Awasthi Gauri, Tyagi Suchi, Kumar Vipin, Patel Sandip Kumar, Rojh Dharmendar, Sakrappanavar Vijeth, Kochar Sanjay Kumar, Talukdar Arunansu, Samanta Biaus, Das Aparup, Srivastava Sanjeeva, Patankar Swati
Molecular Parasitology Lab, Department of Biosciences and Bioengineering, IIT Bombay, Mumbai, Maharashtra, India.
National Institute of Malaria Research, Field Unit, Civil Hospital, Nadiad, Gujarat, India.
Proteomics Clin Appl. 2018 Jul;12(4):e1700077. doi: 10.1002/prca.201700077. Epub 2017 Nov 23.
Haptoglobin (Hp), an acute phase inflammatory protein is associated with malaria pathogenesis in several proteomics and genomics studies. The Hp gene has two co-dominant alleles: Hp1 and Hp2 that produce three genotypes: Hp1/Hp1, Hp1/Hp2 and Hp2/Hp2.
In this study, validation of the proteomics data with Multiple Reaction Monitoring Mass Spectroscopy (MRM-MS) is performed and the association of the Hp gene variants with severe, non-severe malaria and community (healthy) controls using genotyping PCRs and DNA sequencing is analysed.
Highly significant values of Hp is observed in the MRM assay that show a correlation with severity of malaria and is clearly distinguished from another febrile disease, dengue. Moreover, the Hp2/Hp2 genotype is seen in high percentages in non-severe malaria patients (74%) and community controls (72%) whereas patients diagnosed with severe malaria show only (31%) of this genotype. Sequencing of the Hp promoter region reveals three SNPs along with 10 unique haplotypes, out of which five are associated with non-severe and three with severe malaria populations (χ = 130; df = 18; p < 0.0001).
This proteo-genomic study focuses on the correlation of the Hp protein and gene with malaria, thus highlighting the pivotal role of this acute phase immune gene in malaria pathogenesis.
触珠蛋白(Hp)是一种急性期炎症蛋白,在多项蛋白质组学和基因组学研究中与疟疾发病机制相关。Hp基因有两个共显性等位基因:Hp1和Hp2,产生三种基因型:Hp1/Hp1、Hp1/Hp2和Hp2/Hp2。
在本研究中,使用多反应监测质谱(MRM-MS)对蛋白质组学数据进行验证,并通过基因分型PCR和DNA测序分析Hp基因变异与重症疟疾、非重症疟疾及社区(健康)对照之间的关联。
在MRM分析中观察到Hp的高度显著值,其与疟疾严重程度相关,并且与另一种发热性疾病登革热有明显区别。此外,非重症疟疾患者(74%)和社区对照(72%)中Hp2/Hp2基因型的比例较高,而被诊断为重症疟疾的患者中该基因型仅占(31%)。Hp启动子区域的测序揭示了三个单核苷酸多态性(SNP)以及10种独特的单倍型,其中五种与非重症疟疾相关,三种与重症疟疾人群相关(χ = 130;自由度 = 18;p < 0.0001)。
这项蛋白质组学-基因组学研究聚焦于Hp蛋白和基因与疟疾的相关性,从而突出了这种急性期免疫基因在疟疾发病机制中的关键作用。