Jj. Lipuma et al., Disproportionate distribution of Burkholderia cepacia complex species and transmissibility markers in cystic fibrosis, AM J R CRIT, 164(1), 2001, pp. 92-96
Several distinct species (genomovars) comprise bacteria previously identifi
ed merely as Burkholderia cepacia. Understanding how these species, collect
ively referred to as the B. cepacia complex, differ in their epidemiology a
nd pathogenic potential in cystic fibrosis (CF) is important in efforts to
refine management strategies. B. cepacia isolates recovered from 606 CF pat
ients receiving care at 132 treatment centers in 105 cities in the United S
tates were assessed to determine species within the B. cepacia complex and
examined for the presence of putative transmissibility markers (B. cepacia
epidemic strain marker [BCESM] and cable pilin subunit gene [cblA]). Fifty
percent of patients were infected with B. cepacia complex genomovar III, 38
% with B. multivorans (formerly genomovar II), and 5% with B. vietnamiensis
(formerly genomovar V); fewer than 5% of patients were infected with eithe
r genomovar I, B. stabilis (formerly genomovar IV), genomovar VI, or genomo
var VII. BCESM was found in 46% of genomovar III isolates and not in any ot
her species. Only one isolate, from a patient infected with the ET12 epidem
ic lineage, contained the complete cblA pilin subunit gene. Our data indica
te a differential capacity for human infection among the phylogenetically c
losely related species of the B. cepacia complex. The low frequency of BCES
M and cblA suggests that they are not sufficient markers of B. cepacia viru
lence or transmissibility.