Faculty of Pharmacy, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil; Post-Graduation Program of Cellular and Molecular Biology, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil; Center of Experimental Research, Clinical Hospital of Porto Alegre, Porto Alegre, RS, Brazil.
Center of Experimental Research, Clinical Hospital of Porto Alegre, Porto Alegre, RS, Brazil; Tick-Pathogen Transmission Unit, Laboratory of Bacteriology, National Institute of Allergy and Infectious Diseases, Hamilton, MT, United States.
J Proteomics. 2024 Jan 6;290:105022. doi: 10.1016/j.jprot.2023.105022. Epub 2023 Oct 12.
Cryptococcus gattii is a primary pathogenic fungus that causes pneumonia. This species is also responsible for an outbreak in Vancouver, Canada, and spreading to the mainland and United States. The use of medical devices is often complicated by infections with biofilm-forming microbes with increased resistance to antimicrobial agents and host defense mechanisms. This study investigated the comparative proteome of C. gattii R265 (VGIIa) grown under planktonic and biofilm conditions. A brief comparison with C. neoformans H99 biofilm and the use of different culture medium and surface were also evaluated. Using Multidimensional Protein Identification Technology (MudPIT), 1819 proteins were identified for both conditions, where 150 (8.2%) were considered differentially regulated (up- or down-regulated and unique in biofilm cells). Overall, the proteomic approach suggests that C. gattii R265 biofilm cells are maintained by the induction of electron transport chain for reoxidation, and by alternative energy metabolites, such as succinate and acetate. SIGNIFICANCE: Since C. gattii is considered a primary pathogen and is one of the most virulent and less susceptible to antifungals, understanding how biofilms are maintained is fundamental to search for new targets to control this important mode of growth that is difficult to eradicate.
新生隐球菌是一种主要的致病真菌,可引起肺炎。该物种还导致了加拿大温哥华的一次爆发,并传播到了大陆和美国。医疗器械的使用常常伴随着生物膜形成微生物的感染,这些微生物对抗菌药物和宿主防御机制的抵抗力增强。本研究调查了浮游和生物膜条件下培养的新生隐球菌 R265(VGIIa)的比较蛋白质组。还简要比较了新生隐球菌 H99 生物膜,并使用了不同的培养基和表面。使用多维蛋白质鉴定技术(MudPIT),鉴定了两种条件下的 1819 种蛋白质,其中 150 种(8.2%)被认为是差异调节的(上调或下调,并且在生物膜细胞中是独特的)。总的来说,蛋白质组学方法表明,新生隐球菌 R265 生物膜细胞通过诱导电子传递链进行再氧化以及替代能量代谢物(如琥珀酸和乙酸)来维持。意义:由于新生隐球菌被认为是主要病原体之一,而且是最具毒力和对抗真菌药物的敏感性较低的病原体之一,因此了解生物膜是如何维持的对于寻找新的目标来控制这种难以根除的重要生长方式至关重要。