Structure-genetic diversity and recombinant protein of circumsporozoite protein (CSP) of vivax malaria antigen: A potential malaria vaccine candidate

Gene Reports ◽  
2021 ◽  
pp. 101132
Author(s):  
Vahid Raissi ◽  
Soudabeh Etemadi ◽  
Muhammad Ibrahim Getso ◽  
Ahmad Mehravaran ◽  
Omid Raiesi
2021 ◽  
Author(s):  
Nouh Saad Mohamed ◽  
Hanadi AbdElbagi ◽  
Ahad R. Elsadig ◽  
Abdalla Elssir Ahmed ◽  
Yassir Osman Mohammed ◽  
...  

Abstract The currently used malaria vaccine; the RTS,S, is designed based on the Plasmodium falciparum circumsporozoite protein (PfCSP). The PfCSP gene, besides having different polymorphic patterns, can vary between P. falciparum isolates due to geographical origin and host immune response. Such aspects are essential when considering the deployment of the RTS,S vaccine in a certain region. Therefore, in this study we assessed the genetic diversity of P. falciparum in Sudan based on the PfCSP gene by investigating the diversity at the N-terminal, central repeat, and the C-terminal regions. The results of the N-terminal region showed the presence of 2 different haplotypes with a haplotype diversity (Hapd) of 0.425 ± 0.00727. The presence of the unique insertion of NNNGDNGREGKDEDKRDGNN was reported. The KLKQP motif was conserved in all the studied isolates. At the central repeat region, 11 haplotypes were seen with a Hapd of 0.779 ± 0.00097. The analysis of the genetic diversity in the C-terminal region showed the presence of 10 haplotypes with a Hapd of 0.457 ± 0.073. In this study, the results indicated a high conservation at the PfCSP gene. This may further contribute in understanding the genetic polymorphisms of P. falciparum prior to the deployment of the RTS,S vaccine in Sudan.


2021 ◽  
Vol 5 (4) ◽  
pp. 14-17
Author(s):  
Azua Ekokobe Wilfred ◽  
Nkengafac Nyiawung Fobellah ◽  
Omeichu Agwenam Amadeus ◽  
Rose Leke ◽  
Mbatcham Wilfred ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
Rebeka Nazareth ◽  
Pius Horumpende ◽  
Tolbert Sonda ◽  
Arnold Ndaro ◽  
Edson Mollel ◽  
...  

Background. A major challenge to malaria vaccine development is identification of protective epitopes and respective protective immune responses. Objective. To characterize naturally acquired Immunoglobulin G (IgG) responses to the synthetic peptide AS202.11, a malaria vaccine candidate. Methodology. This community based cross-sectional study enrolled 320 participants aged 1 year and above. Demographic information was recorded through interviews. Detection of P. falciparum infection was done by microscopy, malaria rapid diagnostic test, and polymerase chain reaction. ELISA was used to detect IgG antibody. Data was analyzed using STATA. Results. The overall AS202.11 IgG seropositivity was 78.8% (73.9–82.9). Seropositivity by age categories was ≤12 years [74.3% (67.4–80.2)], 13–40 years [85.3% (76.5–91.1)], and >40 years [82.6% (68.7–91.1)]. Compared to the ≤ 12-year-old group, aORs for the other groups were 2.22 (1.14–4.32), p=0.019, and 1.87 (0.81–4.35), p=0.143, for the 13–40-year-old and >40-year-old groups, respectively. The 13–40-year-old group had more seropositive individuals compared to the ≤ 12-year-old group. Conclusion. We report a high degree of recognition of AS202.11 by IgG elicited by field P. falciparum strains, suggesting its close similarity to native P. falciparum antigens and possible suitability of the peptide as a future malaria vaccine candidate.


PLoS ONE ◽  
2014 ◽  
Vol 9 (9) ◽  
pp. e107764 ◽  
Author(s):  
Amy R. Noe ◽  
Diego Espinosa ◽  
Xiangming Li ◽  
Jordana G. A. Coelho-dos-Reis ◽  
Ryota Funakoshi ◽  
...  

2010 ◽  
Vol 78 (5) ◽  
pp. 2182-2188 ◽  
Author(s):  
Marjorie Mauduit ◽  
Rita Tewari ◽  
Nadya Depinay ◽  
Michèle Kayibanda ◽  
Eliette Lallemand ◽  
...  

ABSTRACT Immunization with live Plasmodium sporozoites under chloroquine prophylaxis (Spz plus CQ) induces sterile immunity against sporozoite challenge in rodents and, more importantly, in humans. Full protection is obtained with substantially fewer parasites than with the classic immunization with radiation-attenuated sporozoites. The sterile protection observed comprised a massive reduction in the hepatic parasite load and an additional effect at the blood stage level. Differences in the immune responses induced by the two protocols occur but are as yet little characterized. We have previously demonstrated that in mice immunized with irradiated sporozoites, immune responses against the circumsporozoite protein (CSP), the major component of the sporozoite's surface and the leading malaria vaccine candidate, were not essential for sterile protection. Here, we have employed transgenic P lasmodium berghei parasites in which the endogenous CSP was replaced by that of P lasmodium yoelii, another rodent malaria species, to assess the role of CSP in the sterile protection induced by the Spz-plus-CQ protocol. The data demonstrated that this role was minor because sterile immunity was obtained irrespective of the origin of CSP expressed by the parasites in this model of protection. The immunity was obtained through a single transient exposure of the host to the immunizing parasites (preerythrocytic and erythrocytic), a dose much smaller than that required for immunization with radiation-attenuated sporozoites.


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