Biofilm Antimicrobial Susceptibility Increases With Antimicrobial Exposure Time

被引:80
作者
Castaneda, Paulo [1 ,4 ]
McLaren, Alex [1 ,2 ,3 ,4 ]
Tavaziva, Gamuchirai [4 ]
Overstreet, Derek [3 ,4 ]
机构
[1] Banner Univ Med Ctr Phoenix, 1320 N 10th St, Phoenix, AZ 85006 USA
[2] Univ Arizona, Coll Med Phoenix, Phoenix, AZ USA
[3] Sonoran Biosci, Chandler, AZ USA
[4] Arizona State Univ, Ctr Intervent Biomat, Tempe, AZ USA
基金
美国国家卫生研究院;
关键词
STAPHYLOCOCCUS-AUREUS; VANCOMYCIN; TIGECYCLINE; COMBINATION; GENTAMICIN;
D O I
10.1007/s11999-016-4700-z
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The antimicrobial concentration required to kill all the bacteria in a biofilm, known as the minimum biofilm eradication concentration (MBEC), is typically determined in vitro by exposing the biofilm to serial concentrations of antimicrobials for 24 hours or less. Local delivery is expected to cause high local levels for longer than 24 hours. It is unknown if longer antimicrobial exposures require the same concentration to eradicate bacteria in biofilm. Questions/purposes Does MBEC change with increased antimicrobial exposure time? Biofilms were grown for 24 hours using five pathogens (methicillin-sensitive Staphylococcus aureus, methicillin-resistant Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, and Pseudomonas aeruginosa) and then exposed to four antimicrobials regimens: tobramycin, vancomycin, and tobramycin combined with vancomycin in 3:1 and 1:1 ratios by weight in concentrations of 62.5, 125, 250, 500, 1000, 2000, 4000, and 8000 mu g/mL for three durations, 1, 3, and 5 days, in triplicate. MBEC was measured as the lowest concentration that killed all bacteria in the biofilm determined by 21-day subculture. MBEC was lower when antimicrobial exposure time was longer. For the staphylococcus species, the MBEC was lower when exposure time was 5 days than 1 day in 11 of 12 antimicrobial/microorganism pairs. The MBEC range for these 11 pairs on Day 1 was 4000 to > 8000 mu g/mL and on Day 5 was < 250 to 8000 mu g/mL. MBEC for tobramycin/P. aeruginosa was 2000 mu g/mL on Day 1 and a parts per thousand currency sign 250 mu g/mL on Day 5, and for E. coli, 125 mu g/mL on Day 1 and a parts per thousand currency sign 62.5 on Day 5. Although antimicrobial susceptibility was lower for longer exposure times in the microorganisms we studied, confirmation is required for other pathogens. Clinical Relevance One-day MBEC assays may overestimate the local antimicrobial levels needed to kill organisms in biofilm if local levels are sustained at MBEC or above for longer than 24 hours. Future studies are needed to confirm that antimicrobial levels achieved clinically from local delivery are above the MBEC at relevant time points and to confirm that MBEC for in vitro microorganisms accurately represents MBEC of in vivo organisms in an clinical infection.
引用
收藏
页码:1659 / 1664
页数:6
相关论文
共 21 条
[1]   The Calgary Biofilm Device: New technology for rapid determination of antibiotic susceptibilities of bacterial biofilms [J].
Ceri, H ;
Olson, ME ;
Stremick, C ;
Read, RR ;
Morck, D ;
Buret, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (06) :1771-1776
[2]  
Cockerill F., 2012, Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically: approved standard
[3]   MICROBIAL BIOFILMS [J].
COSTERTON, JW ;
LEWANDOWSKI, Z ;
CALDWELL, DE ;
KORBER, DR ;
LAPPINSCOTT, HM .
ANNUAL REVIEW OF MICROBIOLOGY, 1995, 49 :711-745
[4]   In vitro pharmacokinetics of antimicrobial cationic peptides alone and in combination with antibiotics against methicillin resistant Staphylococcus aureus biofilms [J].
Dosler, Sibel ;
Mataraci, Emel .
PEPTIDES, 2013, 49 :53-58
[5]   EFFECT OF VANCOMYCIN HYDROCHLORIDE ON STAPHYLOCOCCUS-EPIDERMIDIS BIOFILM ASSOCIATED WITH SILICONE ELASTOMER [J].
EVANS, RC ;
HOLMES, CJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (06) :889-894
[6]   Detachment characteristics and oxacillin resistance of Staphyloccocus aureus biofilm emboli in an in vitro catheter infection model [J].
Fux, CA ;
Wilson, S ;
Stoodley, P .
JOURNAL OF BACTERIOLOGY, 2004, 186 (14) :4486-4491
[7]   MIC Versus MBEC to Determine the Antibiotic Sensitivity of Staphylococcus aureus in Peritoneal Dialysis Peritonitis [J].
Girard, Louis P. ;
Ceri, Howard ;
Gibb, Allan P. ;
Olson, Merle ;
Sepandj, Farshad .
PERITONEAL DIALYSIS INTERNATIONAL, 2010, 30 (06) :652-656
[8]   Small colony variants (SCVs) of Staphylococcus aureus - A bacterial survival strategy [J].
Kahl, Barbara C. .
INFECTION GENETICS AND EVOLUTION, 2014, 21 :515-522
[9]  
Kwasny Steven M, 2010, Curr Protoc Pharmacol, VChapter 13, DOI 10.1002/0471141755.ph13a08s50
[10]   Persister cells, dormancy and infectious disease [J].
Lewis, Kim .
NATURE REVIEWS MICROBIOLOGY, 2007, 5 (01) :48-56