南非人、牲畜和野生动物布鲁氏菌全基因组序列分析。

IF 3.3 4区 生物学 Q2 MICROBIOLOGY
Journal of Microbiology Pub Date : 2024-09-01 Epub Date: 2024-07-22 DOI:10.1007/s12275-024-00155-8
Koketso Desiree Mazwi, Kgaugelo Edward Lekota, Barbara Akofo Glover, Francis Babaman Kolo, Ayesha Hassim, Jenny Rossouw, Annelize Jonker, Justnya Maria Wojno, Giuseppe Profiti, Pier Luigi Martelli, Rita Casadio, Katiuscia Zilli, Anna Janowicz, Francesca Marotta, Giuliano Garofolo, Henriette van Heerden
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引用次数: 0

摘要

布鲁氏菌病是一种具有重要经济意义的人畜共患病,影响着全球尤其是非洲的人类、牲畜和野生动物的健康。在南非,从人类、牲畜(牛和山羊)和野生动物(紫貂)身上分离出了流产布鲁氏菌和梅里金布鲁氏菌,但人们对这种病原体在南非的种群基因组结构知之甚少。由于全基因组测序有助于区分和追踪布鲁氏菌属菌株爆发的源头,因此对之前研究中的回顾性分离物(n = 19)进行了全基因组测序。利用平均核苷酸同一性(ANI)、泛基因组学(Pangenomics)和全基因组单核苷酸多态性(wgSNP)对序列进行了分析,以追踪南澳大利亚不同省份人、牛、山羊和黑貂中流行的布鲁氏菌病病例的地理来源。对19株布鲁氏菌(B. melitensis,n = 69)和B. abortus(B. abortus,n = 56)进行了泛基因组学分析,其中包括来自牛的B. abortus(n = 3)和来自人(n = 1)、牛(n = 1)、山羊(n = 1)、Rev1疫苗株(n = 1)和黑貂(n = 12)的B. melitensis。梅里金杆菌基因组的泛基因组学分析突出显示了共享基因,其中包括 10 个假定蛋白和编码黑貂基因组中乙酰辅酶 A 合成酶(acs)和酰酰胺酶(am)的基因。wgSNP 分析证实,与来自豪登省不同病例的 B. melitensis 牛样本相比,从人类身上分离出的 B. melitensis 与西开普省同一疫情中的山羊关系更为密切。黑貂 B. melitensis 株系可与非洲株系区分开来,自成一个非洲亚支系。已测序的堕胎芽孢杆菌菌株属于 C2 系,与莫桑比克和津巴布韦的分离株关系密切。这项研究在南澳大利亚的不同宿主中发现了基因多样的布鲁氏菌属。这项研究扩展了有关南澳大利亚家畜和人类中存在布鲁氏菌的有限已知知识,为今后研究布鲁氏菌属在全球的分布及其进化背景奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Whole Genome Sequence Analysis of Brucella spp. from Human, Livestock, and Wildlife in South Africa.

Whole Genome Sequence Analysis of Brucella spp. from Human, Livestock, and Wildlife in South Africa.

Brucellosis is an economically important zoonotic disease affecting humans, livestock, and wildlife health globally and especially in Africa. Brucella abortus and B. melitensis have been isolated from human, livestock (cattle and goat), and wildlife (sable) in South Africa (SA) but with little knowledge of the population genomic structure of this pathogen in SA. As whole genome sequencing can assist to differentiate and trace the origin of outbreaks of Brucella spp. strains, the whole genomes of retrospective isolates (n = 19) from previous studies were sequenced. Sequences were analysed using average nucleotide identity (ANI), pangenomics, and whole genome single nucleotide polymorphism (wgSNP) to trace the geographical origin of cases of brucellosis circulating in human, cattle, goats, and sable from different provinces in SA. Pangenomics analysis of B. melitensis (n = 69) and B. abortus (n = 56) was conducted with 19 strains that included B. abortus from cattle (n = 3) and B. melitensis from a human (n = 1), cattle (n = 1), goat (n = 1), Rev1 vaccine strain (n = 1), and sable (n = 12). Pangenomics analysis of B. melitensis genomes, highlighted shared genes, that include 10 hypothetical proteins and genes that encodes for acetyl-coenzyme A synthetase (acs), and acylamidase (aam) amongst the sable genomes. The wgSNP analysis confirmed the B. melitensis isolated from human was more closely related to the goat from the Western Cape Province from the same outbreak than the B. melitensis cattle sample from different cases in the Gauteng Province. The B. melitensis sable strains could be distinguished from the African lineage, constituting their own African sub-clade. The sequenced B. abortus strains clustered in the C2 lineage that is closely related to the isolates from Mozambique and Zimbabwe. This study identified genetically diverse Brucella spp. among various hosts in SA. This study expands the limited known knowledge regarding the presence of B. melitensis in livestock and humans in SA, further building a foundation for future research on the distribution of the Brucella spp. worldwide and its evolutionary background.

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来源期刊
Journal of Microbiology
Journal of Microbiology 生物-微生物学
CiteScore
5.70
自引率
3.30%
发文量
0
审稿时长
3 months
期刊介绍: Publishes papers that deal with research on microorganisms, including archaea, bacteria, yeasts, fungi, microalgae, protozoa, and simple eukaryotic microorganisms. Topics considered for publication include Microbial Systematics, Evolutionary Microbiology, Microbial Ecology, Environmental Microbiology, Microbial Genetics, Genomics, Molecular Biology, Microbial Physiology, Biochemistry, Microbial Pathogenesis, Host-Microbe Interaction, Systems Microbiology, Synthetic Microbiology, Bioinformatics and Virology. Manuscripts dealing with simple identification of microorganism(s), cloning of a known gene and its expression in a microbial host, and clinical statistics will not be considered for publication by JM.
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