Lai Kin-Kwan, Davis-Richardson Austin G, Dias Raquel, Triplett Eric W
Microbiology and Cell Science Department, Institute of Food and Agricultural Sciences, University of Florida Gainesville, FL, USA.
Front Microbiol. 2016 Apr 20;7:547. doi: 10.3389/fmicb.2016.00547. eCollection 2016.
Here Tn5 random transposon mutagenesis was used to identify the essential elements for culturing Liberibacter crescens BT-1 that can serve as antimicrobial targets for the closely related pathogens of citrus, Candidatus Liberibacter asiaticus (Las) and tomato and potato, Candidatus Liberibacter solanacearum (Lso). In order to gain insight on the virulence, metabolism, and culturability of the pathogens within the genus Liberibacter, a mini-Tn5 transposon derivative system consisting of a gene specifying resistance to kanamycin, flanked by a 19-base-pair terminal repeat sequence of Tn5, was used for the genome-wide mutagenesis of L. crescens BT-1 and created an insertion mutant library. By analyzing the location of insertions using Sanger and Illumina Mi-Seq sequencing, 314 genes are proposed as essential for the culture of L. crescens BT-1 on BM-7 medium. Of those genes, 76 are not present in the uncultured Liberibacter pathogens and, as a result, suggest molecules necessary for the culturing these pathogens. Those molecules include the aromatic amino acids, several vitamins, histidine, cysteine, lipopolysaccharides, and fatty acids. In addition, the 238 essential genes of L. crescens in common with L. asiaticus are potential targets for the development of therapeutics against the disease.
在这里,Tn5随机转座子诱变被用于鉴定培养渐尖利氏菌BT-1的必需元件,这些元件可作为柑橘的密切相关病原体亚洲韧皮杆菌(Las)以及番茄和马铃薯的茄科韧皮杆菌(Lso)的抗菌靶点。为了深入了解韧皮杆菌属病原体的毒力、代谢和可培养性,一个由指定对卡那霉素抗性的基因组成的mini-Tn5转座子衍生系统,两侧是Tn5的19个碱基对的末端重复序列,用于渐尖利氏菌BT-1的全基因组诱变,并创建了一个插入突变体文库。通过使用桑格测序和Illumina Mi-Seq测序分析插入位点,提出314个基因对渐尖利氏菌BT-1在BM-7培养基上的培养至关重要。在这些基因中,76个在未培养的韧皮杆菌病原体中不存在,因此表明这些分子是培养这些病原体所必需的。这些分子包括芳香族氨基酸、几种维生素、组氨酸、半胱氨酸、脂多糖和脂肪酸。此外,渐尖利氏菌与亚洲韧皮杆菌共有的238个必需基因是开发针对该疾病的治疗方法的潜在靶点。