<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-22T01:41:18Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/12678" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/12678</identifier><datestamp>2024-09-27T23:54:21Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19609</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">O'Brien, Caoimhe E</subfield>
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      <subfield code="a">Oliveira-Pacheco, João</subfield>
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      <subfield code="a">Ó Cinnéide, Eoin</subfield>
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      <subfield code="a">Haase, Max A B</subfield>
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      <subfield code="a">Hittinger, Chris Todd</subfield>
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      <subfield code="a">Rogers, Thomas R</subfield>
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      <subfield code="a">Zaragoza, Oscar</subfield>
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      <subfield code="a">Bond, Ursula</subfield>
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      <subfield code="a">Butler, Geraldine</subfield>
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      <subfield code="c">2021-03-31</subfield>
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      <subfield code="a">Candida tropicalis is a human pathogen that primarily infects the immunocompromised. Whereas the genome of one isolate, C. tropicalis MYA-3404, was originally sequenced in 2009, there have been no large-scale, multi-isolate studies of the genetic and phenotypic diversity of this species. Here, we used whole genome sequencing and phenotyping to characterize 77 isolates of C. tropicalis from clinical and environmental sources from a variety of locations. We show that most C. tropicalis isolates are diploids with approximately 2-6 heterozygous variants per kilobase. The genomes are relatively stable, with few aneuploidies. However, we identified one highly homozygous isolate and six isolates of C. tropicalis with much higher heterozygosity levels ranging from 36-49 heterozygous variants per kilobase. Our analyses show that the heterozygous isolates represent two different hybrid lineages, where the hybrids share one parent (A) with most other C. tropicalis isolates, but the second parent (B or C) differs by at least 4% at the genome level. Four of the sequenced isolates descend from an AB hybridization, and two from an AC hybridization. The hybrids are MTLa/α heterozygotes. Hybridization, or mating, between different parents is therefore common in the evolutionary history of C. tropicalis. The new hybrids were predominantly found in environmental niches, including from soil. Hybridization is therefore unlikely to be associated with virulence. In addition, we used genotype-phenotype correlation and CRISPR-Cas9 editing to identify a genome variant that results in the inability of one isolate to utilize certain branched-chain amino acids as a sole nitrogen source.</subfield>
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      <subfield code="a">PLoS Pathog. 2021 Mar 31;17(3):e1009138.</subfield>
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      <subfield code="a">10.1371/journal.ppat.1009138</subfield>
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      <subfield code="a">1553-7374</subfield>
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      <subfield code="a">PLoS pathogens</subfield>
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      <subfield code="a">33788904</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/12678</subfield>
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      <subfield code="a">Population genomics of the pathogenic yeast Candida tropicalis identifies hybrid isolates in environmental samples.</subfield>
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