Dynamics of long-term colonization of respiratory tract by Haemophilus influenzae in cystic fibrosis patients shows a marked increase in hypermutable strains

被引:73
作者
Román, F
Cantón, R
Pérez-Vázquez, M
Baquero, F
Campos, J
机构
[1] Inst Salud Carlos III, Ctr Nacl Microbiol, Madrid 28220, Spain
[2] Univ Madrid, Hosp Ramon & Cajal, Dept Microbiol, Madrid 3, Spain
关键词
D O I
10.1128/JCM.42.4.1450-1459.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The persistence and variability of 188 Haemophilus influenzae isolates in respiratory tract of 30 cystic fibrosis (CF) patients over the course of 7 years was studied. Antibiotic susceptibility testing, DNA fingerprinting, and analysis of outer membrane protein profiles were performed on all isolates. A total of 115 distinct pulsed-field gel electrophoresis profiles were identified. Ninety percent of patients were cocolonized with two or more clones over the studied period. A third of the patients were cross-colonized with one or two H. influenzae strains; 11% of the clones persisted for 3 or more months. Biotype, outer membrane protein profiles, and resistance profiles showed variation along the studied period, even in persisting clones. Four isolates (2.1%) recovered from 3 patients were type f capsulate, with three of them belonging to the same clone. beta-Lactamase production was detected in 23.9% of isolates while 7% of the beta-lactamase-negative isolates presented diminished susceptibility to ampicillin (beta-lactamase-negative ampicillin resistance phenotype). Remarkably, 21.3% of the H. influenzae isolates presented decreased susceptibility to ciprofloxacin, which was mainly observed in persisting clones. Of the H. influenzae isolates from CF patients, 18 (14.5%) were found to be hypermutable in comparison with 1 (1.4%) from non-CF patients (P < 0.0001). Ten patients (33.3%) were colonized by hypermutable strains over the study period. A multiresistance phenotype and long-term clonal persistence were significantly associated in some cases for up to 7 years. These results suggest that H. influenzae bronchial colonization in CF patients is a dynamic process, but better-adapted clones can persist for long periods of time.
引用
收藏
页码:1450 / 1459
页数:10
相关论文
共 38 条
[1]   SUBTYPING ISOLATES OF HEMOPHILUS-INFLUENZAE TYPE-B BY OUTER-MEMBRANE PROTEIN PROFILES [J].
BARENKAMP, SJ ;
MUNSON, RS ;
GRANOFF, DM .
JOURNAL OF INFECTIOUS DISEASES, 1981, 143 (05) :668-676
[2]  
BILTON D, 1995, EUR RESPIR J, V8, P948
[3]   Antibiotic resistance and clinical significance of Haemophilus influenzae type f [J].
Campos, J ;
Román, F ;
Pérez-Vázquez, M ;
Aracil, B ;
Oteo, J ;
Cercenado, E .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (06) :961-966
[4]   Long-term persistence of ciprofloxacin-resistant Haemophilus influenzae in patients with cystic fibrosis [J].
Campos, J ;
Roman, F ;
Georgiou, M ;
Garcia, C ;
GomezLus, R ;
Canton, R ;
Escobar, H ;
Baquero, F .
JOURNAL OF INFECTIOUS DISEASES, 1996, 174 (06) :1345-1347
[5]   Characterization of non-type B Haemophilus influenzae strains isolated from patients with invasive disease [J].
Cerquetti, M ;
degli Atti, MLC ;
Renna, G ;
Tozzi, AE ;
Garlaschi, ML ;
Mastrantonio, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (12) :4649-4652
[6]  
DOERN GV, 1991, MICROBIOL INFECT DIS, V14, P485
[7]   PCR FOR CAPSULAR TYPING OF HAEMOPHILUS-INFLUENZAE [J].
FALLA, TJ ;
CROOK, DWM ;
BROPHY, LN ;
MASKELL, D ;
KROLL, JS ;
MOXON, ER .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (10) :2382-2386
[8]   Molecular epidemiology of ampicillin-resistant non-β-lactamase-producing Haemophilus influenzae [J].
Gazagne, L ;
Delmas, C ;
Bingen, E ;
Dabernat, H .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (12) :3629-3635
[9]   Ciprofloxacin-resistant Haemophilus influenzae strains possess mutations in analogous positions of GyrA and ParC [J].
Georgiou, M ;
Munoz, R ;
Roman, F ;
Canton, R ;
GomezLus, R ;
Campos, J ;
DelaCampa, AG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (07) :1741-1744
[10]   Persistent and aggressive bacteria in the lungs of cystic fibrosis children [J].
Hart, CA ;
Winstanley, C .
BRITISH MEDICAL BULLETIN, 2002, 61 :81-96