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Single-tube, dual channel pentaplexing for the identification of Candida strains associated with human infection
Invasive candidiasis is one of the most common nosocomial fungal infections worldwide. Delayed implementation of effective antifungal treatment caused by inefficient Candida diagnosis contributes to its notoriously high mortality rates. The availability of better Candida diagnostic tools would posit...
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Published in: | Scientific reports 2019-10, Vol.9 (1), p.14692-14, Article 14692 |
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creator | Jainlabdin, Mohd Hanif Batra, Ambalika Sánchez Paredes, Edith Hernández Hernández, Francisca Fu, Guoliang Tovar-Torres, Jorge |
description | Invasive candidiasis is one of the most common nosocomial fungal infections worldwide. Delayed implementation of effective antifungal treatment caused by inefficient
Candida
diagnosis contributes to its notoriously high mortality rates. The availability of better
Candida
diagnostic tools would positively impact patient outcomes. Here, we report on the development of a single-tube, dual channel pentaplex molecular diagnostic assay based on Multiplex Probe Amplification (MPA) technology. It allows simultaneous identification of
C
.
auris
,
C
.
glabrata
and
C
.
krusei
, at species-level as well as of six additional
albicans
and non-
albicans
pathogenic
Candida
at genus level. The assay overcomes the one-channel one-biomarker limitation of qPCR-based assays. Assay specificities are conferred by unique biomarker probe pairs with characteristic melting temperatures; post-amplification melting curve analysis allows simple identification of the infectious agent. Alerting for the presence of
C
.
auris
, the well-characterised multi-drug resistant outbreak strain, will facilitate informed therapy decisions and aid antifungal stewardship. The MPA
-Candida
assay can also be coupled to a pan-Fungal assay when differentiation between fungal and bacterial infections might be desirable. Its multiplexing capacity, detection range, specificity and sensitivity suggest the potential use of this novel MPA-
Candida
assay in clinical diagnosis and in the control and management of hospital outbreaks. |
doi_str_mv | 10.1038/s41598-019-51198-6 |
format | article |
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Candida
diagnosis contributes to its notoriously high mortality rates. The availability of better
Candida
diagnostic tools would positively impact patient outcomes. Here, we report on the development of a single-tube, dual channel pentaplex molecular diagnostic assay based on Multiplex Probe Amplification (MPA) technology. It allows simultaneous identification of
C
.
auris
,
C
.
glabrata
and
C
.
krusei
, at species-level as well as of six additional
albicans
and non-
albicans
pathogenic
Candida
at genus level. The assay overcomes the one-channel one-biomarker limitation of qPCR-based assays. Assay specificities are conferred by unique biomarker probe pairs with characteristic melting temperatures; post-amplification melting curve analysis allows simple identification of the infectious agent. Alerting for the presence of
C
.
auris
, the well-characterised multi-drug resistant outbreak strain, will facilitate informed therapy decisions and aid antifungal stewardship. The MPA
-Candida
assay can also be coupled to a pan-Fungal assay when differentiation between fungal and bacterial infections might be desirable. Its multiplexing capacity, detection range, specificity and sensitivity suggest the potential use of this novel MPA-
Candida
assay in clinical diagnosis and in the control and management of hospital outbreaks.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-51198-6</identifier><identifier>PMID: 31604994</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>38/22 ; 38/71 ; 38/77 ; 631/326/193 ; 631/337 ; 692/308/2778 ; 9/10 ; Antifungal Agents - therapeutic use ; Antimicrobial Stewardship ; Bacterial diseases ; Bacterial infections ; Biomarkers ; Biomarkers - analysis ; Candida ; Candida - classification ; Candida - genetics ; Candidiasis ; Candidiasis, Invasive - diagnosis ; Candidiasis, Invasive - drug therapy ; Candidiasis, Invasive - microbiology ; Diagnosis ; DNA, Fungal - genetics ; Drug resistance ; Drug Resistance, Multiple, Fungal ; Fungal infections ; Hospitals ; Humanities and Social Sciences ; Humans ; Limit of Detection ; Melting ; Melting curve ; Molecular Diagnostic Techniques - methods ; multidisciplinary ; Multidrug resistance ; Multiplex Polymerase Chain Reaction - methods ; Nosocomial infection ; Outbreaks ; Real-Time Polymerase Chain Reaction - methods ; Science ; Science (multidisciplinary) ; Sensitivity and Specificity ; Transition Temperature</subject><ispartof>Scientific reports, 2019-10, Vol.9 (1), p.14692-14, Article 14692</ispartof><rights>The Author(s) 2019</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-cca6f4e49802333298f07271b11b827b97b82e65fab025dc0273b6a878687dd83</citedby><cites>FETCH-LOGICAL-c474t-cca6f4e49802333298f07271b11b827b97b82e65fab025dc0273b6a878687dd83</cites><orcidid>0000-0001-6798-6714</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2304109643/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2304109643?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31604994$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jainlabdin, Mohd Hanif</creatorcontrib><creatorcontrib>Batra, Ambalika</creatorcontrib><creatorcontrib>Sánchez Paredes, Edith</creatorcontrib><creatorcontrib>Hernández Hernández, Francisca</creatorcontrib><creatorcontrib>Fu, Guoliang</creatorcontrib><creatorcontrib>Tovar-Torres, Jorge</creatorcontrib><title>Single-tube, dual channel pentaplexing for the identification of Candida strains associated with human infection</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Invasive candidiasis is one of the most common nosocomial fungal infections worldwide. Delayed implementation of effective antifungal treatment caused by inefficient
Candida
diagnosis contributes to its notoriously high mortality rates. The availability of better
Candida
diagnostic tools would positively impact patient outcomes. Here, we report on the development of a single-tube, dual channel pentaplex molecular diagnostic assay based on Multiplex Probe Amplification (MPA) technology. It allows simultaneous identification of
C
.
auris
,
C
.
glabrata
and
C
.
krusei
, at species-level as well as of six additional
albicans
and non-
albicans
pathogenic
Candida
at genus level. The assay overcomes the one-channel one-biomarker limitation of qPCR-based assays. Assay specificities are conferred by unique biomarker probe pairs with characteristic melting temperatures; post-amplification melting curve analysis allows simple identification of the infectious agent. Alerting for the presence of
C
.
auris
, the well-characterised multi-drug resistant outbreak strain, will facilitate informed therapy decisions and aid antifungal stewardship. The MPA
-Candida
assay can also be coupled to a pan-Fungal assay when differentiation between fungal and bacterial infections might be desirable. Its multiplexing capacity, detection range, specificity and sensitivity suggest the potential use of this novel MPA-
Candida
assay in clinical diagnosis and in the control and management of hospital outbreaks.</description><subject>38/22</subject><subject>38/71</subject><subject>38/77</subject><subject>631/326/193</subject><subject>631/337</subject><subject>692/308/2778</subject><subject>9/10</subject><subject>Antifungal Agents - therapeutic use</subject><subject>Antimicrobial Stewardship</subject><subject>Bacterial diseases</subject><subject>Bacterial infections</subject><subject>Biomarkers</subject><subject>Biomarkers - analysis</subject><subject>Candida</subject><subject>Candida - classification</subject><subject>Candida - genetics</subject><subject>Candidiasis</subject><subject>Candidiasis, Invasive - diagnosis</subject><subject>Candidiasis, Invasive - drug therapy</subject><subject>Candidiasis, Invasive - microbiology</subject><subject>Diagnosis</subject><subject>DNA, Fungal - genetics</subject><subject>Drug resistance</subject><subject>Drug Resistance, Multiple, Fungal</subject><subject>Fungal infections</subject><subject>Hospitals</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Limit of Detection</subject><subject>Melting</subject><subject>Melting curve</subject><subject>Molecular Diagnostic Techniques - methods</subject><subject>multidisciplinary</subject><subject>Multidrug resistance</subject><subject>Multiplex Polymerase Chain Reaction - methods</subject><subject>Nosocomial infection</subject><subject>Outbreaks</subject><subject>Real-Time Polymerase Chain Reaction - methods</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Sensitivity and Specificity</subject><subject>Transition Temperature</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kctu1TAQhiMEolXpC7BAltiwaMC3-LJBQkfcpEosgLXl-HLiKscOtlPg7etwSiks8GZGnm_-mdHfdU8RfIkgEa8KRYMUPUSyHxBqGXvQnWJIhx4TjB_ey0-681KuYHsDlhTJx90JQQxSKelpt3wOcT-7vq6juwB21TMwk47RzWBxsepldj8aAXzKoE4OBNt-gw9G15AiSB7sdLTBalBq1iEWoEtJJujqLPge6gSm9aAjCNE7s7U86R55PRd3fhvPuq_v3n7ZfegvP73_uHtz2RvKae2N0cxTR6WAmBCCpfCQY45GhEaB-Sh5C44NXo8QD9ZAzMnItOCCCW6tIGfd66Puso4HZ01bO-tZLTkcdP6pkg7q70oMk9qna8W4EFKyJvDiViCnb6srVR1CMW6edXRpLQoTOEACCSMNff4PepXWHNt5G0URlIxuFD5SJqdSsvN3yyCoNk_V0VPVPFW_PFXbFs_un3HX8tvBBpAjUFop7l3-M_s_sjfeOa3g</recordid><startdate>20191011</startdate><enddate>20191011</enddate><creator>Jainlabdin, Mohd Hanif</creator><creator>Batra, Ambalika</creator><creator>Sánchez Paredes, Edith</creator><creator>Hernández Hernández, Francisca</creator><creator>Fu, Guoliang</creator><creator>Tovar-Torres, Jorge</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6798-6714</orcidid></search><sort><creationdate>20191011</creationdate><title>Single-tube, dual channel pentaplexing for the identification of Candida strains associated with human infection</title><author>Jainlabdin, Mohd Hanif ; Batra, Ambalika ; Sánchez Paredes, Edith ; Hernández Hernández, Francisca ; Fu, Guoliang ; Tovar-Torres, Jorge</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-cca6f4e49802333298f07271b11b827b97b82e65fab025dc0273b6a878687dd83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>38/22</topic><topic>38/71</topic><topic>38/77</topic><topic>631/326/193</topic><topic>631/337</topic><topic>692/308/2778</topic><topic>9/10</topic><topic>Antifungal Agents - therapeutic use</topic><topic>Antimicrobial Stewardship</topic><topic>Bacterial diseases</topic><topic>Bacterial infections</topic><topic>Biomarkers</topic><topic>Biomarkers - analysis</topic><topic>Candida</topic><topic>Candida - classification</topic><topic>Candida - genetics</topic><topic>Candidiasis</topic><topic>Candidiasis, Invasive - diagnosis</topic><topic>Candidiasis, Invasive - drug therapy</topic><topic>Candidiasis, Invasive - microbiology</topic><topic>Diagnosis</topic><topic>DNA, Fungal - genetics</topic><topic>Drug resistance</topic><topic>Drug Resistance, Multiple, Fungal</topic><topic>Fungal infections</topic><topic>Hospitals</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Limit of Detection</topic><topic>Melting</topic><topic>Melting curve</topic><topic>Molecular Diagnostic Techniques - methods</topic><topic>multidisciplinary</topic><topic>Multidrug resistance</topic><topic>Multiplex Polymerase Chain Reaction - methods</topic><topic>Nosocomial infection</topic><topic>Outbreaks</topic><topic>Real-Time Polymerase Chain Reaction - methods</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Sensitivity and Specificity</topic><topic>Transition Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jainlabdin, Mohd Hanif</creatorcontrib><creatorcontrib>Batra, Ambalika</creatorcontrib><creatorcontrib>Sánchez Paredes, Edith</creatorcontrib><creatorcontrib>Hernández Hernández, Francisca</creatorcontrib><creatorcontrib>Fu, Guoliang</creatorcontrib><creatorcontrib>Tovar-Torres, Jorge</creatorcontrib><collection>SpringerOpen</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jainlabdin, Mohd Hanif</au><au>Batra, Ambalika</au><au>Sánchez Paredes, Edith</au><au>Hernández Hernández, Francisca</au><au>Fu, Guoliang</au><au>Tovar-Torres, Jorge</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single-tube, dual channel pentaplexing for the identification of Candida strains associated with human infection</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-10-11</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>14692</spage><epage>14</epage><pages>14692-14</pages><artnum>14692</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Invasive candidiasis is one of the most common nosocomial fungal infections worldwide. Delayed implementation of effective antifungal treatment caused by inefficient
Candida
diagnosis contributes to its notoriously high mortality rates. The availability of better
Candida
diagnostic tools would positively impact patient outcomes. Here, we report on the development of a single-tube, dual channel pentaplex molecular diagnostic assay based on Multiplex Probe Amplification (MPA) technology. It allows simultaneous identification of
C
.
auris
,
C
.
glabrata
and
C
.
krusei
, at species-level as well as of six additional
albicans
and non-
albicans
pathogenic
Candida
at genus level. The assay overcomes the one-channel one-biomarker limitation of qPCR-based assays. Assay specificities are conferred by unique biomarker probe pairs with characteristic melting temperatures; post-amplification melting curve analysis allows simple identification of the infectious agent. Alerting for the presence of
C
.
auris
, the well-characterised multi-drug resistant outbreak strain, will facilitate informed therapy decisions and aid antifungal stewardship. The MPA
-Candida
assay can also be coupled to a pan-Fungal assay when differentiation between fungal and bacterial infections might be desirable. Its multiplexing capacity, detection range, specificity and sensitivity suggest the potential use of this novel MPA-
Candida
assay in clinical diagnosis and in the control and management of hospital outbreaks.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31604994</pmid><doi>10.1038/s41598-019-51198-6</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-6798-6714</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Publicly Available Content Database; PubMed Central; Free Full-Text Journals in Chemistry; Springer Nature - nature.com Journals - Fully Open Access |
subjects | 38/22 38/71 38/77 631/326/193 631/337 692/308/2778 9/10 Antifungal Agents - therapeutic use Antimicrobial Stewardship Bacterial diseases Bacterial infections Biomarkers Biomarkers - analysis Candida Candida - classification Candida - genetics Candidiasis Candidiasis, Invasive - diagnosis Candidiasis, Invasive - drug therapy Candidiasis, Invasive - microbiology Diagnosis DNA, Fungal - genetics Drug resistance Drug Resistance, Multiple, Fungal Fungal infections Hospitals Humanities and Social Sciences Humans Limit of Detection Melting Melting curve Molecular Diagnostic Techniques - methods multidisciplinary Multidrug resistance Multiplex Polymerase Chain Reaction - methods Nosocomial infection Outbreaks Real-Time Polymerase Chain Reaction - methods Science Science (multidisciplinary) Sensitivity and Specificity Transition Temperature |
title | Single-tube, dual channel pentaplexing for the identification of Candida strains associated with human infection |
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