Construction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes

ABSTRACT Candida glabrata is the second most common species causing candidiasis. C. glabrata can also readily acquire resistance to azole drugs, complicating its treatment. Here we add to the collection of disruption markers to aid in genetic analysis of this yeast. This new construct is marked with...

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Autores principales: Bao G. Vu, W. Scott Moye-Rowley
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Publicado: American Society for Microbiology 2018
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spelling oai:doaj.org-article:3f5ee69e5b1b40e587400858c065a3dc2021-11-15T15:22:13ZConstruction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes10.1128/mSphere.00099-182379-5042https://doaj.org/article/3f5ee69e5b1b40e587400858c065a3dc2018-04-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00099-18https://doaj.org/toc/2379-5042ABSTRACT Candida glabrata is the second most common species causing candidiasis. C. glabrata can also readily acquire resistance to azole drugs, complicating its treatment. Here we add to the collection of disruption markers to aid in genetic analysis of this yeast. This new construct is marked with a nourseothricin resistance cassette that produces an estrogen-activated form of Cre recombinase in a methionine-regulated manner. This allows eviction and reuse of this cassette in a facile manner. Using this new disruption marker, we have constructed a series of strains lacking different members of the major facilitator superfamily (MFS) of membrane transporter proteins. The presence of 15 MFS proteins that may contribute to drug resistance in C. glabrata placed a premium on development of a marker that could easily be reused to construct multiple gene-disrupted strains. Employing this recyclable marker, we found that loss of the MFS transporter-encoding gene FLR1 caused a dramatic increase in diamide resistance (as seen before), and deletion of two other MFS-encoding genes did not influence this phenotype. Interestingly, loss of FLR1 led to an increase in levels of oxidized glutathione, suggesting a possible molecular explanation for this enhanced oxidant sensitivity. We also found that while overproduction of the transcription factor Yap1 could suppress the fluconazole sensitivity caused by loss of the important ATP-binding cassette transporter protein Cdr1, this required the presence of FLR1. IMPORTANCE Export of drugs is a problem for chemotherapy of infectious organisms. A class of membrane proteins called the major facilitator superfamily contains a large number of proteins that often elevate drug resistance when overproduced but do not impact this phenotype when the gene is removed. We wondered if this absence of a phenotype for a disruption allele might be due to the redundancy of this group of membrane proteins. We describe the production of an easy-to-use recyclable marker cassette that will allow construction of strains lacking multiple members of the MFS family of transporter proteins.Bao G. VuW. Scott Moye-RowleyAmerican Society for MicrobiologyarticleCandida glabratamajor facilitator superfamilyselectable markertranscriptional regulationtransportersMicrobiologyQR1-502ENmSphere, Vol 3, Iss 2 (2018)
institution DOAJ
collection DOAJ
language EN
topic Candida glabrata
major facilitator superfamily
selectable marker
transcriptional regulation
transporters
Microbiology
QR1-502
spellingShingle Candida glabrata
major facilitator superfamily
selectable marker
transcriptional regulation
transporters
Microbiology
QR1-502
Bao G. Vu
W. Scott Moye-Rowley
Construction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes
description ABSTRACT Candida glabrata is the second most common species causing candidiasis. C. glabrata can also readily acquire resistance to azole drugs, complicating its treatment. Here we add to the collection of disruption markers to aid in genetic analysis of this yeast. This new construct is marked with a nourseothricin resistance cassette that produces an estrogen-activated form of Cre recombinase in a methionine-regulated manner. This allows eviction and reuse of this cassette in a facile manner. Using this new disruption marker, we have constructed a series of strains lacking different members of the major facilitator superfamily (MFS) of membrane transporter proteins. The presence of 15 MFS proteins that may contribute to drug resistance in C. glabrata placed a premium on development of a marker that could easily be reused to construct multiple gene-disrupted strains. Employing this recyclable marker, we found that loss of the MFS transporter-encoding gene FLR1 caused a dramatic increase in diamide resistance (as seen before), and deletion of two other MFS-encoding genes did not influence this phenotype. Interestingly, loss of FLR1 led to an increase in levels of oxidized glutathione, suggesting a possible molecular explanation for this enhanced oxidant sensitivity. We also found that while overproduction of the transcription factor Yap1 could suppress the fluconazole sensitivity caused by loss of the important ATP-binding cassette transporter protein Cdr1, this required the presence of FLR1. IMPORTANCE Export of drugs is a problem for chemotherapy of infectious organisms. A class of membrane proteins called the major facilitator superfamily contains a large number of proteins that often elevate drug resistance when overproduced but do not impact this phenotype when the gene is removed. We wondered if this absence of a phenotype for a disruption allele might be due to the redundancy of this group of membrane proteins. We describe the production of an easy-to-use recyclable marker cassette that will allow construction of strains lacking multiple members of the MFS family of transporter proteins.
format article
author Bao G. Vu
W. Scott Moye-Rowley
author_facet Bao G. Vu
W. Scott Moye-Rowley
author_sort Bao G. Vu
title Construction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes
title_short Construction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes
title_full Construction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes
title_fullStr Construction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes
title_full_unstemmed Construction and Use of a Recyclable Marker To Examine the Role of Major Facilitator Superfamily Protein Members in <named-content content-type="genus-species">Candida glabrata</named-content> Drug Resistance Phenotypes
title_sort construction and use of a recyclable marker to examine the role of major facilitator superfamily protein members in <named-content content-type="genus-species">candida glabrata</named-content> drug resistance phenotypes
publisher American Society for Microbiology
publishDate 2018
url https://doaj.org/article/3f5ee69e5b1b40e587400858c065a3dc
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