“Phylogenomic insights into brucellaceae: The Pseudochrobactrum algeriensis case”

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
Maite Loperena-Barber , Aitor Elizalde-Bielsa , Miriam Salvador-Bescós , Paula Ruiz-Rodríguez , Joaquin Miguel Pellegrini , Chantal Renau-Mínguez , Rebecca Lancaster , Amaia Zúñiga-Ripa , Maite Iriarte , Jose A. Bengoechea , Mireia Coscollá , Jean-Pierre Gorvel , Ignacio Moriyón , Raquel Conde-Álvarez
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引用次数: 0

Abstract

The genus Pseudochrobactrum encompasses free-living bacteria phylogenetically close to Ochrobactrum opportunistic pathogens and to Brucella, facultative intracellular parasites causing brucellosis, a worldwide-extended and grave zoonosis. Recently, Pseudochrobactrum strains were isolated from Brucella natural hosts on Brucella selective media, potentially causing diagnostic confusions. Strikingly, P. algeriensis was isolated from cattle lymph nodes, organs that are inimical to bacteria. Here, we analyse P. algeriensis potential virulence factors in comparison with Ochrobactrum and Brucella. Consistent with genomic analyses, Western-Blot analyses confirmed that P. algeriensis lacks the ability to synthesize the N-formylperosamine O-polysaccharide characteristic of the lipopolysaccharide (LPS) of smooth Brucella core species. However, unlike other Pseudochrobactrum but similar to some early diverging brucellae, P. algeriensis carries genes potentially synthetizing a rhamnose-based O-polysaccharide LPS. Lipid A analysis by MALDI-TOF demonstrated that P. algeriensis LPS bears a lipid A with a reduced pathogen-associated molecular pattern, a trait shared with Ochrobactrum and Brucella that is essential to generate a highly stable outer membrane and to delay immune activation. Also, although not able to multiply intracellularly in macrophages, the analysis of P. algeriensis cell lipid envelope revealed the presence of large amounts of cationic aminolipids, which may account for the extremely high resistance of P. algeriensis to bactericidal peptides and could favor colonization of mucosae and transient survival in Brucella hosts. However, two traits critical in Brucella pathogenicity are either significantly different (T4SS [VirB]) or absent (erythritol catabolic pathway) in P. algeriensis. This work shows that, while diverging in other characteristics, lipidic envelope features relevant in Brucella pathogenicity are conserved in Brucellaceae. The constant presence of these features strongly suggests that reinforcement of the envelope integrity as an adaptive advantage in soil was maintained in Brucella because of the similarity of some environmental challenges, such as the action of cationic peptide antibiotics and host defense peptides. This information adds knowledge about the evolution of Brucellaceae, and also underlines the taxonomical differences of the three genera compared.

"对布鲁氏菌科的系统发生组学研究:阿尔及利亚假丝酵母菌(Pseudochrobactrum algeriensis)"。
假核金黄色葡萄球菌属(Pseudochrobactrum)包括自由生活的细菌,在系统发育上与机会致病菌赭曲霉(Ochrobactrum)和布鲁氏菌(Brucella)接近,后者是引起布鲁氏菌病(一种遍及全球的严重人畜共患疾病)的细胞内寄生虫。最近,在布鲁氏菌选择性培养基上从布鲁氏菌自然宿主中分离出假包囊菌株,可能会造成诊断上的混乱。令人震惊的是,从牛的淋巴结中分离出了 P. algeriensis,而淋巴结是不适宜细菌生长的器官。在此,我们分析了 P. algeriensis 与 Ochrobactrum 和布鲁氏菌的潜在毒力因子。与基因组分析一致,Western-Blot 分析证实,P. algeriensis 缺乏合成 N-formylperosamine O 型多糖的能力,而这种多糖是平滑布鲁氏菌核心菌种脂多糖(LPS)的特征。然而,与其他假杆菌不同,但与一些早期分化的布鲁氏菌类似,阿尔及尔假杆菌携带有可能合成鼠李糖基 O 型多糖 LPS 的基因。通过 MALDI-TOF 进行的脂质 A 分析表明,P. algeriensis LPS 所携带的脂质 A 具有较低的病原体相关分子模式,这是与 Ochrobactrum 和布鲁氏菌共有的特性,对于生成高度稳定的外膜和延迟免疫激活至关重要。此外,虽然不能在巨噬细胞内繁殖,但对阿耳戈螺旋体细胞脂质包膜的分析表明,阿耳戈螺旋体存在大量阳离子氨基脂,这可能是阿耳戈螺旋体对杀菌肽具有极强抵抗力的原因,并可能有利于在布鲁氏菌宿主的粘膜上定植和短暂存活。然而,对布鲁氏菌致病性至关重要的两个性状(T4SS [VirB])在阿尔盖氏痢疾杆菌中要么存在显著差异,要么不存在(赤藓糖醇分解途径)。这项工作表明,布鲁氏菌致病性相关的脂质包膜特征虽然在其他特征上存在差异,但在布鲁氏菌科中是保守的。这些特征的持续存在有力地表明,由于某些环境挑战(如阳离子肽抗生素和宿主防御肽的作用)的相似性,布鲁氏菌保持了包膜的完整性,这也是布鲁氏菌在土壤中的一种适应优势。这些信息增加了对布鲁氏菌科演化的了解,同时也强调了所比较的三个属在分类学上的差异。
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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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