Zhou Yumei, Wang Yang, Li Yuan, Nick Nwankpa, Zou Xiaohui, Bai Fan, Wu Jindi, Xin Jiuqing
National Contagious Bovine Pleuropneumonia Reference Laboratory, Division of Bacterial Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, CAAS, Harbin, China.
Pan African Veterinary Vaccine Center, Debre Zeit, Ethiopia.
Microb Pathog. 2016 Apr;93:13-21. doi: 10.1016/j.micpath.2016.01.011. Epub 2016 Jan 19.
Mycoplasma mycoides subsp. mycoides (Mmm) is the causative agent of contagious bovine pleuropneumonia (CBPP). The virulent Mmm Ben-1 strain was isolated from the lung of a CBPP-infected cow in China in the 1950s. To attenuate the virulence of the Ben-1 strain and preserve its protective ability, the isolate was re-isolated after inoculation into the testicles of rabbits and into the rabbit thorax. As a result, after the subsequent isolates were continuously passaged 468 times in rabbits, its pathogenicity to cattle decreased. However, the molecular mechanisms leading to attenuation of the Mmm Ben-1 remain unknown. We compared the entire genomes of the Ben-1 strain and the 468 th generation strain passaged in rabbits (Ben-468) and discovered that a putative protein gene named p19 was absent from the Ben-468 strain. The p19 gene was cloned and expressed in Escherichia coli to obtain recombinant P19 (rP19). Western blot analysis demonstrated that the P19 protein is detected in the cell-membrane fraction, the cell-soluble cytosolic fraction and whole-cell lysate of the Mmm Ben-1 strain. The rP19 can interact with international standard serum against CBPP. Immunostaining visualised via confocal laser scanning microscopy indicated that P19 is able to adhere to embryonic bovine lung (EBL) cells, and this finding was also confirmed by a sandwich ELISA. We also found that anti-rP19 serum could inhibit the adhesion of the Mmm Ben-1 total proteins to EBL cells.
丝状支原体丝状亚种(Mmm)是牛传染性胸膜肺炎(CBPP)的病原体。强毒Mmm Ben-1菌株于20世纪50年代从中国一头感染CBPP的奶牛的肺中分离得到。为了减弱Ben-1菌株的毒力并保留其保护能力,将该分离株接种到兔睾丸和兔胸腔后进行再次分离。结果,后续分离株在兔体内连续传代468次后,其对牛的致病性降低。然而,导致Mmm Ben-1毒力减弱的分子机制仍不清楚。我们比较了Ben-1菌株和在兔体内传代至第468代的菌株(Ben-468)的全基因组,发现Ben-468菌株中缺失一个名为p19的假定蛋白基因。将p19基因克隆并在大肠杆菌中表达以获得重组P19(rP19)。蛋白质免疫印迹分析表明,在Mmm Ben-1菌株的细胞膜组分、细胞可溶性胞质组分和全细胞裂解物中可检测到P19蛋白。rP19能与抗CBPP国际标准血清相互作用。通过共聚焦激光扫描显微镜观察的免疫染色表明,P19能够粘附于胚胎牛肺(EBL)细胞,这一发现也通过夹心ELISA得到证实。我们还发现抗rP19血清能够抑制Mmm Ben-1总蛋白对EBL细胞的粘附。