The origin of extracellular DNA in bacterial biofilm infections in vivo

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The origin of extracellular DNA in bacterial biofilm infections in vivo. / Alhede, Maria; Alhede, Morten; Qvortrup, Klaus; Kragh, Kasper Nørskov; Jensen, Peter Østrup; Stewart, Philip Shook; Bjarnsholt, Thomas.

In: Pathogens and Disease, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Alhede, M, Alhede, M, Qvortrup, K, Kragh, KN, Jensen, PØ, Stewart, PS & Bjarnsholt, T 2020, 'The origin of extracellular DNA in bacterial biofilm infections in vivo', Pathogens and Disease. https://doi.org/10.1093/femspd/ftaa018

APA

Alhede, M., Alhede, M., Qvortrup, K., Kragh, K. N., Jensen, P. Ø., Stewart, P. S., & Bjarnsholt, T. (2020). The origin of extracellular DNA in bacterial biofilm infections in vivo. Pathogens and Disease, [ftaa018]. https://doi.org/10.1093/femspd/ftaa018

Vancouver

Alhede M, Alhede M, Qvortrup K, Kragh KN, Jensen PØ, Stewart PS et al. The origin of extracellular DNA in bacterial biofilm infections in vivo. Pathogens and Disease. 2020. ftaa018. https://doi.org/10.1093/femspd/ftaa018

Author

Alhede, Maria ; Alhede, Morten ; Qvortrup, Klaus ; Kragh, Kasper Nørskov ; Jensen, Peter Østrup ; Stewart, Philip Shook ; Bjarnsholt, Thomas. / The origin of extracellular DNA in bacterial biofilm infections in vivo. In: Pathogens and Disease. 2020.

Bibtex

@article{e517cdd34c90440abc81039aa3280f13,
title = "The origin of extracellular DNA in bacterial biofilm infections in vivo",
abstract = "Extracellular DNA (eDNA) plays an important role in both the aggregation of bacteria and in the interaction of the resulting biofilms with polymorphonuclear leukocytes (PMNs) during an inflammatory response. Here, transmission electron and confocal scanning laser microscopy were used to examine the interaction between biofilms of Pseudomonas aeruginosa and PMNs in a murine implant model and in lung tissue from chronically infected cystic fibrosis patients. PNA FISH, DNA staining, labeling of PMN DNA with a thymidine analogue, and immunohistochemistry were applied to localize bacteria, eDNA, PMN-derived eDNA, PMN-derived histone H3 (H3), neutrophil elastase (NE), and citrullinated H3 (citH3). Host-derived eDNA was observed surrounding bacterial biofilms but not within the biofilms. H3 localized to the lining of biofilms while NE was found throughout biofilms. CitH3, a marker for neutrophil extracellular traps (NETs) was detected only sporadically indicating that most host-derived eDNA in vivo was not a result of NETosis. Together these observations show that, in these in vivo biofilm infections with P. aeruginosa, the majority of eDNA is found external to the biofilm and derives from the host.",
author = "Maria Alhede and Morten Alhede and Klaus Qvortrup and Kragh, {Kasper N{\o}rskov} and Jensen, {Peter {\O}strup} and Stewart, {Philip Shook} and Thomas Bjarnsholt",
note = "{\textcopyright} FEMS 2020.",
year = "2020",
doi = "10.1093/femspd/ftaa018",
language = "English",
journal = "FEMS Immunology and Medical Microbiology",
issn = "2049-632X",
publisher = "Oxford University Press",

}

RIS

TY - JOUR

T1 - The origin of extracellular DNA in bacterial biofilm infections in vivo

AU - Alhede, Maria

AU - Alhede, Morten

AU - Qvortrup, Klaus

AU - Kragh, Kasper Nørskov

AU - Jensen, Peter Østrup

AU - Stewart, Philip Shook

AU - Bjarnsholt, Thomas

N1 - © FEMS 2020.

PY - 2020

Y1 - 2020

N2 - Extracellular DNA (eDNA) plays an important role in both the aggregation of bacteria and in the interaction of the resulting biofilms with polymorphonuclear leukocytes (PMNs) during an inflammatory response. Here, transmission electron and confocal scanning laser microscopy were used to examine the interaction between biofilms of Pseudomonas aeruginosa and PMNs in a murine implant model and in lung tissue from chronically infected cystic fibrosis patients. PNA FISH, DNA staining, labeling of PMN DNA with a thymidine analogue, and immunohistochemistry were applied to localize bacteria, eDNA, PMN-derived eDNA, PMN-derived histone H3 (H3), neutrophil elastase (NE), and citrullinated H3 (citH3). Host-derived eDNA was observed surrounding bacterial biofilms but not within the biofilms. H3 localized to the lining of biofilms while NE was found throughout biofilms. CitH3, a marker for neutrophil extracellular traps (NETs) was detected only sporadically indicating that most host-derived eDNA in vivo was not a result of NETosis. Together these observations show that, in these in vivo biofilm infections with P. aeruginosa, the majority of eDNA is found external to the biofilm and derives from the host.

AB - Extracellular DNA (eDNA) plays an important role in both the aggregation of bacteria and in the interaction of the resulting biofilms with polymorphonuclear leukocytes (PMNs) during an inflammatory response. Here, transmission electron and confocal scanning laser microscopy were used to examine the interaction between biofilms of Pseudomonas aeruginosa and PMNs in a murine implant model and in lung tissue from chronically infected cystic fibrosis patients. PNA FISH, DNA staining, labeling of PMN DNA with a thymidine analogue, and immunohistochemistry were applied to localize bacteria, eDNA, PMN-derived eDNA, PMN-derived histone H3 (H3), neutrophil elastase (NE), and citrullinated H3 (citH3). Host-derived eDNA was observed surrounding bacterial biofilms but not within the biofilms. H3 localized to the lining of biofilms while NE was found throughout biofilms. CitH3, a marker for neutrophil extracellular traps (NETs) was detected only sporadically indicating that most host-derived eDNA in vivo was not a result of NETosis. Together these observations show that, in these in vivo biofilm infections with P. aeruginosa, the majority of eDNA is found external to the biofilm and derives from the host.

U2 - 10.1093/femspd/ftaa018

DO - 10.1093/femspd/ftaa018

M3 - Journal article

C2 - 32196074

JO - FEMS Immunology and Medical Microbiology

JF - FEMS Immunology and Medical Microbiology

SN - 2049-632X

M1 - ftaa018

ER -

ID: 238530178