Biofilm Formation and Effect of Caspofungin on Biofilm Structure of Candida Species Bloodstream Isolates

被引:65
作者
Ferreira, J. A. G. [1 ,2 ]
Carr, J. H. [3 ]
Starling, C. E. F. [2 ]
de Resende, M. A. [1 ]
Donlan, R. M. [3 ]
机构
[1] Univ Fed Minas Gerais, Dept Microbiol, BR-31270901 Belo Horizonte, MG, Brazil
[2] Hosp Vera Cruz, Dept Doencas Infecciosas, Belo Horizonte, MG, Brazil
[3] Ctr Dis Control & Prevent, Div Healthcare Qual Promot, Atlanta, GA USA
关键词
ALBICANS BIOFILMS; ANTIFUNGAL AGENTS; IN-VITRO; PERSISTER CELLS; UNITED-STATES; FLUCONAZOLE RESISTANCE; PARAPSILOSIS BIOFILMS; EFFLUX PUMPS; INFECTIONS; SUSCEPTIBILITY;
D O I
10.1128/AAC.00316-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Candida biofilms are microbial communities, embedded in a polymeric matrix, growing attached to a surface, and are highly recalcitrant to antimicrobial therapy. These biofilms exhibit enhanced resistance against most antifungal agents except echinocandins and lipid formulations of amphotericin B. In this study, biofilm formation by different Candida species, particularly Candida albicans, C. tropicalis, and C. parapsilosis, was evaluated, and the effect of caspofungin (CAS) was assessed using a clinically relevant in vitro model system. CAS displayed in vitro activity against C. albicans and C. tropicalis cells within biofilms. Biofilm formation was evaluated after 48 h of antifungal drug exposure, and the effects of CAS on preformed Candida species biofilms were visualized using scanning electron microscopy (SEM). Several species-specific differences in the cellular morphologies associated with biofilms were observed. Our results confirmed the presence of paradoxical growth (PG) in C. albicans and C. tropicalis biofilms in the presence of high CAS concentrations. These findings were also confirmed by SEM analysis and were associated with the metabolic activity obtained by biofilm susceptibility testing. Importantly, these results suggest that the presence of atypical, enlarged, conical cells could be associated with PG and with tolerant cells in Candida species biofilm populations. The clinical implications of these findings are still unknown.
引用
收藏
页码:4377 / 4384
页数:8
相关论文
共 56 条
[1]   Development and characterization of an in vivo central venous catheter Candida albicans biofilm model [J].
Andes, D ;
Nett, J ;
Oschel, P ;
Albrecht, R ;
Marchillo, K ;
Pitula, A .
INFECTION AND IMMUNITY, 2004, 72 (10) :6023-6031
[2]   In vitro activity of caspofungin against Candida albicans biofilms [J].
Bachmann, SP ;
VandeWalle, K ;
Ramage, G ;
Patterson, TF ;
Wickes, BL ;
Graybill, JR ;
López-Ribot, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (11) :3591-3596
[3]   Matrix polymers of Candida biofilms and their possible role in biofilm resistance to antifungal agents [J].
Baillie, GS ;
Douglas, LJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2000, 46 (03) :397-403
[4]   Role of dimorphism in the development of Candida albicans biofilms [J].
Baillie, GS ;
Douglas, LJ .
JOURNAL OF MEDICAL MICROBIOLOGY, 1999, 48 (07) :671-679
[5]   Effect of growth rate on resistance of Candida albicans biofilms to antifungal agents [J].
Baillie, GS ;
Douglas, LJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (08) :1900-1905
[6]   SECULAR TRENDS IN NOSOCOMIAL PRIMARY BLOOD-STREAM INFECTIONS IN THE UNITED-STATES, 1980-1989 [J].
BANERJEE, SN ;
EMORI, TG ;
CULVER, DH ;
GAYNES, RP ;
JARVIS, WR ;
HORAN, T ;
EDWARDS, JR ;
TOLSON, J ;
HENDERSON, T ;
MARTONE, WJ .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 :S86-S89
[7]   How to build a biofilm: a fungal perspective [J].
Blankenship, Jill R. ;
Mitchell, Aaron P. .
CURRENT OPINION IN MICROBIOLOGY, 2006, 9 (06) :588-594
[8]  
Calderone Richard A., 2002, P3
[9]   The antibiotic-lock technique for therapy of 'highly needed' infected catheters [J].
Carratalà, J .
CLINICAL MICROBIOLOGY AND INFECTION, 2002, 8 (05) :282-289
[10]   In vitro efficacies of caspofungin or micafungin catheter lock solutions on Candida albicans biofilm growth [J].
Cateau, Estelle ;
Rodier, Marie-Helene ;
Imbert, Christine .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 62 (01) :153-155