Sporothrix schenckii complex and sporotrichosis, an emerging health problem

被引:115
作者
Lopez-Romero, Everardo [2 ]
del Rocio Reyes-Montes, Maria [1 ]
Perez-Torres, Armando [1 ]
Ruiz-Baca, Estela [3 ]
Villagomez-Castro, Julio C. [2 ]
Mora-Montes, Hector M. [2 ]
Flores-Carreon, Arturo [2 ]
Toriello, Conchita [1 ]
机构
[1] Univ Nacl Autonoma Mexico, Mexico City 04510, DF, Mexico
[2] Univ Guanajuato, Guanajuato, Mexico
[3] Univ Juarez Estado Durango, Durango, Mexico
关键词
adhesin; emerging mycosis; glucosamine-6-P synthase; protein glycosylation; Sporothrix schenckii; sporotrichosis; RIO-DE-JANEIRO; MITOCHONDRIAL-DNA ANALYSIS; UNITED-STATES EPIDEMIC; CELL-WALL COMPONENTS; CANDIDA-ALBICANS; IN-VITRO; GLUCOSAMINE-6-PHOSPHATE SYNTHASE; BIOCHEMICAL-CHARACTERIZATION; HEXOSAMINE BIOSYNTHESIS; MOLECULAR CHARACTERIZATION;
D O I
10.2217/FMB.10.157
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Sporothrix schenckii, now named the S. schenckii species complex, has largely been known as the etiological agent of sporotrichosis, which is an acute or chronic subcutaneous mycosis of humans and other mammals. Gene sequencing has revealed the following species in the S. schenckii complex: Sporothrix albicans, Sporothrix brasiliensis, Sporothrix globosa, Sporothrix luriel, Sporothrix mexicana and S. schenckii. The increasing number of reports of Sporothrix infection in immunocompromised patients, mainly the HIV-infected population, suggests sporotrichosis as an emerging global health problem concomitant with the AIDS pandemic. Molecular studies have demonstrated a high level of intraspecific variability. Components of the S. schenckii cell wall that act as adhesins and immunogenic inducers, such as a 70-kDa glycoprotein, are apparently specific to this fungus. The main glycan peptidorhamnomannan cell wall component is the only O-linked glycan structure known in S. schenckii. It contains an a-mannobiose core followed by one a-glucuronic acid unit, which may be mono- or di-rhamnosylated. The oligomeric structure of glucosamine-6-P synthase has led to a significant advance in the development of antifungals targeted to the enzyme's catalytic domain in S. schenckii.
引用
收藏
页码:85 / 102
页数:18
相关论文
共 168 条
[1]   Biochemical characterization, membrane association and identification of amino acids essential for the function of Alg11 from Saccharomyces cerevisiae, an α1,2-mannosyltransferase catalysing two sequential glycosylation steps in the formation of the lipid-linked core oligosaccharide [J].
Absmanner, Birgit ;
Schmeiser, Verena ;
Kaempf, Michael ;
Lehle, Ludwig .
BIOCHEMICAL JOURNAL, 2010, 426 :205-217
[2]   Growth conditions influence melanization of Brazilian clinical Sporothrix schenckii isolates [J].
Almeida-Paes, Rodrigo ;
Frases, Susana ;
Fialho Monteiro, Paulo Cezar ;
Gutierrez-Galhardo, Maria Clara ;
Zancope-Oliveira, Rosely Maria ;
Nosanchuk, Joshua D. .
MICROBES AND INFECTION, 2009, 11 (05) :554-562
[3]   NOVEL ANTIGENIC DETERMINANTS FROM PEPTIDORHAMNOMANNANS OF SPOROTHRIX-SCHENCKII [J].
ALVER, LL ;
TRAVASSOS, LR ;
PREVIATO, JO ;
MENDONCAPREVIATO, L .
GLYCOBIOLOGY, 1994, 4 (03) :281-288
[4]   Inhibition of toll-like receptor signaling in primary murine microglia [J].
Aravalli, Rajagopal N. ;
Hu, Shuxian ;
Lokensgard, James R. .
JOURNAL OF NEUROIMMUNE PHARMACOLOGY, 2008, 3 (01) :5-11
[5]  
ARENAS G, 1986, Revista Mexicana de Micologia, V2, P131
[6]  
Arenas R, 2007, INT J DERMATOL, V46, P177
[7]   Different virulence levels of the species of Sporothrix in a murine model [J].
Arrillaga-Moncrieff, I. ;
Capilla, J. ;
Mayayo, E. ;
Marimon, R. ;
Marine, M. ;
Gene, J. ;
Cano, J. ;
Guarro, J. .
CLINICAL MICROBIOLOGY AND INFECTION, 2009, 15 (07) :651-655
[8]   Endoplasmic reticulum (ER) mannosidase I is compartmentalized and required for N-glycan trimming to Man5-6GlcNAc2 in glycoprotein ER-associated degradation [J].
Avezov, Edward ;
Frenkel, Zehavit ;
Ehrlich, Marcelo ;
Herscovics, Annette ;
Lederkremer, Gerardo Z. .
MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (01) :216-225
[9]  
Baroni Adone, 2007, Skinmed, V6, P41, DOI 10.1111/j.1540-9740.2007.05665.x
[10]  
Barros MBD, 2004, CLIN INFECT DIS, V38, P529, DOI 10.1086/381200