Xu Hai, Bao Xi, Hong Weiming, Wang Anping, Wang Kaimin, Dong Hongyan, Hou Jibo, Govinden Roshini, Deng Bihua, Chenia Hafizah Y
Jiangsu Key Laboratory for High-Tech Research and Development of Veterinary Biopharmaceuticals, Jiangsu Agri-Animal Husbandry Vocational College, Taizhou, China.
Institute of Veterinary Immunology & Engineering, Jiangsu Academy of Agricultural Science, Nanjing, China.
Front Microbiol. 2021 Aug 2;12:705310. doi: 10.3389/fmicb.2021.705310. eCollection 2021.
Bacteriophage T7 gene coding for the only known holin is one of the components of its lysis system, but the holin activity in T7 is more complex than a single gene, and evidence points to the existence of additional T7 genes with holin activity. In this study, a T7 phage with a gene deletion (T7-△holin) was rescued and its biological characteristics and effect on cell lysis were determined. Furthermore, the genomic evolution of mutant phage T7-△holin during serial passage was assessed by whole-genome sequencing analysis. It was observed that deletion of gene from phage T7 delays lysis time and enlarges the phage burst size; however, this biological characteristic recovered to normal lysis levels during serial passage. Scanning electron microscopy showed that the two opposite ends of BL21 cells swell post-T7-△holin infection rather than drilling holes on cell membrane when compared with T7 wild-type infection. No visible progeny phage particle accumulation was observed inside the BL21 cells by transmission electron microscopy. Following serial passage of T7-△holin from the 1st to 20th generations, the mRNA levels of gene and gene were upregulated and several mutation sites were discovered, especially two missense mutations in gene , which indicate a potential contribution to the evolution of the T7-△holin. Although the burst size of T7-△holin increased, high titer cultivation of T7-△holin was not achieved by optimizing the culture process. Accordingly, these results suggest that gene is a potential lysis-related component that needs to be studied further and that the T7-△holin strain with its gene deletion is not adequate to establish the high-titer phage cultivation process.
编码唯一已知孔蛋白的噬菌体T7基因是其裂解系统的组成部分之一,但T7中的孔蛋白活性比单个基因更为复杂,有证据表明存在具有孔蛋白活性的其他T7基因。在本研究中,拯救了一个具有基因缺失的T7噬菌体(T7-△holin),并确定了其生物学特性及对细胞裂解的影响。此外,通过全基因组测序分析评估了突变噬菌体T7-△holin在连续传代过程中的基因组进化。观察到从噬菌体T7中缺失该基因会延迟裂解时间并增大噬菌体的爆发量;然而,这一生物学特性在连续传代过程中恢复到了正常裂解水平。扫描电子显微镜显示,与T7野生型感染相比,T7-△holin感染后BL21细胞的两端肿胀,而不是在细胞膜上钻孔。通过透射电子显微镜未观察到BL21细胞内有可见的子代噬菌体颗粒积累。T7-△holin从第1代连续传代至第20代后,该基因和另一基因的mRNA水平上调,并发现了几个突变位点,特别是该基因中的两个错义突变,这表明其对T7-△holin的进化有潜在贡献。尽管T7-△holin的爆发量增加,但通过优化培养过程并未实现T7-△holin的高滴度培养。因此,这些结果表明该基因是一个需要进一步研究的潜在裂解相关成分,并且缺失该基因的T7-△holin菌株不足以建立高滴度噬菌体培养过程。