Hostname: page-component-8448b6f56d-gtxcr Total loading time: 0 Render date: 2024-04-25T01:31:17.069Z Has data issue: false hasContentIssue false

Staphylococcus aureus adheres avidly to decellularised cardiac homograft tissue in vitro in the fibrinogen-dependent manner

Published online by Cambridge University Press:  21 September 2020

Bartosz Ditkowski*
Affiliation:
Cardiovascular Developmental Biology, Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium Centre for Molecular and Vascular Biology, Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium
Kirsten Leeten
Affiliation:
Cardiovascular Developmental Biology, Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium Centre for Molecular and Vascular Biology, Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium
Ramadan Jashari
Affiliation:
European Homograft Bank, Saint Jean Clinique, Brussels, Belgium
Elizabeth Jones
Affiliation:
Centre for Molecular and Vascular Biology, Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium
Ruth Heying
Affiliation:
Cardiovascular Developmental Biology, Department of Cardiovascular Sciences, KU Leuven, Leuven, Belgium
*
Author for correspondence: Bartosz Ditkowski, PhD, Cardiovascular Developmental Biology/Centre for Molecular and Vascular Biology, Department of Cardiovascular Sciences, KU Leuven, Herestraat 49-3000, Leuven, Belgium. E-mail: bartosz.ditkowski@gmail.com

Abstract

Objective:

Infective endocarditis remains a severe complication associated with a high morbidity and mortality in patients after heart valve replacement. Exploration of the pathogenesis is of high demand and we, therefore, present a competent model that allows studying bacterial adherence and the role of plasma fibrinogen in this process using a new in-house designed low-volume flow chamber. Three cardiac graft tissues used for pulmonary valve replacement have been tested under shear conditions to investigate the impact of surface composition on the adhesion events.

Methods:

Tissue pieces of cryopreserved homograft (non-decellularised), decellularised homograft and bovine pericardium patch were investigated for fibrinogen binding. Adherence of Staphylococcus aureus to these graft tissues was studied quantitatively under flow conditions in our newly fabricated chamber based on a parallel plates’ modality. The method of counting colony-forming units was reliable and reproducible to assess the propensity of different graft materials for bacterial attachment under shear.

Results:

Bacterial perfusions over all plasma-precoated tissues identified cryopreserved homograft with the lowest affinity for S. aureus compared to decellularised homograft presenting a significantly higher bacterial adhesion (p < 0.05), which was linked to a more avid fibrinogen binding (p < 0.01). Bovine pericardial patch, as a reference tissue in this study, was confirmed to be the most susceptible tissue graft for the bacterial adhesion, which was in line with our previous work.

Conclusion:

The two studied homograft tissues showed different levels of bacterial attachment, which might be postulated by the involvement of fibrinogen in the adhesion mechanism(s) shown previously for bovine tissues.

Type
Original Article
Copyright
© The Author(s), 2020. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Moreillon, P, Que, YA. Infective endocarditis. Lancet 2004; 363: 139149.CrossRefGoogle ScholarPubMed
Toyoda, N, Chikwe, J, Itagaki, S, Gelijns, AC, Adams, DH, Egorova, NN. Trends in infective endocarditis in California and New York State, 1998–2013. JAMA 2017; 317: 16521660.CrossRefGoogle ScholarPubMed
Mery, CM, Guzman-Pruneda, FA, De Leon, LE, et al. Risk factors for development of endocarditis and reintervention in patients undergoing right ventricle to pulmonary artery valved conduit placement. J Thorac Cardiovasc Surg 2016; 151: 432439, 441.e431–432.CrossRefGoogle ScholarPubMed
Van Dijck, I, Budts, W, Cools, B, et al. Infective endocarditis of a transcatheter pulmonary valve in comparison with surgical implants. Heart 2015; 101: 788793.CrossRefGoogle ScholarPubMed
Sarikouch, S, Theodoridis, K, Hilfiker, A, et al. Early insight into in vivo recellularization of cell-free allogenic heart valves. Ann Thorac Surg 2019; 108: 581589.CrossRefGoogle ScholarPubMed
Boethig, D, Horke, A, Hazekamp, M, et al. A European study on decellularized homografts for pulmonary valve replacement: initial results from the prospective ESPOIR Trial and ESPOIR Registry datadagger. Eur J Cardiothorac Surg 2019; 56: 503509.CrossRefGoogle Scholar
Schneider, H, Vogt, M, Boekenkamp, R, et al. Melody transcatheter valve: histopathology and clinical implications of nine explanted devices. Int J Cardiol 2015; 189: 124131.CrossRefGoogle ScholarPubMed
Pislaru, SV, Pellikka, PA, Schaff, HV, Connolly, HM. Bioprosthetic valve thrombosis: the eyes will not see what the mind does not know. J Thorac Cardiovasc Surg 2015; 149: e86e87.CrossRefGoogle Scholar
Ditkowski, B, Bezulska-Ditkowska, M, Jashari, R, et al. Antiplatelet therapy abrogates platelet-assisted Staphylococcus aureus infectivity of biological heart valve conduits. J Thorac Cardiovasc Surg 2019; S0022–5223: 33112 33115.Google ScholarPubMed
Xu, LC, Bauer, JW, Siedlecki, CA Proteins, platelets, and blood coagulation at biomaterial interfaces. Colloids and surfaces. B, Biointerfaces 2014; 124: 4968.CrossRefGoogle ScholarPubMed
Neumann, A, Cebotari, S, Tudorache, I, Haverich, A, Sarikouch, S. Heart valve engineering: decellularized allograft matrices in clinical practice. Biomed Tech (Berl) 2013; 58: 453456.CrossRefGoogle ScholarPubMed
Sarikouch, S, Horke, A, Tudorache, I, et al. Decellularized fresh homografts for pulmonary valve replacement: a decade of clinical experience. Eur J Cardiothorac Surg 2016; 50: 281290.CrossRefGoogle ScholarPubMed
Cahill, TJ, Baddour, LM, Habib, G, et al. Challenges in Infective Endocarditis. J Am Coll Cardiol 2017; 69: 325344.CrossRefGoogle ScholarPubMed
Ditkowski, B, Veloso, TR, Bezulska-Ditkowska, M, et al. An in vitro model of a parallel-plate perfusion system to study bacterial adherence to graft tissues. J Vis Exp 2019; 143: 1-8.e58476.Google Scholar
Que, YA, Moreillon, P. Infective endocarditis. Nat Rev Cardiol 2011; 8: 322336.CrossRefGoogle ScholarPubMed
Jalal, Z, Galmiche, L, Beloin, C, Boudjemline, Y. Impact of percutaneous pulmonary valve implantation procedural steps on leaflets histology and mechanical behaviour: an in vitro study. Archives of cardiovascular diseases 2016; 109: 465475.CrossRefGoogle ScholarPubMed
Entenza, JM, Moreillon, P, Senn, MM, et al. Role of sigmaB in the expression of Staphylococcus aureus cell wall adhesins ClfA and FnbA and contribution to infectivity in a rat model of experimental endocarditis. Infect Immun 2005; 73: 990998.CrossRefGoogle Scholar
Veloso, TR, Claes, J, Van Kerckhoven, S, et al. Bacterial adherence to graft tissues in static and flow conditions. J Thorac Cardiovasc Surg 2018; 155: 325332.e324.CrossRefGoogle ScholarPubMed
Jalal, Z, Galmiche, L, Lebeaux, D, et al. Selective propensity of bovine jugular vein material to bacterial adhesions: an in-vitro study. Int J Cardiol 2015; 198: 201205.CrossRefGoogle ScholarPubMed
Tsai, WB, Grunkemeier, JM, Horbett, TA. Human plasma fibrinogen adsorption and platelet adhesion to polystyrene. J Biomed Mater Res 1999; 44: 130139.3.0.CO;2-9>CrossRefGoogle ScholarPubMed
Kasimir, MT, Weigel, G, Sharma, J, et al. The decellularized porcine heart valve matrix in tissue engineering: platelet adhesion and activation. Thromb Haemost 2005; 94: 562567.CrossRefGoogle ScholarPubMed
Tudorache, I, Cebotari, S, Sturz, G, et al. Tissue engineering of heart valves: biomechanical and morphological properties of decellularized heart valves. J Heart Valve Dis 2007; 16: 567573.Google ScholarPubMed
Ramm, R, Goecke, T, Theodoridis, K, et al. Decellularization combined with enzymatic removal of N-linked glycans and residual DNA reduces inflammatory response and improves performance of porcine xenogeneic pulmonary heart valves in an ovine in vivo model. Xenotransplantation 2019; 27: e12571.Google Scholar
Veloso, TR, Ditkowski, B, Mela, P, Hoylaerts, MF, Heying, R Are plasma proteins key players in the pathogenesis of infective endocarditis? J Thorac Cardiovasc Surg 2018; 156: 738739.CrossRefGoogle ScholarPubMed
Sharma, A, Cote, AT, Hosking, MCK, Harris, KC. A systematic review of infective endocarditis in patients with bovine jugular vein valves compared with other valve types. JACC. Cardiovascular interventions 2017; 10: 14491458.CrossRefGoogle ScholarPubMed
da Costa, FDA, Etnel, JRG, Torres, R, et al. Decellularized allografts for right ventricular outflow tract reconstruction in children. World J Pediatr Cong Heart Surg 2017; 8: 605612.CrossRefGoogle ScholarPubMed
d’Udekem, Y Decellularized homografts: in fashion or really superior? Eur J Cardiothorac Surg 2016; 50: 291292.CrossRefGoogle ScholarPubMed
Sarikouch, S, Haverich, A, Pepper, J, et al. Every like is not the same. J Thorac Cardiovasc Surg 2017; 153: 15531555.CrossRefGoogle Scholar
Supplementary material: File

Ditkowski et al. supplementary material

Ditkowski et al. supplementary material

Download Ditkowski et al. supplementary material(File)
File 22.6 KB