Distribution of genes encoding putative transmissibility factors among epidemic and nonepidemic strains of Burkholderia cepacia from cystic fibrosis patients in the United Kingdom

Citation
Fe. Clode et al., Distribution of genes encoding putative transmissibility factors among epidemic and nonepidemic strains of Burkholderia cepacia from cystic fibrosis patients in the United Kingdom, J CLIN MICR, 38(5), 2000, pp. 1763-1766
Citations number
16
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
JOURNAL OF CLINICAL MICROBIOLOGY
ISSN journal
00951137 → ACNP
Volume
38
Issue
5
Year of publication
2000
Pages
1763 - 1766
Database
ISI
SICI code
0095-1137(200005)38:5<1763:DOGEPT>2.0.ZU;2-Y
Abstract
In the last 15 years, Burkholderia cepacia has emerged as a significant pat hogen in cystic fibrosis (CF) patients, mainly due to the severity of infec tion observed in a subset of patients and the fear of transmission of the o rganism to noncolonized patients. Although patients who deteriorate rapidly cannot be predicted by microbiological characteristics, three genetic mark ers have been described for strains that spread between patients. These are the cblA gene, encoding giant cable pill; a hybrid of two insertion sequen ces, IS1356 and IS402; and a 1.4-kb open reading frame known as the B. cepa cia epidemic strain marker (BCESM), The latter two are of unknown function. An epidemic strain lineage was previously identified among CF patients in the United Kingdom that apparently had spread from North America and that w as characterized by a specific random amplified polymorphic DNA (RAPD) patt ern. We searched for the described genetic markers using specific PCR assay s with 117 patient isolates of B. cepacia from 40 United Kingdom hospitals. Isolates were grouped according to genomovar and epidemic strain lineage R APD pattern with a 10-base primer, P272, A total of 41 isolates from patien ts in 12 hospitals were classified as the epidemic strain, and 40 of these were distributed in genomovars IIIa (11 isolates), IIIb (1 isolate), and II Ic (28 isolates). All isolates of the epidemic strain were positive for the cblA gene and BCESM, but two lacked the insertion sequence hybrid. None of the 76 sporadic isolates contained cblA or the insertion sequence hybrid, but 11 of them were positive for BCESM, Nonepidemic isolates were distribut ed among genomovars I or IV (9), II (49), IIIa (11), IIIb (3), and IIIc (4) . There were three clusters of cross-infection (one involving two patients and two involving three patients) with isolates of genomovar II. We conclud e that in the United Kingdom, a single clonal lineage has spread between an d within some hospitals providing care for CF patients. The presence of the cblA gene is the most specific marker for the epidemic strain. We recommen d that all isolates of B. cepacia from CF patients should be screened by PC R to influence segregation and infection control strategies.