Di Dong-Dong, Jiang Hai, Tian Li-Li, Kang Jing-Li, Zhang Wen, Yi Xin-Ping, Ye Feng, Zhong Qi, Ni Bo, He You-Yu, Xia Lin, Yu Yao, Cui Bu-Yun, Mao Xiang, Fan Wei-Xing
Laboratory of Zoonoses, China Animal Health and Epidemiology Center, Qingdao, Shandong, China.
State Key Laboratory for Infectious Disease Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Beijing, China.
BMC Genomics. 2016 Sep 20;17(1):741. doi: 10.1186/s12864-016-3076-5.
Brucellosis is a bacterial disease caused by Brucella infection. In the late fifties, Brucella suis vaccine strain S2 with reduced virulence was obtained by serial transfer of a virulent B. suis biovar 1 strain in China. It has been widely used for vaccination in China since 1971. Until now, the mechanisms underlie virulence attenuation of S2 are still unknown.
In this paper, the whole genome sequencing of S2 was carried out by Illumina Hiseq2000 sequencing method. We further performed the comparative genomic analysis to find out the differences between S2 and the virulent Brucella suis strain 1330. We found premature stops in outer membrane autotransporter omaA and eryD genes. Single mutations were found in phosphatidylcholine synthase, phosphorglucosamine mutase, pyruvate kinase and FliF, which have been reported to be related to the virulence of Brucella or other bacteria. Of the other different proteins between S2 and 1330, such as Omp2b, periplasmic sugar-binding protein, and oligopeptide ABC transporter, no definitive implications related to bacterial virulence were found, which await further investigation.
The data presented here provided the rational basis for designing Brucella vaccines that could be used in other strains.
布鲁氏菌病是由布鲁氏菌感染引起的一种细菌性疾病。20世纪50年代后期,中国通过对强毒猪布鲁氏菌生物变种1菌株进行连续传代获得了减毒猪布鲁氏菌疫苗株S2。自1971年以来,它在中国已被广泛用于疫苗接种。迄今为止,S2毒力减弱的机制仍不清楚。
本文采用Illumina Hiseq2000测序方法对S2进行了全基因组测序。我们进一步进行了比较基因组分析,以找出S2与强毒猪布鲁氏菌菌株1330之间的差异。我们发现外膜自转运蛋白omaA和eryD基因存在提前终止。在磷脂酰胆碱合酶、磷酸葡糖胺变位酶、丙酮酸激酶和FliF中发现了单突变,这些已被报道与布鲁氏菌或其他细菌的毒力有关。在S2和1330之间的其他不同蛋白质中,如Omp2b、周质糖结合蛋白和寡肽ABC转运蛋白,未发现与细菌毒力有明确关联,有待进一步研究。
本文提供的数据为设计可用于其他菌株的布鲁氏菌疫苗提供了合理依据。