Ninomiya Akihiro, Urayama Syun-Ichi, Suo Rei, Itoi Shiro, Fuji Shin-Ichi, Moriyama Hiromitsu, Hagiwara Daisuke
Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Japan.
Microbiology Research Center for Sustainability, University of Tsukuba, Tsukuba, Japan.
Front Microbiol. 2020 Jul 17;11:1641. doi: 10.3389/fmicb.2020.01641. eCollection 2020.
Fungi are a rich source of natural products with biological activities. In this study, we evaluated viral effects on secondary metabolism of the rice blast fungus using an isolate of APU10-199A co-infected with three types of mycoviruses: a totivirus, a chrysovirus, and a partitivirus. Comparison of the secondary metabolite profile of APU10-199A with that of the strain lacking the totivirus and chrysovirus showed that a mycotoxin tenuazonic (TeA) acid was produced in a manner dependent on the mycoviruses. Virus reinfection experiments verified that TeA production was dependent on the totivirus. Quantitative reverse transcription PCR and RNA-sequencing analysis indicated the regulatory mechanism underlying viral induction of TeA: the totivirus activates the TeA synthetase gene by upregulating the transcription of the gene encoding a Zn(II)-Cys-type transcription factor, . To our knowledge, this is the first report that confirmed mycovirus-associated regulation of secondary metabolism at a transcriptional level by viral reinfection. Because only treatment with dimethyl sulfoxide has been reported to trigger TeA production in this fungus without gene manipulation, our finding highlights the potential of mycoviruses as an epigenomic regulator of fungal secondary metabolism.
真菌是具有生物活性的天然产物的丰富来源。在本研究中,我们使用与三种类型的真菌病毒(一种双链RNA病毒、一种黄病毒和一种分体病毒)共同感染的APU10 - 199A分离株,评估了病毒对稻瘟病菌次生代谢的影响。将APU10 - 199A的次生代谢产物谱与缺乏双链RNA病毒和黄病毒的菌株的次生代谢产物谱进行比较,结果表明,一种霉菌毒素细交链孢菌酮酸(TeA)的产生方式依赖于真菌病毒。病毒再感染实验证实,TeA的产生依赖于双链RNA病毒。定量逆转录PCR和RNA测序分析表明了病毒诱导TeA的调控机制:双链RNA病毒通过上调编码Zn(II)-Cys型转录因子的基因的转录来激活TeA合成酶基因。据我们所知,这是第一份通过病毒再感染在转录水平上证实真菌病毒对次生代谢进行调控的报告。因为据报道,在这种真菌中,仅用二甲基亚砜处理可在不进行基因操作的情况下触发TeA的产生,我们的发现突出了真菌病毒作为真菌次生代谢的表观基因组调节剂的潜力。