Bacterial biofilms predominate in both acute and chronic human lung infections

Research output: Contribution to journalJournal articleResearchpeer-review

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Bacterial biofilms predominate in both acute and chronic human lung infections. / Kolpen, M.; Kragh, K. N.; Enciso, J. B.; Faurholt-Jepsen, D.; Lindegaard, B.; Egelund, G. B.; Jensen, A.V.; Ravn, P.; Mathiesen, I. H. M.; Gheorghe, A. G.; Hertz, F. B.; Qvist, T.; Whiteley, M.; Jensen, P. Ø.; Bjarnsholt, T.

In: European Respiratory Journal. Supplement, Vol. 60, No. Suppl. 66, 4, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kolpen, M, Kragh, KN, Enciso, JB, Faurholt-Jepsen, D, Lindegaard, B, Egelund, GB, Jensen, AV, Ravn, P, Mathiesen, IHM, Gheorghe, AG, Hertz, FB, Qvist, T, Whiteley, M, Jensen, PØ & Bjarnsholt, T 2022, 'Bacterial biofilms predominate in both acute and chronic human lung infections', European Respiratory Journal. Supplement, vol. 60, no. Suppl. 66, 4. https://doi.org/10.1183/13993003.congress-2022.4

APA

Kolpen, M., Kragh, K. N., Enciso, J. B., Faurholt-Jepsen, D., Lindegaard, B., Egelund, G. B., Jensen, A. V., Ravn, P., Mathiesen, I. H. M., Gheorghe, A. G., Hertz, F. B., Qvist, T., Whiteley, M., Jensen, P. Ø., & Bjarnsholt, T. (2022). Bacterial biofilms predominate in both acute and chronic human lung infections. European Respiratory Journal. Supplement, 60(Suppl. 66), [4]. https://doi.org/10.1183/13993003.congress-2022.4

Vancouver

Kolpen M, Kragh KN, Enciso JB, Faurholt-Jepsen D, Lindegaard B, Egelund GB et al. Bacterial biofilms predominate in both acute and chronic human lung infections. European Respiratory Journal. Supplement. 2022;60(Suppl. 66). 4. https://doi.org/10.1183/13993003.congress-2022.4

Author

Kolpen, M. ; Kragh, K. N. ; Enciso, J. B. ; Faurholt-Jepsen, D. ; Lindegaard, B. ; Egelund, G. B. ; Jensen, A.V. ; Ravn, P. ; Mathiesen, I. H. M. ; Gheorghe, A. G. ; Hertz, F. B. ; Qvist, T. ; Whiteley, M. ; Jensen, P. Ø. ; Bjarnsholt, T. / Bacterial biofilms predominate in both acute and chronic human lung infections. In: European Respiratory Journal. Supplement. 2022 ; Vol. 60, No. Suppl. 66.

Bibtex

@article{cea23ca583114199845b51bad49beae5,
title = "Bacterial biofilms predominate in both acute and chronic human lung infections",
abstract = "Background: A basic paradigm of human infection is that acute bacterial disease is caused by fast growing planktonic bacteria while chronic infections are caused by slow-growing, aggregated bacteria; a phenomenon known as a biofilm. For lung infections, this paradigm has been thought to be supported by observations of how bacteria proliferate in well-established growth media in the laboratory - the gold standard of microbiology.Aim: To investigate the bacterial architecture in sputum from patients with acute and chronic lung infections.Methods: Advanced imaging technology was used for quantification and direct comparison of infection types on fresh sputum samples thereby directly testing the acute versus chronic paradigm.Results: In this study we compared the bacterial lifestyle (planktonic or biofilm), growth rate and inflammatory response of bacteria in freshly collected sputum (n=43) from patient groups presenting with acute or chronic lung infections. We found that both acute and chronic lung infections are dominated by biofilms although planktonic cells were observed in both sample types. Bacteria grew faster in sputum from acute infections, but these fast-growing bacteria were enriched in biofilms similar to the architecture thought to be reserved for chronic infections. Cellular inflammation in the lungs was also similar across patient groups, but systemic inflammatory markers were only elevated in acute infections.Conclusions: Our findings indicate that the current paradigm of equating planktonic with acute and biofilm with chronic infection needs to be revisited as the difference lies primarily in metabolic rates, not bacterial architecture",
keywords = "Bacteria, COPD, Cystic fibrosis",
author = "M. Kolpen and Kragh, {K. N.} and Enciso, {J. B.} and D. Faurholt-Jepsen and B. Lindegaard and Egelund, {G. B.} and A.V. Jensen and P. Ravn and Mathiesen, {I. H. M.} and Gheorghe, {A. G.} and Hertz, {F. B.} and T. Qvist and M. Whiteley and Jensen, {P. {\O}.} and T. Bjarnsholt",
year = "2022",
doi = "10.1183/13993003.congress-2022.4",
language = "English",
volume = "60",
journal = "European Respiratory Journal. Supplement",
issn = "0904-1850",
publisher = "European Respiratory Society",
number = "Suppl. 66",
note = "International Congress of the European-Respiratory-Society (ERS) ; Conference date: 04-09-2022 Through 06-09-2022",

}

RIS

TY - JOUR

T1 - Bacterial biofilms predominate in both acute and chronic human lung infections

AU - Kolpen, M.

AU - Kragh, K. N.

AU - Enciso, J. B.

AU - Faurholt-Jepsen, D.

AU - Lindegaard, B.

AU - Egelund, G. B.

AU - Jensen, A.V.

AU - Ravn, P.

AU - Mathiesen, I. H. M.

AU - Gheorghe, A. G.

AU - Hertz, F. B.

AU - Qvist, T.

AU - Whiteley, M.

AU - Jensen, P. Ø.

AU - Bjarnsholt, T.

PY - 2022

Y1 - 2022

N2 - Background: A basic paradigm of human infection is that acute bacterial disease is caused by fast growing planktonic bacteria while chronic infections are caused by slow-growing, aggregated bacteria; a phenomenon known as a biofilm. For lung infections, this paradigm has been thought to be supported by observations of how bacteria proliferate in well-established growth media in the laboratory - the gold standard of microbiology.Aim: To investigate the bacterial architecture in sputum from patients with acute and chronic lung infections.Methods: Advanced imaging technology was used for quantification and direct comparison of infection types on fresh sputum samples thereby directly testing the acute versus chronic paradigm.Results: In this study we compared the bacterial lifestyle (planktonic or biofilm), growth rate and inflammatory response of bacteria in freshly collected sputum (n=43) from patient groups presenting with acute or chronic lung infections. We found that both acute and chronic lung infections are dominated by biofilms although planktonic cells were observed in both sample types. Bacteria grew faster in sputum from acute infections, but these fast-growing bacteria were enriched in biofilms similar to the architecture thought to be reserved for chronic infections. Cellular inflammation in the lungs was also similar across patient groups, but systemic inflammatory markers were only elevated in acute infections.Conclusions: Our findings indicate that the current paradigm of equating planktonic with acute and biofilm with chronic infection needs to be revisited as the difference lies primarily in metabolic rates, not bacterial architecture

AB - Background: A basic paradigm of human infection is that acute bacterial disease is caused by fast growing planktonic bacteria while chronic infections are caused by slow-growing, aggregated bacteria; a phenomenon known as a biofilm. For lung infections, this paradigm has been thought to be supported by observations of how bacteria proliferate in well-established growth media in the laboratory - the gold standard of microbiology.Aim: To investigate the bacterial architecture in sputum from patients with acute and chronic lung infections.Methods: Advanced imaging technology was used for quantification and direct comparison of infection types on fresh sputum samples thereby directly testing the acute versus chronic paradigm.Results: In this study we compared the bacterial lifestyle (planktonic or biofilm), growth rate and inflammatory response of bacteria in freshly collected sputum (n=43) from patient groups presenting with acute or chronic lung infections. We found that both acute and chronic lung infections are dominated by biofilms although planktonic cells were observed in both sample types. Bacteria grew faster in sputum from acute infections, but these fast-growing bacteria were enriched in biofilms similar to the architecture thought to be reserved for chronic infections. Cellular inflammation in the lungs was also similar across patient groups, but systemic inflammatory markers were only elevated in acute infections.Conclusions: Our findings indicate that the current paradigm of equating planktonic with acute and biofilm with chronic infection needs to be revisited as the difference lies primarily in metabolic rates, not bacterial architecture

KW - Bacteria

KW - COPD

KW - Cystic fibrosis

U2 - 10.1183/13993003.congress-2022.4

DO - 10.1183/13993003.congress-2022.4

M3 - Journal article

VL - 60

JO - European Respiratory Journal. Supplement

JF - European Respiratory Journal. Supplement

SN - 0904-1850

IS - Suppl. 66

M1 - 4

T2 - International Congress of the European-Respiratory-Society (ERS)

Y2 - 4 September 2022 through 6 September 2022

ER -

ID: 341838258