Analysis of Inteins in the Candida parapsilosis Complex for Simple and Accurate Species Identification
Author(s) -
Tâmara Heloísa Rocha Prandini,
Raquel Cordeiro Theodoro,
Ariane Bruder-Nascimento,
Christina M. Scheel,
Eduardo Bagagli
Publication year - 2013
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.00981-13
Subject(s) - intein , biology , genetics , computational biology , gene , rna splicing , rna
Inteins are coding sequences that are transcribed and translated with flanking sequences and then are excised by an autocatalytic process. There are two types of inteins in fungi, mini-inteins and full-length inteins, both of which present a splicing domain containing well-conserved amino acid sequences. Full-length inteins also present a homing endonuclease domain that makes the intein a mobile genetic element. These parasitic genetic elements are located in highly conserved genes and may allow for the differentiation of closely related species of theCandida parapsilosis (psilosis) complex. The correct identification of the three psilosis complex speciesC. parapsilosis ,Candida metapsilosis , andCandida orthopsilosis is very important in the clinical setting for improving antifungal therapy and patient care. In this work, we analyzed inteins that are present in the vacuolar ATPase geneVMA and in the threonyl-tRNA synthetase geneThrRS in 85 strains of theCandida psilosis complex (46C. parapsilosis , 17C. metapsilosis , and 22C. orthopsilosis ). Here, we describe an accessible and accurate technique based on a single PCR that is able to differentiate the psilosis complex based on the VMA intein. Although the ThrRS intein does not distinguish the three species of the psilosis complex by PCR product size, it can differentiate them by sequencing and phylogenetic analysis. Furthermore, this intein is unusually present as both mini- and full-length forms inC. orthopsilosis . Additional population studies should be performed to address whether this represents a common intraspecific variability or the presence of subspecies withinC. orthopsilosis .
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