间日疟原虫表面蛋白 8 在全球种群中的遗传多样性和自然选择。

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Infection Genetics and Evolution Pub Date : 2024-05-15 DOI:10.1016/j.meegid.2024.105605
Man Zhang , Yue Wang , Hai-Mo Shen , Shen-Bo Chen , Tian-Yu Wang , Kokouvi Kassegne , Jun-Hu Chen
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引用次数: 0

摘要

间日疟原虫表面蛋白8(PvMSP8)是开发多组分疫苗的一个很有希望的候选靶标。因此,确定 msp8 的遗传变异模式至关重要,可为合理设计间日疟原虫疟疾疫苗提供参考。本研究深入探讨了 Pvmsp8 基因的遗传特征,特别关注来自中缅边境地区(CMB)的样本,并将这些发现与更广泛的全球模式进行对比。研究发现,Pvmsp8 在不同人群中表现出明显的保守性,多态性有限,核苷酸多样性相对较低(0.00023-0.0012)。这种保护性与 msp1 等其他间日疟原虫抗原的高多态性形成了鲜明对比。在全球样本中总共发现了 25 个单倍型和 14 个氨基酸突变位点,所有突变位点都局限于非功能区。研究还注意到,缅甸、柬埔寨、泰国和越南人群共享大多数 CMB Pvmsp8 单倍型,表明地域差异较小,但与太平洋岛屿地区或巴拿马的单倍型差异明显。这些发现强调了在开发有针对性的疟疾疫苗时考虑间日疟原虫区域遗传多样性的重要性。塔吉玛检验没有发现偏离中性进化的情况,但在 kn 和 ks 率之间观察到了显著的统计学差异。这项研究的发现对于了解 Pvmsp8 基因的进化和种群结构至关重要,尤其是在地区性疟疾消除工作中。Pvmsp8 基因的高度保守性,加上其功能域缺乏突变,使其有希望成为开发广泛而有效的间日疟原虫疫苗的候选基因。因此,这项研究为合理开发针对这一基因稳定抗原的多价疟疾疫苗奠定了基础。
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Genetic Diversity and Natural Selection of Plasmodium vivax Merozoite Surface Protein 8 in Global Populations

Plasmodium vivax Merozoite Surface Protein 8 (PvMSP8) is a promising candidate target for the development of multi-component vaccines. Therefore, determining the genetic variation pattern of Pvmsp8 is essential in providing a reference for the rational design of the P. vivax malaria vaccines. This study delves into the genetic characteristics of the Pvmsp8 gene, specifically focusing on samples from the China-Myanmar border (CMB) region, and contrasts these findings with broader global patterns. The study uncovers that Pvmsp8 exhibits a notable level of conservation across different populations, with limited polymorphisms and relatively low nucleotide diversity (0.00023–0.00120). This conservation contrasts starkly with the high polymorphisms found in other P. vivax antigens such as Pvmsp1. A total of 25 haplotypes and 14 amino acid mutation sites were identified in the global populations, and all mutation sites were confined to non-functional regions. The study also notes that most CMB Pvmsp8 haplotypes are shared among Burmese, Cambodian, Thai, and Vietnamese populations, indicating less geographical variance, but differ notably from those found in Pacific island regions or the Panama. The findings underscore the importance of considering regional genetic diversity in P. vivax when developing targeted malaria vaccines. Non departure from neutral evolution were found by Tajima's D test, however, statistically significant differences were observed between the kn/ks rates. The study's findings are crucial in understanding the evolution and population structure of the Pvmsp8 gene, particularly during regional malaria elimination efforts. The highly conserved nature of Pvmsp8, combined with the lack of mutations in its functional domain, presents it as a promising candidate for developing a broad and effective P. vivax vaccine. This research thus lays a foundation for the rational development of multivalent malaria vaccines targeting this genetically stable antigen.

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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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