UMR1331 TOXALIM, French National Institute for Agricultural Research, INP, UPS, Toulouse, France.
PLoS One. 2012;7(2):e29906. doi: 10.1371/journal.pone.0029906. Epub 2012 Feb 3.
Inhalation of Aspergillus fumigatus conidia can cause severe aspergillosis in immunosuppressed people. A. fumigatus produces a large number of secondary metabolites, some of which are airborne by conidia and whose toxicity to the respiratory tract has not been investigated. We found that spores of A. fumigatus contain five main compounds, tryptoquivaline F, fumiquinazoline C, questin, monomethylsulochrin and trypacidin. Fractionation of culture extracts using RP-HPLC and LC-MS showed that samples containing questin, monomethylsulochrin and trypacidin were toxic to the human A549 lung cell line. These compounds were purified and their structure verified using NMR in order to compare their toxicity against A549 cells. Trypacidin was the most toxic, decreasing cell viability and triggering cell lysis, both effects occurring at an IC₅₀ close to 7 µM. Trypacidin toxicity was also observed in the same concentration range on human bronchial epithelial cells. In the first hour of exposure, trypacidin initiates the intracellular formation of nitric oxide (NO) and hydrogen peroxide (H₂O₂). This oxidative stress triggers necrotic cell death in the following 24 h. The apoptosis pathway, moreover, was not involved in the cell death process as trypacidin did not induce apoptotic bodies or a decrease in mitochondrial membrane potential. This is the first time that the toxicity of trypacidin to lung cells has been reported.
吸入烟曲霉分生孢子可导致免疫抑制人群发生严重的曲霉病。烟曲霉产生大量的次生代谢产物,其中一些由分生孢子释放到空气中,其对呼吸道的毒性尚未得到研究。我们发现烟曲霉孢子含有五种主要化合物,即 tryptoquivaline F、fumiquinazoline C、questin、monomethylsulochrin 和 trypacidin。使用反相高效液相色谱法(RP-HPLC)和液质联用(LC-MS)对培养提取物进行分级,结果表明含有 questin、monomethylsulochrin 和 trypacidin 的样品对人 A549 肺细胞系具有毒性。这些化合物被分离纯化并用 NMR 确定其结构,以比较它们对 A549 细胞的毒性。Trypacidin 的毒性最强,可降低细胞活力并引发细胞裂解,这两种作用均发生在接近 7 µM 的 IC₅₀。在相同的浓度范围内,Trypacidin 对人支气管上皮细胞也具有毒性。在暴露的最初 1 小时内,Trypacidin 引发细胞内形成一氧化氮(NO)和过氧化氢(H₂O₂)。这种氧化应激在接下来的 24 小时内引发坏死性细胞死亡。此外,凋亡途径并未参与细胞死亡过程,因为 Trypacidin 不会诱导凋亡小体或线粒体膜电位降低。这是首次报道 Trypacidin 对肺细胞的毒性。