Current methods for determining the identity of substrains of Mycobacterium
bovis BCG (BCG) vaccine are labour intensive, or provide only limited subs
train differentiation. In this paper we describe a multiplex PCR that disti
nguishes between M. tuberculosis (TB) and M. bovis and the non-pathogenic B
CG strain, and also subdivides the BCG vaccine substrains investigated into
seven distinct fingerprints based on six target regions in the DNA. This t
est is specific, rapid, reproducible and portable and is proposed as a nove
l test for BCG vaccine control. It offers substantial advantages over the m
ethods currently in use. Using this test we have characterised a number of
commercial BCG vaccines. (C) 2001 Elsevier Science Ltd. All rights reserved
.