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首页> 外文期刊>Journal of Clinical Microbiology >Polymorphism in the Gene Coding for the Immunodominant Antigen gp43 from the Pathogenic FungusParacoccidioides brasiliensis
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Polymorphism in the Gene Coding for the Immunodominant Antigen gp43 from the Pathogenic FungusParacoccidioides brasiliensis

机译:巴西病原真菌Paracoccidioides brasiliensis的免疫抗原gp43基因编码中的多态性

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摘要

The gp43 glycoprotein is an immune-dominant antigen in patients with paracoccidioidomycosis (PCM). It is protective against murine PCM and is a putative virulence factor. The gp43 gene ofParacoccidioides brasiliensis B-339 is located in a 1,329-bp DNA fragment that includes two exons, a 78-bp intron, and a leader peptide-coding region of 105 bp. Polymorphism in gp43 has been suggested by the occurrence, in the same isolate or among different fungal samples, of isoforms with distinct isoelectric points. In the present study we aligned and compared with a consensus sequence the gp43 precursor genes of 17 P. brasiliensis isolates after sequencing two PCR products from each fungal sample. The genotypic types detected showed 1 to 4 or 14 to 15 informative substitution sites, preferentially localized between 578 and 1166 bp. Some nucleotide differences within individual isolates (noninformative sites) resulted in a second isoelectric point for the deduced protein. The most polymorphic sequences were also phylogenetically distant from the others and encoded basic gp43 isoforms. The three isolates in this group were from patients with chronic PCM, and their DNA restriction patterns were distinct in Southern blots. The nucleotides encoding the inner core of the murine T-cell-protective epitope of gp43 were conserved, offering hope for the development of a universal vaccine.
机译:gp43糖蛋白是副球菌病(PCM)患者的一种免疫优势抗原。它对鼠类PCM具有保护作用,是一种假定的致病因子。巴西巴拉圭球菌B-339的gp43基因位于一个1,329 bp的DNA片段中,该片段包含两个外显子,一个78 bp的内含子和一个105 bp的前导肽编码区。通过在同一个分离株中或在不同真菌样品中出现具有不同等电点的同工型,已经表明了gp43的多态性。在本研究中,我们比对并比较了共有序列的17 p的gp43前体基因。在对每个真菌样品中的两种PCR产物进行测序后,分离出巴西利亚。检测到的基因型类型显示1至4或14至15个信息性取代位点,优先位于578和1166 bp之间。个别分离物中的某些核苷酸差异(非信息性位点)导致了推导蛋白质的第二个等电点。大多数多态性序列在系统发育上也与其他序列相距甚远,并编码基本的gp43同工型。该组中的三个分离株来自慢性PCM患者,其DNA限制模式在Southern印迹中不同。编码gp43的鼠T细胞保护性抗原决定簇的内核的核苷酸被保守,为开发通用疫苗提供了希望。

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