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本文引用的文献

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Brucellosis at the animal/ecosystem/human interface at the beginning of the 21st century.21 世纪初动物/生态系统/人类界面的布鲁氏菌病。
Prev Vet Med. 2011 Nov 1;102(2):118-31. doi: 10.1016/j.prevetmed.2011.04.007. Epub 2011 May 14.
2
Characterization of novel Brucella strains originating from wild native rodent species in North Queensland, Australia.鉴定源自澳大利亚北昆士兰州野生本地啮齿动物的新型布鲁氏菌菌株。
Appl Environ Microbiol. 2010 Sep;76(17):5837-45. doi: 10.1128/AEM.00620-10. Epub 2010 Jul 16.
3
Identification of an unusual Brucella strain (BO2) from a lung biopsy in a 52 year-old patient with chronic destructive pneumonia.从一名患有慢性破坏性肺炎的 52 岁患者的肺活检中鉴定出一种不寻常的布鲁氏菌菌株(BO2)。
BMC Microbiol. 2010 Jan 27;10:23. doi: 10.1186/1471-2180-10-23.
4
Brucella inopinata sp. nov., isolated from a breast implant infection.意外布鲁菌,新种,从乳房植入物感染中分离得到。
Int J Syst Evol Microbiol. 2010 Apr;60(Pt 4):801-808. doi: 10.1099/ijs.0.011148-0. Epub 2009 Aug 6.
5
Current understanding of the genetic diversity of Brucella, an expanding genus of zoonotic pathogens.当前对布鲁氏菌属(一个不断扩大的人畜共患病病原体属)遗传多样性的认识。
Infect Genet Evol. 2009 Dec;9(6):1168-84. doi: 10.1016/j.meegid.2009.07.001. Epub 2009 Jul 21.
6
DNA polymorphism analysis of Brucella lipopolysaccharide genes reveals marked differences in O-polysaccharide biosynthetic genes between smooth and rough Brucella species and novel species-specific markers.布鲁氏菌脂多糖基因的DNA多态性分析揭示了光滑型和粗糙型布鲁氏菌属之间O-多糖生物合成基因的显著差异以及新的种特异性标记。
BMC Microbiol. 2009 May 13;9:92. doi: 10.1186/1471-2180-9-92.
7
A novel Brucella isolate in association with two cases of stillbirth in non-human primates - first report.一种与两例非人灵长类动物死产相关的新型布鲁氏菌分离株——首例报告。
J Med Primatol. 2009 Feb;38(1):70-3. doi: 10.1111/j.1600-0684.2008.00314.x.
8
Isolation of Brucella microti from mandibular lymph nodes of red foxes, Vulpes vulpes, in lower Austria.在下奥地利州赤狐(Vulpes vulpes)的下颌淋巴结中分离出微小布鲁氏菌。
Vector Borne Zoonotic Dis. 2009 Apr;9(2):153-6. doi: 10.1089/vbz.2008.0036.
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Isolation of Brucella microti from soil.从土壤中分离出微小布鲁氏菌。
Emerg Infect Dis. 2008 Aug;14(8):1316-7. doi: 10.3201/eid1408.080286.
10
Brucellosis vaccines: assessment of Brucella melitensis lipopolysaccharide rough mutants defective in core and O-polysaccharide synthesis and export.布鲁氏菌病疫苗:对核心及O-多糖合成与输出存在缺陷的粗糙型羊种布鲁氏菌脂多糖突变体的评估
PLoS One. 2008 Jul 23;3(7):e2760. doi: 10.1371/journal.pone.0002760.

新出现的非典型布鲁氏菌属中的脂多糖异质性

Lipopolysaccharide heterogeneity in the atypical group of novel emerging Brucella species.

作者信息

Zygmunt Michel S, Jacques Isabelle, Bernardet Nelly, Cloeckaert Axel

机构信息

INRA, UMR1282 Infectiologie et Santé Publique, Nouzilly, France.

出版信息

Clin Vaccine Immunol. 2012 Sep;19(9):1370-3. doi: 10.1128/CVI.00300-12. Epub 2012 Jul 3.

DOI:10.1128/CVI.00300-12
PMID:22761298
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3428386/
Abstract

Recently, novel Brucella strains with phenotypic characteristics that were atypical for strains belonging to the genus Brucella have been reported. Phenotypically many of these strains were initially misidentified as Ochrobactrum spp. Two novel species have been described so far for these strains, i.e., B. microti and B. inopinata, and other strains genetically related to B. inopinata may constitute other novel species as well. In this study, we analyzed the lipopolysaccharides (LPS) (smooth LPS [S-LPS] and rough LPS [R-LPS]) of these atypical strains using different methods and a panel of monoclonal antibodies (MAbs) directed against several epitopes of the Brucella O-polysaccharide (O-PS) and R-LPS. Among the most striking results, Brucella sp. strain BO2, isolated from a patient with chronic destructive pneumonia, showed a completely distinct S-LPS profile in silver stain gels that looked more similar to that of enterobacterial S-LPS. This strain also failed to react with MAbs against Brucella O-PS epitopes and showed weak reactivity with anti-R-LPS MAbs. B. inopinata reference strain BO1 displayed an M-dominant S-LPS type with some heterogeneity relative to the classical M-dominant Brucella S-LPS type. Australian wild rodent strains belonging also to the B. inopinata group showed a classical A-dominant S-LPS but lacked the O-PS common (C) epitopes, as previously reported for B. suis biovar 2 strains. Interestingly, some strains also failed to react with anti-R-LPS MAbs, such as the B. microti reference strain and B. inopinata BO1, suggesting modifications in the core-lipid A moieties of these strains. These results have several implications for serological typing and serological diagnosis and underline the need for novel tools for detection and correct identification of such novel emerging Brucella spp.

摘要

最近,有报道称出现了具有非典型布鲁氏菌属菌株表型特征的新型布鲁氏菌菌株。从表型上看,其中许多菌株最初被误鉴定为苍白杆菌属。到目前为止,已针对这些菌株描述了两个新物种,即微小布鲁氏菌和意外布鲁氏菌,其他与意外布鲁氏菌有遗传关系的菌株可能也构成其他新物种。在本研究中,我们使用不同方法和一组针对布鲁氏菌O-多糖(O-PS)和粗糙型脂多糖(R-LPS)多个表位的单克隆抗体(MAb),分析了这些非典型菌株的脂多糖(LPS)(光滑型LPS [S-LPS]和粗糙型LPS [R-LPS])。在最显著的结果中,从一名慢性破坏性肺炎患者分离出的松材线虫菌株BO2在银染凝胶中显示出完全不同的S-LPS图谱,看起来更类似于肠杆菌科细菌的S-LPS。该菌株也不与针对布鲁氏菌O-PS表位的MAb发生反应,并且与抗R-LPS MAb的反应较弱。意外布鲁氏菌参考菌株BO1显示出M型占主导的S-LPS类型,相对于经典的M型占主导的布鲁氏菌S-LPS类型存在一些异质性。同样属于意外布鲁氏菌群落的澳大利亚野生啮齿动物菌株显示出典型的A占主导的S-LPS,但缺乏O-PS共同(C)表位,如先前针对猪布鲁氏菌生物变种2菌株所报道的那样。有趣的是,一些菌株也不与抗R-LPS MAb发生反应,如微小布鲁氏菌参考菌株和意外布鲁氏菌BO1,这表明这些菌株的核心脂质A部分存在修饰。这些结果对血清学分型和血清学诊断有若干影响,并强调需要新的工具来检测和正确鉴定此类新出现的布鲁氏菌属物种。