| Autor: |
Kasraian Fard, Sara, Tinguely, Regula, Donà, Valentina, Bernasconi, Odette Joëlle, Endimiani, Andrea |
| Jazyk: |
angličtina |
| Rok vydání: |
2017 |
| Předmět: |
|
| DOI: |
10.7892/boris.93325 |
| Popis: |
Background: The aim of this study was to design a rapid and sensitive real-time PCR (RT-PCR) method for colistin resistance mcr-1 gene detection in human fecal samples. Methods: Stools (n=88) from 36 volunteers were analyzed. To isolate mcr-1-producing Enterobacteriaceae samples were enriched overnight in LB broth containing 2 mg/L colistin and then plated in selective agar plates with 4 mg/L colistin. We then designed a SYBRGreen-based RT-PCR targeting the mcr-1. For method validation and to establish the limit of detection (LOD), total DNA was extracted from mcr-1-negative and mcr-1-positive E. coli. RT-PCR was also performed with DNA extracted from the 88 native stools and after enriching them in LB broth containing colistin. Results: Based on the culture approach, 3 unique volunteers resulted colonized with mcr-1-harboring E. coli strains. For culture isolates, our RT-PCR exhibited a LOD of 10 genomic copies/reaction with both sensitivity and specificity of 100%. Nevertheless, when testing native stools, only two out of the three mcr-1-positive specimens were detected. However, after enrichment in LB containing colistin, the RT-PCR was strongly positive for all culture-positive samples. The average cycle threshold was 22, granting rapid and confident detection of positive specimens within 30 cycles. No false-positives were observed for the remaining 85 culture-negative specimens. Conclusions: We developed a rapid RT-PCR for the detection of mcr-1 from stool specimens. We increased the detection rate by testing selective broth enrichments. This approach has also the advantage of concomitant isolation of the mcr-1-harboring strains for further antimicrobial susceptibility and genetic tests. |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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