Population genetic analysis of Plasmodium falciparum cell-traversal protein for ookinetes and sporozoite among malaria patients from southern Nigeria

被引:3
作者
Oboh, Mary A. [1 ,6 ]
Isaac, Clement [2 ]
Schroeter, Marissa N. [1 ]
Morenikeji, Olanrewaju B. [3 ]
Amambua-Ngwa, Alfred [4 ]
Meremikwu, Martin M. [5 ]
Thomas, Bolaji N. [1 ,6 ]
机构
[1] Rochester Inst Technol, Dept Biomed Sci, Rochester, NY USA
[2] Ambrose Ali Univ, Fac Life Sci, Dept Zool, Ekpoma, Nigeria
[3] Univ Pittsburgh, Div Biol & Hlth Sci, Bradford, PA 16701 USA
[4] London Sch Hyg & Trop Med, Med Res Council Unit, Fajara, Gambia
[5] Univ Calabar, Teaching Hosp, Calabar, Cross River, Nigeria
[6] Rochester Inst Technol, Dept Biomed Sci, 153 Lomb Mem Dr, Rochester, NY 14623 USA
关键词
Plasmodium falciparum; genetic diversity; polymorphism; phylogenetic relatedness; sub-Saharan Africa  celtos; VACCINE DEVELOPMENT; DIVERSITY; POLYMORPHISM; EFFICACY; PFCRT;
D O I
10.1016/j.meegid.2022.105369
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Plasmodium falciparum immune escape mechanisms affect antigens being prioritized for vaccine design. As a result of the multiple surface antigens the parasite exhibits at different life cycle stages, designing a vaccine that would efficiently boost the immune system in clearing infections has been challenging. The P. falciparum cell -traversal protein for ookinetes and sporozoite (Pfceltos) is instrumental for ookinete traversal of the mosquito midgut and sporozoites invasion of the human liver cells. Pfceltos elicits both humoral and cellular immune response but has been reported with multiple single nucleotide polymorphisms in global isolates. A cross-sectional survey, conducted in southern Nigeria, between January-March 2021 recruited 283 individuals. Of this, 166 demonstrated P. falciparum infections (86 from Cross River and 80 from Edo), 48 (55.8%) while only 36 (45%) were amplified for Pfceltos gene from both sites respectively. Fifty amplified samples were sequenced and analysed for their diversity, polymorphisms and population structure of the gene. The number of segregating sites in Edo State was higher (34) than that of Cross River State. Though nucleotide diversity was higher for Edo compared to Cross River State (Ow = 0.02505; 7C = 0.03993 versus Ow = 0.00930; 7C = 0.01033 respectively), the reverse was the case for haplotype diversity (0.757 versus 0.890 for Edo and Cross River respectively). Of the twelve haplotypes observed from both states, only two (KASLPVEK and NAFLSFEK) were shared, with haplotype prevalence higher in Edo (16% and 36%) than Cross River (8% and 4%). The Tajima's D test was positive for both states, with Fst value showing a strong genetic differentiation (Fst = 0.25599), indicating the occurrence of balancing selection favoring haplotype circulation at a low frequency. The shared haplotypes, low Hst and Fst values presents a challenge to predict the extent of gene flow. High LD values present a grim public health consequence should a Pfceltos-conjugated vaccine be considered for prophylaxis in Nigeria.
引用
收藏
页数:7
相关论文
共 50 条
[1]   Genetic Diversity of Plasmodium falciparum Populations in Malaria Declining Areas of Sabah, East Malaysia [J].
Abd Razak, Mohd Ridzuan Mohd ;
Sastu, Umi Rubiah ;
Norahmad, Nor Azrina ;
Abdul-Karim, Abass ;
Muhammad, Amirrudin ;
Muniandy, Prem Kumar ;
Jelip, Jenarun ;
Rundi, Christina ;
Imwong, Mallika ;
Mudin, Rose Nani ;
Abdullah, Noor Rain .
PLOS ONE, 2016, 11 (03)
[2]  
[Anonymous], 2021, LANCET, V398, P1381, DOI 10.1016/S0140-6736(21)02235-2
[3]  
[Anonymous], 2017, PLOS MED, V14
[4]   Synergism between Pfcrt and Pfmdr 1 genes could account for the slow recovery of chloroquine sensitive Plasmodium falciparum strains in Ghana after chloroquine withdrawal [J].
Asare, Kwame K. ;
Boampong, Johnson N. ;
Duah, Nancy O. ;
Afoakwah, Richmond ;
Sehgal, Rakesh ;
Quashie, Neils B. .
JOURNAL OF INFECTION AND PUBLIC HEALTH, 2017, 10 (01) :110-119
[5]   Changing Prevalence of Potential Mediators of Aminoquinoline, Antifolate, and Artemisinin Resistance Across Uganda [J].
Asua, Victor ;
Conrad, Melissa D. ;
Aydemir, Ozkan ;
Duvalsaint, Marvin ;
Legac, Jennifer ;
Duarte, Elias ;
Tumwebaze, Patrick ;
Chin, Deborah M. ;
Cooper, Roland A. ;
Yeka, Adoke ;
Kamya, Moses R. ;
Dorsey, Grant ;
Nsobya, Sam L. ;
Bailey, Jeffrey ;
Rosenthal, Philip J. .
JOURNAL OF INFECTIOUS DISEASES, 2021, 223 (06) :985-994
[6]   Evidence of Artemisinin-Resistant Malaria in Africa [J].
Balikagala, Betty ;
Fukuda, Naoyuki ;
Ikeda, Mie ;
Katuro, Osbert T. ;
Tachibana, Shin-Ichiro ;
Yamauchi, Masato ;
Opio, Walter ;
Emoto, Sakurako ;
Anywar, Denis A. ;
Kimura, Eisaku ;
Palacpac, Nirianne M. Q. ;
Odongo-Aginya, Emmanuel, I ;
Ogwang, Martin ;
Horii, Toshihiro ;
Mita, Toshihiro .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 385 (13) :1163-1171
[7]   Haploview: analysis and visualization of LD and haplotype maps [J].
Barrett, JC ;
Fry, B ;
Maller, J ;
Daly, MJ .
BIOINFORMATICS, 2005, 21 (02) :263-265
[8]   Cellular and humoral immune effector mechanisms required for sterile protection against sporozoite challenge induced with the novel malaria vaccine candidate CelTOS [J].
Bergmann-Leitner, Elke S. ;
Legler, Patricia M. ;
Savranskaya, Tatyana ;
Ockenhouse, Christian F. ;
Angov, Evelina .
VACCINE, 2011, 29 (35) :5940-5949
[9]   Immunization with Pre-Erythrocytic Antigen CelTOS from Plasmodium falciparum Elicits Cross-Species Protection against Heterologous Challenge with Plasmodium berghei [J].
Bergmann-Leitner, Elke S. ;
Mease, Ryan M. ;
De La Vega, Patricia ;
Savranskaya, Tatyana ;
Polhemus, Mark ;
Ockenhouse, Christian ;
Angov, Evelina .
PLOS ONE, 2010, 5 (08)
[10]  
Chauhan VS, 2010, HUM VACCINES, V6, P757, DOI [10.4161/hv.6.9.12468, 10.4161.hv.6.9.12468]