Department of Microbiology and Molecular Genetics, McGovern Medical School, The University of Texas Health Science Center, Houston, Texas, USA.
Department of Microbiology and Molecular Genetics, McGovern Medical School, The University of Texas Health Science Center, Houston, Texas, USA
Infect Immun. 2020 Apr 20;88(5). doi: 10.1128/IAI.00763-19.
Nutrient acquisition is a central challenge for all organisms. For the fungal pathogen , utilization of amino acids has been shown to be critical for survival, immune evasion, and escape, while the importance of catabolism of host-derived proteins and peptides is less well understood. Stp1 and Stp2 are paralogous transcription factors (TFs) regulated by the sy1-tr3-sy5 (SPS) amino acid sensing system and have been proposed to have distinct, if uncertain, roles in protein and amino acid utilization. We show here that Stp1 is required for proper utilization of peptides but has no effect on amino acid catabolism. In contrast, Stp2 is critical for utilization of both carbon sources. Commensurate with this observation, we found that Stp1 controls a very limited set of genes, while Stp2 has a much more extensive regulon that is partly dependent on the Ssy1 amino acid sensor (amino acid uptake and catabolism) and partly Ssy1 independent (genes associated with filamentous growth, including the regulators and ). The Δ/Δ and Δ/Δ mutants showed reduced fitness in a gastrointestinal (GI) colonization model, yet induced greater damage to epithelial cells and macrophages in a manner that was highly dependent on the growth status of the fungal cells. Surprisingly, the Δ/Δ mutant was better able to colonize the gut but the mutation had no effect on host cell damage. Thus, proper protein and amino acid utilization are both required for normal host interaction and are controlled by an interrelated network that includes Stp1 and Stp2.
营养物质的获取是所有生物面临的核心挑战。对于真菌病原体来说,利用氨基酸对于生存、免疫逃避和逃逸至关重要,而宿主来源的蛋白质和肽的分解代谢的重要性则知之甚少。Stp1 和 Stp2 是由 sy1-tr3-sy5(SPS)氨基酸感应系统调控的同源转录因子(TFs),它们在蛋白质和氨基酸利用方面可能具有不同但不确定的作用。我们在这里表明,Stp1 是正确利用肽所必需的,但对氨基酸分解代谢没有影响。相比之下,Stp2 对两种碳源的利用都至关重要。与这一观察结果一致,我们发现 Stp1 控制着非常有限的一组基因,而 Stp2 具有更广泛的调控组,部分依赖于 Ssy1 氨基酸传感器(氨基酸摄取和分解代谢),部分独立于 Ssy1(与丝状生长相关的基因,包括调节剂 和 )。Δ/Δ 和 Δ/Δ 突变体在胃肠道(GI)定植模型中表现出较低的适应性,但以高度依赖真菌细胞生长状态的方式对上皮细胞和巨噬细胞造成更大的损伤。令人惊讶的是,Δ/Δ 突变体能够更好地定植肠道,但该突变对宿主细胞损伤没有影响。因此,适当的蛋白质和氨基酸利用对于正常的宿主相互作用都是必需的,并且受到包括 Stp1 和 Stp2 在内的相互关联的网络的控制。