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噬菌体T7-△溶菌酶在连续传代过程中的生物学特性及进化

Biological Characterization and Evolution of Bacteriophage T7-△holin During the Serial Passage Process.

作者信息

Xu Hai, Bao Xi, Hong Weiming, Wang Anping, Wang Kaimin, Dong Hongyan, Hou Jibo, Govinden Roshini, Deng Bihua, Chenia Hafizah Y

机构信息

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.

出版信息

Front Microbiol. 2021 Aug 2;12:705310. doi: 10.3389/fmicb.2021.705310. eCollection 2021.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b566/8365609/f90e6203b1e2/fmicb-12-705310-g001.jpg

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