Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5915355 | Molecular and Biochemical Parasitology | 2015 | 4 Pages |
â¢Inactivation of the Leishmania AQP1 gene was difficult.â¢Leishmania cells without AQP1 are viable.â¢Leishmania AQP1 is involved in cellular volume regulation.â¢Leishmania AQP1 null mutants are resistant to antimony.
The Leishmania aquaglyceroporin AQP1 plays an important physiological role in water and uncharged polar solutes transport, volume regulation, osmotaxis, and is a key determinant of antimony resistance. By targeted gene disruption, we generated a Leishmania major promastigote AQP1 null mutant. This required several attempts but a chromosomal null AQP1 mutant was obtained by loss of heterozygosity in the presence of a rescue plasmid encoding AQP1. Growth in the absence of selection led to the loss of the rescuing plasmid, indicating that AQP1 is not essential for Leishmania viability. The AQP1-null mutant was resistant to antimonyl tartrate (SbIII) and arsenite (AsIII) due to a decrease import of these metalloids. It also exhibited alterations in its osmoregulation abilities compared with wild-type cells. This is the first report of the generation of a genetic AQP1 null mutant in Leishmania parasite, confirming its physiological function and role in resistance to antimonials, the therapeutic mainstay against Leishmania.
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