Inefficient delivery of yeast cells as an explanation for reduced plating efficiency of Candida albicans

被引:4
作者
Bhatti, MA
Hjertstedt, J
Hahn, BL
Sohnle, PG [1 ]
机构
[1] Vet Affairs Med Ctr, Res Serv 151, Milwaukee, WI 53295 USA
[2] Med Coll Wisconsin, Dept Med, Div Infect Dis, Milwaukee, WI 53226 USA
[3] Marquette Univ, Sch Dent, Milwaukee, WI 53233 USA
关键词
plating efficiency; Candida albicans; yeast cells;
D O I
10.1080/714031136
中图分类号
R51 [传染病];
学科分类号
100401 [流行病与卫生统计学];
摘要
The plating efficiency for fungal yeast cells is usually less than that expected from microscopic counts, and a number of explanations for this phenomenon have been proposed. The present study was undertaken to explore possible reasons for reduced plating efficiency of Candida albicans. Explanations that we evaluated and found unlikely included: ineffectiveness of different culture media and/or incubation temperatures for growing colonies, insufficient area of the plate available for expression of individual colonies, production of microcolonies, and inaccurate counting of the organisms in the inoculum. An assay for delivery of the inoculum into tissue culture plate wells indicated that reduced delivery of the organisms accounted for lower than expected plating efficiency. C albicans yeast cells grown under low glucose conditions and expected to have reduced adhesiveness were found to have higher values for both delivery and plating efficiency in our assays. In summary, our results indicate that reduced plating efficiency for C albicans under the conditions used for these experiments is best explained by the loss of some yeast cells during preparation of the inocula or delivery of the yeast cells onto the plates.
引用
收藏
页码:465 / 469
页数:5
相关论文
共 16 条
[1]
INCREASE IN COLONY-FORMING-UNITS OF CANDIDA-ALBICANS AFTER TREATMENT WITH POLYENE ANTIBIOTICS [J].
BRAJTBURG, J ;
ELBERG, S ;
MEDOFF, G ;
KOBAYASHI, GS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1981, 19 (01) :199-200
[2]
CASTANEDA E, 1988, J MED VET MYCOL, V26, P351
[3]
Flow cytometric quantitation of yeast a novel technique for use in animal model work and in vitro immunologic assays [J].
Chang, WL ;
van der Heyde, HC ;
Klein, BS .
JOURNAL OF IMMUNOLOGICAL METHODS, 1998, 211 (1-2) :51-63
[4]
The action of methylene-blue and certain other dyes on living and dead yeast [J].
Fraser, CG .
JOURNAL OF PHYSICAL CHEMISTRY, 1920, 24 (09) :741-748
[5]
Hjertstedt J, 1998, MYCOSES, V41, P487, DOI 10.1111/j.1439-0507.1998.tb00711.x
[6]
KURITA N, 1993, J MED VET MYCOL, V31, P201
[7]
A RAPID COLORIMETRIC ASSAY OF FUNGAL VIABILITY WITH THE TETRAZOLIUM SALT MTT [J].
LEVITZ, SM ;
DIAMOND, RD .
JOURNAL OF INFECTIOUS DISEASES, 1985, 152 (05) :938-945
[8]
KILLING OF ASPERGILLUS-FUMIGATUS SPORES AND CANDIDA-ALBICANS YEAST PHASE BY THE IRON-HYDROGEN-PEROXIDE-IODIDE CYTO-TOXIC SYSTEM - COMPARISON WITH THE MYELOPEROXIDASE-HYDROGEN PEROXIDE-HALIDE SYSTEM [J].
LEVITZ, SM ;
DIAMOND, RD .
INFECTION AND IMMUNITY, 1984, 43 (03) :1100-1102
[9]
RELATIONSHIP BETWEEN CELL-SURFACE COMPOSITION OF CANDIDA-ALBICANS AND ADHERENCE TO ACRYLIC AFTER GROWTH ON DIFFERENT CARBON-SOURCES [J].
MCCOURTIE, J ;
DOUGLAS, LJ .
INFECTION AND IMMUNITY, 1981, 32 (03) :1234-1241
[10]
MCCOURTIE J, 1985, J GEN MICROBIOL, V131, P495