2016
DOI: 10.1093/femsec/fiw020
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Antimicrobial resistance dashboard application for mapping environmental occurrence and resistant pathogens

Abstract: An antibiotic resistance (AR) Dashboard application is being developed regarding the occurrence of antibiotic resistance genes (ARG) and bacteria (ARB) in environmental and clinical settings. The application gathers and geospatially maps AR studies, reported occurrence and antibiograms, which can be downloaded for offline analysis. With the integration of multiple data sets, the database can be used on a regional or global scale to identify hot spots for ARGs and ARB; track and link spread and transmission, qu… Show more

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Cited by 33 publications
(22 citation statements)
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“…The cphA gene (β‐lactam resistance) has been found to be intrinsic in environmental isolates of A. jandaei and Aeromonas hydrophila (Balsalobre et al ., ). The mexF and oprD multidrug resistance genes were proposed to naturally occur in water (Stedtfeld et al ., ). The vanC gene can encode resistance to vancomycin, which is considered as one of the last‐resort defence against organisms like Streptococcus pneumonia and Enterococcus (Gilmore and Hoch, ), and this gene is ancient in natural environments (D'Costa et al ., ).…”
Section: Discussionmentioning
confidence: 97%
“…The cphA gene (β‐lactam resistance) has been found to be intrinsic in environmental isolates of A. jandaei and Aeromonas hydrophila (Balsalobre et al ., ). The mexF and oprD multidrug resistance genes were proposed to naturally occur in water (Stedtfeld et al ., ). The vanC gene can encode resistance to vancomycin, which is considered as one of the last‐resort defence against organisms like Streptococcus pneumonia and Enterococcus (Gilmore and Hoch, ), and this gene is ancient in natural environments (D'Costa et al ., ).…”
Section: Discussionmentioning
confidence: 97%
“…Sample and primers were dispensed into the SmartChip™ using a Multi-sample Nano-dispenser (Wafergen Biosystems, Fremont, CA). PCR cycling conditions and initial data processing were performed as previously described (Wang et al 2014; Stedtfeld et al 2016). Amplification reactions on the SmartChip™ consisted of 1×LightCycler 480 SYBR® Green I Master Mix (Roche Inc., USA), nuclease-free PCR-grade water, 10 ng/μl cDNA template per sample in the qPCR reaction (0.5 ng per reaction well), and 0.5 μM of each forward and reverse primer.…”
Section: Methodsmentioning
confidence: 99%
“…Another study quantified the intI1 gene abundance in different land use, with higher abundance observed in agricultural, industrial, and urban settings compared to national parks (Borruso et al, 2016). We previously observed a high correlation (R 2 = 0.76) between total ARGs and intI1 gene measured using qPCR in water samples collected from 30 fresh surface water and influent lines from three waste water treatment plants (WWTPs) in Michigan (Stedtfeld et al, 2016b). Selective reduction of ARGs using anaerobic digestion also correlated with reduced counts of the intI1 gene (Burch et al, 2016).…”
Section: Discussionmentioning
confidence: 99%