Thirty-minute screening of antibiotic resistance genes in bacterial isolates with minimal sample preparation in static self-dispensing 64 and 384 assay cards

Verfasser / Beitragende:
[Tanja Kostić, Michael Ellis, Maggie Williams, Tiffany Stedtfeld, John Kaneene, Robert Stedtfeld, Syed Hashsham]
Ort, Verlag, Jahr:
2015
Enthalten in:
Applied Microbiology and Biotechnology, 99/18(2015-09-01), 7711-7722
Format:
Artikel (online)
ID: 605501459
LEADER caa a22 4500
001 605501459
003 CHVBK
005 20210128100601.0
007 cr unu---uuuuu
008 210128e20150901xx s 000 0 eng
024 7 0 |a 10.1007/s00253-015-6774-z  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00253-015-6774-z 
245 0 0 |a Thirty-minute screening of antibiotic resistance genes in bacterial isolates with minimal sample preparation in static self-dispensing 64 and 384 assay cards  |h [Elektronische Daten]  |c [Tanja Kostić, Michael Ellis, Maggie Williams, Tiffany Stedtfeld, John Kaneene, Robert Stedtfeld, Syed Hashsham] 
520 3 |a In a clinical setting, molecular assays such as polymerase chain reaction offer a rapid means to infer or confirm identity and therapeutic decisions. Accordingly, a number of molecular assays targeting identity and antibiotic resistance (AR) genes have been developed; however, these methods can be technically complex and relatively expensive. Herein, we describe a diagnostic concept utilizing isothermal amplification technology with non-purified heat-lysed cells and self-dispensing cards for testing multiple primers in parallel. This proof-of-concept study, performed with Staphylococcus aureus isolates and associated AR genes, was compared with culture-based susceptibility and quantitative PCR (qPCR). Results demonstrate reduced sample processing steps resulting in a turnaround time (starting from bacterial culture to ending in the antibiotic resistance gene profile) in less than 30min. For antibiotics tested in which an associated AR gene was targeted on the Gene-Z card, 69% (18/26) of culture-based resistance events were positive for related AR genes. A comparison of loop-mediated isothermal amplification (LAMP) and qPCR assays targeting the same antibiotic resistance genes showed a 98.2% agreement in terms of presence and absence calls. Identity-based discrepancies between conventional (phenotypic) and molecular (genotypic) results were further resolved, and we were able to demonstrate higher accuracy in identification with the molecular analysis. 
540 |a The Author(s), 2015 
690 7 |a Antibiotic resistance  |2 nationallicence 
690 7 |a Rapid genetic testing  |2 nationallicence 
690 7 |a LAMP  |2 nationallicence 
690 7 |a Point of care  |2 nationallicence 
690 7 |a Gene-Z  |2 nationallicence 
690 7 |a S. aureus  |2 nationallicence 
690 7 |a E. faecalis  |2 nationallicence 
690 7 |a E. faecium  |2 nationallicence 
700 1 |a Kostić  |D Tanja  |u AIT Austrian Institute of Technology GmbH, Bioresources Unit, Konrad Lorenz Strasse 24, A-3430, Tulln an der Donau, Austria  |4 aut 
700 1 |a Ellis  |D Michael  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
700 1 |a Williams  |D Maggie  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
700 1 |a Stedtfeld  |D Tiffany  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
700 1 |a Kaneene  |D John  |u Center for Comparative Epidemiology, College of Veterinary Medicine, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
700 1 |a Stedtfeld  |D Robert  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
700 1 |a Hashsham  |D Syed  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
773 0 |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/18(2015-09-01), 7711-7722  |x 0175-7598  |q 99:18<7711  |1 2015  |2 99  |o 253 
856 4 0 |u https://doi.org/10.1007/s00253-015-6774-z  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00253-015-6774-z  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kostić  |D Tanja  |u AIT Austrian Institute of Technology GmbH, Bioresources Unit, Konrad Lorenz Strasse 24, A-3430, Tulln an der Donau, Austria  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Ellis  |D Michael  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Williams  |D Maggie  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Stedtfeld  |D Tiffany  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kaneene  |D John  |u Center for Comparative Epidemiology, College of Veterinary Medicine, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Stedtfeld  |D Robert  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hashsham  |D Syed  |u Civil and Environmental Engineering, Michigan State University, 48824, East Lansing, MI, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Applied Microbiology and Biotechnology  |d Springer Berlin Heidelberg  |g 99/18(2015-09-01), 7711-7722  |x 0175-7598  |q 99:18<7711  |1 2015  |2 99  |o 253