Qinghai Institute for Endemic Disease Prevention and Control, The department of brucellosis prevention and control, Xining, 810021, Qinghai, China.
Key Laboratory of Plague Prevention and Research, Qinghai Institute for Endemic Disease Prevention and Control, National Health Commission (2019PT310004) and Key Laboratory for Plague Prevention and Control of Qinghai Province, Xining, 810021, Qinghai, China.
Infect Dis Poverty. 2021 Mar 26;10(1):42. doi: 10.1186/s40249-021-00829-0.
The prevalence of human brucellosis in Qinghai Province of China has been increasing rapidly, with confirmed cases distributed across 31 counties. However, the epidemiology of brucellosis transmission has not been fully elucidated. To characterize the infecting strains isolated from humans, multiple-locus variable-number tandem repeats analysis (MLVA) and whole-genome single-nucleotide polymorphism (SNP)-based approaches were employed.
Strains were isolated from two males blood cultures that were confirmed Brucella melitensis positive following biotyping and MLVA. Genomic DNA was extracted from these two strains, and whole-genome sequencing was performed. Next, SNP-based phylogenetic analysis was performed to compare the two strains to 94 B. melitensis strains (complete genome and draft genome) retrieved from online databases.
The two Brucella isolates were identified as B. melitensis biovar 3 (QH2019001 and QH2019005) following conventional biotyping and were found to have differences in their variable number tandem repeats (VNTRs) using MLVA-16. Phylogenetic examination assigned the 96 strains to five genotype groups, with QH2019001 and QH2019005 assigned to the same group, but different subgroups. Moreover, the QH2019005 strain was assigned to a new subgenotype, IIj, within genotype II. These findings were then combined to determine the geographic origin of the two Brucella strains.
Utilizing a whole-genome SNP-based approach enabled differences between the two B. melitensis strains to be more clearly resolved, and facilitated the elucidation of their different evolutionary histories. This approach also revealed that QH2019005 is a member of a new subgenotype (IIj) with an ancient origin in the eastern Mediterranean Sea.
中国青海省的人类布鲁氏菌病患病率迅速上升,确诊病例分布在 31 个县。然而,布鲁氏菌病传播的流行病学尚未完全阐明。为了描述从人类中分离出的感染株,采用多位点可变数目串联重复分析(MLVA)和全基因组单核苷酸多态性(SNP)为基础的方法。
从两名男性的血液培养物中分离出菌株,这两名男性的生物型和 MLVA 检测均证实为布鲁氏菌 melitensis 阳性。从这两个菌株中提取基因组 DNA,并进行全基因组测序。然后,对这两个菌株与从在线数据库中检索到的 94 株布鲁氏菌 melitensis 菌株(完整基因组和草图基因组)进行基于 SNP 的系统发育分析。
这两个布鲁氏菌分离株经常规生物型鉴定为布鲁氏菌 melitensis 生物型 3(QH2019001 和 QH2019005),并通过 MLVA-16 检测到它们在可变数串联重复(VNTR)方面存在差异。系统发育分析将 96 株菌分为五个基因型组,QH2019001 和 QH2019005 被分为同一组,但属于不同的亚组。此外,QH2019005 株被分配到基因型 II 内的一个新的亚基因型 IIj。然后将这些发现结合起来,以确定这两个布鲁氏菌菌株的地理起源。
利用全基因组 SNP 为基础的方法,可以更清楚地分辨出这两个布鲁氏菌菌株之间的差异,并阐明它们不同的进化历史。该方法还揭示 QH2019005 是一个新的亚基因型(IIj)的成员,其起源于地中海东部的古老地区。