Cargando…

Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence

Neisseria meningitidis can utilize haem, haemoglobin and haemoglobin–haptoglobin complexes as sources of iron via two TonB-dependent phase variable haemoglobin receptors, HmbR and HpuAB. HmbR is over-represented in disease isolates, suggesting a link between haemoglobin acquisition and meningococcal...

Descripción completa

Detalles Bibliográficos
Autores principales: Tauseef, Isfahan, Harrison, Odile B., Wooldridge, Karl G., Feavers, Ian M., Neal, Keith R., Gray, Stephen J., Kriz, Paula, Turner, David P. J., Ala’Aldeen, Dlawer A. A., Maiden, Martin C. J., Bayliss, Christopher D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for General Microbiology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352162/
https://www.ncbi.nlm.nih.gov/pubmed/21310784
http://dx.doi.org/10.1099/mic.0.046946-0
_version_ 1782232858428964864
author Tauseef, Isfahan
Harrison, Odile B.
Wooldridge, Karl G.
Feavers, Ian M.
Neal, Keith R.
Gray, Stephen J.
Kriz, Paula
Turner, David P. J.
Ala’Aldeen, Dlawer A. A.
Maiden, Martin C. J.
Bayliss, Christopher D.
author_facet Tauseef, Isfahan
Harrison, Odile B.
Wooldridge, Karl G.
Feavers, Ian M.
Neal, Keith R.
Gray, Stephen J.
Kriz, Paula
Turner, David P. J.
Ala’Aldeen, Dlawer A. A.
Maiden, Martin C. J.
Bayliss, Christopher D.
author_sort Tauseef, Isfahan
collection PubMed
description Neisseria meningitidis can utilize haem, haemoglobin and haemoglobin–haptoglobin complexes as sources of iron via two TonB-dependent phase variable haemoglobin receptors, HmbR and HpuAB. HmbR is over-represented in disease isolates, suggesting a link between haemoglobin acquisition and meningococcal disease. This study compared the distribution of HpuAB and phase variation (PV) status of both receptors in disease and carriage isolates. Meningococcal disease (n = 214) and carriage (n = 305) isolates representative of multiple clonal complexes (CCs) were investigated for the distribution, polyG tract lengths and ON/OFF status of both haemoglobin receptors, and for the deletion mechanism for HpuAB. Strains with both receptors or only hmbR were present at similar frequencies among meningococcal disease isolates as compared with carriage isolates. However, >90 % of isolates from the three CCs CC5, CC8 and CC11 with the highest disease to carriage ratios contained both receptors. Strains with an hpuAB-only phenotype were under-represented among disease isolates, suggesting selection against this receptor during systemic disease, possibly due to the receptor having a high level of immunogenicity or being inefficient in acquisition of iron during systemic spread. Absence of hpuAB resulted from either complete deletion or replacement by an insertion element. In an examination of PV status, one or both receptors were found in an ON state in 91 % of disease and 71 % of carriage isolates. We suggest that expression of a haemoglobin receptor, either HmbR or HpuAB, is of major importance for systemic spread of meningococci, and that the presence of both receptors contributes to virulence in some strains.
format Online
Article
Text
id pubmed-3352162
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Society for General Microbiology
record_format MEDLINE/PubMed
spelling pubmed-33521622012-05-29 Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence Tauseef, Isfahan Harrison, Odile B. Wooldridge, Karl G. Feavers, Ian M. Neal, Keith R. Gray, Stephen J. Kriz, Paula Turner, David P. J. Ala’Aldeen, Dlawer A. A. Maiden, Martin C. J. Bayliss, Christopher D. Microbiology (Reading) Microbial Pathogenicity Neisseria meningitidis can utilize haem, haemoglobin and haemoglobin–haptoglobin complexes as sources of iron via two TonB-dependent phase variable haemoglobin receptors, HmbR and HpuAB. HmbR is over-represented in disease isolates, suggesting a link between haemoglobin acquisition and meningococcal disease. This study compared the distribution of HpuAB and phase variation (PV) status of both receptors in disease and carriage isolates. Meningococcal disease (n = 214) and carriage (n = 305) isolates representative of multiple clonal complexes (CCs) were investigated for the distribution, polyG tract lengths and ON/OFF status of both haemoglobin receptors, and for the deletion mechanism for HpuAB. Strains with both receptors or only hmbR were present at similar frequencies among meningococcal disease isolates as compared with carriage isolates. However, >90 % of isolates from the three CCs CC5, CC8 and CC11 with the highest disease to carriage ratios contained both receptors. Strains with an hpuAB-only phenotype were under-represented among disease isolates, suggesting selection against this receptor during systemic disease, possibly due to the receptor having a high level of immunogenicity or being inefficient in acquisition of iron during systemic spread. Absence of hpuAB resulted from either complete deletion or replacement by an insertion element. In an examination of PV status, one or both receptors were found in an ON state in 91 % of disease and 71 % of carriage isolates. We suggest that expression of a haemoglobin receptor, either HmbR or HpuAB, is of major importance for systemic spread of meningococci, and that the presence of both receptors contributes to virulence in some strains. Society for General Microbiology 2011-05 /pmc/articles/PMC3352162/ /pubmed/21310784 http://dx.doi.org/10.1099/mic.0.046946-0 Text en © 2011 SGM http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Microbial Pathogenicity
Tauseef, Isfahan
Harrison, Odile B.
Wooldridge, Karl G.
Feavers, Ian M.
Neal, Keith R.
Gray, Stephen J.
Kriz, Paula
Turner, David P. J.
Ala’Aldeen, Dlawer A. A.
Maiden, Martin C. J.
Bayliss, Christopher D.
Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence
title Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence
title_full Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence
title_fullStr Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence
title_full_unstemmed Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence
title_short Influence of the combination and phase variation status of the haemoglobin receptors HmbR and HpuAB on meningococcal virulence
title_sort influence of the combination and phase variation status of the haemoglobin receptors hmbr and hpuab on meningococcal virulence
topic Microbial Pathogenicity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352162/
https://www.ncbi.nlm.nih.gov/pubmed/21310784
http://dx.doi.org/10.1099/mic.0.046946-0
work_keys_str_mv AT tauseefisfahan influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT harrisonodileb influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT wooldridgekarlg influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT feaversianm influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT nealkeithr influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT graystephenj influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT krizpaula influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT turnerdavidpj influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT alaaldeendlaweraa influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT maidenmartincj influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence
AT baylisschristopherd influenceofthecombinationandphasevariationstatusofthehaemoglobinreceptorshmbrandhpuabonmeningococcalvirulence