Abstract
PCR primers targeting loci in the current Burkholderia cepacia complex multilocus sequence typing scheme were redesigned to (i) more reliably amplify these loci from B. cepacia complex species, (ii) amplify these same loci from additional Burkholderia species, and (iii) enable the use of a single primer set per locus for both amplification and DNA sequencing.
Publication types
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Bacterial Typing Techniques / methods*
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Burkholderia / classification*
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Burkholderia / genetics*
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Cluster Analysis
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DNA Fingerprinting / methods*
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DNA Primers / genetics
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DNA, Bacterial / chemistry
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DNA, Bacterial / genetics*
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Phylogeny
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Sequence Analysis, DNA
Substances
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DNA Primers
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DNA, Bacterial