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Abstract
Current methods for determining the identity of substrains of Mycobacterium bovis
BCG (BCG) vaccine are labour intensive, or provide only limited substrain differentiation.
In this paper we describe a multiplex PCR that distinguishes between M. tuberculosis
(TB) and M. bovis and the non-pathogenic BCG strain, and also subdivides the BCG vaccine
substrains investigated into seven distinct fingerprints based on six target regions
in the DNA. This test is specific, rapid, reproducible and portable and is proposed
as a novel test for BCG vaccine control. It offers substantial advantages over the
methods currently in use. Using this test we have characterised a number of commercial
BCG vaccines.