Genome-wide analysis of PTR transporters in Candida species and their functional characterization in Candida auris
The peptide transport (PTR) or proton-dependent oligopeptide transporter (POT) family exploits the inwardly directed proton motive force to facilitate the cellular uptake of di/tripeptides. Interestingly, some representatives are also shown to import peptide-based antifungals in certain Candida spec...
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Veröffentlicht in: | Applied microbiology and biotechnology 2022-06, Vol.106 (11), p.4223-4235 |
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Sprache: | eng |
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Zusammenfassung: | The peptide transport (PTR) or proton-dependent oligopeptide transporter (POT) family exploits the inwardly directed proton motive force to facilitate the cellular uptake of di/tripeptides. Interestingly, some representatives are also shown to import peptide-based antifungals in certain
Candida
species. Thus, the identification and characterization of PTR transporters serve as an essential first step for their potential usage as antifungal peptide uptake systems. Herein, we present a genome-wide inventory of the PTR transporters in five prominent
Candida
species. Our study identifies 2 PTR transporters each in
C. albicans
and
C. dubliniensis
, 1 in
C. glabrata
, 4 in
C. parapsilosis
, and 3 in
C. auris
. Notably, despite all representatives retaining the conserved features seen in the PTR family, there exist two distinct classes of PTR transporters that differ in terms of their sequence identities and lengths of certain extracellular and intracellular segments. Further, we also evaluated the contribution of each PTR protein of the newly emerged multi-drug-resistant
C. auris
in di/tripeptide uptake. Notably, deletion of two
PTR
genes BNJ08_003830 and BNJ08_005124 led to a marked reduction in the transport capabilities of several tested di/tripeptides. However, all three genes could complement the role of native
PTR2
gene of
Saccharomyces cerevisiae
, albeit to varied levels. Besides, BNJ08_005124 deletion also resulted in increased resistance toward the peptide-nucleoside drug Nikkomycin Z as well as the glucosamine-6-phosphate synthase inhibitor, L-norvalyl-N3-(4-methoxyfumaroyl)-L-2,3-diaminopropionoic acid (Nva-FMDP), pointing toward its predominant role in their uptake mechanism. Altogether, the study provides an important template for future structure–function investigations of PTR transporters in
Candida
species.
Key points
•
Candida genome encodes for two distinct classes of PTR transporters.
•
Candida auris encodes for 3 PTR transporters with different specificities.
•
BNJ08_005124 in C. auris is involved in the uptake of Nikkomycin Z and Nva-FMDP. |
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ISSN: | 0175-7598 1432-0614 |
DOI: | 10.1007/s00253-022-11998-9 |