Use of synthesized double-stranded gene fragments as qPCR standards for the quantification of antibiotic resistance genes.
Anti-Bacterial Agents
/ pharmacology
Cloning, Molecular
DNA, Bacterial
/ isolation & purification
Drug Resistance, Microbial
/ genetics
Environmental Monitoring
Feces
/ microbiology
Genes, Bacterial
/ genetics
Molecular Biology
/ methods
Real-Time Polymerase Chain Reaction
/ methods
Reproducibility of Results
Sensitivity and Specificity
Soil
Soil Microbiology
Water Microbiology
Antibiotic resistance genes
Chemically synthesized gene fragments
Gene cloning
qPCR
Journal
Journal of microbiological methods
ISSN: 1872-8359
Titre abrégé: J Microbiol Methods
Pays: Netherlands
ID NLM: 8306883
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
07
05
2019
revised:
13
07
2019
accepted:
16
07
2019
pubmed:
22
7
2019
medline:
23
6
2020
entrez:
21
7
2019
Statut:
ppublish
Résumé
Pollution of various environmental matrices by antibiotic resistance genes (ARGs) has become a growing threat to human health. For the quantitative analysis of the presence of ARGs, there is a need for sensitive and robust qPCR assays which can detect various genes from different types of DNA extracts. Fourteen ARGs were selected as target genes in this study including: bla
Identifiants
pubmed: 31325465
pii: S0167-7012(19)30374-4
doi: 10.1016/j.mimet.2019.105670
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
DNA, Bacterial
0
Soil
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
105670Informations de copyright
Copyright © 2019 Elsevier B.V. All rights reserved.