Burkholderia cepacia has become an increasingly recognized pathogen am
ong cystic fibrosis (CF) patients and its potential role in declining
pulmonary function or unexpected fatal outcome has caused widespread c
oncern. Direct person-to-person transmission has been documented and a
segregation policy of CF patients colonized with B.cepacia from non-c
olonized CF patients is widely adopted. Since this policy has a dramat
ic impact on social behaviour of CF patients it is imperative that cli
nical laboratories accurately isolate and identify B.cepacia in the re
spiratory secretions. In order to comprehend the epidemiology of B.cep
acia in the Belgian CF population a multicentre study was conducted du
ring a period of 1 year (March'93-February'94). B.cepacia was isolated
in only 12 of 465 CF patients (2.6%). Routine biochemical tests ident
ified these strains as authentic B.cepacia. However, the combined data
from protein and DNA-DNA hybridization analyses revealed that the Bel
gian CF ''B.cepacia'' isolates showed patterns different from referenc
e B.cepacia isolates and belong to 3 different, newly identified Burkh
olderia genomovars, but not to B.cepacia. Comparative analysis of the
selective media used for recovery of these ''B.cepacia'' strains from
respiratory secretions indicated that the commercial medium (Mast) con
taining polymyxin B and ticarcillin as the selective agents was the be
st and most user-friendly. Molecular typing of these Burkholderia isol
ates by arbitrarily-primed PCR (AP-PCR) and pulsed-field gel electroph
oresis (PFGE) showed that spread of a single strain within a same cent
re occurred but the mode of transmission remains unknown; inter-centre
spread of strains was not observed. Interestingly, neither colonizati
on with a distinct or an epidemic strain (belonging to either of the t
hree newly identified Burkholderia genomovars) nor colonization for a
prolonged period of time, led to a rapid deterioration of lung functio
n in these CF patients. It appears essential to determine the prevalen
ce of these ''new'' Burkholderia genomovars in larger populations of C
F patients and to evaluate their virulence and other features as this
may have important clinical and practical implications.