Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, 58038 Morelia, Michoacán, Mexico.
Departamento de Genética y Microbiología, Facultad de Biología, Universidad de Murcia, 30100 Murcia, Spain.
Fungal Genet Biol. 2019 Aug;129:40-51. doi: 10.1016/j.fgb.2019.04.011. Epub 2019 Apr 20.
Mucor circinelloides is an etiologic agent of mucormycosis, a fungal infection produced by Mucorales often associated with mortality due to unavailability of antifungal drugs. Arl proteins belong to the Arf family and are involved in vesicle trafficking and tubulin assembly. This study identified two Arl (Arf-like)-encoding genes, arl1 and arl2, in M. circinelloides and explored their function in morphogenesis, virulence, and antifungal susceptibility. Although Arl1 and Arl2 proteins shared 55% amino acid sequence identity, arl1 and arl2 genes showed distinct transcriptional expression patterns. arl1 was expressed at higher levels than arl2 and induced in mycelia, suggesting a role in morphological transitions. Disruption of the arl1 and arl2 genes led to heterokaryon (Δarl1) and homokaryon (Δarl2) genotypes, respectively. The incapacity to generate homokaryon mutants for arl1 suggested that it is essential for growth of M. circinelloides. Deletion of each gene reduced the expression of the other, suggesting the existence of a positive cross-regulation between them. Thus, deletion of arl2 resulted in a ~60% reduction of arl1 expression, whereas the Δarl1 showed ∼90% reduction of arl1 expression. Mutation of arl2 showed no phenotype or a mild phenotype between Δarl1 and wild-type (WT), suggesting that all observed phenotypes in both mutant strains corresponded to arl1 low expression. The Δarl1 produced a small amount of spores that showed increased sensitivity to dodecyl-sulfate and azoles, suggesting a defect in the cell wall that was further supported by decrease in saccharide content. These defects in the cell wall were possibly originated by abnormal vesicle trafficking since FM4-64 staining of both mutants Δarl1 and Δarl2 revealed less well-localized endosomes compared to the WT. Moreover, aberrant vesicle trafficking may be responsible for the secretion of specific virulence-related proteins since cell-free medium from Δarl1 were found to increase killing of Caenorhabditis elegans compared to WT.
卷枝毛霉是毛霉病的病原体,毛霉病是一种由毛霉目真菌引起的真菌感染,由于抗真菌药物的缺乏,通常与死亡率有关。Arl 蛋白属于 Arf 家族,参与囊泡运输和微管组装。本研究在卷枝毛霉中鉴定了两个 Arl(Arf 样)编码基因 arl1 和 arl2,并探讨了它们在形态发生、毒力和抗真菌敏感性中的功能。尽管 Arl1 和 Arl2 蛋白具有 55%的氨基酸序列同一性,但 arl1 和 arl2 基因表现出不同的转录表达模式。arl1 的表达水平高于 arl2,并在菌丝中诱导表达,提示其在形态转变中发挥作用。arl1 和 arl2 基因的缺失分别导致异核体(Δarl1)和同核体(Δarl2)基因型。无法产生 arl1 的同核体突变体表明它对卷枝毛霉的生长是必需的。每个基因的缺失都会降低另一个基因的表达,表明它们之间存在正交叉调节。因此,arl2 的缺失导致 arl1 表达降低约 60%,而 Δarl1 则导致 arl1 表达降低约 90%。arl2 的突变在 Δarl1 和野生型(WT)之间没有表现型或表现出轻度表型,这表明在两个突变株中观察到的所有表型都对应于 arl1 的低表达。Δarl1 产生的孢子数量很少,对十二烷基硫酸钠和唑类药物的敏感性增加,表明细胞壁存在缺陷,糖含量的减少进一步支持了这一观点。细胞壁的这些缺陷可能是由于囊泡运输异常引起的,因为与 WT 相比,两种突变体Δarl1 和Δarl2 的 FM4-64 染色显示内体定位较差。此外,异常的囊泡运输可能是导致特定毒力相关蛋白分泌的原因,因为与 WT 相比,来自Δarl1 的无细胞培养基发现可增加对秀丽隐杆线虫的杀伤作用。