Analysis of immunogenicity of different protein groups from malaria parasite Plasmodium falciparum

被引:6
|
作者
Krzyczmonik, Katarzyna [1 ]
Switnicki, Michal [1 ]
Kaczanowski, Szymon [1 ]
机构
[1] Polish Acad Sci, Inst Biochem & Biophy, Bioinformat Dept, PL-02106 Warsaw, Poland
关键词
Plasmodium falciparum; Malaria; Diversifying selection; Polymorphism; Immunogenicity; DIVERSIFYING SELECTION; MEMBRANE-PROTEINS; NATURAL-SELECTION; EVOLUTION; IDENTIFICATION; DATABASE; GENES;
D O I
10.1016/j.meegid.2012.07.023
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
It was observed that pressure of host immune system leads to diversifying selection (which can be measured in terms of pN/pS ratio). In this research we checked whether Plasmodium falciparum proteins containing experimentally evident epitopes from the IEDB database are subject to diversifying selection. We also investigated which life stage of this parasite and which proteins are subject to the strongest immune pressure. To answer these questions we used information about experimentally evident epitopes from P. falciparum, that interact with human immune system and sequences of different isolates of P. falciparum obtained from PlasmoDB. We confirmed the expectations that proteins containing IEDB epitopes are subject to stronger diversifying selection which is evidenced by higher pN/pS ratio. A stage characterized by the highest average pN/pS ratio is that of the sporozoite. The greatest fraction of putative antigens is also present at this stage. We also found that the sporozoite stage is particularly interesting for further analysis as it potentially contains the highest number of unidentified epitopes. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1911 / 1916
页数:6
相关论文
共 50 条
  • [1] Systematic Analysis of Proteomes with Emphasis on Insertions in Malaria Parasite Plasmodium falciparum
    Kapil, Charu
    Hussain, Tahir
    Jairajpuri, Mohamad Aman
    Yogavel, Manickam
    Chatterjee, Samrat
    Sharma, Amit
    PROTEIN AND PEPTIDE LETTERS, 2013, 20 (10) : 1088 - 1097
  • [2] Helicases involved in splicing from malaria parasite Plasmodium falciparum
    Tuteja, Renu
    PARASITOLOGY INTERNATIONAL, 2011, 60 (04) : 335 - 340
  • [3] Defining the protein interaction network of human malaria parasite Plasmodium falciparum
    Ramaprasad, Abhinay
    Pain, Arnab
    Ravasi, Timothy
    GENOMICS, 2012, 99 (02) : 69 - 75
  • [4] Protein phosphorylation during sexual differentiation in the malaria parasite Plasmodium falciparum
    Kumar, N
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1997, 87 (02) : 205 - 210
  • [5] From malaria parasite point of view - Plasmodium falciparum evolution
    Zerka, Agata
    Kaczmarek, Radoslaw
    Jaskiewicz, Ewa
    POSTEPY HIGIENY I MEDYCYNY DOSWIADCZALNEJ, 2015, 69 : 1519 - 1529
  • [6] Polysome profiling of the malaria parasite Plasmodium falciparum
    Lacsina, Joshua R.
    LaMonte, Gregory
    Nicchitta, Christopher V.
    Chi, Jen-Tsan
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2011, 179 (01) : 42 - 46
  • [7] Method for the separation of mitochondria and apicoplast from the malaria parasite Plasmodium falciparum
    Hata, Masayuki
    Sato, Shigeharu
    Kita, Kiyoshi
    PARASITOLOGY INTERNATIONAL, 2019, 69 : 99 - 102
  • [8] Proteomic Analysis of Urine from Patients with Plasmodium vivax Malaria Unravels a Unique Plasmodium vivax Protein That Is Absent from Plasmodium falciparum
    Fantin, Raianna F.
    Abeijon, Claudia
    Pereira, Dhelio B.
    Fujiwara, Ricardo T.
    Bueno, Lilian L.
    Campos-Neto, Antonio
    TROPICAL MEDICINE AND INFECTIOUS DISEASE, 2022, 7 (10)
  • [9] Co-expression network with protein-protein interaction and transcription regulation in malaria parasite Plasmodium falciparum
    Yu, Fu-Dong
    Yang, Shao-You
    Li, Yuan-Yuan
    Hu, Wei
    GENE, 2013, 518 (01) : 7 - 16
  • [10] ACTIN IN THE MEROZOITE OF THE MALARIA PARASITE, PLASMODIUM-FALCIPARUM
    FIELD, SJ
    PINDER, JC
    CLOUGH, B
    DLUZEWSKI, AR
    WILSON, RJM
    GRATZER, WB
    CELL MOTILITY AND THE CYTOSKELETON, 1993, 25 (01): : 43 - 48