DNA restriction endonuclease analysis of Mycobacterium bovis and other members of the tuberculosis complex

59Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

DNA preparations from 24 New Zealand isolates, two reference strains of Mycobacterium bovis, and one reference strain each of Mycobacterium microti, Mycobacterium africanum, and Mycobacterium tuberculosis were characterized by restriction endonuclease analysis. Twenty-five restriction enzymes were investigated. The clearest differences in M. bovis patterns were obtained with the enzymes BstEII and BclI. These produced four and five different patterns, respectively, for the 24 local isolates. When the results from both enzymes were considered, seven different combinations were obtained. The patterns produced for the two reference strains of M. bovis could be distinguished from each other and also from the patterns produced for the local isolates. All patterns were reproducible and are now being used for typing M. bovis isolates. With either enzyme, the patterns produced for the M. tuberculosis, M. bovis, and M. africanum strains had many features in common, but all the M. bovis patterns were clearly more similar to each other than to the M. tuberculosis patterns. The patterns produced for the M. microti strain were markedly different from those produced for the other species. Restriction endonuclease analysis is clearly a useful method for inter- and intraspecific classifications of the tuberculosis complex.

Cite

CITATION STYLE

APA

Collins, D. M., & De Lisle, G. W. (1985). DNA restriction endonuclease analysis of Mycobacterium bovis and other members of the tuberculosis complex. Journal of Clinical Microbiology, 21(4), 562–564. https://doi.org/10.1128/jcm.21.4.562-564.1985

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free