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A biphasic epigenetic switch controls immunoevasion, virulence and niche adaptation in non-typeable Haemophilus influenzae

机译:双相表观遗传开关控制不可分型的流感嗜血杆菌的免疫逃避,毒力和生态位适应

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Non-typeable Haemophilus influenzae contains an N6-adenine DNA-methyltransferase (ModA) that is subject to phase-variable expression (random ON/OFF switching). Five modA alleles, modA2 , modA4, modA5 , modA9 and modA10 , account for over two-thirds of clinical otitis media isolates surveyed. Here, we use single molecule, real-time (SMRT) methylome analysis to identify the DNA-recognition motifs for all five of these modA alleles. Phase variation of these alleles regulates multiple proteins including vaccine candidates, and key virulence phenotypes such as antibiotic resistance ( modA2 , modA5 , modA10 ), biofilm formation ( modA2 ) and immunoevasion ( modA4 ). Analyses of a modA2 strain in the chinchilla model of otitis media show a clear selection for ON switching of modA2 in the middle ear. Our results indicate that a biphasic epigenetic switch can control bacterial virulence, immunoevasion and niche adaptation in an animal model system.
机译:不可分型的流感嗜血杆菌含有N 6 -腺嘌呤DNA-甲基转移酶(ModA),可进行相变表达(随机ON / OFF切换)。五个modA等位基因modA2,modA4,modA5,modA9和modA10占所调查临床中耳炎分离株的三分之二以上。在这里,我们使用单分子实时(SMRT)甲基化组分析来识别所有这五个modA等位基因的DNA识别基序。这些等位基因的相变调节着多种蛋白质,包括候选疫苗和关键毒力表型,例如抗生素抗性(modA2,modA5,modA10),生物膜形成(modA2)和免疫逃避(modA4)。在中耳炎的黄鼠模型中对modA2菌株的分析显示,中耳中modA2的ON切换是一个明确的选择。我们的结果表明,在动物模型系统中,双相表观遗传开关可以控制细菌毒力,免疫逃逸和生态位适应。

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