TY - JOUR
T1 - Cathodic voltage-controlled electrical stimulation of titanium for prevention of methicillin-resistant Staphylococcus aureus and Acinetobacter baumannii biofilm infections
AU - Canty, Mary
AU - Luke-Marshall, Nicole
AU - Campagnari, Anthony
AU - Ehrensberger, Mark
N1 - Publisher Copyright:
© 2016 Acta Materialia Inc.
PY - 2017/1/15
Y1 - 2017/1/15
N2 - Antibiotic resistance of bacterial biofilms limits available treatment methods for implant-associated orthopaedic infections. This study evaluated the effects of applying cathodic voltage-controlled electrical stimulations (CVCES) of −1.5 V and −1.8 V (vs. Ag/AgCl) to coupons of commercially pure titanium (cpTi) incubated in cultures of methicillin-resistant Staphylococcus aureus (MRSA) and Acinetobacter baumannii (A. baumannii) as a method of preventing bacterial attachment. Stimulations were applied for 2, 4, and 8 h and coupon-associated and planktonic colony-forming units (CFU) were enumerated following stimulation. Compared to open circuit potential (OCP) controls, CVCES for 4 h at −1.8 V significantly reduced coupon-associated MRSA CFU by 99.9% (1.30 × 104 vs. 4.45 × 107, p = 0.047) and A. baumannii coupon-associated CFU by 99.9% (1.64 × 104 vs. 5.93 × 107, p = 0.001) and reduced planktonic CFU below detectable levels for both strains. CVCES at −1.8 V for 8 h also reduced coupon-associated and planktonic CFU below detectable levels for each strain. CVCES at −1.5 V for 4 and 8 h, and −1.8 V for 2 h did not result in clinically relevant reductions. For 4 and 8 h stimulations, the current density was significantly higher for −1.8 V than −1.5 V, an effect directly related to the rate of water and oxygen reduction on the cpTi surface. This significantly increased the pH, a suspected influence in decreased CFU viability. The voltage-dependent electrochemical properties of cpTi likely contribute to the observed antimicrobial effects of CVCES. This study revealed that CVCES of titanium could prevent coupon-associated and planktonic CFU of Gram-positive MRSA and Gram-negative A. baumannii from reaching detectable levels in a magnitude-dependent and time-dependent manner. Statement of Significance Periprosthetic joint infection is a devastating outcome of total joint arthroplasty and has led to increased patient morbidity and rising healthcare costs. Current treatments are limited by the growing prevalence of antimicrobial resistant biofilms. Therefore, there is a growing interest in the prevention of bacterial colonization of implants. Previous work has shown that cathodic voltage-controlled electrical stimulation (CVCES) of titanium is effective both in vitro and in vivo as an antimicrobial strategy to eradicate established implant-associated biofilm infections. The present study revealed that CVCES of titanium coupons also has utility in preventing coupon-associated and planktonic colony-forming units of Gram-positive methicillin-resistant Staphylococcus aureus and Gram-negative Acinetobacter baumannii from reaching detectable levels in a magnitude-dependent and time-dependent manner.
AB - Antibiotic resistance of bacterial biofilms limits available treatment methods for implant-associated orthopaedic infections. This study evaluated the effects of applying cathodic voltage-controlled electrical stimulations (CVCES) of −1.5 V and −1.8 V (vs. Ag/AgCl) to coupons of commercially pure titanium (cpTi) incubated in cultures of methicillin-resistant Staphylococcus aureus (MRSA) and Acinetobacter baumannii (A. baumannii) as a method of preventing bacterial attachment. Stimulations were applied for 2, 4, and 8 h and coupon-associated and planktonic colony-forming units (CFU) were enumerated following stimulation. Compared to open circuit potential (OCP) controls, CVCES for 4 h at −1.8 V significantly reduced coupon-associated MRSA CFU by 99.9% (1.30 × 104 vs. 4.45 × 107, p = 0.047) and A. baumannii coupon-associated CFU by 99.9% (1.64 × 104 vs. 5.93 × 107, p = 0.001) and reduced planktonic CFU below detectable levels for both strains. CVCES at −1.8 V for 8 h also reduced coupon-associated and planktonic CFU below detectable levels for each strain. CVCES at −1.5 V for 4 and 8 h, and −1.8 V for 2 h did not result in clinically relevant reductions. For 4 and 8 h stimulations, the current density was significantly higher for −1.8 V than −1.5 V, an effect directly related to the rate of water and oxygen reduction on the cpTi surface. This significantly increased the pH, a suspected influence in decreased CFU viability. The voltage-dependent electrochemical properties of cpTi likely contribute to the observed antimicrobial effects of CVCES. This study revealed that CVCES of titanium could prevent coupon-associated and planktonic CFU of Gram-positive MRSA and Gram-negative A. baumannii from reaching detectable levels in a magnitude-dependent and time-dependent manner. Statement of Significance Periprosthetic joint infection is a devastating outcome of total joint arthroplasty and has led to increased patient morbidity and rising healthcare costs. Current treatments are limited by the growing prevalence of antimicrobial resistant biofilms. Therefore, there is a growing interest in the prevention of bacterial colonization of implants. Previous work has shown that cathodic voltage-controlled electrical stimulation (CVCES) of titanium is effective both in vitro and in vivo as an antimicrobial strategy to eradicate established implant-associated biofilm infections. The present study revealed that CVCES of titanium coupons also has utility in preventing coupon-associated and planktonic colony-forming units of Gram-positive methicillin-resistant Staphylococcus aureus and Gram-negative Acinetobacter baumannii from reaching detectable levels in a magnitude-dependent and time-dependent manner.
KW - Antimicrobial
KW - Biofilm
KW - Electrical stimulation
KW - Infection prevention
KW - Titanium
UR - http://www.scopus.com/inward/record.url?scp=85007493609&partnerID=8YFLogxK
U2 - 10.1016/j.actbio.2016.11.056
DO - 10.1016/j.actbio.2016.11.056
M3 - Article
C2 - 27890730
AN - SCOPUS:85007493609
SN - 1742-7061
VL - 48
SP - 451
EP - 460
JO - Acta Biomaterialia
JF - Acta Biomaterialia
ER -