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本文引用的文献

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Transposon mutagenesis of the anaerobic commensal, Bacteroides fragilis, using the EZ::TN5 transposome.利用 EZ::TN5 转座体对厌氧共生菌脆弱拟杆菌进行转座子诱变。
FEMS Microbiol Lett. 2012 Aug;333(2):94-100. doi: 10.1111/j.1574-6968.2012.02602.x. Epub 2012 Jun 18.
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MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods.MEGA5:用于最大似然法、进化距离法和最大简约法的分子进化遗传学分析。
Mol Biol Evol. 2011 Oct;28(10):2731-9. doi: 10.1093/molbev/msr121. Epub 2011 May 4.
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Antibiotic resistance and adhesion potential of Bacteroides fragilis clinical isolates from Cape Town, South Africa.南非开普敦脆弱拟杆菌临床分离株的抗生素耐药性和黏附潜力。
Anaerobe. 2011 Aug;17(4):142-6. doi: 10.1016/j.anaerobe.2011.02.009. Epub 2011 Apr 28.
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Enterotypes of the human gut microbiome.人类肠道微生物组的肠型。
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Multi-drug resistant Bacteroides fragilis recovered from blood and severe leg wounds caused by an improvised explosive device (IED) in Afghanistan.从血液和阿富汗简易爆炸装置(IED)造成的严重腿部创伤中分离出的多药耐药脆弱拟杆菌。
Anaerobe. 2011 Aug;17(4):152-5. doi: 10.1016/j.anaerobe.2011.02.007. Epub 2011 Mar 3.
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Anaerobic bacteria and antibiotics: What kind of unexpected resistance could I find in my laboratory tomorrow?厌氧菌和抗生素:明天在我的实验室里,我可能会发现什么样的意外耐药性呢?
Anaerobe. 2010 Dec;16(6):555-9. doi: 10.1016/j.anaerobe.2010.10.002. Epub 2010 Oct 28.
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Trans locus inhibitors limit concomitant polysaccharide synthesis in the human gut symbiont Bacteroides fragilis.转座子抑制剂限制了人类肠道共生菌脆弱拟杆菌的多糖同时合成。
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Bacteroides fragilis RecA protein overexpression causes resistance to metronidazole.脆弱拟杆菌 RecA 蛋白过表达导致对甲硝唑的耐药性。
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A human gut microbial gene catalogue established by metagenomic sequencing.宏基因组测序建立的人类肠道微生物基因目录。
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10
Biophysical characterization and mutational analysis of the antibiotic resistance protein NimA from Deinococcus radiodurans.耐辐射球菌抗生素抗性蛋白NimA的生物物理特性及突变分析
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脆弱拟杆菌的两株多药耐药临床分离株携带一种新型甲硝唑耐药 nim 基因(nimJ)。

Two multidrug-resistant clinical isolates of Bacteroides fragilis carry a novel metronidazole resistance nim gene (nimJ).

机构信息

GLAVAHCS, Los Angeles, California, USA.

出版信息

Antimicrob Agents Chemother. 2013 Aug;57(8):3767-74. doi: 10.1128/AAC.00386-13. Epub 2013 May 28.

DOI:10.1128/AAC.00386-13
PMID:23716049
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3719759/
Abstract

Two multidrug-resistant Bacteroides fragilis clinical isolates contain and express a novel nim gene, nimJ, that is not recognized by the "universal" nim primers and can confer increased resistance to metronidazole when introduced into a susceptible strain on a multicopy plasmid. HMW615, an appendiceal isolate, contains at least two copies of nimJ on its genome, while HMW616, an isolate from a patient with sepsis, contains one genomic copy of nimJ. B. fragilis NimJ is phylogenetically closer to Prevotella baroniae NimI and Clostridium botulinum NimA than to the other known Bacteroides Nim proteins. The predicted protein structure of NimJ, based on fold recognition analysis, is consistent with the crystal structures derived for known Nim proteins, and specific amino acid residues important for substrate binding in the active site are conserved. This study demonstrates that the "universal" nim primers will not detect all nim genes with the ability to confer metronidazole resistance, but nimJ alone cannot account for the very high metronidazole MICs of these resistant clinical isolates.

摘要

两株多药耐药脆弱拟杆菌临床分离株含有并表达一种新型 nim 基因 nimJ,该基因不能被“通用” nim 引物识别,当它被引入敏感菌株的多拷贝质粒中时,可赋予对甲硝唑的增加抗性。HMW615 是阑尾分离株,其基因组中至少含有两个 nimJ 拷贝,而 HMW616 是来自脓毒症患者的分离株,含有一个基因组拷贝的 nimJ。脆弱拟杆菌 NimJ 在系统发育上与 prevotella baroniae nimI 和梭状芽胞杆菌 nimA 比其他已知的拟杆菌 Nim 蛋白更接近。基于折叠识别分析预测的 NimJ 蛋白结构与已知 Nim 蛋白的晶体结构一致,并且在活性位点中对底物结合很重要的特定氨基酸残基保守。这项研究表明,“通用”nim 引物不能检测所有具有赋予甲硝唑抗性能力的 nim 基因,但 nimJ 本身不能解释这些耐药临床分离株非常高的甲硝唑 MIC 值。