A patatin-like phospholipase functions during gametocyte induction in the malaria parasite Plasmodium falciparum

被引:21
|
作者
Flammersfeld, Ansgar [1 ]
Panyot, Atscharah [1 ]
Yamaryo-Botte, Yoshiki [2 ]
Aurass, Philipp [4 ]
Przyborski, Jude M. [3 ]
Flieger, Antje [4 ]
Botte, Cyrille [2 ]
Pradel, Gabriele [1 ]
机构
[1] Rhein Westfal TH Aachen, Inst Zool, Div Cellular, Appl Infection Biol, Aachen, Germany
[2] Univ Grenoble Alpes, Inst Adv Biosciences, ApicoLipid Team, La Tronche, France
[3] Inst, Div Entropathogn Bacteria, Robert Koch, Legionella, Wernigerode, Germany
[4] Heidelberg Univ Hosp, Centre Infect Dis, Heidelberg, Germany
关键词
malaria; Plasmodium falciparum; gametocyte induction; patatin-like phospholipase; sexual commitment; phosphatidylcholine; PROTECTS TOXOPLASMA-GONDII; SEXUAL COMMITMENT; LEGIONELLA-PNEUMOPHILA; LIPOLYTIC ENZYMES; XANTHURENIC ACID; TOBACCO-LEAVES; FATTY-ACIDS; IN-VIVO; PROTEINS; TRANSMISSION;
D O I
10.1111/cmi.13146
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Patatin-like phospholipases (PNPLAs) are highly conserved enzymes of prokaryotic and eukaryotic organisms with major roles in lipid homeostasis. The genome of the malaria parasite Plasmodium falciparum encodes four putative PNPLAs with predicted functions during phospholipid degradation. We here investigated the role of one of the plasmodial PNPLAs, a putative PLA(2) termed PNPLA1, during blood stage replication and gametocyte development. PNPLA1 is present in the asexual and sexual blood stages and here localizes to the cytoplasm. PNPLA1-deficiency due to gene disruption or conditional gene-knockdown had no effect on intraerythrocytic growth, gametocyte development and gametogenesis. However, parasites lacking PNPLA1 were impaired in gametocyte induction, while PNPLA1 overexpression promotes gametocyte formation. The loss of PNPLA1 further leads to transcriptional down-regulation of genes related to gametocytogenesis, including the gene encoding the sexual commitment regulator AP2-G. Additionally, lipidomics of PNPLA1-deficient asexual blood stage parasites revealed overall increased levels of major phospholipids, including phosphatidylcholine (PC), which is a substrate of PLA(2). PC synthesis is known to be pivotal for erythrocytic replication, while the reduced availability of PC precursors drives the parasite into gametocytogenesis; we thus hypothesize that the higher PC levels due to PNPLA1-deficiency prevent the blood stage parasites from entering the sexual pathway.
引用
收藏
页数:20
相关论文
共 50 条
  • [41] Changes in lipid composition during sexual development of the malaria parasite Plasmodium falciparum
    Phuong N. Tran
    Simon H. J. Brown
    Melanie Rug
    Melanie C. Ridgway
    Todd W. Mitchell
    Alexander G. Maier
    Malaria Journal, 15
  • [42] Dynamics of DNA Replication during Male Gametogenesis in the Malaria Parasite Plasmodium Falciparum
    Matthews, Holly
    McDonald, Jennifer
    Totanes, Francis Isidore G.
    Merrick, Catherine J.
    CELLULAR MICROBIOLOGY, 2022, 2022
  • [43] Molecular function of a translational regulator during gametocytogenesis of the malaria parasite plasmodium falciparum
    Cui, Liwang
    Li, Jinfang
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2005, 73 (06): : 134 - 135
  • [44] Human erythrocyte remodelling during Plasmodium falciparum malaria parasite growth and egress
    Mbengue, Alassane
    Yam, Xue Y.
    Braun-Breton, Catherine
    BRITISH JOURNAL OF HAEMATOLOGY, 2012, 157 (02) : 171 - 179
  • [45] A protein interaction network of the malaria parasite Plasmodium falciparum
    Douglas J. LaCount
    Marissa Vignali
    Rakesh Chettier
    Amit Phansalkar
    Russell Bell
    Jay R. Hesselberth
    Lori W. Schoenfeld
    Irene Ota
    Sudhir Sahasrabudhe
    Cornelia Kurschner
    Stanley Fields
    Robert E. Hughes
    Nature, 2005, 438 : 103 - 107
  • [46] Genome sequence of the human malaria parasite Plasmodium falciparum
    Malcolm J. Gardner
    Neil Hall
    Eula Fung
    Owen White
    Matthew Berriman
    Richard W. Hyman
    Jane M. Carlton
    Arnab Pain
    Karen E. Nelson
    Sharen Bowman
    Ian T. Paulsen
    Keith James
    Jonathan A. Eisen
    Kim Rutherford
    Steven L. Salzberg
    Alister Craig
    Sue Kyes
    Man-Suen Chan
    Vishvanath Nene
    Shamira J. Shallom
    Bernard Suh
    Jeremy Peterson
    Sam Angiuoli
    Mihaela Pertea
    Jonathan Allen
    Jeremy Selengut
    Daniel Haft
    Michael W. Mather
    Akhil B. Vaidya
    David M. A. Martin
    Alan H. Fairlamb
    Martin J. Fraunholz
    David S. Roos
    Stuart A. Ralph
    Geoffrey I. McFadden
    Leda M. Cummings
    G. Mani Subramanian
    Chris Mungall
    J. Craig Venter
    Daniel J. Carucci
    Stephen L. Hoffman
    Chris Newbold
    Ronald W. Davis
    Claire M. Fraser
    Bart Barrell
    Nature, 2002, 419 : 498 - 511
  • [47] Genome variation and evolution of the malaria parasite Plasmodium falciparum
    Jeffares, Daniel C.
    Pain, Arnab
    Berry, Andrew
    Cox, Anthony V.
    Stalker, James
    Ingle, Catherine E.
    Thomas, Alan
    Quail, Michael A.
    Siebenthall, Kyle
    Uhlemann, Anne-Catrin
    Kyes, Sue
    Krishna, Sanjeev
    Newbold, Chris
    Dermitzakis, Emmanouil T.
    Berriman, Matthew
    NATURE GENETICS, 2007, 39 (01) : 120 - 125
  • [48] Complete gene map of the plastid-like DNA of the malaria parasite Plasmodium falciparum
    Wilson, RJM
    Denny, PW
    Preiser, PR
    Rangachari, K
    Roberts, K
    Roy, A
    Whyte, A
    Strath, M
    Moore, DJ
    Moore, PW
    Williamson, DH
    JOURNAL OF MOLECULAR BIOLOGY, 1996, 261 (02) : 155 - 172
  • [49] Polyamine uptake by the intraerythrocytic malaria parasite, Plasmodium falciparum
    Niemand, J.
    Louw, A. I.
    Birkholtz, L.
    Kirk, K.
    INTERNATIONAL JOURNAL FOR PARASITOLOGY, 2012, 42 (10) : 921 - 929
  • [50] Characterisation of a δ-COP homologue in the malaria parasite, Plasmodium falciparum
    Adisa, A
    Rug, M
    Foley, M
    Tilley, L
    MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2002, 123 (01) : 11 - 21