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Phase Variations of the Mycoplasma penetrans Main Surface Lipoprotein Increase Antigenic Diversity

机译:支原体支反主表面脂蛋白的相变增加抗原多样性

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Mycoplasma penetrans is a recently identified mycoplasma, isolated from urine samples collected from human immunodeficiency virus (HIV)-infected patients. Its presence is significantly associated with HIV infection. The major antigen recognized during natural and experimental infections is an abundant P35 lipoprotein which, upon extraction, segregates in the Triton X-114 detergent phase and is the basis of M. penetrans-specific serological assays. We report here that the P35 antigen undergoes spontaneous and reversible phase variation at high frequency, leading to heterogeneous populations of mycoplasmas, even when derived from a clonal lineage. This variation was found to be determined at the transcription level, and although this property is not unique among the members of the class Mollicutes, the mechanism by which it occurs in M. penetrans differs from those previously described for other Mycoplasma species. Indeed, the P35 phase variation was due neither to a p35 gene rearrangement nor to point mutations within the gene itself or its promoter. The P35 phase variation in the different variants obtained was concomitant with modifications in the pattern of other expressed lipoproteins, probably due to regulated expression of selected members of a gene family which was found to potentially encode similar lipoproteins. M. penetrans variants could be selected on the basis of their lack of colony immunoreactivity with a polyclonal antiserum against a Triton X-114 extract, strongly suggesting that the mechanisms involved in altering surface antigen expression might allow evasion of the humoral immune response of the infected host.
机译:支原体支原体是最近鉴定出的支原体,是从感染了人类免疫缺陷病毒(HIV)的患者的尿液样本中分离出来的。它的存在与HIV感染显着相关。在自然和实验感染过程中公认的主要抗原是丰富的P35脂蛋白,提取后会分离在Triton X-114去污剂相中,是 M的基础。 penetrans 特异性血清学检测。我们在这里报告说,P35抗原在高频下经历自发和可逆的相变,即使从克隆谱系衍生出来也导致支原体的异质种群。发现这种变异是在转录水平上确定的,尽管该性质在 Mollicutes 类的成员中不是唯一的,但它是在 M中发生的机制。 penetrans 与先前针对其他支原体物种所描述的不同。确实,P35相位变化既不是由于 p35 基因重排,也不是由于基因本身或其启动子内部的点突变。在获得的不同变体中的P35相变伴随着其他表达的脂蛋白的模式的改变,这可能是由于发现了可能编码相似脂蛋白的基因家族的选定成员的表达调控。 M。可以根据与抗Triton X-114提取物的多克隆抗血清缺乏菌落免疫反应性来选择penetrans 变体,强烈表明与改变表面抗原表达有关的机制可能有助于规避小鼠的体液免疫反应。被感染的主机。

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