Dormancy of Candida albicans cells in the presence of the polyene antibiotic amphotericin B:: simple demonstration by flow cytometry

被引:9
作者
Boucherit, Zahia [1 ]
Seksek, Olivier [1 ]
Bolard, Jacques [1 ]
机构
[1] Univ Paris 06, CNRS, UMR 7033, BIOMOCETI, F-91030 Evry, France
关键词
Candida albicans; dormancy; amphotericin B; flow cytometry;
D O I
10.1080/13693780701487821
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Flow cytometry light scattering was used to monitor size increase of Candida albicans (isolate ATCC 10231) cells in the presence or absence of the antifungal drug amphotericin B (AmB). This non-invasive and descriptive method allowed for the differentiation of dead and dormant sub-populations of cells. When inoculated into a growth medium without AmB, a progressive increase in light scattering was observed over a period of approximately 4 h, but without proliferation of the yeast. After this period, the light scattering distribution regressed to baseline level, whereas cell proliferation started. In the presence of AmB, all the cells shrank in size within approximately 4 h and proliferation was temporarily halted. However, in the presence of 0.4 mu M AmB, a progressive increase of light scattering occurred after 21 h which was similar to that observed within the first 4 h in the absence of the antifungal. After approximately 24 h of incubation at this concentration of AmB, proliferation resumed. These observations indicate that this renewed cell proliferation was due to the reawakening of dormant cells in the presence of AmB (45% in the presence of 0.4 mM AmB) rather than the result of the development of viable cells that had escaped detection. This simple descriptive approach could be extended to other fungal strains or species, to other antifungal drugs and possibly to bacteria.
引用
收藏
页码:525 / 533
页数:9
相关论文
共 43 条
[1]   Applications of flow cytometry to clinical microbiology [J].
Alvarez-Barrientos, A ;
Arroyo, J ;
Cantón, R ;
Nombela, C ;
Sánchez-Pérez, M .
CLINICAL MICROBIOLOGY REVIEWS, 2000, 13 (02) :167-+
[2]  
ARSENY S, 1994, FEMS MICROBIOL LETT, V115, P347
[3]   THE REGULATION OF NUCLEAR MIGRATION AND DIVISION DURING SYNCHRONOUS BUD FORMATION IN RELEASED STATIONARY PHASE CULTURES OF THE YEAST CANDIDA-ALBICANS [J].
BEDELL, GW ;
WERTH, A ;
SOLL, DR .
EXPERIMENTAL CELL RESEARCH, 1980, 127 (01) :103-113
[4]   RECOVERY OF HEPATOCYTES FROM ATTACK BY THE PORE FORMER AMPHOTERICIN-B [J].
BINET, A ;
BOLARD, J .
BIOCHEMICAL JOURNAL, 1988, 253 (02) :435-440
[5]  
Bolard J., 1991, Candida albicans. Cellular and molecular biology., P214
[6]   Pharmacodynamics of fluconazole, itraconazole, and amphotericin B against Candida albicans [J].
Burgess, DS ;
Hastings, RW ;
Summers, KK ;
Hardin, TC ;
Rinaldi, MG .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2000, 36 (01) :13-18
[7]  
Carter Elizabeth A., 1993, P111
[8]  
CHAFFIN WL, 1980, CAN J MICROBIOL, V30, P192
[9]   New automated method for determining postantifungal effect of amphotericin B against Candida species:: Effects of concentration, exposure time, and area under the curve [J].
Chryssanthou, E ;
Cars, O ;
Sjölin, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (12) :4016-4018
[10]  
Davey Hazel M., 2003, Current Issues in Molecular Biology, V5, P9