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1.
Genome ; 59(11): 1049-1061, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27809602

ABSTRACT

Here, we present a new approach for increasing the rate and lowering the cost of identifying, cataloging, and monitoring global biodiversity. These advances, which we call Closed-Tube Barcoding, are one application of a suite of proven PCR-based technologies invented in our laboratory. Closed-Tube Barcoding builds on and aims to enhance the profoundly important efforts of the International Barcode of Life initiative. Closed-Tube Barcoding promises to be particularly useful when large numbers of small or rare specimens need to be screened and characterized at an affordable price. This approach is also well suited for automation and for use in portable devices.


Subject(s)
Biodiversity , DNA Barcoding, Taxonomic/methods , Animals , Bacterial Proteins/genetics , Cluster Analysis , Computational Biology/methods , DNA-Directed RNA Polymerases/genetics , Electron Transport Complex IV/genetics , High-Throughput Nucleotide Sequencing , Humans , Polymerase Chain Reaction/methods , Workflow
2.
J Clin Microbiol ; 42(8): 3626-34, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15297508

ABSTRACT

This paper presents Etest determinations of MICs of selected antimicrobial agents for 76 isolates of Bacillus anthracis chosen for their diverse histories and 67, 12, and 4 cultures, respectively, of its close relatives B. cereus, B. thuringiensis, and B. mycoides derived from a range of clinical and environmental sources. NCCLS breakpoints are now available for B. anthracis and ciprofloxacin, penicillin, and tetracycline; based on these breakpoints, the B. anthracis isolates were all fully susceptible to ciprofloxacin and tetracycline, and all except four cultures, three of which had a known history of penicillin resistance and were thought to originate from the same original parent, were susceptible to penicillin. Based on NCCLS interpretive standards for gram-positive and/or aerobic bacteria, all cultures were susceptible to amoxicillin-clavulanic acid and gentamicin and 99% (one with intermediate sensitivity) of cultures were susceptible to vancomycin. No group trends were apparent among the different categories of B. cereus (isolates from food poisoning incidents and nongastrointestinal infections and food and environmental specimens not associated with illness). Differences between B. anthracis and the other species were as expected for amoxicillin and penicillin, with all B. anthracis cultures, apart from the four referred to above, being susceptible versus high proportions of resistant isolates for the other three species. Four of the B. cereus and one of the B. thuringiensis cultures were resistant to tetracycline and a further six B. cereus and one B. thuringiensis cultures fell into the intermediate category. There was a slightly higher resistance to azithromycin among the B. anthracis strains than for the other species. The proportion of B. anthracis strains fully susceptible to erythromycin was also substantially lower than for the other species, although just a single B. cereus strain was fully resistant. The Etest compared favorably with agar dilution in a subsidiary test set up to test the readings, and it compared with other published studies utilizing a variety of test methods.


Subject(s)
Bacillus anthracis/drug effects , Bacillus cereus/drug effects , Bacillus thuringiensis/drug effects , Anti-Bacterial Agents/pharmacology , Bacillus anthracis/isolation & purification , Bacillus cereus/isolation & purification , Bacillus thuringiensis/isolation & purification , Foodborne Diseases/diagnosis , Foodborne Diseases/microbiology , Humans , Microbial Sensitivity Tests
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