Yong H Y, Bakar F D A, Illias R M, Mahadi N M, Murad A M A
School of Biosciences and Biotechnology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Selangor, Malaysia.
Department of Bioprocess Engineering, Faculty of Chemical and Natural Resources Engineering, Universiti Teknologi Malaysia, Skudai, Johor, Malaysia.
Braz J Microbiol. 2014 Mar 10;44(4):1241-50. doi: 10.1590/s1517-83822013000400031. eCollection 2013 Dec.
The mitogen-activated protein (MAP) kinase pathways has been implicated in the pathogenicity of various pathogenic fungi and plays important roles in regulating pathogenicity-related morphogenesis. This work describes the isolation and characterization of MAP kinase gene, Cgl-SLT2, from Colletotrichum gloeosporioides. A DNA sequence, including 1,633 bp of Cgl-SLT2 open-reading frame and its promoter and terminator regions, was isolated via DNA walking and cloned. To analyze gene function, a gene disruption cassette containing hygromycin-resistant gene was constructed, and Cgl-SLT2 was inactivated via gene deletion. Analysis on Cgl-slt2 mutant revealed a defect in vegetative growth and sporulation as compared to the wild-type strain. When grown under nutrient-limiting conditions, hyperbranched hyphal morphology was observed in the mutant. Conidia induction for germination on rubber wax-coated hard surfaces revealed no differences in the percentage of conidial germination between the wild-type and Cgl-slt2 mutant. However, the percentage of appressorium formation in the mutant was greatly reduced. Bipolar germination in the mutant was higher than in the wild-type at 8-h post-induction. A pathogenicity assay revealed that the mutant was unable to infect either wounded or unwounded mangoes. These results suggest that the Cgl-SLT2 MAP kinase is required for C. gloeosporioides conidiation, polarized growth, appressorium formation and pathogenicity.
丝裂原活化蛋白(MAP)激酶途径与多种致病真菌的致病性有关,并在调节致病性相关的形态发生中发挥重要作用。本研究描述了从胶孢炭疽菌中分离和鉴定MAP激酶基因Cgl-SLT2的过程。通过染色体步移法分离并克隆了一段包含Cgl-SLT2开放阅读框1633 bp及其启动子和终止子区域的DNA序列。为了分析基因功能,构建了一个含有潮霉素抗性基因的基因敲除盒,并通过基因缺失使Cgl-SLT2失活。对Cgl-slt2突变体的分析表明,与野生型菌株相比,其在营养生长和孢子形成方面存在缺陷。在营养限制条件下生长时,突变体中观察到菌丝形态高度分支。在涂有橡胶蜡的硬表面上诱导分生孢子萌发,结果显示野生型和Cgl-slt2突变体之间的分生孢子萌发率没有差异。然而,突变体中附着胞形成的百分比大大降低。诱导8小时后,突变体中的双极萌发高于野生型。致病性测定表明,该突变体无法感染受伤或未受伤的芒果。这些结果表明,Cgl-SLT2 MAP激酶是胶孢炭疽菌分生孢子形成、极性生长、附着胞形成和致病性所必需的。