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Pneumococcal neuraminidase A: an essential upper airway colonization factor for Streptococcus pneumoniae
Author(s) -
Brittan J.L.,
Buckeridge T.J.,
Finn A.,
Kadioglu A.,
Jenkinson H.F.
Publication year - 2012
Publication title -
molecular oral microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 77
eISSN - 2041-1014
pISSN - 2041-1006
DOI - 10.1111/j.2041-1014.2012.00658.x
Subject(s) - streptococcus pneumoniae , microbiology and biotechnology , neuraminidase , biology , bacterial adhesin , pneumococcal infections , biofilm , streptococcus gordonii , colonization , streptococcaceae , respiratory tract , immunology , bacteria , escherichia coli , respiratory system , gene , virus , biochemistry , genetics , anatomy , antibiotics
Summary Streptococcus pneumoniae colonizes the upper respiratory tract from where the organisms may disseminate systemically to cause life threatening infections. The mechanisms by which pneumococci colonize epithelia are not understood, but neuraminidase A (NanA) has a major role in promoting growth and survival in the upper respiratory tract. In this article we show that mutants of S. pneumoniae D39 deficient in NanA or neuraminidase B (NanB) are abrogated in adherence to three epithelial cell lines, and to primary nasopharyngeal cells. Adherence levels were partly restored by nanA complementation in trans. Enzymic activity of NanA was shown to be necessary for pneumococcal adherence to epithelial cells, and adherence of the nanA mutant was restored to wild‐type level by pre‐incubation of epithelial cells with Lactococcus lactis cells expressing NanA. Pneumococcal nanA or nanB mutants were deficient in biofilm formation, while expression of NanA on L. lactis or Streptococcus gordonii promoted biofilm formation by these heterologous host organisms. The results suggest that NanA is an enzymic factor mediating adherence to epithelial cells by decrypting receptors for adhesion, and functions at least in part as an adhesin in biofilm formation. Neuraminidase A thus appears to play multiple temporal roles in pneumococcal infection, from adherence to host tissues, colonization, and community development, to systemic spread and crossing of the blood‐brain barrier.