The developmentally regulated alb1 gene of Aspergillus fumigatus:: Its role in modulation of conidial morphology and virulence

被引:270
作者
Tsai, HF
Chang, YC
Washburn, RG
Wheeler, MH
Kwon-Chung, KJ
机构
[1] NIAID, Clin Invest Lab, NIH, Bethesda, MD 20892 USA
[2] Wake Forest Univ, Sch Med, Dept Internal Med, Infect Dis Sect, Winston Salem, NC 27006 USA
[3] USDA ARS, Cotton Pathol Res Unit, So Crops Res Lab, College Stn, TX 77845 USA
关键词
D O I
10.1128/JB.180.12.3031-3038.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Aspergillus fumigatus, an important opportunistic pathogen which commonly affects neutropenic patients, produces conidia with a bluish-green color. We identified a gene, alb1, which is required for conidial pigmentation. The alb1 gene encodes a putative polyketide synthase, and disruption of alb1 resulted in an albino conidial phenotype. Expression of alb1 is developmentally regulated, and the 7-kb transcript is detected only during the conidiation stage. The alb1 mutation was found to block 1,3,6,8-tetrahydroxynaphthalene production, indicating that alb1 is involved in dihydroxynaphthalene-melanin biosynthesis. Scanning electron microscopy studies showed that the alb1 disruptant exhibited a smooth conidial surface, whereas complementation of the alb1 deletion restored the echinulate wild-type surface. Disruption of alb1 resulted in a significant increase in C3 binding on conidial surfaces, and the conidia of the alb1 disruptant were ingested by human neutrophils at a higher rate than were those of the wild type. The alb1-complemented strain producing bluish-green conidia exhibited inefficient C3 binding and neutrophil-mediated phagocytosis quantitatively similar to those of the wild type. Importantly, the alb1 disruptant had a statistically significant loss of virulence compared to the wild-type and alb1-complemented strains in a murine model. These results suggest that disruption of alb1 causes pleiotropic effects on conidial morphology and fungal virulence.
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页码:3031 / 3038
页数:8
相关论文
共 69 条
[41]   ISOLATION, CHARACTERIZATION, AND CLONING OF CDNA AND THE GENE FOR AN ELASTINOLYTIC SERINE PROTEINASE FROM ASPERGILLUS-FLAVUS [J].
RAMESH, MV ;
SIRAKOVA, T ;
KOLATTUKUDY, PE .
INFECTION AND IMMUNITY, 1994, 62 (01) :79-85
[42]  
RAPER KB, 1965, GENUS ASPERGILLUS, P238
[43]   Effect of the laccase gene, CNLAC1, on virulence of Cryptococcus neoformans [J].
Salas, SD ;
Bennett, JE ;
KwonChung, KJ ;
Perfect, JR ;
Williamson, PR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (02) :377-386
[44]  
Sambrook J., 1989, MOL CLONING
[45]  
Silar P., 1995, Fungal Genet. Rep, V42, P73, DOI [10.4148/1941-4765.1353, DOI 10.4148/1941-4765.1353]
[46]   VIRULENCE OF ASPERGILLUS-FUMIGATUS DOUBLE MUTANTS LACKING RESTRICTOCIN AND AN ALKALINE PROTEASE IN A LOW-DOSE MODEL OF INVASIVE PULMONARY ASPERGILLOSIS [J].
SMITH, JM ;
TANG, CM ;
VANNOORDEN, S ;
HOLDEN, DW .
INFECTION AND IMMUNITY, 1994, 62 (12) :5247-5254
[47]   CONSTRUCTION AND PATHOGENICITY OF ASPERGILLUS-FUMIGATUS MUTANTS THAT DO NOT PRODUCE THE RIBOTOXIN RESTRICTOCIN [J].
SMITH, JM ;
DAVIES, JE ;
HOLDEN, DW .
MOLECULAR MICROBIOLOGY, 1993, 9 (05) :1071-1077
[48]   DEWA ENCODES A FUNGAL HYDROPHOBIN COMPONENT OF THE ASPERGILLUS SPORE WALL [J].
STRINGER, MA ;
TIMBERLAKE, WE .
MOLECULAR MICROBIOLOGY, 1995, 16 (01) :33-44
[49]   INTERACTIONS BETWEEN CONIDIA OF ASPERGILLUS-FUMIGATUS AND HUMAN-COMPLEMENT COMPONENT-C3 [J].
STURTEVANT, JE ;
LATGE, JP .
INFECTION AND IMMUNITY, 1992, 60 (05) :1913-1918
[50]   STRUCTURAL-ANALYSIS OF PKS1, A POLYKETIDE SYNTHASE GENE INVOLVED IN MELANIN BIOSYNTHESIS IN COLLETOTRICHUM-LAGENARIUM [J].
TAKANO, Y ;
KUBO, Y ;
SHIMIZU, K ;
MISE, K ;
OKUNO, T ;
FURUSAWA, I .
MOLECULAR & GENERAL GENETICS, 1995, 249 (02) :162-167