Glucose-6-phosphate Dehydrogenase Variants: Analysing in Indian Plasmodium vivax Patients

• Published in: Acta parasitologica 2024-09, Vol.69 (3), p.1522-1529
• Main Authors: Jakhan, Jahnvi, Kojom Foko, Loick Pradel, Narang, Geetika, Singh, Vineeta
• Format: Article
• Language: English
• Subjects: Adult; Anemia; Animal Systematics/Taxonomy/Biogeography; Bioinformatics; Biomedical and Life Sciences; Biomedicine; Dehydrogenase; Dehydrogenases; DNA sequencing; Ecology; Exons; Female; Gene sequencing; Genetic analysis; Genetic diversity; Genetic variance; Genetic Variation; Genotype; Glucose 6 phosphate dehydrogenase; Glucosephosphate dehydrogenase; Glucosephosphate Dehydrogenase - genetics; Glucosephosphate Dehydrogenase Deficiency - genetics; Hemolytic anemia; Humans; India - epidemiology; Malaria; Malaria, Vivax - parasitology; Male; Medical Microbiology; Microbiology; Mutation; Original Paper; Parasitology; Plasmodium vivax; Plasmodium vivax - enzymology; Plasmodium vivax - genetics; Population studies; Primaquine; Retrospective Studies; Vector-borne diseases
• ISSN: 1230-2821; 1896-1851; 1896-1851
• DOI: 10.1007/s11686-024-00883-2

Purpose Primaquine (PQ) is recommended for radical cure of Plasmodium vivax ( Pv ) malaria, but its utilization is still limited due to high risk of severe haemolytic anaemia in patients with glucose-6-phosphate dehydrogenase deficiency (G6PD-d). The aim of the present study is to assess the different genotypic variants leading to G6PD-d in Delhi and Goa regions of India. Methods A total of 46 samples (34 retrospective Pv -mono-infected samples and 12 Pv -uninfected samples) were included in the study. Various genetic variants leading to G6PD-d were analysed by PCR amplification and DNA sequencing of different targeted exons of G6PD gene. Results Molecular analysis showed presence of four mutations in study population viz. 1311 C > T, 34.1% & IVSXI 93T > C, 45.5% and two novel mutations 1388G > T, 2.3% and 1398 C > T, 2.3% (silent mutation). The bioinformatics and computational analysis demonstrate that the slight conformational changes caused by R643L mutation in protein are deleterious in nature. Conclusion The observed mutations do not clarify the role or association between G6PD-d and Pv -infected cases. Further investigation is required in order to fully comprehend and analyse the precise role of these mutations with context to malaria infections.