Objective-To assess phylogenetic relationships among Mycobacterium bovis is
olates by use of random amplified polymorphic DNA polymerase chain reaction
(RAPD-PCR) fingerprinting and to relate genetic profiles of isolates to ep
idemiologic characteristics.
Animals-400 cattle with tuberculosis.
Procedure-Mycobacterium bovis was isolated from various organs of cattle sl
aughtered in 6 geographic regions of Mexico. Most cattle were adult Holstei
ns from large herds that did not participate in a tuberculosis control prog
ram. Four random primers and 2 selected primers were used in RAPD-PCR finge
rprinting of 88 isolates. Pairwise genetic distance between isolates was ob
tained and subjected to cluster analysis with bootstrapping to test for lev
els of support.
Results-98 different fragments were obtained; there was broad genetic diver
sity among isolates, and each isolate had a unique RAPD-genotype, including
those originating from the same herd. Clustering by geographic location, a
ffected organ, or severity of lesion was not detected. linkage disequilibri
um analysis suggested that M bovis was highly clonal and that mutations dev
elop at a rapid rate among isolates.
Conclusions and Clinical Relevance-Use of RAPD-PCR could not differentiate
M bovis isolates by epidemiologic characteristics or identify common source
s of infection.