Speaker
Description
The requirement of an efficient P. vivax vaccine is crucial as evidenced from reports of drug resistance globally. PvDBPII, a leading vaccine candidate for P. vivax, has cleared Phase I clinical trial and is reported to be highly polymorphic, which might be a major obstacle on the way of attaining a successful vaccine. India, a significant contributor to P. vivax malaria burden in the WHO-SEAR, exhibits varying P. vivax endemicity. Hence, understanding the pattern of diversity and selection in Pvdbp in India would be vital for developing a DBP-based vaccine.
Genetic diversity and natural selection of PvDBP-II was investigated in 73 P. vivax isolates collected from different parts of India. Out of a total of 57 SNPs identified, 18 were non-synonymous and 3 were synonymous mutations. The overall nucleotide diversity of 73 PvDBP-II isolates was 0.00609 with 22 haplotypes (Hd=0.87) identified. The high ratio of non-synonymous to synonymous mutations suggests that PvDBPII had evolved under positive selection.
Polymorphisms of PvDBP-II shows that isolates from India were genetically diverse. Also, findings from this study further confirmed that mutations and natural selection might increase and sustain evasion of host immunity. These results expand our understanding of P. vivax evolution in India and, more crucially, solidify the rationale for the development of a blood-stage P. vivax malaria vaccine.
Keywords
Malaria, India, P.vivax, PvDBPII, genetic diversity, natural selection
Junior Scientist Status | Yes, I am a Junior Scientist. |
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Professional Status of the Speaker | PhD Student |
Registration-ID code | #596 |
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Co-authors
External references
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