Development of flow cytometric opsonophagocytosis and antibody-mediated complement deposition assays for non-typeable Haemophilus influenzae
Development of flow cytometric opsonophagocytosis and antibody-mediated complement deposition assays for non-typeable Haemophilus influenzae
Background: Haemophilus influenzae is found in the nasopharynx of 80% of the human population. While colonisation with non-typeable Haemophilus influenzae (NTHi) is usually asymptomatic, it is capable of causing acute and chronic otitis media (OM) in infants, invasive disease in susceptible groups and is the leading cause of exacerbations of patients with chronic obstructive pulmonary disease (COPD). Current methods for assessing functional antibody immunity to NTHi are limited and labour intensive. Flow cytometric assays could provide an attractive alternative to evaluate immune responses to candidate vaccines in clinical trials.Results: We have developed a duplexed flow-cytometric uptake and oxidative burst opsonophagocytosis assay (fOPA). We have also developed a duplexed antibody-mediated complement C3b/iC3b and C5b-9 deposition assay (CDA). Antibody-mediated C3b/iC3b deposition correlated with opsonophagocytic uptake (r = 0.65) and with opsonophagocytic oxidative burst (r = 0.69). Both fOPA and CDA were reproducible, with the majority of samples giving a coefficient of variation (CV) of < 20% and overall assay CVs of 14% and 16% respectively.Conclusions: The high-throughput flow cytometric assays developed here were successfully optimised for use with NTHi. Assays proved to be sensitive and highly reproducible for the measurement of bacterial uptake and oxidative burstopsonophagocytosis and antibody-mediated deposition of C3b/iC3b and C5b-9. These assays are useful tools for use in large scale epidemiological studies and to assist in the assessment of functional antibody induced by NTHi candidate vaccines.
Non-typeableHaemophilus influenzae, Antibody, Opsonophagocytosis, Complement, Flow cytometry, Vaccine
1-11
Thomas, Stephen R
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Leung, Stephanie
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Knox, Katy
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Wilkinson, Tom MA
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Staples, Karl J.
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Lestrate, Pascal
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Wauters, Dominique
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Gorringe, Andrew
503cb828-4e75-44e9-a8af-61f814e02bc6
Taylor, Stephen C.
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29 October 2018
Thomas, Stephen R
effeb4ca-ca6b-4b21-b399-4f56cecc5d31
Leung, Stephanie
1d370c56-70c6-47f6-bc39-9366358dec31
Knox, Katy
742dd062-aa5a-4911-ac0b-425a0e036d88
Wilkinson, Tom MA
8c55ebbb-e547-445c-95a1-c8bed02dd652
Staples, Karl J.
e0e9d80f-0aed-435f-bd75-0c8818491fee
Lestrate, Pascal
5b0486f2-6b92-4201-b201-3d17d1c2efcc
Wauters, Dominique
1aedd157-e071-45d6-bcf5-add288c7466a
Gorringe, Andrew
503cb828-4e75-44e9-a8af-61f814e02bc6
Taylor, Stephen C.
4bc69d42-be21-4f26-b13e-a7e99e8fd173
Thomas, Stephen R, Leung, Stephanie, Knox, Katy, Wilkinson, Tom MA, Staples, Karl J., Lestrate, Pascal, Wauters, Dominique, Gorringe, Andrew and Taylor, Stephen C.
(2018)
Development of flow cytometric opsonophagocytosis and antibody-mediated complement deposition assays for non-typeable Haemophilus influenzae.
BMC Microbiology, 18 (167), , [doi].
(doi:10.1186/s12866-018-1314-5).
Abstract
Background: Haemophilus influenzae is found in the nasopharynx of 80% of the human population. While colonisation with non-typeable Haemophilus influenzae (NTHi) is usually asymptomatic, it is capable of causing acute and chronic otitis media (OM) in infants, invasive disease in susceptible groups and is the leading cause of exacerbations of patients with chronic obstructive pulmonary disease (COPD). Current methods for assessing functional antibody immunity to NTHi are limited and labour intensive. Flow cytometric assays could provide an attractive alternative to evaluate immune responses to candidate vaccines in clinical trials.Results: We have developed a duplexed flow-cytometric uptake and oxidative burst opsonophagocytosis assay (fOPA). We have also developed a duplexed antibody-mediated complement C3b/iC3b and C5b-9 deposition assay (CDA). Antibody-mediated C3b/iC3b deposition correlated with opsonophagocytic uptake (r = 0.65) and with opsonophagocytic oxidative burst (r = 0.69). Both fOPA and CDA were reproducible, with the majority of samples giving a coefficient of variation (CV) of < 20% and overall assay CVs of 14% and 16% respectively.Conclusions: The high-throughput flow cytometric assays developed here were successfully optimised for use with NTHi. Assays proved to be sensitive and highly reproducible for the measurement of bacterial uptake and oxidative burstopsonophagocytosis and antibody-mediated deposition of C3b/iC3b and C5b-9. These assays are useful tools for use in large scale epidemiological studies and to assist in the assessment of functional antibody induced by NTHi candidate vaccines.
Text
Thomas et al 2018 BMC Microbiology
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More information
Accepted/In Press date: 11 October 2018
e-pub ahead of print date: 29 October 2018
Published date: 29 October 2018
Keywords:
Non-typeableHaemophilus influenzae, Antibody, Opsonophagocytosis, Complement, Flow cytometry, Vaccine
Identifiers
Local EPrints ID: 425745
URI: http://eprints.soton.ac.uk/id/eprint/425745
ISSN: 1471-2180
PURE UUID: edd6e7de-9663-48fe-b627-94744f2fa4d2
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Date deposited: 02 Nov 2018 17:30
Last modified: 16 Mar 2024 03:52
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Contributors
Author:
Stephen R Thomas
Author:
Stephanie Leung
Author:
Katy Knox
Author:
Pascal Lestrate
Author:
Dominique Wauters
Author:
Andrew Gorringe
Author:
Stephen C. Taylor
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