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The hsp65 gene patterns of less common Mycobacterium and Nocardia spp. by polymerase chain reaction-restriction fragment length polymorphism analysis with capillary electrophoresis.
- Source :
-
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2007 Jul; Vol. 58 (3), pp. 315-23. Date of Electronic Publication: 2007 Mar 26. - Publication Year :
- 2007
-
Abstract
- To rapidly identify Mycobacterium and Nocardia spp. without costly probes, we had implemented capillary electrophoresis (CE) in polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) analysis to analyze their 65-kDa heat shock protein (hsp65) gene. The PCR-RFLP analysis with CE (PRACE) involved only one restriction enzyme, HaeIII, and a single electrophoretic separation less than 10 min. Full-range (10-200 bp) RFLP patterns of 12 less common Mycobacterium and 7 Nocardia spp. were investigated. A good agreement was observed between the sizes of restriction fragments resolved by CE and the real sizes deduced from sequence analysis. Including hsp65 gene patterns of 12 Mycobacterium spp. published earlier, differentiation was distinct among 24 Mycobacterium and 7 Nocardia spp. Some closely related species exhibiting similar biochemical characteristics could be well discriminated by an extra HaeIII digestion site. Thus, PRACE offers a nonprobe alternative for rapid identification of various cultured Mycobacterium and Nocardia to the species level.
- Subjects :
- Chaperonin 60
DNA, Bacterial genetics
Deoxyribonucleases, Type II Site-Specific
Mycobacterium genetics
Nocardia genetics
Polymerase Chain Reaction
Bacterial Proteins genetics
Chaperonins genetics
Electrophoresis, Capillary methods
Mycobacterium classification
Nocardia classification
Polymorphism, Restriction Fragment Length
Subjects
Details
- Language :
- English
- ISSN :
- 0732-8893
- Volume :
- 58
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Diagnostic microbiology and infectious disease
- Publication Type :
- Academic Journal
- Accession number :
- 17382507
- Full Text :
- https://doi.org/10.1016/j.diagmicrobio.2007.02.004