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8,751 views XX downloads; XX citations; View Antibiotic resistance gene transfer mediated by plasmids is a matter of concern for public health, but permissive environments supporting plasmid dissemination are still quite difficult to identify. Lately, we have reported a molecular approach based on quantitative PCR (qPCR) to monitor the fate of the IncP-1β plasmid pB10 in natural microbial communities maintained in microcosms. 2017-07-12 2014-02-10 Novel assay to measure the plasmid mobilizing potential of mixed microbial communities. By Barth Smets, Arnaud Dechesne, and Uli Klümper. Novel Assay To Assess Permissiveness of a Soil Microbial Community toward Receipt of Mobile Genetic Elements. By Arnaud Dechesne. 2021-01-08 1998-03-01 2016-09-23 2018-11-23 Moreover, conjugation via plasmid transfer is postulated to be prevalent in complex microbial communities (e.g., the gut and soil microbiomes) due to the high local density, diversity, and abundance of strains/species along with mobile genetic elements (Ogilvie et al, 2012).
Authors: Uli Klümper, Ariadni Droumpali, Arnaud Dechesne, Barth F. Smets Abstract: Novel assay to measure the plasmid mobilizing potential of mixed microbial communities. Uli Klümper; Ariadni Droumpali; Arnaud Dechesne; Barth F. Smets; Frontiers in Microbiology. Published on 21 Dec 2014. 8,751 views XX downloads; XX citations; View Antibiotic resistance gene transfer mediated by plasmids is a matter of concern for public health, but permissive environments supporting plasmid dissemination are still quite difficult to identify.
We compare the transfer frequency of a mobilizable plasmid to that of a mobilizing and conjugal plasmid measured for a model strain and for the assayed community.
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Authors: Uli Klümper, Ariadni Droumpali, Arnaud Dechesne, Barth F. Smets Abstract:
Novel assay to measure the plasmid mobilizing potential of mixed microbial communities. Uli Klümper; Ariadni Droumpali; Arnaud Dechesne; Barth F. Smets; Frontiers in Microbiology. Published on 21 Dec 2014. 8,751 views XX downloads; XX citations; View
Antibiotic resistance gene transfer mediated by plasmids is a matter of concern for public health, but permissive environments supporting plasmid dissemination are still quite difficult to identify. Lately, we have reported a molecular approach based on quantitative PCR (qPCR) to monitor the fate of the IncP-1β plasmid pB10 in natural microbial communities maintained in microcosms. 2017-07-12
2014-02-10
Novel assay to measure the plasmid mobilizing potential of mixed microbial communities.
Johan isaksson marjavaara
mcr-3 expression confers a lower fitness cost than mcr-1, as determined by competitive Methods for the robust quantification of bacterial communities are still under development. In this context, the present study aimed to evaluate a method combining competitive PCR (cPCR) and microarray assays for the determination of absolute content of total bacteria and individual bacterial species in samples. Plasmid Transfer and Conjugation Assays. Large plasmids were transferred to clinical isolates via either conjugation or direct electroporation when possible. For transfer by conjugation, the TOP10 strain (Life Technologies, USA) was used as donor strain due to its high competence and leucine auxotrophy.
Uli Klümper, Ariadni Droumpali, Arnaud Dechesne, Barth F. Smets. Department of Environmental Engineering; Research output: Contribution to journal › Journal article › Research › peer-review.
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Antibiotic resistance gone wild - Diva Portal
Novel assay to measure the plasmid mobilizing potential of mixed microbial communities Uli Klümper * , Ariadni Droumpali , Arnaud Dechesne and Barth F. Smets * Department of Environmental Engineering, Technical University of Denmark, Kongens Lyngby, Denmark Direct mobilization of mobilizable plasmids into 91 indigenous bacteria within mixed natural communities has been detected before (Hill et al., 1992; van 92 Elsas et al., 1998), but was never directly quantified. 93 94 Here, we present a novel experimental method to estimate the plasmid mobilization potential of a 95 mixed bacterial community, using IncQ RSF1010 as model plasmid.