Real-time PCR assays of single-nucleotide polymorphisms defining the major Brucella clades

被引:52
作者
Foster, Jeffrey T. [1 ]
Okinaka, Richard T. [2 ]
Svensson, Rita [2 ]
Shaw, Kathryn [2 ]
De, Barun K. [3 ]
Robison, Richard A. [4 ]
Probert, William S. [5 ]
Brown, William D.
Keim, Paul [1 ]
机构
[1] No Arizona Univ, Ctr Microbial Genet & Genom, Flagstaff, AZ 86011 USA
[2] Los Alamos Natl Lab, Biosci Div, Los Alamos, NM 87545 USA
[3] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
[4] Brigham Young Univ, Dept Mol Biol & Microbiol, Provo, UT 84602 USA
[5] Calif Dept Publ Hlth, Microbial Dis Lab, Richmond, CA 94804 USA
关键词
D O I
10.1128/JCM.01496-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Members of the genus Brucella are known worldwide as pathogens of wildlife and livestock and are the most common organisms of zoonotic infection in humans. In general, brucellae exhibit a range of host specificity in animals that has led to the identification of at least seven Brucella species. The genomes of the various Brucella species are highly conserved, which makes the differentiation of species highly challenging. However, we found single-nucleotide polymorphisms (SNPs) in housekeeping and other genes that differentiated the seven main Brucella species or clades and thus enabled us to develop real-time PCR. assays based around these SNPs. Screening of a diverse panel of 338 diverse isolates with these assays correctly identified each isolate with its previously determined Brucella clade. Six of the seven clade-specific assays detected DNA concentrations of less than 10 fg, indicating a high level of sensitivity. This SNP-based approach places samples into a phylogenetic framework, allowing reliable comparisons to be made among the lineages of clonal bacteria and providing a solid basis for genotyping. These PCR assays provide a rapid and highly sensitive method of differentiating the major Brucella groups that will be valuable for clinical and forensic applications.
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收藏
页码:296 / 301
页数:6
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