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巴西副球孢子菌致病真菌免疫显性抗原gp43编码基因的多态性。

Polymorphism in the gene coding for the immunodominant antigen gp43 from the pathogenic fungus Paracoccidioides brasiliensis.

作者信息

Morais F V, Barros T F, Fukada M K, Cisalpino P S, Puccia R

机构信息

Departamento de Microbiologia, Imunologia e Parasitologia da Universidade Federal de São Paulo, São Paulo, SP, Brazil.

出版信息

J Clin Microbiol. 2000 Nov;38(11):3960-6. doi: 10.1128/JCM.38.11.3960-3966.2000.

Abstract

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 of Paracoccidioides 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.

摘要

gp43糖蛋白是副球孢子菌病(PCM)患者的一种免疫优势抗原。它对小鼠PCM具有保护作用,是一种假定的毒力因子。巴西副球孢子菌B - 339的gp43基因位于一个1329 bp的DNA片段中,该片段包括两个外显子、一个78 bp的内含子和一个105 bp的前导肽编码区。在同一分离株或不同真菌样本中出现具有不同等电点的同工型,提示gp43存在多态性。在本研究中,我们对每个真菌样本的两个PCR产物进行测序后,将17株巴西副球孢子菌分离株的gp43前体基因与一个共有序列进行比对和比较。检测到的基因型类型显示有1至4个或14至15个信息性替换位点,优先定位在578至1166 bp之间。个别分离株内的一些核苷酸差异(非信息性位点)导致推导蛋白出现第二个等电点。多态性最高的序列在系统发育上也与其他序列相距较远,编码碱性gp43同工型。该组中的三株分离株来自慢性PCM患者,它们在Southern印迹中的DNA限制性图谱不同。编码gp43小鼠T细胞保护性表位内核的核苷酸是保守的,这为开发通用疫苗带来了希望。

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