Department of Dermatology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.
Dermatology Hospital of Southern Medical University, Guangzhou, China.
Med Mycol. 2020 Apr 1;58(3):351-361. doi: 10.1093/mmy/myz063.
Talaromyces marneffei (T. marneffei), which used to be known as Penicillium marneffei, is the causative agent of the fatal systemic mycosis known as talaromycosis. For the purpose of understanding the role of methylcitrate cycle in the virulence of T. marneffei, we generated MCD deletion (ΔMCD) and complementation (ΔMCD+) mutants of T. marneffei. Growth in different carbon sources showed that ΔMCD cannot grow on propionate media and grew slowly on the valerate, valine, methionine, isoleucine, cholesterol, and YNB (carbon free) media. The macrophage killing assay showed that ΔMCD was attenuated in macrophages of mice in vitro, especially at the presence of propionate. Finally, virulence studies in a murine infection experiment revealed attenuated virulence of the ΔMCD, which indicates MCD is essential for T. marneffei virulence in the host. This experiment laid the foundation for the further study of the specific mechanisms underlying the methylcitrate cycle of T. marneffei and may provide suitable targets for new antifungals.
马尔尼菲青霉(Talaromyces marneffei),以前被称为 Penicillium marneffei,是一种致命的系统性真菌病——马尔尼菲青霉病的病原体。为了了解甲基柠檬酸循环在马尔尼菲青霉毒力中的作用,我们生成了 T. marneffei 的 MCD 缺失(ΔMCD)和互补(ΔMCD+)突变体。在不同碳源中的生长表明,ΔMCD 不能在丙酸介质中生长,并且在戊酸盐、缬氨酸、蛋氨酸、异亮氨酸、胆固醇和 YNB(无碳)介质中生长缓慢。巨噬细胞杀伤试验表明,ΔMCD 在体外小鼠巨噬细胞中减毒,特别是在存在丙酸的情况下。最后,在小鼠感染实验中的毒力研究表明,ΔMCD 的毒力减弱,这表明 MCD 对 T. marneffei 在宿主中的毒力至关重要。该实验为进一步研究 T. marneffei 甲基柠檬酸循环的具体机制奠定了基础,并可能为新型抗真菌药物提供合适的靶点。