scholarly journals Antibiotic Resistance Genes in the Bacteriophage DNA Fraction of Environmental Samples

PLoS ONE ◽  
2011 ◽  
Vol 6 (3) ◽  
pp. e17549 ◽  
Author(s):  
Marta Colomer-Lluch ◽  
Juan Jofre ◽  
Maite Muniesa
2021 ◽  
Author(s):  
Schuyler D. Smith ◽  
Jin Choi ◽  
Nicole Ricker ◽  
Fan Yang ◽  
Shannon Hinsa-Leasure ◽  
...  

Effective monitoring of antibiotic resistance genes and their dissemination in environmental ecosystems has been hindered by the cost and efficiency of methods available for the task. We developed a method entitled the Diversity of Antibiotic Resistance genes and Transfer Elements-Quantitative Monitoring (DARTE-QM), a system implementing high-throughput sequencing to simultaneously sequence thousands of antibiotic resistant genes representing a full-spectrum of antibiotic resistance classes commonly seen in environmental systems. In this study, we demonstrated DARTE-QM by screening 662 antibiotic resistance genes within environmental samples originated from manure, soil, and animal feces, in addition to a mock-community used as a control to test performance. DARTE-QM offers a new approach to studying antibiotic resistance in environmental microbiomes, showing advantages in efficiency and the ability to scale for many samples. This method provides a means of data acquisition that will alleviate the obstacles that many researchers in this area currently face.


CourseSource ◽  
2016 ◽  
Vol 3 ◽  
Author(s):  
Jessica H. Bell ◽  
Lori Thrun ◽  
Michelle LeBeau ◽  
Irina Makarevitch ◽  
Jodi Goldberg ◽  
...  

2019 ◽  
Vol 12 (2) ◽  
pp. 356-363 ◽  
Author(s):  
Adinortey Cynthia Ayefoumi ◽  
Amewowor Damian H.A ◽  
Galyuon Isaac K.A. ◽  
Otwe Emmanuel Plas ◽  
Asante Daniel K.A ◽  
...  

2021 ◽  
pp. 101485
Author(s):  
Ting Zhu ◽  
Tao Chen ◽  
Zhen Cao ◽  
Shan Zhong ◽  
Xin Wen ◽  
...  

2016 ◽  
Vol 1 (2) ◽  
pp. 22 ◽  
Author(s):  
Navindra Kumari Palanisamy ◽  
Parasakthi Navaratnam ◽  
Shamala Devi Sekaran

Introduction: Streptococcus pneumoniae is an important bacterial pathogen, causing respiratory infection. Penicillin resistance in S. pneumoniae is associated with alterations in the penicillin binding proteins, while resistance to macrolides is conferred either by the modification of the ribosomal target site or efflux mechanism. This study aimed to characterize S. pneumoniae and its antibiotic resistance genes using 2 sets of multiplex PCRs. Methods: A quintuplex and triplex PCR was used to characterize the pbp1A, ermB, gyrA, ply, and the mefE genes. Fifty-eight penicillin sensitive strains (PSSP), 36 penicillin intermediate strains (PISP) and 26 penicillin resistance strains (PRSP) were used. Results: Alteration in pbp1A was only observed in PISP and PRSP strains, while PCR amplification of the ermB or mefE was observed only in strains with reduced susceptibility to erythromycin. The assay was found to be sensitive as simulated blood cultures showed the lowest level of detection to be 10cfu. Conclusions: As predicted, the assay was able to differentiate penicillin susceptible from the non-susceptible strains based on the detection of the pbp1A gene, which correlated with the MIC value of the strains.


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