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Contribution of PCR Denaturing Gradient Gel Electrophoresis Combined with Mixed Chromatogram Software Separation for Complex Urinary Sample Analysis
I. Kotásková, B. Mališová, H. Obručová, V. Holá, T. Peroutková, F. Růžička, T. Freiberger,
Language English Country Switzerland
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
NV16-31593A
MZ0
CEP Register
PubMed
29258075
DOI
10.1159/000484524
Knihovny.cz E-resources
- MeSH
- Bacteria classification genetics isolation & purification MeSH
- Denaturing Gradient Gel Electrophoresis methods MeSH
- Molecular Diagnostic Techniques methods MeSH
- Diagnostic Techniques, Urological MeSH
- DNA, Bacterial MeSH
- Humans MeSH
- Urine chemistry microbiology MeSH
- Urinary Catheters microbiology MeSH
- Polymerase Chain Reaction methods MeSH
- Software * MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Complex samples are a challenge for sequencing-based broad-range diagnostics. We analysed 19 urinary catheter, ureteral Double-J catheter, and urine samples using 3 methodological approaches. Out of the total 84 operational taxonomic units, 37, 61, and 88% were identified by culture, PCR-DGGE-SS (PCR denaturing gradient gel electrophoresis followed by Sanger sequencing), and PCR-DGGE-RM (PCR- DGGE combined with software chromatogram separation by RipSeq Mixed tool), respectively. The latter approach was shown to be an efficient tool to complement culture in complex sample assessment.
References provided by Crossref.org
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