Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17722
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dc.contributor.authorZozaya-Valdés, Enrique-
dc.contributor.authorPorter, Jessica L-
dc.contributor.authorCoventry, John-
dc.contributor.authorFyfe, Janet A M-
dc.contributor.authorCarter, Glen P-
dc.contributor.authorGonçalves da Silva, Anders-
dc.contributor.authorSchultz, Mark B-
dc.contributor.authorSeemann, Torsten-
dc.contributor.authorJohnson, Paul D R-
dc.contributor.authorStewardson, Andrew J-
dc.contributor.authorBastian, Ivan-
dc.contributor.authorRoberts, Sally A-
dc.contributor.authorHowden, Benjamin P-
dc.contributor.authorWilliamson, Deborah A-
dc.contributor.authorStinear, Timothy P-
dc.date2017-04-05-
dc.date.accessioned2018-05-15T06:33:55Z-
dc.date.available2018-05-15T06:33:55Z-
dc.date.issued2017-06-
dc.identifier.citationJournal of clinical microbiology 2017; 55(6): 1847-1856-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17722-
dc.description.abstractMycobacterium chimaera is an opportunistic environmental mycobacterium belonging to the Mycobacterium avium-M. intracellulare complex. Although most commonly associated with pulmonary disease, there has been growing awareness of invasive M. chimaera infections following cardiac surgery. Investigations suggest worldwide spread of a specific M. chimaera clone, associated with contaminated hospital heater-cooler units used during the surgery. Given the global dissemination of this clone, its potential to cause invasive disease, and the laboriousness of current culture-based diagnostic methods, there is a pressing need to develop rapid and accurate diagnostic assays specific for M. chimaera Here, we assessed 354 mycobacterial genome sequences and confirmed that M. chimaera is a phylogenetically coherent group. In silico comparisons indicated six DNA regions present only in M. chimaera We targeted one of these regions and developed a TaqMan quantitative PCR (qPCR) assay for M. chimaera with a detection limit of 100 CFU/ml in whole blood spiked with bacteria. In vitro screening against DNA extracted from 40 other mycobacterial species and 22 bacterial species from 21 diverse genera confirmed the in silico-predicted specificity for M. chimaera Screening 33 water samples from heater-cooler units with this assay highlighted the increased sensitivity of PCR compared to culture, with 15 of 23 culture-negative samples positive by M. chimaera qPCR. We have thus developed a robust molecular assay that can be readily and rapidly deployed to screen clinical and environmental specimens for M. chimaera.-
dc.language.isoeng-
dc.subjectdiagnostics-
dc.subjectgenomics-
dc.subjectinfectious disease-
dc.subjectmycobacterium-
dc.titleTarget-Specific Assay for Rapid and Quantitative Detection of Mycobacterium chimaera DNA.-
dc.typeJournal Article-
dc.identifier.journaltitleJournal of clinical microbiology-
dc.identifier.affiliationDepartment of Microbiology and Immunology, The Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia-
dc.identifier.affiliationMicrobiological Diagnostic Unit Public Health Laboratory, Department of Microbiology and Immunology, The Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia-
dc.identifier.affiliationVictorian Infectious Diseases Laboratory, The Doherty Institute for Infection and Immunity, Victoria, Australia-
dc.identifier.affiliationVictorian Life Sciences Computational Initiative, University of Melbourne, Melbourne, Victoria, Australia-
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationSA Pathology, Adelaide, South Australia, Australia-
dc.identifier.affiliationMycobacterial Laboratory, LabPlus, Auckland, New Zealand-
dc.identifier.affiliationDoherty Applied Microbial Genomics, The Doherty Institute for Infection and Immunity, University of Melbourne, Victoria, Australia-
dc.identifier.doi10.1128/JCM.00197-17-
dc.identifier.pubmedid28381604-
dc.type.austinEvaluation Studies-
dc.type.austinJournal Article-
dc.type.austinResearch Support, Non-U.S. Gov't-
local.name.researcherHowden, Benjamin P
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMicrobiology-
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