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Molecular characteristics of Brucella melitensis isolates from humans in Qinghai Province, China

机译:中国青海省人类的Brucella melitensis分离株的分子特征

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摘要

Abstract Background 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. Methods 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. Results 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. Conclusions 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.
机译:摘要背景中国青海省人布鲁氏病的患病率迅速增加,确认案件分布在31个县。然而,布鲁氏菌病传播的流行病学尚未完全阐明。为了表征从人分离的感染菌株,使用多基因座可变数量串联分析(MLVA)和全基因组单核苷酸多态性(SNP)的基础方法。方法从两种男性血液培养物中分离出菌株,该血液培养物证实了Brucella melitensis阳性的生物型和MLVA。从这两个菌株中提取基因组DNA,并进行全基因组测序。接下来,进行基于SNP的系统发育分析,以将两个菌株与在线数据库中检索的甜发菌菌株(完全基因组和草案)进行比较。结果,在常规生物型化后,将两种布鲁氏菌和QH2019001和QH2019005)鉴定为B.Melitensis Biovar 3(QH2019001和QH2019005),并且发现使用MLVA-16具有它们的可变数量串联重复(VNTRS)的差异。系统发育检查将96个菌株分配给五种基因型组,QH2019001和QH2019005分配给同一组,但不同的亚组。此外,QH2019005菌株被分配给基因型II中的新亚型型IIJ。然后将这些发现组合以确定两种布鲁氏菌株的地理来源。结论利用全基因组的SNP的方法使得两种B.Melitensis菌株之间的差异更明确地解决,并促进了他们不同的进化历史的阐明。这种方法还透露,Q2019005是新亚型(IIJ)的成员,位于地中海东部的古代起源。

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