Baker Lorina G, Specht Charles A, Lodge Jennifer K
Department of Molecular Microbiology, Washington University School of Medicine, 660 S. Euclid Avenue, Campus Box 8230, St. Louis, MO 63104, USA.
Eukaryot Cell. 2009 Nov;8(11):1692-705. doi: 10.1128/EC.00227-09. Epub 2009 Sep 4.
Cryptococcus neoformans is an opportunistic pathogen that mainly infects immunocompromised individuals. The fungal cell wall of C. neoformans is an excellent target for antifungal therapies since it is an essential organelle that provides cell structure and integrity. Importantly, it is needed for localization or attachment of known virulence factors, including melanin, phospholipase, and the polysaccharide capsule. The polysaccharide fraction of the cryptococcal cell wall is a complex structure composed of chitin, chitosan, and glucans. Chitin is an indispensable component of many fungal cell walls that contributes significantly to cell wall strength and integrity. Fungal cell walls are very dynamic, constantly changing during cell division and morphogenesis. Hydrolytic enzymes, such as chitinases, have been implicated in the maintenance of cell wall plasticity and separation of the mother and daughter cells at the bud neck during vegetative growth in yeast. In C. neoformans we identified four predicted endochitinases, CHI2, CHI21, CHI22, and CHI4, and a predicted exochitinase, hexosaminidase, HEX1. Enzymatic analysis indicated that Chi2, Chi22, and Hex1 actively degraded chitinoligomeric substrates. Chi2 and Hex1 activity was associated mostly with the cellular fraction, and Chi22 activity was more prominent in the supernatant. The enzymatic activity of Hex1 increased when grown in media containing only N-acetylglucosamine as a carbon source, suggesting that its activity may be inducible by chitin degradation products. Using a quadruple endochitinase deletion strain, we determined that the endochitinases do not affect the growth or morphology of C. neoformans during asexual reproduction. However, mating assays indicated that Chi2, Chi21, and Chi4 are each involved in sexual reproduction. In summary, the endochitinases were found to be dispensable for routine vegetative growth but not sexual reproduction.
新型隐球菌是一种机会性致病病原体,主要感染免疫功能低下的个体。新型隐球菌的真菌细胞壁是抗真菌治疗的理想靶点,因为它是一种重要的细胞器,可提供细胞结构和完整性。重要的是,它是已知毒力因子(包括黑色素、磷脂酶和多糖荚膜)定位或附着所必需的。隐球菌细胞壁的多糖部分是一种由几丁质、壳聚糖和葡聚糖组成的复杂结构。几丁质是许多真菌细胞壁中不可或缺的成分,对细胞壁的强度和完整性有重要贡献。真菌细胞壁非常动态,在细胞分裂和形态发生过程中不断变化。水解酶,如几丁质酶,参与维持细胞壁的可塑性,并在酵母营养生长期间在芽颈处分离母细胞和子细胞。在新型隐球菌中,我们鉴定出四种预测的内切几丁质酶CHI2、CHI21、CHI22和CHI4,以及一种预测的外切几丁质酶己糖胺酶HEX1。酶活性分析表明,Chi2、Chi22和Hex1可有效降解几丁质寡聚底物。Chi2和Hex1的活性主要与细胞部分相关,而Chi22的活性在上清液中更为突出。当在仅含有N-乙酰葡糖胺作为碳源的培养基中生长时,Hex1的酶活性增加,这表明其活性可能受几丁质降解产物诱导。使用四重重组内切几丁质酶缺失菌株,我们确定内切几丁质酶在无性繁殖过程中不影响新型隐球菌的生长或形态。然而,交配试验表明,Chi2、Chi21和Chi4各自参与有性繁殖。总之,发现内切几丁质酶对于常规营养生长并非必需,但对有性繁殖是必需的。