Sato'o Yusuke, Aiba Yoshifumi, Kiga Kotaro, Watanabe Shinya, Sasahara Teppei, Hayakawa Yasuhiko, Cui Longzhu
Division of Bacteriology, Department of Infection and Immunity, Faculty of Medicine, Jichi Medical University, 3311-1, Yakushiji, Shimotsuke-shi, Tochigi 329-0498, Japan.
NEPA GENE Co., Ltd., Chiba, Japan.
J Microbiol Methods. 2018 Mar;146:25-32. doi: 10.1016/j.mimet.2018.01.006. Epub 2018 Feb 3.
Electroporation is a common technique necessary for genomic manipulation of Staphylococci. However, because this technique has too low efficiency to be applied to some Staphylococcal species and strains, especially to coagulase-negative Staphylococcus (CNS) isolates, basic researches on these clinically important Staphylococci are limited. Here we report on the optimization of electroporation parameters and conditions as well as on the generation of a universal protocol that can be efficiently applicable to both CNS and Coagulase-positive Staphylococci (CPS). This protocol could generate transformants of clinical Staphylococcus epidermidis isolate, with an efficiency of up to 1400 CFU/μg of plasmid DNA. Transformants of 12 other clinically important Staphylococcal species, including CNS and CPS, were also generated with this protocol. To our knowledge, this is the first report on successful electroporation in nine these Staphylococcal species.
电穿孔是葡萄球菌基因组操作所必需的一种常用技术。然而,由于该技术效率过低,无法应用于某些葡萄球菌种类和菌株,尤其是凝固酶阴性葡萄球菌(CNS)分离株,因此对这些具有临床重要性的葡萄球菌的基础研究受到限制。在此,我们报告了电穿孔参数和条件的优化,以及一种通用方案的产生,该方案可有效应用于CNS和凝固酶阳性葡萄球菌(CPS)。该方案能够产生临床表皮葡萄球菌分离株的转化子,效率高达每微克质粒DNA 1400 CFU。使用该方案还产生了包括CNS和CPS在内的其他12种具有临床重要性的葡萄球菌的转化子。据我们所知,这是关于在这9种葡萄球菌中成功进行电穿孔的首次报道。