens and Disease, 2021; 79(1):1-8
Publisher: Oxford University Press
Issue Date: 2021
ISSN: 2049-632X
2049-632X
Statement of
Responsibility: 
Alexandra Tikhomirova, Claudia Trappetti, James C Paton, Nathan Watson-Haigh, David Wabnitz, Jake Jervis-Bardy ... et al.
Abstract: Factors facilitating the chronicity of otitis media (OM) in children are, to date, not fully understood. An understanding of molecular factors aiding bacterial persistence within the middle ear during OM could reveal pathways required for disease. This study performed a detailed analysis of Streptococcus pneumoniae populations isolated from the nasopharynx and middle ear of one OM case. Isolates were assessed for growth in vitro and infection in a mouse intranasal challenge model. Whole genome sequencing was performed to compare the nasopharyngeal and middle ear isolates. The middle ear isolate displayed a reduced rate of growth and enhanced potential to transit to the middle ear in a murine model. The middle ear population possessed a single nucleotide polymorphism (SNP) in the IgA1 protease gene igA, predicted to render its product non-functional. Allelic exchange mutagenesis of the igA alleles from the genetic variant middle ear and nasopharyngeal isolates was able to reverse the niche-adaptation phenotype in the murine model. These results indicate the potential role of a SNP in the gene encoding the IgA1 protease, in determining S. pneumoniae adaptation to the middle ear during chronic OM. In contrast, a functional IgA1 protease was associated with increased colonisation of the nasopharynx.
Keywords: Pneumococcus
bacterial persistence
otitis media
Rights: © The Author(s) 2020. Published by Oxford University Press on behalf of FEMS. All rights reserved.
DOI: 10.1093/femspd/ftaa077
Grant ID: http://purl.org/au-research/grants/nhmrc/1071659
Published version: http://dx.doi.org/10.1093/femspd/ftaa077
Appears in Collections:Aurora harvest 8
Microbiology and Immunology publications

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