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猕猴桃溃疡病菌丁香假单胞菌猕猴桃致病变种5的基因组分析。

Genome analysis of the kiwifruit canker pathogen Pseudomonas syringae pv. actinidiae biovar 5.

作者信息

Fujikawa Takashi, Sawada Hiroyuki

机构信息

NARO Institute of Fruit Tree Science, National Agriculture and Food Research Organization (NARO), Fujimoto 2-1, Tsukuba, Ibaraki 305-8605, Japan.

National Institute of Agrobiological Sciences, Kannondai 2-1-2, Tsukuba, Ibaraki 305-8602, Japan.

出版信息

Sci Rep. 2016 Feb 19;6:21399. doi: 10.1038/srep21399.

Abstract

Pseudomonas syringae pv. actinidiae (Psa) is a destructive pathogen of kiwifruit bacterial canker disease, causing severe economic losses to kiwifruit industry worldwide. Biovar 5 is the most recently reported biovar of Psa, and is found in only a local area of Japan at present. There is not much information of genetic characteristics of biovar 5. Thus, the genome of biovar 5 was sequenced and analyzed to clarify its detailed genetic characteristics. Here, the genomes of strain MAFF 212056 and MAFF 212061 of biovar 5 were estimated to be about 6.3 Mbp and 6.5 Mbp, respectively, and their phylogenetic positions were proved to be near that of biovar 2 in the phylogenetic tree. However, it was confirmed that biovar 5 had neither the coronatine biosynthetic genes conserved in biovar 2, its phylogenetic neighbor, nor the phaseolotoxin biosynthetic genes conserved in biovar 1, Japanese native pathogen. In addition, 45 genes of type III secreted effectors were identified in biovar 5 genomes, showing that their composition is different from that in the other biovars. Moreover, some biovar 5-specific regions were identified. Then, biovar 5-specific PCR primers for targeting these regions were designed, and proved to be applicable for detecting biovar 5 specifically.

摘要

猕猴桃溃疡病菌(Pseudomonas syringae pv. actinidiae,简称Psa)是猕猴桃细菌性溃疡病的一种毁灭性病原菌,给全球猕猴桃产业造成了严重的经济损失。生物变种5是最近报道的Psa生物变种,目前仅在日本局部地区发现。关于生物变种5的遗传特征信息不多。因此,对生物变种5的基因组进行了测序和分析,以阐明其详细的遗传特征。在此,生物变种5的MAFF 212056和MAFF 212061菌株的基因组估计分别约为630万碱基对和650万碱基对,并且在系统发育树中它们的系统发育位置被证明与生物变种2接近。然而,已证实生物变种5既没有在其系统发育邻种生物变种2中保守的冠毒素生物合成基因,也没有在日本本土病原菌生物变种1中保守的菜豆毒素生物合成基因。此外,在生物变种5的基因组中鉴定出45个III型分泌效应子基因,表明它们的组成与其他生物变种不同。而且,鉴定出了一些生物变种5特有的区域。然后,针对这些区域设计了生物变种5特异性PCR引物,并证明可用于特异性检测生物变种5。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2ac/4759546/ce590650846e/srep21399-f1.jpg

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