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潜在贾第虫疫苗候选物囊壁蛋白2和α1-贾第虫蛋白的基因变异

Genetic variation in potential Giardia vaccine candidates cyst wall protein 2 and α1-giardin.

作者信息

Radunovic Matej, Klotz Christian, Saghaug Christina Skår, Brattbakk Hans-Richard, Aebischer Toni, Langeland Nina, Hanevik Kurt

机构信息

Department of Clinical Science, University of Bergen, 8th floor, Lab-building, N-5021, Bergen, Norway.

Department of Infectious Diseases, Unit 16 Mycotic and Parasitic Agents and Mycobacteria, Robert Koch-Institute, Berlin, Germany.

出版信息

Parasitol Res. 2017 Aug;116(8):2151-2158. doi: 10.1007/s00436-017-5516-9. Epub 2017 Jun 3.

Abstract

Giardia is a prevalent intestinal parasitic infection. The trophozoite structural protein a1-giardin (a1-g) and the cyst protein cyst wall protein 2 (CWP2) have shown promise as Giardia vaccine antigen candidates in murine models. The present study assesses the genetic diversity of a1-g and CWP2 between and within assemblages A and B in human clinical isolates. a1-g and CWP2 sequences were acquired from 15 Norwegian isolates by PCR amplification and 20 sequences from German cultured isolates by whole genome sequencing. Sequences were aligned to reference genomes from assemblage A2 and B to identify genetic variance. Genetic diversity was found between assemblage A and B reference sequences for both a1-g (90.8% nucleotide identity) and CWP2 (82.5% nucleotide identity). However, for a1-g, this translated into only 3 amino acid (aa) substitutions, while for CWP2 there were 41 aa substitutions, and also one aa deletion. Genetic diversity within assemblage B was larger; nucleotide identity 92.0% for a1-g and 94.3% for CWP2, than within assemblage A (nucleotide identity 99.0% for a1-g and 99.7% for CWP2). For CWP2, the diversity on both nucleotide and protein level was higher in the C-terminal end. Predicted antigenic epitopes were not affected for a1-g, but partially for CWP2. Despite genetic diversity in a1-g, we found aa sequence, characteristics, and antigenicity to be well preserved. CWP2 showed more aa variance and potential antigenic differences. Several CWP2 antigens might be necessary in a future Giardia vaccine to provide cross protection against both Giardia assemblages infecting humans.

摘要

贾第虫是一种常见的肠道寄生虫感染。滋养体结构蛋白a1-贾第虫蛋白(a1-g)和包囊蛋白包囊壁蛋白2(CWP2)在小鼠模型中已显示出作为贾第虫疫苗抗原候选物的潜力。本研究评估了人类临床分离株中A群和B群之间以及群内a1-g和CWP2的遗传多样性。通过PCR扩增从15株挪威分离株中获取a1-g和CWP2序列,并通过全基因组测序从20株德国培养分离株中获取20个序列。将序列与A2群和B群的参考基因组进行比对以识别遗传变异。在a1-g(核苷酸同一性为90.8%)和CWP2(核苷酸同一性为82.5%)的A群和B群参考序列之间发现了遗传多样性。然而,对于a1-g,这仅转化为3个氨基酸(aa)替代,而对于CWP2则有41个aa替代,还有1个aa缺失。B群内的遗传多样性更大;a1-g的核苷酸同一性为92.0%,CWP2为94.3%,高于A群内(a1-g的核苷酸同一性为99.0%,CWP2为99.7%)。对于CWP2,C末端的核苷酸和蛋白质水平的多样性都更高。预测的抗原表位对a1-g没有影响,但对CWP2有部分影响。尽管a1-g存在遗传多样性,但我们发现其氨基酸序列、特征和抗原性保存良好。CWP2显示出更多的氨基酸变异和潜在的抗原差异。未来的贾第虫疫苗可能需要几种CWP2抗原,以提供针对感染人类的两种贾第虫群的交叉保护。

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