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RNA-seq analyses of gene expression in the microsclerotia of Verticillium dahliae

机译:黄萎病菌小核盘菌基因表达的RNA-seq分析

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Background The soilborne fungus, Verticillium dahliae, causes Verticillium wilt disease in plants. Verticillium wilt is difficult to control since V. dahliae is capable of persisting in the soil for 10 to 15 years as melanized microsclerotia, rendering crop rotation strategies for disease control ineffective. Microsclerotia of V. dahliae overwinter and germinate to produce infectious hyphae that give rise to primary infections. Consequently, microsclerotia formation, maintenance, and germination are critically important processes in the disease cycle of V. dahliae. Results To shed additional light on the molecular processes that contribute to microsclerotia biogenesis and melanin synthesis in V. dahliae, three replicate RNA-seq libraries were prepared from 10?day-old microsclerotia (MS)-producing cultures of V. dahliae, strain VdLs.17 (average?=?52.23 million reads), and those not producing microsclerotia (NoMS, average?=?50.58 million reads). Analyses of these libraries for differential gene expression revealed over 200 differentially expressed genes, including up-regulation of melanogenesis-associated genes tetrahydroxynaphthalene reductase (344-fold increase) and scytalone dehydratase (231-fold increase), and additional genes located in a 48.8 kilobase melanin biosynthetic gene cluster of strain VdLs.17. Nearly 50% of the genes identified as differentially expressed in the MS library encode hypothetical proteins. Additional comparative analyses of gene expression in V. dahliae, under growth conditions that promote or preclude microsclerotial development, were conducted using a microarray approach with RNA derived from V. dahliae strain Dvd-T5, and from the amicrosclerotial vdh1 strain. Differential expression of selected genes observed by RNA-seq or microarray analysis was confirmed using RT-qPCR or Northern hybridizations. Conclusion Collectively, the data acquired from these investigations provide additional insight into gene expression and molecular processes that occur during MS biogenesis and maturation in V. dahliae. The identified gene products could therefore potentially represent new targets for disease control through prevention of survival structure development.
机译:背景技术土壤传播的真菌黄萎病菌在植物中引起黄萎病。黄萎病很难控制,因为大黄弧菌能够像黑色素菌核一样在土壤中保持10至15年,使作物轮作策略无法有效控制疾病。大丽花弧菌的菌核越冬并发芽产生感染菌丝,从而引起原发感染。因此,小核盘菌的形成,维持和萌发是大疱弧菌病周期中至关重要的过程。结果为进一步揭示有助于大隐孢子虫微菌核的生物发生和黑色素合成的分子过程,从10天大的小枝菌核(MS)产生的VdLs菌株中,制备了三个重复的RNA-seq文库。 0.17(平均?=?5,223万次读取),以及那些不产生微核硬化症(NoMS,平均?=?5,058万读取)。对这些基因库中差异基因表达的分析揭示了200多种差异表达基因,包括黑色素生成相关基因四羟基萘还原酶(增加了344倍)和鞘氨醇脱水酶(增加了231倍)的上调,以及位于48.8 kb内的其他基因VdLs菌株黑色素生物合成基因簇17。在MS文库中鉴定为差异表达的基因中,近50%编码假想蛋白质。使用微阵列方法,利用衍生自大隐孢子虫菌株Dvd-T5和非微囊病vdh1菌株的RNA的微阵列方法,在促进或排除微菌核发育的生长条件下,进行了大丽菌基因表达的其他比较分析。使用RT-qPCR或Northern杂交证实了通过RNA-seq或微阵列分析观察到的所选基因的差异表达。结论总的来说,从这些调查中获得的数据为V. dahliae的MS生物发生和成熟过程中发生的基因表达和分子过程提供了更多的见解。因此,通过预防存活结构的发展,鉴定出的基因产物可能潜在地代表了疾病控制的新目标。

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