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The Moraxella catarrhalis Immunoglobulin D-Binding Protein MID Has Conserved Sequences and Is Regulated by a Mechanism Corresponding to Phase Variation

机译:卡他莫拉菌免疫球蛋白D结合蛋白MID具有保守的序列,并受相变机制的调节。

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摘要

The prevalence of the Moraxella catarrhalis immunoglobulin D (IgD)-binding outer membrane protein MID and its gene was determined in 91 clinical isolates and in 7 culture collection strains. Eighty-four percent of the clinical Moraxella strains expressed MID-dependent IgD binding. The mid gene was detected in all strains as revealed by homology of the signal peptide sequence and a conserved area in the 3′ end of the gene. When MID proteins from five different strains were compared, an identity of 65.3 to 85.0% and a similarity of 71.2 to 89.1% were detected. Gene analyses showed several amino acid repeat motifs in the open reading frames, and MID could be called a putative autotransport protein. Interestingly, homopolymeric {polyguanine [poly(G)]} tracts were detected at the 5′ ends within the open reading frames. By flow cytometry, using human IgD and fluorescein isothiocyanate-conjugated anti-IgD polyclonal antibodies, most strains showed two peaks: one high- and one low-intensity peak. All isolates expressing high levels of MID had 1, 2, or 3 triplets of G's in their poly(G) tracts, while strains not expressing MID had 4, 7, 8, or 10 G’s in their poly(G) tracts or point mutations causing a putative preterminated translation. Northern blot analysis revealed that the mid gene was regulated at the transcriptional level. Experiments with nonclumping variants of M. catarrhalis proved that bacteria lost their MID expression by removing a G in their poly(G) tracts. Moraxella strains isolated from the nasopharynx or from blood and sputum specimens expressed MID at approximately the same frequency. In addition, no variation was observed between strains of different geographical origins (Australia, Europe, Japan, or the United States). MID and the mid gene were found solely in M. catarrhalis, whereas related Neisseria and Moraxella species did not express MID. Taken together, MID appears to be a conserved protein that can be found in essentially all M. catarrhalis strains. Furthermore, MID is governed by poly(G) tracts when bacteria undergo phase variation.
机译:确定了91株临床分离株和7株培养菌株中卡他莫拉菌免疫球蛋白D(IgD)结合的外膜蛋白MID及其基因的发生率。百分之八十四的临床莫拉氏菌菌株表达了MID依赖的IgD结合。通过信号肽序列的同源性和基因3'末端的保守区揭示了在所有菌株中都检测到了中间基因。比较来自五个不同菌株的MID蛋白时,检出的同一性为65.3%至85.0%,相似度为71.2%至89.1%。基因分析显示在开放阅读框中有多个氨基酸重复基序,MID可以称为推定的自转运蛋白。有趣的是,在开放阅读框内的5'端检测到均聚物{polyguanine [poly(G)]}片段。通过流式细胞术,使用人IgD和荧光素异硫氰酸荧光素偶联的抗IgD多克隆抗体,大多数菌株显示两个峰:一个高强度峰和一个低强度峰。所有表达高水平MID的分离株在其poly(G)道中具有1、2或3个三联体G,而未表达MID的菌株在其poly(G)道中具有4、7、8或10G。导致假定的翻译终止。 Northern印迹分析表明,中间基因在转录水平受到调控。卡他氏菌的非结块变体实验证明,细菌通过去除其poly(G)区域中的G而失去了其MID表达。从鼻咽或从血液和痰标本中分离出的莫拉氏菌菌株以大约相同的频率表达MID。此外,在不同地理起源的菌株(澳大利亚,欧洲,日本或美国)之间未观察到变异。 MID和mid基因仅在粘膜炎莫拉氏菌中发现,而相关的奈瑟氏菌和莫拉氏菌则不表达MID。两者合计,MID似乎是一种保守的蛋白质,基本上可以在所有卡他莫拉氏菌菌株中找到。此外,当细菌发生相变时,MID受聚(G)束支配。

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