Abstract
Cryptococcus neoformans is a facultative intracellular pathogen, which can replicate in the acidic environment inside phagolysosomes. Deletion of the enzyme inositol-phosphosphingolipid-phospholipase-C (Isc1) makes C. neoformans hypersensitive to acidic pH likely by inhibiting the function of the proton pump, plasma membrane ATPase (Pma1). In this work, we examined the role of Isc1 on Pma1 transport and oligomerization. Our studies showed that Isc1 deletion did not affect Pma1 synthesis or transport, but significantly inhibited Pma1 oligomerization. Interestingly, Pma1 oligomerization could be restored by supplementing the medium with phytoceramide. These results offer insight into the mechanism of intracellular survival of C. neoformans.
| Original language | English |
|---|---|
| Pages (from-to) | 3932-3938 |
| Number of pages | 7 |
| Journal | FEBS Letters |
| Volume | 588 |
| Issue number | 21 |
| DOIs | |
| State | Published - Nov 3 2014 |
Keywords
- Cryptococcus neoformans
- Inositiol phosphosphingolipid
- phospholipase C (Isc1)
- Plasma membrane
- Plasma membrane ATPase (Pma1)
- Sphingolipid
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