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来自五例孤立性淋巴细胞瘤患者的伯氏疏螺旋体狭义种分离株的分子分型

Molecular subtyping of Borrelia burgdorferi sensu lato isolates from five patients with solitary lymphocytoma.

作者信息

Picken R N, Strle F, Ruzic-Sabljic E, Maraspin V, Lotric-Furlan S, Cimperman J, Cheng Y, Picken M M

机构信息

Section of Infectious Disease, Rush-Presbyterian-St. Luke's Medical Center, Chicago, Illinois, USA.

出版信息

J Invest Dermatol. 1997 Jan;108(1):92-7. doi: 10.1111/1523-1747.ep12285646.

Abstract

Solitary lymphocytoma is a rare cutaneous manifestation of Lyme borreliosis that has been reported almost exclusively from Europe. This suggests that its etiologic agent may be absent or extremely rare on the North American continent. All three species of B. burgdorferi sensu lato known to be associated with human Lyme borreliosis (B. burgdorferi sensu stricto, B. garinii, and B. afzelii have been isolated in Europe, whereas only B. burgdorferi sensu stricto has been found in North America. This suggests that either B. garinii or B. afzelii might be the etiologic agent of borrelial lymphocytoma. To investigate this hypothesis we characterized five strains of B. burgdorferi sensu lato isolated from lymphocytoma lesions of patients residing in Slovenia. The methods used included: large restriction fragment pattern analysis of restriction enzyme MluI-digested genomic DNA, plasmid profiling, protein profiling, ribotyping using 5S, 16S, and 23S rDNA probes, and polymerase chain reaction amplification of the rrf (5S)-rrl (23S) intergenic spacer region. Molecular subtyping showed that four of the five isolates belonged to the species B. afzelii; however, this species is the predominant patient isolate in Slovenia and, therefore, may not represent a preferential association with lymphocytoma. The fifth isolate appeared to be most closely related to the DN127 genomic group of organisms. Further characterization of the isolate revealed that it possessed a unique molecular "fingerprint." The results not only show that borrelial lymphocytoma can be caused by B. afzelii but also demonstrate an association with another genomic group of B. burgdorferi sensu lato that is present in North America as well.

摘要

孤立性淋巴细胞瘤是莱姆病的一种罕见皮肤表现,几乎仅在欧洲有报道。这表明其病原体在北美大陆可能不存在或极为罕见。已知与人类莱姆病相关的三种狭义伯氏疏螺旋体(狭义伯氏疏螺旋体、伽氏疏螺旋体和阿氏疏螺旋体)在欧洲均有分离,而在北美仅发现了狭义伯氏疏螺旋体。这表明伽氏疏螺旋体或阿氏疏螺旋体可能是伯氏淋巴细胞瘤的病原体。为了研究这一假设,我们对从斯洛文尼亚患者淋巴细胞瘤病变中分离出的五株狭义伯氏疏螺旋体进行了特征分析。所采用的方法包括:用限制性内切酶MluI消化基因组DNA后的大片段限制性图谱分析、质粒图谱分析、蛋白质图谱分析、使用5S、16S和23S rDNA探针的核糖体分型,以及rrf(5S)-rrl(23S)基因间隔区的聚合酶链反应扩增。分子亚型分析表明,五株分离株中有四株属于阿氏疏螺旋体;然而,该菌种是斯洛文尼亚患者的主要分离株,因此可能并不代表与淋巴细胞瘤有优先关联。第五株分离株似乎与DN127基因组的生物体关系最为密切。对该分离株的进一步特征分析表明,它具有独特的分子“指纹”。结果不仅表明伯氏淋巴细胞瘤可由阿氏疏螺旋体引起,还证明了与北美也存在的另一个狭义伯氏疏螺旋体基因组群有关联。

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