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The rise and spread of a new pathogen: seroresistant Moraxella catarrhalis.一种新型病原体:血清抗性卡他莫拉菌的出现与传播。
Genome Res. 2007 Nov;17(11):1647-56. doi: 10.1101/gr.6122607. Epub 2007 Sep 25.
2
Moraxella (Branhamella) catarrhalis--clinical and molecular aspects of a rediscovered pathogen.卡他莫拉菌(布兰汉菌属)——一种重新被发现的病原体的临床及分子学特征
J Med Microbiol. 1997 May;46(5):360-71. doi: 10.1099/00222615-46-5-360.
3
Virulence factors of Moraxella catarrhalis outer membrane vesicles are major targets for cross-reactive antibodies and have adapted during evolution.卡他莫拉菌外膜囊泡的毒力因子是交叉反应性抗体的主要靶标,并在进化过程中发生了适应性变化。
Sci Rep. 2018 Mar 21;8(1):4955. doi: 10.1038/s41598-018-23029-7.
4
Comparative Genomic Analyses of the Moraxella catarrhalis Serosensitive and Seroresistant Lineages Demonstrate Their Independent Evolution.卡他莫拉菌血清敏感和血清抗性谱系的比较基因组分析表明它们的独立进化。
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Moraxella catarrhalis: from interactions with the host immune system to vaccine development.卡他莫拉菌:从与宿主免疫系统的相互作用到疫苗开发。
Future Microbiol. 2012 Sep;7(9):1073-100. doi: 10.2217/fmb.12.80.
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Moraxella catarrhalis, a human respiratory tract pathogen.卡他莫拉菌,一种人类呼吸道病原体。
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Distribution of genes encoding virulence factors ompB2, ompCD, ompE, β-lactamase and serotype in pathogenic and colonizing strains of Moraxella catarrhalis.黏膜炎莫拉菌毒力因子编码基因 ompB2、ompCD、ompE、β-内酰胺酶和血清型在其致病性菌株和定植菌株中的分布。
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Antimicrobial resistance of Moraxella catarrhalis isolates in Taiwan.台湾卡他莫拉菌分离株的抗菌药物耐药性。
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A global perspective on the genomics of .关于……基因组学的全球视角。 你提供的原文“A global perspective on the genomics of.”似乎不完整,请补充完整以便我能更准确地翻译。
Microb Genom. 2025 Aug;11(8). doi: 10.1099/mgen.0.001488.
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Understanding the population structure of using core genome multilocus sequence typing (cgMLST) and a life identification number (LIN) code classification system.使用核心基因组多位点序列分型(cgMLST)和生命识别号(LIN)编码分类系统来了解……的种群结构。 注:原文中“Understanding the population structure of ”后面缺少具体内容。
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Moraxella catarrhalis phase-variable loci show differences in expression during conditions relevant to disease.卡他莫拉菌相变异位在与疾病相关的条件下表现出表达差异。
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Moraxella catarrhalis NucM is an entry nuclease involved in extracellular DNA and RNA degradation, cell competence and biofilm scaffolding.卡他莫拉菌 NucM 是一种参与细胞外 DNA 和 RNA 降解、细胞感受态和生物膜支架的进入核酸酶。
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9
Moraxella catarrhalis Restriction-Modification Systems Are Associated with Phylogenetic Lineage and Disease.卡他莫拉菌的限制修饰系统与系统发育谱系和疾病相关。
Genome Biol Evol. 2018 Nov 1;10(11):2932-2946. doi: 10.1093/gbe/evy226.
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Virulence factors of Moraxella catarrhalis outer membrane vesicles are major targets for cross-reactive antibodies and have adapted during evolution.卡他莫拉菌外膜囊泡的毒力因子是交叉反应性抗体的主要靶标,并在进化过程中发生了适应性变化。
Sci Rep. 2018 Mar 21;8(1):4955. doi: 10.1038/s41598-018-23029-7.

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GENETIC EVIDENCE FOR A PLEISTOCENE POPULATION EXPLOSION.更新世人口爆炸的遗传学证据。
Evolution. 1995 Aug;49(4):608-615. doi: 10.1111/j.1558-5646.1995.tb02297.x.
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Arlequin (version 3.0): an integrated software package for population genetics data analysis.Arlequin(版本 3.0):一个用于群体遗传学数据分析的集成软件包。
Evol Bioinform Online. 2007 Feb 23;1:47-50.
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An African origin for the intimate association between humans and Helicobacter pylori.人类与幽门螺杆菌密切关联起源于非洲。
Nature. 2007 Feb 22;445(7130):915-918. doi: 10.1038/nature05562. Epub 2007 Feb 7.
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Multilocus sequence typing of bacteria.细菌多位点序列分型
Annu Rev Microbiol. 2006;60:561-88. doi: 10.1146/annurev.micro.59.030804.121325.
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Sex and virulence in Escherichia coli: an evolutionary perspective.大肠杆菌中的性别与毒力:进化视角
Mol Microbiol. 2006 Jun;60(5):1136-51. doi: 10.1111/j.1365-2958.2006.05172.x.
6
Human SNPs reveal no evidence of frequent positive selection.人类单核苷酸多态性未显示出频繁正向选择的证据。
Mol Biol Evol. 2005 Dec;22(12):2504-7. doi: 10.1093/molbev/msi240. Epub 2005 Aug 17.
7
Mutator phenotype confers advantage in Escherichia coli chronic urinary tract infection pathogenesis.突变体表型在大肠杆菌慢性尿路感染发病机制中赋予优势。
FEMS Immunol Med Microbiol. 2005 Jun 1;44(3):317-21. doi: 10.1016/j.femsim.2005.01.003.
8
Moraxella catarrhalis strains with reduced expression of the UspA outer membrane proteins belong to a distinct subpopulation.外膜蛋白UspA表达降低的卡他莫拉菌菌株属于一个独特的亚群。
Vaccine. 2005 Mar 14;23(16):2000-8. doi: 10.1016/j.vaccine.2004.09.036.
9
Microevolution and history of the plague bacillus, Yersinia pestis.鼠疫杆菌耶尔森氏菌的微进化与历史
Proc Natl Acad Sci U S A. 2004 Dec 21;101(51):17837-42. doi: 10.1073/pnas.0408026101. Epub 2004 Dec 14.
10
Silent nucleotide polymorphisms and a phylogeny for Mycobacterium tuberculosis.结核分枝杆菌的沉默核苷酸多态性与系统发育
Emerg Infect Dis. 2004 Sep;10(9):1568-77. doi: 10.3201/eid1009.040046.

一种新型病原体:血清抗性卡他莫拉菌的出现与传播。

The rise and spread of a new pathogen: seroresistant Moraxella catarrhalis.

作者信息

Wirth Thierry, Morelli Giovanna, Kusecek Barica, van Belkum Alex, van der Schee Cindy, Meyer Axel, Achtman Mark

机构信息

Department of Biology, University Konstanz, D-78457 Konstanz, Germany.

出版信息

Genome Res. 2007 Nov;17(11):1647-56. doi: 10.1101/gr.6122607. Epub 2007 Sep 25.

DOI:10.1101/gr.6122607
PMID:17895425
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2045147/
Abstract

The nosocomial human pathogen Moraxella catarrhalis is one the most important agents of human respiratory tract infections. This species is composed of two distinct lineages, one of only moderate virulence, the so-called serosensitive subpopulation, and a second, the seroresistant one, which is enriched among strains that harbor two major virulence traits: complement resistance and adherence to epithelial cells. Using a suite of population genetics tools, we show that the seroresistant lineage is also characterized by higher homologous recombination and mutation rates at housekeeping genes relative to its less pathogenic counterpart. Thus, sex and virulence have evolved in tandem in M. catarrhalis. Moreover, phylogenetic and Bayesian analyses that take into account recombination between the two clades show that the ancestral group was avirulent, is possibly 70 million years old, and must have infected mammals prior to the evolution of humans, which occurred later. The younger seroresistant isolates went through an important population expansion some 5 million years ago, coincident with the hominid expansion. This rise and spread was possibly coupled with a host shift and the acquisition of virulence genes.

摘要

医院内感染的人类病原体卡他莫拉菌是人类呼吸道感染最重要的病原体之一。该菌种由两个不同的谱系组成,一个谱系的毒力仅为中等,即所谓的血清敏感亚群,另一个是血清抗性亚群,在具有两种主要毒力特征(补体抗性和对上皮细胞的粘附)的菌株中更为富集。使用一系列群体遗传学工具,我们发现血清抗性谱系相对于致病性较低的对应谱系,在管家基因处也具有更高的同源重组和突变率。因此,在卡他莫拉菌中,有性生殖和毒力是协同进化的。此外,考虑到两个进化枝之间重组的系统发育和贝叶斯分析表明,祖先群体无毒力,可能有7000万年历史,并且肯定在人类进化(较晚发生)之前就已感染哺乳动物。较年轻的血清抗性分离株在约500万年前经历了一次重要的群体扩张,这与原始人类的扩张同时发生。这种增长和传播可能与宿主转移以及毒力基因的获得有关。