ICMR-National Institute of Malaria Research, Delhi, India.
Indian Foundation for Fundamental Research, Uttar Pradesh, India.
Transl Res. 2022 Nov;249:28-36. doi: 10.1016/j.trsl.2022.06.008. Epub 2022 Jun 10.
Malaria is still a global challenge with significant morbidity and mortality, especially in the African, South-East Asian, and Latin American regions. Malaria diagnosis is a crucial pillar in the control and elimination efforts, often accomplished by the administration of mass-scale Rapid diagnostic tests (RDTs). The inherent limitations of RDTs- insensitivity in scenarios of low transmission settings and deletion of one of the target proteins- Histidine rich protein 2/3 (HRP-2/3) are evident from multiple reports, thus necessitating the need to explore novel diagnostic tools/targets. The present study used peptide microarray to screen potential epitopes from 13 antigenic proteins (CSP, EXP1, LSA1, TRAP, AARP, AMA1, GLURP, MSP1, MSP2, MSP3, MSP4, P48/45, HAP2) of P. falciparum. Three cyclic constrained immunoreactive peptides- C6 (EXP1), A8 (MSP2), B7 (GLURP) were identified from 5458 cyclic constrained peptides (in duplicate) against P. falciparum-infected sera. Peptides (C6, A8, B7- cyclic constrained) and (G11, DSQ, NQN- corresponding linear peptides) were fairly immunoreactive towards P. falciparum-infected sera in dot-blot assay. Using direct ELISA, cyclic constrained peptides (C6 and B7) were found to be specific to P. falciparum-infected sera. A substantial number of samples were tested and the peptides successfully differentiated the P. falciparum positive and negative samples with high confidence. In conclusion, the study identified 3 cyclic constrained immunoreactive peptides (C6, B7, and A8) from P. falciparum secretory/surface proteins and further validated for diagnostic potential of 2 peptides (C6 and B7) with field-collected P. falciparum-infected sera samples.
疟疾仍然是一个具有重大发病率和死亡率的全球挑战,特别是在非洲、东南亚和拉丁美洲地区。疟疾诊断是控制和消除疟疾努力的重要支柱,通常通过大规模快速诊断检测(RDT)来实现。多项报告表明,RDT 存在固有局限性——在低传播环境下不敏感,以及目标蛋白之一(富含组氨酸蛋白 2/3(HRP-2/3))缺失,因此需要探索新的诊断工具/靶点。本研究使用肽微阵列从恶性疟原虫的 13 种抗原蛋白(CSP、EXP1、LSA1、TRAP、AARP、AMA1、GLURP、MSP1、MSP2、MSP3、MSP4、P48/45、HAP2)中筛选潜在的表位。从针对恶性疟原虫感染血清的 5458 个(重复)环状约束肽中鉴定出 3 个环状约束免疫反应肽-C6(EXP1)、A8(MSP2)和 B7(GLURP)。肽(C6、A8、B7-环状约束)和(G11、DSQ、NQN-对应线性肽)在斑点印迹分析中对恶性疟原虫感染血清具有相当的免疫反应性。使用直接 ELISA,发现环状约束肽(C6 和 B7)对恶性疟原虫感染血清具有特异性。对大量样本进行了测试,这些肽成功地区分了恶性疟原虫阳性和阴性样本,具有很高的置信度。总之,该研究从恶性疟原虫分泌/表面蛋白中鉴定出 3 个环状约束免疫反应肽(C6、B7 和 A8),并进一步验证了 2 个肽(C6 和 B7)在野外采集的恶性疟原虫感染血清样本中的诊断潜力。