Affiliation:
1. Institut für Molekulare Infektionsbiologie, Universität Würzburg, Würzburg, Germany
Abstract
ABSTRACT
Fungi possess two distinct proton-coupled peptide transport systems, the dipeptide/tripeptide transporters (PTR) and the oligopeptide transporters (OPT), which enable them to utilize peptides as nutrients. In the pathogenic yeast
Candida albicans
, peptide transporters are encoded by gene families consisting of two
PTR
genes and eight
OPT
genes. To gain insight into the functions and importance of specific peptide transporters, we generated mutants lacking the two dipeptide/tripeptide transporters Ptr2 and Ptr22, as well as the five major oligopeptide transporters Opt1 to Opt5. These mutants were unable to grow in media containing peptides as the sole nitrogen source. Forced expression of individual peptide transporters in the septuple mutants showed that Ptr2 and Ptr22 could utilize all tested dipeptides as substrates but differed in their abilities to transport specific tripeptides. Interestingly, several oligopeptide transporters, which are thought to transport peptides consisting of more than three amino acids, also mediated the uptake of tripeptides. Opt1 especially turned out to be a highly flexible transporter that enabled growth on all tripeptides tested and could even utilize a dipeptide, a function that has never been ascribed to this family of peptide transporters. Despite their inability to grow on proteins or peptides, the
opt1
Δ
opt2
Δ
opt3
Δ
opt4
Δ
opt5
Δ
ptr2
Δ
ptr22
Δ septuple mutants had no
in vivo
fitness defect in a mouse model of gastrointestinal colonization. Therefore, the nutritional versatility of
C. albicans
enables it to utilize alternative nitrogen sources in this host niche, which probably contributes to its success as a commensal and pathogen in mammalian hosts.
Publisher
American Society for Microbiology
Subject
Molecular Biology,General Medicine,Microbiology
Cited by
29 articles.
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