Identification of Brucella by ribosomal-spacer-region PCR and differentiation of Brucella canis from other Brucella spp. pathogenic for humans by carbohydrate profiles

被引:21
作者
Fox, KF
Fox, A [1 ]
Nagpal, M
Steinberg, P
Heroux, K
机构
[1] Univ S Carolina, Sch Med, Dept Microbiol & Immunol, Columbia, SC 29208 USA
[2] USA, Ctr Dev & Engn, Aberdeen Proving Ground, MD 21010 USA
关键词
D O I
10.1128/JCM.36.11.3217-3222.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Molecular and chemical characteristics often provide complementary information in the differentiation of closely related organisms. The genus Brucella consists of a highly conserved group of organisms. Identification of the four species pathogenic in humans (Brucella melitensis, Brucella abortus, Brucella suis, and Brucella canis) is problematic for many clinical laboratories that depend primarily on serology and phenotypic characteristics to differentiate species. PCR amplification of the 16S-23S ribosomal DNA interspace region was evaluated for species-specific polymorphism. B, abortus, B, melitensis, B. suis, and B, canis produced identical PCR interspace profiles, However, these PCR products were unique to brucellae, allowing them to be readily distinguished from other gram-negative bacteria (including Bartonella spp. and Agrobacterium spp,), Carbohydrate profiles differentiated B, canis from the other three Brucella species due to the absence of the rare amino sugar quinovosamine in the three other species. PCR of the rRNA interspace region is useful in identification of the genus Brucella, while carbohydrate profiling is capable of differentiating B. canis from the other Brucella species.
引用
收藏
页码:3217 / 3222
页数:6
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