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Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei.

Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei. Research Abstract Details 

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  • Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei. Abstract Text:

    dominique promeneurDominique Promeneur,yangjian liuYangjian Liu,jorge macielJorge Maciel,peter agrePeter Agre,landon s kingLandon S King,nirbhay kumarNirbhay Kumar,

    The malaria parasite can use host plasma glycerol for lipid biosynthesis and membrane biogenesis during the asexual intraerythrocytic development. The molecular basis for glycerol uptake into the parasite is undefined. We hypothesize that the Plasmodium aquaglyceroporin provides the pathway for glycerol uptake into the malaria parasite. To test this hypothesis, we identified the orthologue of Plasmodium falciparum aquaglyceroporin (PfAQP) in the rodent malaria parasite, Plasmodium berghei (PbAQP), and examined the biological role of PbAQP by performing a targeted deletion of the PbAQP gene. PbAQP and PfAQP are 62% identical in sequence. In contrast to the canonical NPA (Asn-Pro-Ala) motifs in most aquaporins, the PbAQP has NLA (Asn-Leu-Ala) and NPS (Asn-Leu-Ser) in those positions. PbAQP expressed in Xenopus oocytes was permeable to water and glycerol, suggesting that PbAQP is an aquaglyceroporin. In P. berghei, PbAQP was localized to the parasite plasma membrane. The PbAQP-null parasites were viable; however, they were highly deficient in glycerol transport. In addition, they proliferated more slowly compared with the WT parasites, and mice infected with PbAQP-null parasites survived longer. Taken together, these findings suggest that PbAQP provides the pathway for the entry of glycerol into P. berghei and contributes to the growth of the parasite during the asexual intraerythrocytic stages of infection. In conclusion, we demonstrate here that PbAQP plays an important role in the blood-stage development of the rodent malaria parasite during infection in mice and could be added to the list of targets for the design of antimalarial drugs.

    Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei. Publishing Authors By Initials

    d promeneurD Promeneur,y liuY Liu,j macielJ Maciel,p agreP Agre,ls kingLS King,n kumarN Kumar,

    For similar proteins: protozoan proteins research abstracts see: proteins: protozoan proteins research

    PUBMED ID PMID:

    MEDLINE DATE:

    Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Proceedings of the National Academy of Sciences of

    VOLUME: 104

    Page Numbers: 2211-6

    Journal Abbreviation: Proc. Natl. Acad. Sci. U.S.A.

    ISSN: 0027-8424

    DAY: 6

    MONTH: 02

    YEAR: 2007

    Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7505876

    Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei. Keywords Mesh Terms:

    KEYWORDS: Protozoan Proteins

    MESH TERMS: pathogenicity

    Chemical & Substance for Abstract: Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei. Information

    Substance Name: Glycerol

    Registry Number: 56-81-5

    Grant and Affiliation Information for Aquaglyceroporin PbAQP during intraerythrocytic development of the malaria parasite Plasmodium berghei.

    AFFILIATION: Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, MD 21205-2185, USA. d.promeneur@cellbio.duke.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: HL48268

    ACRONYM: HL

    MEDLINETA: Proc Natl Acad Sci U S A

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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