Laboratory of Plant Pathology, Faculty of Agriculture, Graduate School, Kyushu University, Fukuoka 819-0395, Japan.
Aino Potato Branch, Nagasaki Prefectural Agricultural and Forestry Experiment Station, Nagasaki 854-0302, Japan.
FEMS Microbiol Lett. 2021 Feb 4;368(2). doi: 10.1093/femsle/fnaa223.
Pseudomonas cichorii is divided into two subclades based on the 16S ribosomal RNA gene sequence and core genome multilocus sequence typing. It was shown that subclade 2 strains utilize d-tartrate as a sole carbon source, whereas subclade 1 strains do not. Draft genome sequencing was performed with P. cichorii strains to identify d-tartrate utilization genes. By genome comparative and homology search studies, an ∼7.1-kb region was identified to be involved in d-tartrate utilization. The region is subclade 2 specific, and contains tarD and dctA genes, which encode a putative enzyme and transporter of d-tartrate, respectively. When the region was introduced into subclade 1 strains, the transformants were able to utilize d-tartrate. Partial fragments of tarD and dctA were amplified from all subclade 2 strains tested in this study by PCR using gene-specific primers, but not from subclade 1 strains. This is the first report on the genetic analysis of biochemical characteristics corresponding to a specific phylogenetic group in P. cichorii.
菊欧文氏菌可根据 16S 核糖体 RNA 基因序列和核心基因组多位点序列分型划分为两个亚群。研究表明,亚群 2 菌株利用 d-酒石酸盐作为唯一碳源,而亚群 1 菌株则不能。对菊欧文氏菌菌株进行了草案基因组测序,以鉴定 d-酒石酸盐利用基因。通过基因组比较和同源性搜索研究,确定了一个约 7.1kb 的区域与 d-酒石酸盐利用有关。该区域是亚群 2 特异性的,包含 tarD 和 dctA 基因,分别编码 d-酒石酸盐的假定酶和转运蛋白。当该区域被引入亚群 1 菌株时,转化体能够利用 d-酒石酸盐。通过使用基因特异性引物的 PCR 从本研究中测试的所有亚群 2 菌株中扩增了 tarD 和 dctA 的部分片段,但不能从亚群 1 菌株中扩增。这是菊欧文氏菌中特定系统发育群生化特征的遗传分析的首次报道。