Prasanna Honnavar, Arunaloke Chakrabarti, Jillwin Joseph, Sheetal Thakur, Sunil Dogra, P V M Lakshmi, Shivaprakash M Rudramurthy
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In total, 154 isolates representing M. globosa (n = 85), M. restricta (n = 55), and M. arunalokei (n = 14) from lesional/non-lesional areas of SD/D patients and healthy controls residing in the rural (n = 77) and urban (n = 77) areas of northern India were included. A strategy based on the FAFLP methodology was developed using two endonuclease enzymes (EcoRI and HindIII). M. globosa, M. restricta, and M. arunalokei formed 11, 3, and 2 FAFLP clusters, respectively. Disease-specific strains of M. restricta and M. arunalokei preferentially tend to cause SD/D. M. restricta and M. arunalokei showed less genetic variation. M.globosa showed higher genetic diversity. FAFLP clusters revealed the existence of geographically specific strains in M. restricta, M. arunalokei, and M. globosa. 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引用次数: 0
摘要
马拉色菌是一种共生菌,有时会在各种因素的影响下成为致病菌。有几种马拉色菌很难培养,因此传统的鉴定方法具有挑战性。与脂溢性皮炎/头皮屑(SD/D)相关的马拉色菌的分子分型问题是由于无法获得这些快速培养的酵母菌。本研究的目的是调查荧光扩增片段长度多态性(FAFLP)基因型、疾病状态(SD/D)与 M. globosa、M. restricta 和 M. arunalokei 的地理分布之间的关联。研究共纳入了 154 个分离株,分别代表 M. globosa(n = 85)、M. restricta(n = 55)和 M. arunalokei(n = 14),这些分离株来自 SD/D 患者的病变/非病变区域,以及居住在印度北部农村(n = 77)和城市(n = 77)地区的健康对照组。使用两种内切酶(EcoRI 和 HindIII)制定了基于 FAFLP 方法的策略。M.globosa、M.restricta 和 M.arunalokei 分别形成了 11 个、3 个和 2 个 FAFLP 簇。M. restricta 和 M. arunalokei 的疾病特异性菌株更倾向于引起 SD/D。M. restricta 和 M. arunalokei 的遗传变异较小。M.globosa的遗传多样性较高。FAFLP 群显示,M. restricta、M. arunalokei 和 M. globosa 中存在地理特异性菌株。我们的研究结果表明,某些马拉色菌菌株不仅具有疾病特异性,而且还具有地域差异性。
Molecular epidemiology of seborrheic dermatitis/dandruff associated Malassezia species from northern India.
Malassezia is a commensal that sometimes becomes pathogenic under the influence of diverse factors. Several species of Malassezia are difficult to culture, making traditional methods of identification challenging. The problem with molecular typing of Malassezia in association with seborrheic dermatitis/dandruff (SD/D) arises due to the unavailability of these fastidious yeast cultures. The aim of the study was to investigate the association between fluorescent amplified fragment length polymorphism (FAFLP) genotypes, disease state (SD/D), and the geographic distribution of M. globosa, M. restricta, and M. arunalokei. In total, 154 isolates representing M. globosa (n = 85), M. restricta (n = 55), and M. arunalokei (n = 14) from lesional/non-lesional areas of SD/D patients and healthy controls residing in the rural (n = 77) and urban (n = 77) areas of northern India were included. A strategy based on the FAFLP methodology was developed using two endonuclease enzymes (EcoRI and HindIII). M. globosa, M. restricta, and M. arunalokei formed 11, 3, and 2 FAFLP clusters, respectively. Disease-specific strains of M. restricta and M. arunalokei preferentially tend to cause SD/D. M. restricta and M. arunalokei showed less genetic variation. M.globosa showed higher genetic diversity. FAFLP clusters revealed the existence of geographically specific strains in M. restricta, M. arunalokei, and M. globosa. Our findings suggest that certain Malassezia strains are not only disease-specific but also geographically distinct.
期刊介绍:
Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.