Kottom Theodore J, Limper Andrew H
Thoracic Diseases Research Unit, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Infect Immun. 2004 Aug;72(8):4628-36. doi: 10.1128/IAI.72.8.4628-4636.2004.
Pneumocystis species remain an important cause of life-threatening pneumonia in immunocompromised hosts, including those with AIDS. Responses of the organism to environmental cues both within the lung and elsewhere have been poorly defined. Herein, we report the identification of a cell wall biosynthesis kinase gene (CBK1) homologue in Pneumocystis carinii, isolated by differential display PCR, that is expressed optimally at physiological pH (7 to 8) as opposed to more acidic environments. Expression of Pneumocystis CBK1 was also induced by contact with lung epithelial cells and extracellular matrix. Translation of this gene revealed extensive homology to other fungal CBK1 kinases. Pneumocystis CBK1 expression was equal in the cyst and trophic life forms of the organisms. We further demonstrate that Pneumocystis CBK1 expressed in cbk1 Delta Saccharomyces cerevisiae cells restored defective cell wall separation during proliferation. Consistent with this, Pneumocystis CBK1 expression also stimulated transcription of the CTS1 chitinase in cbk1 Delta mutant yeast cells, an event necessary for cell wall separation. In addition, Pneumocystis CBK1 cDNA supported normal mating projection formation in response to alpha-factor in the cbk1 Delta yeast cells. Site-directed mutations of serine-303 and threonine-494, potential regulatory phosphorylation sites in Pneumocystis CBK1, abolished mating projection formation, indicating a role for these amino acid residues in CBK1 activity. These findings indicate that Pneumocystis CBK1 is an environmentally responsive gene that may function in signaling pathways necessary for cell growth and mating.
肺孢子菌属仍然是免疫功能低下宿主(包括艾滋病患者)中危及生命的肺炎的重要病因。该生物体对肺内及其他部位环境信号的反应一直未得到充分阐明。在此,我们报告通过差异显示PCR分离出卡氏肺孢子菌中一个细胞壁生物合成激酶基因(CBK1)的同源物,该基因在生理pH值(7至8)下而非更酸性环境中表达最佳。肺孢子菌CBK1的表达也可由与肺上皮细胞和细胞外基质接触诱导。该基因的翻译产物显示与其他真菌CBK1激酶有广泛同源性。肺孢子菌CBK1在该生物体的包囊和滋养体生命形式中的表达相同。我们进一步证明,在cbk1Δ酿酒酵母细胞中表达的肺孢子菌CBK1可恢复增殖过程中有缺陷的细胞壁分离。与此一致的是,肺孢子菌CBK1的表达还刺激了cbk1Δ突变酵母细胞中CTS1几丁质酶的转录,这是细胞壁分离所必需的事件。此外,肺孢子菌CBK1 cDNA支持cbk1Δ酵母细胞对α因子作出正常的交配突起形成反应。肺孢子菌CBK1中潜在的调节性磷酸化位点丝氨酸-303和苏氨酸-494的定点突变消除了交配突起的形成,表明这些氨基酸残基在CBK1活性中起作用。这些发现表明,肺孢子菌CBK1是一个对环境有反应的基因,可能在细胞生长和交配所需的信号通路中发挥作用。