Toopaang Wachiraporn, Phonghanpot Suranat, Punya Juntira, Panyasiri Cheerapha, Klamchao Kewarin, Wasuwan Rudsamee, Srisuksam Chettida, Sangsrakru Duangjai, Sonthirod Chutima, Tangphatsornruang Sithichoke, Tanticharoen Morakot, Amnuaykanjanasin Alongkorn
National Center for Genetic Engineering and Biotechnology, National Science and Technology Development Agency, 113 Paholyothin Road, Klong 1, Klong Luang, Pathumthani 12120, Thailand.
School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok 10140, Thailand.
Fungal Biol. 2017 Aug;121(8):664-675. doi: 10.1016/j.funbio.2017.04.007. Epub 2017 May 6.
The reducing clade III polyketide synthase genes, including pks15, are highly conserved among entomopathogenic fungi. To examine the function of pks15, we used targeted disruption to investigate the impact of Beauveria bassiana pks15 on insect pathogenesis. Southern analysis verified that the Δpks15 mutant was disrupted by a single integration of the transformation cassette at the pks15 locus. The Δpks15 mutant had a slight reduction in radial growth, and it produced fewer spores. Our insect bioassays indicated the Δpks15 mutant to be significantly reduced in virulence against beet armyworms compared to wild type (WT), which could be partially accounted for by its markedly decreased ability to survive phagocytosis. Total haemocyte count decreased sharply by 50-fold from days 1-3 post-inoculation in insects infected with WT, compared to a 5-fold decrease in the Δpks15 mutant. The mutant also produced fewer hemolymph hyphal bodies than WT by 3-fold. In co-culture studies with amoebae that have phagocytic ability similar to that of insect haemocytes, at 48 h the mortality rate of amoebae engulfing Δpks15 decreased by 72 %, and Δpks15 CFU decreased by 83 % compared to co-culture with WT. Thus, the Δpks15 mutant had a reduced ability to cope with phagocytosis and highly reduced virulence in an insect host. These data elucidate a mechanism of insect pathogenesis associated with polyketide biosynthesis.
包括pks15在内的还原性进化枝III聚酮合酶基因在昆虫病原真菌中高度保守。为了研究pks15的功能,我们使用靶向破坏来研究球孢白僵菌pks15对昆虫致病作用的影响。Southern分析证实,Δpks15突变体在pks15基因座处通过转化盒的单整合而被破坏。Δpks15突变体的径向生长略有降低,并且产生的孢子较少。我们的昆虫生物测定表明,与野生型(WT)相比,Δpks15突变体对甜菜夜蛾的毒力显著降低,这可能部分归因于其吞噬作用存活能力的明显下降。与感染WT的昆虫相比,接种后第1 - 3天,总血细胞计数急剧下降50倍,而Δpks15突变体下降了5倍。该突变体产生的血淋巴菌丝体也比WT少3倍。在与具有与昆虫血细胞相似吞噬能力的变形虫的共培养研究中,在48小时时,吞噬Δpks15的变形虫死亡率降低了72%,与与WT共培养相比,Δpks15的CFU减少了83%。因此,Δpks15突变体应对吞噬作用的能力降低,并且在昆虫宿主中的毒力大大降低。这些数据阐明了与聚酮生物合成相关的昆虫致病机制。