Jores Joerg, Ma Li, Ssajjakambwe Paul, Schieck Elise, Liljander Anne, Chandran Suchismita, Stoffel Michael H, Cippa Valentina, Arfi Yonathan, Assad-Garcia Nacyra, Falquet Laurent, Sirand-Pugnet Pascal, Blanchard Alain, Lartigue Carole, Posthaus Horst, Labroussaa Fabien, Vashee Sanjay
Department of Infectious Diseases and Pathobiology, Institute of Veterinary Bacteriology, University of Bern, Bern, Switzerland.
International Livestock Research Institute, Nairobi, Kenya.
Front Microbiol. 2019 Apr 3;10:664. doi: 10.3389/fmicb.2019.00664. eCollection 2019.
Mycoplasmas are the smallest free-living organisms and cause a number of economically important diseases affecting humans, animals, insects, and plants. Here, we demonstrate that highly virulent subspecies () can be fully attenuated targeted deletion of non-essential genes encoding, among others, potential virulence traits. Five genomic regions, representing approximately 10% of the original genome, were successively deleted using as an engineering platform. Specifically, a total of 68 genes out of the 432 genes verified to be individually non-essential in the JCVI-Syn3.0 minimal cell, were excised from the genome. characterization showed that this mutant was similar to its parental strain in terms of its doubling time, even though 10% of the genome content were removed. A novel challenge model in goats revealed that the wild-type parental strain caused marked necrotizing inflammation at the site of inoculation, septicemia and all animals reached endpoint criteria within 6 days after experimental infection. This is in contrast to the mutant strain, which caused no clinical signs nor pathomorphological lesions. These results highlight, for the first time, the rational design, construction and complete attenuation of a strain via synthetic genomics tools. Trait addition using the yeast-based genome engineering platform and subsequent or trials employing the chassis will allow us to dissect the role of individual candidate virulence factors and lead the way for the development of an attenuated designer vaccine.
支原体是最小的自由生活生物体,可引发多种对人类、动物、昆虫和植物具有经济重要性的疾病。在此,我们证明,通过靶向缺失编码潜在毒力特征等非必需基因,高毒力亚种()可被完全减毒。以作为工程平台,依次删除了代表原始基因组约10%的五个基因组区域。具体而言,从基因组中切除了在JCVI-Syn3.0最小细胞中经验证为单个非必需的432个基因中的总共68个基因。表征显示,尽管去除了10%的基因组内容,但该突变体在倍增时间方面与其亲本菌株相似。一种新的山羊攻毒模型显示,野生型亲本菌株在接种部位引起明显的坏死性炎症、败血症,并且所有动物在实验感染后6天内达到终点标准。这与突变株形成对比,突变株未引起任何临床症状或病理形态学损伤。这些结果首次突出了通过合成基因组学工具对菌株进行合理设计、构建和完全减毒。使用基于酵母的基因组工程平台添加性状,以及随后使用底盘进行或试验,将使我们能够剖析单个候选毒力因子的作用,并为开发减毒设计疫苗铺平道路。