Bcmfs1, a novel major facilitator superfamily transporter from Botrytis cinerea, provides tolerance towards the natural toxic compounds camptothecin and cercosporin and towards fungicides

被引:108
作者
Hayashi, K [1 ]
Schoonbeek, HJ [1 ]
De Waard, MA [1 ]
机构
[1] Univ Wageningen & Res Ctr, Phytopathol Lab, NL-6700 EE Wageningen, Netherlands
关键词
D O I
10.1128/AEM.68.10.4996-5004.2002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Bcmfs1, a novel major facilitator superfamily gene from Botrytis cinerea, was cloned, and replacement and overexpression mutants were constructed to study its function. Replacement mutants showed increased sensitivity to the natural toxic compounds camptothecin and cercosporin, produced by the plant Camptotheca acuminata and the plant pathogenic fungus Cercospora kikuchii, respectively. Overexpression mutants displayed decreased sensitivity to these compounds and to structurally unrelated fungicides, such as sterol demethylation inhibitors (DMIs). A double-replacement mutant of Bcmfs1 and the ATP-binding cassette (ABC) transporter gene BcatrD was more sensitive to DMI fungicides than a single-replacement mutant of BcatrD, known to encode an important ABC transporter of DMIs. The sensitivity of the wild-type strain and mutants to DMI fungicides correlated with Bcmfs1 expression levels and with the initial accumulation of oxpoconazole by germlings of these isolates. The results indicate that Bcmfs1 is a major facilitator superfamily multidrug transporter involved in protection against natural toxins and fungicides and has a substrate specificity that overlaps with the ABC transporter BcatrD. Bcmfs1 may be involved in protection of B. cinerea against plant defense compounds during the pathogenic phase of growth on host plants and against fungitoxic antimicrobial metabolites during its saprophytic phase of growth.
引用
收藏
页码:4996 / 5004
页数:9
相关论文
共 34 条
[1]   AP1-mediated multidrug resistance in Saccharomyces cerevisiae requires FLR1 encoding a transporter of the major facilitator superfamily [J].
Alarco, AM ;
Balan, I ;
Talibi, D ;
Mainville, N ;
Raymond, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (31) :19304-19313
[2]   TRI12, a trichothecene efflux pump from Fusarium sporotrichioides:: gene isolation and expression in yeast [J].
Alexander, NJ ;
McCormick, SP ;
Hohn, TM .
MOLECULAR AND GENERAL GENETICS, 1999, 261 (06) :977-984
[3]   The ABC transporter AtrB from Aspergillus nidulans mediates resistance to all major classes of fungicides and some natural toxic compounds [J].
Andrade, AC ;
Del Sorbo, G ;
Van Nistelrooy, JGM ;
De Waard, MA .
MICROBIOLOGY-SGM, 2000, 146 :1987-1997
[4]   VARIATIONS IN PLOIDY AMONG ISOLATES OF BOTRYTIS-CINEREA - IMPLICATIONS FOR GENETIC AND MOLECULAR ANALYSES [J].
BUTTNER, P ;
KOCH, F ;
VOIGT, K ;
QUIDDE, T ;
RISCH, S ;
BLAICH, R ;
BRUCKNER, B ;
TUDZYNSKI, P .
CURRENT GENETICS, 1994, 25 (05) :445-450
[5]   A novel multidrug efflux transporter gene of the major facilitator superfamily from Candida albicans (FLU1) conferring resistance to fluconazole [J].
Calabrese, D ;
Bille, J ;
Sanglard, D .
MICROBIOLOGY-UK, 2000, 146 :2743-2754
[6]   CFP, the putative cercosporin transporter of Cercospora kikuchii, is required for wild type cercosporin production, resistance, and virulence on soybean [J].
Callahan, TM ;
Rose, MS ;
Meade, MJ ;
Ehrenshaft, M ;
Upchurch, RG .
MOLECULAR PLANT-MICROBE INTERACTIONS, 1999, 12 (10) :901-910
[7]   Inheritance and mechanisms of resistance to anilinopyrimidine fungicides in Botrytis cinerea (Botryotinia fuckeliana) [J].
Chapeland, F ;
Fritz, R ;
Lanen, C ;
Gredt, M ;
Leroux, P .
PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, 1999, 64 (02) :85-100
[8]  
Coley-Smith J.R., 1980, The Biology of Botrytis
[9]   The photoactivated Cercospora toxin cercosporin:: Contributions to plant disease and fundamental biology [J].
Daub, ME ;
Ehrenshaft, M .
ANNUAL REVIEW OF PHYTOPATHOLOGY, 2000, 38 :461-+
[10]   Botrydial is produced in plant tissues infected by Botrytis cinerea [J].
Deighton, N ;
Muckenschnabel, I ;
Colmenares, AJ ;
Collado, IG ;
Williamson, B .
PHYTOCHEMISTRY, 2001, 57 (05) :689-692