TY - JOUR
T1 - Ornithine decarboxylase gene deletion mutants of Leishmania donovani
AU - Jiang, Yuqui
AU - Roberts, Sigrid C.
AU - Jardim, Armande
AU - Carter, Nicola S.
AU - Shin, Sarah
AU - Ariyanayagam, Mark
AU - Fairlamb, Alan H.
AU - Ullman, Buddy
PY - 1999/2/5
Y1 - 1999/2/5
N2 - A knockout strain of Leishmania donovani lacking both ornithine decarboxylase (ODC) alleles has been created by targeted gene replacement. Growth of Δodc cells in polyamine-deficient medium resulted in a rapid and profound depletion of cellular putrescine pools, although levels of spermidine were relatively unaffected. Concentrations of trypanothione, a spermidine conjugate, were also reduced, whereas glutathione concentrations were augmented. The Δodc L. donovani exhibited an auxotrophy for polyamines that could be circumvented by the addition of the naturally occurring polyamines, putrescine or spermidine, to the culture medium. Whereas putrescine supplementation restored intracellular pools of both putrescine and spermidine, exogenous spermidine was not converted back to putrescine, indicating that spermidine alone is sufficient to meet the polyamine requirement, and that L. donovani does not express the enzymatic machinery for polyamine degradation. The lack of a polyamine catabolic pathway in intact parasites was confirmed radiometrically. In addition, the Δodc strain could grow in medium supplemented with either 1,3-diaminopropane or 1,5diaminopentane (cadaverine), but polyamine auxotrophy could not be overcome by other aliphatic diamines or spermine. These data establish genetically that ODC is an essential gene in L. donovani, define the polyamine requirements of the parasite, and reveal the absence of a polyamine-degradative pathway.
AB - A knockout strain of Leishmania donovani lacking both ornithine decarboxylase (ODC) alleles has been created by targeted gene replacement. Growth of Δodc cells in polyamine-deficient medium resulted in a rapid and profound depletion of cellular putrescine pools, although levels of spermidine were relatively unaffected. Concentrations of trypanothione, a spermidine conjugate, were also reduced, whereas glutathione concentrations were augmented. The Δodc L. donovani exhibited an auxotrophy for polyamines that could be circumvented by the addition of the naturally occurring polyamines, putrescine or spermidine, to the culture medium. Whereas putrescine supplementation restored intracellular pools of both putrescine and spermidine, exogenous spermidine was not converted back to putrescine, indicating that spermidine alone is sufficient to meet the polyamine requirement, and that L. donovani does not express the enzymatic machinery for polyamine degradation. The lack of a polyamine catabolic pathway in intact parasites was confirmed radiometrically. In addition, the Δodc strain could grow in medium supplemented with either 1,3-diaminopropane or 1,5diaminopentane (cadaverine), but polyamine auxotrophy could not be overcome by other aliphatic diamines or spermine. These data establish genetically that ODC is an essential gene in L. donovani, define the polyamine requirements of the parasite, and reveal the absence of a polyamine-degradative pathway.
UR - http://www.scopus.com/inward/record.url?scp=0033525089&partnerID=8YFLogxK
U2 - 10.1074/jbc.274.6.3781
DO - 10.1074/jbc.274.6.3781
M3 - Article
C2 - 9920931
AN - SCOPUS:0033525089
SN - 0021-9258
VL - 274
SP - 3781
EP - 3788
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 6
ER -