Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model

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Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model. / Sunnerhagen, Torgny; Schwartz, Franziska; Christophersen, Lars; Bjarnsholt, Thomas; Qvortrup, Klaus; Eldrup, Nikolaj; Vogt, Katja; Moser, Claus.

In: Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, Vol. 29, No. 12, 2023, p. 1600.e1-1600.e6.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Sunnerhagen, T, Schwartz, F, Christophersen, L, Bjarnsholt, T, Qvortrup, K, Eldrup, N, Vogt, K & Moser, C 2023, 'Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model', Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, vol. 29, no. 12, pp. 1600.e1-1600.e6. https://doi.org/10.1016/j.cmi.2023.09.012

APA

Sunnerhagen, T., Schwartz, F., Christophersen, L., Bjarnsholt, T., Qvortrup, K., Eldrup, N., Vogt, K., & Moser, C. (2023). Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 29(12), 1600.e1-1600.e6. https://doi.org/10.1016/j.cmi.2023.09.012

Vancouver

Sunnerhagen T, Schwartz F, Christophersen L, Bjarnsholt T, Qvortrup K, Eldrup N et al. Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model. Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases. 2023;29(12):1600.e1-1600.e6. https://doi.org/10.1016/j.cmi.2023.09.012

Author

Sunnerhagen, Torgny ; Schwartz, Franziska ; Christophersen, Lars ; Bjarnsholt, Thomas ; Qvortrup, Klaus ; Eldrup, Nikolaj ; Vogt, Katja ; Moser, Claus. / Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model. In: Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases. 2023 ; Vol. 29, No. 12. pp. 1600.e1-1600.e6.

Bibtex

@article{5a97a16926624faa8d0f9cdfdf4488d0,
title = "Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model",
abstract = "OBJECTIVES: An endovascular aneurysm repair (EVAR) graft is a catheter-implanted vascular prosthesis and is the preferred treatment for patients with aortic aneurysm. If an EVAR graft becomes the focus of infection, the treatment possibilities are limited as it is technically difficult to remove the graft to obtain source control. This study examines whether Pseudomonas aeruginosa and Staphylococcus aureus form biofilm on EVAR prostheses.METHODS: EVAR graft sections were exposed to bacteria at 102 or 108 colony forming units (CFU)/ml in lysogeny broth and Krebs-Ringer at 37°C, bacterial biofilm formation was evaluated by scanning electron microscopy (SEM) and counting CFU on the graft sections following antibiotic exposure at x10 minimal inhibitory concentration (MIC). Bacteria were tested for tolerance to benzyl penicillin, tobramycin and ciprofloxacin.RESULTS: Bacterial exposure for 15 minutes established biofilms on all prosthesis fragments (6/6 replicates). After 4 hours, bacteria were firmly attached to the EVAR prostheses and resisted washing. After 18 to 24 hours the median CFU/g of EVAR graft reached 5.2 x 108 (1.15 x 108 - 1.1 x 109) for S. aureus and 9.1 x 107 (3.5 x 107 - 6.25 x 108) for P. aeruginosa. SEM showed bacterial attachment to the graft pieces. There was a time-dependent development of tolerance with approximately 20 (tobramycin), 560 (benzyl penicillin), and 600 (ciprofloxacin) times more S. aureus surviving antibiotic exposure in 24 compared to 0 hours old biofilm. Five (tobramycin) and 170 times (ciprofloxacin) more P. aeruginosa survived antibiotic exposure in 24 compared to 0 hours old biofilms.CONCLUSIONS: Our results show that bacteria can rapidly adhere to and subsequently form antibiotic tolerant biofilms on EVAR graft material in concentrations equivalent to levels seen in transient bacteremia in vivo. Potentially, the system can be used for identifying optimal treatment combinations for infected EVAR prosthesis.",
author = "Torgny Sunnerhagen and Franziska Schwartz and Lars Christophersen and Thomas Bjarnsholt and Klaus Qvortrup and Nikolaj Eldrup and Katja Vogt and Claus Moser",
note = "Corrigendum https://www.sciencedirect.com/science/article/pii/S1198743X2300602X?via%3Dihub",
year = "2023",
doi = "10.1016/j.cmi.2023.09.012",
language = "English",
volume = "29",
pages = "1600.e1--1600.e6",
journal = "Clinical Microbiology and Infection",
issn = "1198-743X",
publisher = "Elsevier",
number = "12",

}

RIS

TY - JOUR

T1 - Biofilm formation on endovascular aneurysm repair (EVAR) grafts- a proof of concept in vitro model

AU - Sunnerhagen, Torgny

AU - Schwartz, Franziska

AU - Christophersen, Lars

AU - Bjarnsholt, Thomas

AU - Qvortrup, Klaus

AU - Eldrup, Nikolaj

AU - Vogt, Katja

AU - Moser, Claus

N1 - Corrigendum https://www.sciencedirect.com/science/article/pii/S1198743X2300602X?via%3Dihub

PY - 2023

Y1 - 2023

N2 - OBJECTIVES: An endovascular aneurysm repair (EVAR) graft is a catheter-implanted vascular prosthesis and is the preferred treatment for patients with aortic aneurysm. If an EVAR graft becomes the focus of infection, the treatment possibilities are limited as it is technically difficult to remove the graft to obtain source control. This study examines whether Pseudomonas aeruginosa and Staphylococcus aureus form biofilm on EVAR prostheses.METHODS: EVAR graft sections were exposed to bacteria at 102 or 108 colony forming units (CFU)/ml in lysogeny broth and Krebs-Ringer at 37°C, bacterial biofilm formation was evaluated by scanning electron microscopy (SEM) and counting CFU on the graft sections following antibiotic exposure at x10 minimal inhibitory concentration (MIC). Bacteria were tested for tolerance to benzyl penicillin, tobramycin and ciprofloxacin.RESULTS: Bacterial exposure for 15 minutes established biofilms on all prosthesis fragments (6/6 replicates). After 4 hours, bacteria were firmly attached to the EVAR prostheses and resisted washing. After 18 to 24 hours the median CFU/g of EVAR graft reached 5.2 x 108 (1.15 x 108 - 1.1 x 109) for S. aureus and 9.1 x 107 (3.5 x 107 - 6.25 x 108) for P. aeruginosa. SEM showed bacterial attachment to the graft pieces. There was a time-dependent development of tolerance with approximately 20 (tobramycin), 560 (benzyl penicillin), and 600 (ciprofloxacin) times more S. aureus surviving antibiotic exposure in 24 compared to 0 hours old biofilm. Five (tobramycin) and 170 times (ciprofloxacin) more P. aeruginosa survived antibiotic exposure in 24 compared to 0 hours old biofilms.CONCLUSIONS: Our results show that bacteria can rapidly adhere to and subsequently form antibiotic tolerant biofilms on EVAR graft material in concentrations equivalent to levels seen in transient bacteremia in vivo. Potentially, the system can be used for identifying optimal treatment combinations for infected EVAR prosthesis.

AB - OBJECTIVES: An endovascular aneurysm repair (EVAR) graft is a catheter-implanted vascular prosthesis and is the preferred treatment for patients with aortic aneurysm. If an EVAR graft becomes the focus of infection, the treatment possibilities are limited as it is technically difficult to remove the graft to obtain source control. This study examines whether Pseudomonas aeruginosa and Staphylococcus aureus form biofilm on EVAR prostheses.METHODS: EVAR graft sections were exposed to bacteria at 102 or 108 colony forming units (CFU)/ml in lysogeny broth and Krebs-Ringer at 37°C, bacterial biofilm formation was evaluated by scanning electron microscopy (SEM) and counting CFU on the graft sections following antibiotic exposure at x10 minimal inhibitory concentration (MIC). Bacteria were tested for tolerance to benzyl penicillin, tobramycin and ciprofloxacin.RESULTS: Bacterial exposure for 15 minutes established biofilms on all prosthesis fragments (6/6 replicates). After 4 hours, bacteria were firmly attached to the EVAR prostheses and resisted washing. After 18 to 24 hours the median CFU/g of EVAR graft reached 5.2 x 108 (1.15 x 108 - 1.1 x 109) for S. aureus and 9.1 x 107 (3.5 x 107 - 6.25 x 108) for P. aeruginosa. SEM showed bacterial attachment to the graft pieces. There was a time-dependent development of tolerance with approximately 20 (tobramycin), 560 (benzyl penicillin), and 600 (ciprofloxacin) times more S. aureus surviving antibiotic exposure in 24 compared to 0 hours old biofilm. Five (tobramycin) and 170 times (ciprofloxacin) more P. aeruginosa survived antibiotic exposure in 24 compared to 0 hours old biofilms.CONCLUSIONS: Our results show that bacteria can rapidly adhere to and subsequently form antibiotic tolerant biofilms on EVAR graft material in concentrations equivalent to levels seen in transient bacteremia in vivo. Potentially, the system can be used for identifying optimal treatment combinations for infected EVAR prosthesis.

U2 - 10.1016/j.cmi.2023.09.012

DO - 10.1016/j.cmi.2023.09.012

M3 - Journal article

C2 - 37734593

VL - 29

SP - 1600.e1-1600.e6

JO - Clinical Microbiology and Infection

JF - Clinical Microbiology and Infection

SN - 1198-743X

IS - 12

ER -

ID: 367598154