巴基斯坦恶性疟原虫分离株顶端膜抗原-1的基因结构。

0 PARASITOLOGY Parasites, hosts and diseases Pub Date : 2024-08-01 Epub Date: 2024-08-26 DOI:10.3347/PHD.24028
Komal Zaib, Asifullah Khan, Muhammad Umair Khan, Ibrar Ullah, Tuấn Cường Võ, Jung-Mi Kang, Hương Giang Lê, Byoung-Kuk Na, Sahib Gul Afridi
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引用次数: 0

摘要

恶性疟原虫顶端膜抗原-1(PfAMA-1)是血期疟疾疫苗的主要候选抗原。全球 pfama-1 的遗传多态性表明,该基因的遗传多样性会干扰针对该抗原的疫苗的有效开发。本研究旨在探索巴基斯坦开伯尔-普赫图赫瓦(KP)省收集的恶性疟原虫分离株中 pfama-1 的遗传多样性和基因结构。研究人员从巴基斯坦开伯尔巴图克瓦省的恶性疟原虫分离株中获得了 19 个全长 pfama-1 序列,并对其遗传多态性和自然选择进行了研究。KP-Pakistan的pfama-1表现出遗传多样性,其中发现了58个氨基酸变化,大部分位于外结构域和结构域I、II和III。在全球 pfama-1 外结构域中常见的氨基酸变化也在 KP-Pakistan pfama-1 中检测到。有趣的是,在 KP-Pakistan pfama-1 中发现了 13 个在全球群体中未报道的新的氨基酸变化。KP-Pakistan pfama-1 与全球 pfama-1 的遗传多样性水平相似。在 KP-Pakistan pfama-1 中还发现了自然选择和重组事件的证据。
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Genetic structure of apical membrane antigen-1 in Plasmodium falciparum isolates from Pakistan.

Plasmodium falciparum apical membrane antigen-1 (PfAMA-1) is a major candidate for the blood-stage malaria vaccine. Genetic polymorphisms of global pfama-1suggest that the genetic diversity of the gene can disturb effective vaccine development targeting this antigen. This study was conducted to explore the genetic diversity and gene structure of pfama-1 among P. falciparum isolates collected in the Khyber Pakhtunkhwa (KP) province of Pakistan. A total of 19 full-length pfama-1 sequences were obtained from KP-Pakistan P. falciparum isolates, and genetic polymorphism and natural selection were investigated. KP-Pakistan pfama-1 exhibited genetic diversity, wherein 58 amino acid changes were identified, most of which were located in ectodomains, and domains I, II, and III. The amino acid changes commonly found in the ectodomain of global pfama-1 were also detected in KP-Pakistan pfama-1. Interestingly, 13 novel amino acid changes not reported in the global population were identified in KP-Pakistan pfama-1. KP-Pakistan pfama-1 shared similar levels of genetic diversity with global pfama-1. Evidence of natural selection and recombination events were also detected in KP-Pakistan pfama-1.

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A novel kit for enrichment of fecal helminth eggs. Alterations in immunized antigens of Anisakis pegreffii by ampicillin-induced gut microbiome changes in mice. CysLT receptor-mediated NOX2 activation is required for IL-8 production in HMC-1 cells induced by Trichomonas vaginalis-derived secretory products. Dynamin 2-mediated endocytosis of BLT1 is required for IL-8 production in HMC-1 cells induced by Trichomonas vaginalis-derived secretory products. Genetic structure of apical membrane antigen-1 in Plasmodium falciparum isolates from Pakistan.
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