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NTHi killing activity is reduced in COPD patients and is associated with a differential microbiome

NTHi killing activity is reduced in COPD patients and is associated with a differential microbiome
NTHi killing activity is reduced in COPD patients and is associated with a differential microbiome

Chronic obstructive pulmonary disease (COPD) is a chronic lung disease characterized by airway obstruction and inflammation. Non-typeable Haemophilus influenzae (NTHi) lung infections are common in COPD, promoting frequent exacerbations and accelerated lung function decline. The relationship with immune responses and NTHi are poorly understood. Herein, we comprehensively characterized the respiratory microbiome and mycobiome of patients while investigating microbial dynamics and host immune changes attributable to NTHi killing activity. Mild-to-moderate COPD patients encompassing frequent and infrequent exacerbators and healthy volunteers (HV) were enrolled. Microbial composition, proteomics and NTHi killing activity was analyzed using bronchoalveolar lavage fluid (BALF). In addition, antigen-antibody titers in sera to COPD pathogens were determined using a multiplex assay. Differential abundance analysis revealed an enrichment of Actinobacteria and Bacteroidetes in the BALF of COPD and HV subjects respectively. Significant differences in the IgA titer response were observed against NTHi antigens in COPD vs. HV. Notably, there was also significantly greater killing activity against NTHi in BALF from COPD vs. HV subjects (OR = 5.64; 95% CI = 1.75-20.20; p = 0.001). Stratification of COPD patients by NTHi killing activity identified unique microbial and protein signatures wherein Firmicutes, Actinobacteria and haptoglobin were enriched in patients with killing activity. We report that differences in host immune responses and NTHi-killing activity are associated with microbiome changes in mild-to-moderate COPD. This is suggestive of a potential link between the respiratory microbiome and immune activity against NTHi in the context of COPD pathogenesis even at this disease stage.

Aged, Bronchoalveolar Lavage Fluid/immunology, Female, Haemophilus Infections/immunology, Haemophilus influenzae/immunology, Humans, Male, Microbiota/physiology, Middle Aged, Pulmonary Disease, Chronic Obstructive/microbiology, Non-typeable Haemophilus influenzae, Exacerbations, COPD, Microbiome
1465-9921
Gopalakrishnan, Vancheswaran
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Sparklin, Ben
debf74bb-42e5-4cd5-9ea6-1094fd7086fe
Kim, Jung Hwan
b28e15de-9b82-4289-9f62-fac98596df02
Kehl, Margaret
adad2128-c6c5-443e-b869-c0e71b6b8fb0
Kenny, Tara
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Morehouse, Christopher
148c1c83-d0c1-4a1a-a8c8-af6f7d1a0718
Caceres, Carolina
e0b7e113-db14-4d69-88c3-3421850b345e
Warrener, Paul
ae3d329d-e79a-41ba-9bcf-0bb1de91d3b8
Hristova, Ventzislava A.
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Wilson, Susan
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Shandilya, Harini
69034c2a-7abd-4f57-95eb-89f976e5b08d
Barnes, Arnita
75ebf490-369a-4721-a55a-4e90878bc385
Ruzin, Alexey
11b473e3-d598-47d8-813f-490067b1fe2b
Wang, Junmin
39779780-8cf1-4ed2-a20a-bd8bb1f417aa
Öberg, Lisa
431ae4a1-6024-4cd8-bf43-7b387f03dc3e
Angermann, Bastian
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McCrae, Christopher
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Platt, Adam
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Muthas, Daniel
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Hess, Sonja
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Tkaczyk, Christine
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Sellman, Bret R.
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Ostridge, Kristoffer
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Belvisi, Maria G.
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Wilkinson, Tom M.A.
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Staples, Karl J.
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DiGiandomenico, Antonio
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MICA II Study Group
Gopalakrishnan, Vancheswaran
849d2ecb-df92-4bed-bb2c-e4c92a9e6496
Sparklin, Ben
debf74bb-42e5-4cd5-9ea6-1094fd7086fe
Kim, Jung Hwan
b28e15de-9b82-4289-9f62-fac98596df02
Kehl, Margaret
adad2128-c6c5-443e-b869-c0e71b6b8fb0
Kenny, Tara
8c5c880f-f880-41f5-b9b0-bac5019f44f8
Morehouse, Christopher
148c1c83-d0c1-4a1a-a8c8-af6f7d1a0718
Caceres, Carolina
e0b7e113-db14-4d69-88c3-3421850b345e
Warrener, Paul
ae3d329d-e79a-41ba-9bcf-0bb1de91d3b8
Hristova, Ventzislava A.
c30fdb39-c86f-4049-aaa9-0a46a9c68844
Wilson, Susan
b9b23e2c-42d7-46d4-ad28-d85d7a686ee2
Shandilya, Harini
69034c2a-7abd-4f57-95eb-89f976e5b08d
Barnes, Arnita
75ebf490-369a-4721-a55a-4e90878bc385
Ruzin, Alexey
11b473e3-d598-47d8-813f-490067b1fe2b
Wang, Junmin
39779780-8cf1-4ed2-a20a-bd8bb1f417aa
Öberg, Lisa
431ae4a1-6024-4cd8-bf43-7b387f03dc3e
Angermann, Bastian
14d8db65-ad90-4484-b7d8-638b31113058
McCrae, Christopher
905349d4-6151-412b-b146-7f1481d8472b
Platt, Adam
1cf7f1f0-5b57-407d-b6f1-51b5bebc204d
Muthas, Daniel
6928e069-9767-4a26-85f6-b5407073612d
Hess, Sonja
67385379-45f1-4c34-bfed-cfa033187cc1
Tkaczyk, Christine
088776db-b22f-44a6-b50b-3eec638dc79d
Sellman, Bret R.
e620964f-253f-4ea9-b5c9-e7035a0e9999
Ostridge, Kristoffer
10231477-1554-43ed-9d23-35258f101b16
Belvisi, Maria G.
5db9e025-50e5-4433-84ae-e19a57402a1e
Wilkinson, Tom M.A.
8c55ebbb-e547-445c-95a1-c8bed02dd652
Staples, Karl J.
e0e9d80f-0aed-435f-bd75-0c8818491fee
DiGiandomenico, Antonio
acabdd32-e84d-495a-b3aa-5e36fb59f8bc

Gopalakrishnan, Vancheswaran, Sparklin, Ben and Kim, Jung Hwan , MICA II Study Group (2025) NTHi killing activity is reduced in COPD patients and is associated with a differential microbiome. Respiratory Research, 26 (1), [45]. (doi:10.1186/s12931-025-03113-z).

Record type: Article

Abstract

Chronic obstructive pulmonary disease (COPD) is a chronic lung disease characterized by airway obstruction and inflammation. Non-typeable Haemophilus influenzae (NTHi) lung infections are common in COPD, promoting frequent exacerbations and accelerated lung function decline. The relationship with immune responses and NTHi are poorly understood. Herein, we comprehensively characterized the respiratory microbiome and mycobiome of patients while investigating microbial dynamics and host immune changes attributable to NTHi killing activity. Mild-to-moderate COPD patients encompassing frequent and infrequent exacerbators and healthy volunteers (HV) were enrolled. Microbial composition, proteomics and NTHi killing activity was analyzed using bronchoalveolar lavage fluid (BALF). In addition, antigen-antibody titers in sera to COPD pathogens were determined using a multiplex assay. Differential abundance analysis revealed an enrichment of Actinobacteria and Bacteroidetes in the BALF of COPD and HV subjects respectively. Significant differences in the IgA titer response were observed against NTHi antigens in COPD vs. HV. Notably, there was also significantly greater killing activity against NTHi in BALF from COPD vs. HV subjects (OR = 5.64; 95% CI = 1.75-20.20; p = 0.001). Stratification of COPD patients by NTHi killing activity identified unique microbial and protein signatures wherein Firmicutes, Actinobacteria and haptoglobin were enriched in patients with killing activity. We report that differences in host immune responses and NTHi-killing activity are associated with microbiome changes in mild-to-moderate COPD. This is suggestive of a potential link between the respiratory microbiome and immune activity against NTHi in the context of COPD pathogenesis even at this disease stage.

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More information

Accepted/In Press date: 11 January 2025
Published date: 30 January 2025
Keywords: Aged, Bronchoalveolar Lavage Fluid/immunology, Female, Haemophilus Infections/immunology, Haemophilus influenzae/immunology, Humans, Male, Microbiota/physiology, Middle Aged, Pulmonary Disease, Chronic Obstructive/microbiology, Non-typeable Haemophilus influenzae, Exacerbations, COPD, Microbiome

Identifiers

Local EPrints ID: 498372
URI: http://eprints.soton.ac.uk/id/eprint/498372
ISSN: 1465-9921
PURE UUID: a5b52281-bf67-45d2-a947-13485dbbaa65
ORCID for Karl J. Staples: ORCID iD orcid.org/0000-0003-3844-6457

Catalogue record

Date deposited: 17 Feb 2025 17:46
Last modified: 22 Aug 2025 01:56

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Contributors

Author: Vancheswaran Gopalakrishnan
Author: Ben Sparklin
Author: Jung Hwan Kim
Author: Margaret Kehl
Author: Tara Kenny
Author: Christopher Morehouse
Author: Carolina Caceres
Author: Paul Warrener
Author: Ventzislava A. Hristova
Author: Susan Wilson
Author: Harini Shandilya
Author: Arnita Barnes
Author: Alexey Ruzin
Author: Junmin Wang
Author: Lisa Öberg
Author: Bastian Angermann
Author: Christopher McCrae
Author: Adam Platt
Author: Daniel Muthas
Author: Sonja Hess
Author: Christine Tkaczyk
Author: Bret R. Sellman
Author: Kristoffer Ostridge
Author: Maria G. Belvisi
Author: Karl J. Staples ORCID iD
Author: Antonio DiGiandomenico
Corporate Author: MICA II Study Group

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