Sporothrix schenckii complex and sporotrichosis, an emerging health problem. (January 2011)

• Record Type: Journal Article
• Authors: López-Romero, Everardo; Reyes-Montes, María del Rocío; Pérez-Torres, Armando; Ruiz-Baca, Estela; Villagómez-Castro, Julio C; Mora-Montes, Héctor M; Flores-Carreón, Arturo; Toriello, Conchita
• Is Part Of: Future microbiology. Volume 6:Number 1(2011)
• Page Start: 85
• Page End: 102
• Publication Date: 2011-01
• Subjects: adhesin -- emerging mycosis -- glucosamine-6-P synthase -- protein glycosylation -- Sporothrix schenckii -- sporotrichosis; Microbiology -- Research -- Periodicals; 616.9041
• DOI: 10.2217/fmb.10.157
• Languages: English
• ISSNs: 1746-0913

Abstract

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 luriei, 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 α-mannobiose core followed by one α-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 .