Population genetic analyses inferred a limited genetic diversity across the pvama-1 DI domain among Plasmodium vivax isolates from Khyber Pakhtunkhwa regions of Pakistanopen access
- Authors
- Ullah, Ibrar; Afridi, Sahib Gul; Israr, Muhammad; Khan, Hizbullah; Shams, Sulaiman; Zaib, Komal; Le, Huong Giang; Kang, Jung-Mi; Na, Byoung-Kuk; Khan, Asifullah
- Issue Date
- Oct-2022
- Publisher
- BioMed Central
- Keywords
- Plasmodium vivax; Apical membrane antigen-1; Genetic diversity; Khyber Pakhtunkhwa; Pakistan
- Citation
- BMC Infectious Diseases, v.22, no.1
- Indexed
- SCIE
SCOPUS
- Journal Title
- BMC Infectious Diseases
- Volume
- 22
- Number
- 1
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/29808
- DOI
- 10.1186/s12879-022-07798-1
- ISSN
- 1471-2334
1471-2334
- Abstract
- Background Plasmodium vivax apical membrane antigen-1 (pvama-1) is an important vaccine candidate against Malaria. The genetic composition assessment of pvama-1 from wide-range geography is vital to plan the antigen based vaccine designing against Malaria. Methods The blood samples were collected from 84 P. vivax positive malaria patients from different districts of Khyber Pakhtunkhwa (KP) province of Pakistan. The highly polymorphic and immunogenic domain-I (DI) region of pvama-1 was PCR amplified and DNA sequenced. The QC based sequences raw data filtration was done using DNASTAR package. The downstream population genetic analyses were performed using MEGA4, DnaSP, Arlequin v3.5 and Network.5 resources. Results The analyses unveiled total 57 haplotypes of pvama-1 (DI) in KP samples with majorly prevalent H-14 and H-5 haplotypes. Pairwise comparative population genetics analyses identified limited to moderate genetic distinctions among the samples collected from different districts of KP, Pakistan. In context of worldwide available data, the KP samples depicted major genetic differentiation against the Korean samples with Fst = 0.40915 (P-value = 0.0001), while least distinction was observed against Indian and Iranian samples. The statistically significant negative values of Fu and Li's D* and F* tests indicate the evidence of population expansion and directional positive selection signature. The slow LD decay across the nucleotide distance in KP isolates indicates low nucleotide diversity. In context of reference pvama-1 sequence, the KP samples were identified to have 09 novel non-synonymous single nucleotide polymorphisms (nsSNPs), including several trimorphic and tetramorphic substitutions. Few of these nsSNPs are mapped within the B-cell predicted epitopic motifs of the pvama-1, and possibly modulate the immune response mechanism. Conclusion Low genetic differentiation was observed across the pvama-1 DI among the P. vivax isolates acquired from widespread regions of KP province of Pakistan. The information may implicate in future vaccine designing strategies based on antigenic features of pvama-1.
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