Phenotypic switching in Cryptococcus neoformans

被引:28
作者
Fries, BC
Goldman, DL
Casadevall, A
机构
[1] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Pediat, Bronx, NY 10461 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
关键词
phenotypic switching; fungus; colony morphology; virulence; microevolution;
D O I
10.1016/S1286-4579(02)00006-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Coptococcus neoformans strains exhibit considerable phenotype variability with regards to the capsular polysaccharide, sterol composition of the cell wall, and cell and colony morphology. Phenotypic changes can occur spontaneously during in vitro passage of strains or during chronic infection in vivo and may be associated with differences in virulence. Studies from our laboratory have demonstrated that phenotype variability can be the result of phenotypic switching. Phenotypic switching is defined as a reversible change of an observable colony phenotype that occurs at a frequency above the expected frequency for somatic mutations. This implies that phenotypic switching represents controlled and programmed changes in this pathogenic yeast rather than random mutations. We have shown that a phenotypic switch from a smooth colony phenotype to a mucoid colony phenotype occurs in vitro and in vivo during chronic infection of mice. More importantly we have now demonstrated that the switch is associated with an increase in virulence and a change in the host immune response. Implications of these findings for the pathogenesis of cryptococcosis are discussed. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
引用
收藏
页码:1345 / 1352
页数:8
相关论文
共 49 条
[21]   Karyotype instability in Cryptococcus neoformans infection [J].
Fries, BC ;
Chen, FY ;
Currie, BP ;
Casadevall, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (06) :1531-1534
[22]   Phenotypic switching in the human pathogenic fungus Cryptococcus neoformans is associated with changes in virulence and pulmonary inflammatory response in rodents [J].
Goldman, DL ;
Fries, BC ;
Franzot, SP ;
Montella, L ;
Casadevall, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14967-14972
[23]   Modulation of cell surface sialic acid expression in Neisseria meningitidis via a transposable genetic element [J].
Hammerschmidt, S ;
Hilse, R ;
vanPutten, JPM ;
GerardySchahn, R ;
Unkmeir, A ;
Frosch, M .
EMBO JOURNAL, 1996, 15 (01) :192-198
[24]  
HOWARD DRB, J GEN MICROBIOL, V139, P1195
[25]  
Klar AJS, 2001, GENETICS, V158, P919
[26]   Phenotypic variation and intracellular parasitism by Histoplasma capsulatum [J].
Kügler, S ;
Sebghati, TS ;
Eissenberg, LG ;
Goldman, WE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :8794-8798
[27]   Phenotypic switching in Candida glabrata involves phase-specific regulation of the metallothionein gene MT-II and the newly discovered hemolysin gene HLP [J].
Lachke, SA ;
Srikantha, T ;
Tsai, LK ;
Daniels, K ;
Soll, DR .
INFECTION AND IMMUNITY, 2000, 68 (02) :884-895
[28]   Cryptococcus neoformans resides in an acidic phagolysosome of human macrophages [J].
Levitz, SM ;
Nong, SH ;
Seetoo, KF ;
Harrison, TS ;
Speizer, RA ;
Simons, ER .
INFECTION AND IMMUNITY, 1999, 67 (02) :885-890
[29]   Phenotypic switching of variable surface lipoproteins in Mycoplasma bovis involves high-frequency chromosomal rearrangements [J].
Lysnyansky, I ;
Rosengarten, R ;
Yogev, D .
JOURNAL OF BACTERIOLOGY, 1996, 178 (18) :5395-5401
[30]   MECHANISM OF CONVERSION TO MUCOIDY IN PSEUDOMONAS-AERUGINOSA INFECTING CYSTIC-FIBROSIS PATIENTS [J].
MARTIN, DW ;
SCHURR, MJ ;
MUDD, MH ;
GOVAN, JRW ;
HOLLOWAY, BW ;
DERETIC, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (18) :8377-8381