Hypermutable Haemophilus influenzae with mutations in mutS are found in cystic fibrosis sputum
被引:66
作者:
Watson, ME
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机构:Seattle Biomed Res Inst, Seattle, WA 98109 USA
Watson, ME
Burns, JL
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机构:Seattle Biomed Res Inst, Seattle, WA 98109 USA
Burns, JL
Smith, AL
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机构:Seattle Biomed Res Inst, Seattle, WA 98109 USA
Smith, AL
机构:
[1] Seattle Biomed Res Inst, Seattle, WA 98109 USA
[2] Univ Missouri, Sch Med, Dept Mol Microbiol & Immunol, Columbia, MO 65212 USA
[3] Childrens Hosp & Reg Med Ctr, Div Infect Dis, Seattle, WA 98105 USA
来源:
MICROBIOLOGY-SGM
|
2004年
/
150卷
关键词:
D O I:
10.1099/mic.0.27230-0
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Hypermutable bacterial pathogens exist at surprisingly high prevalence and benefit bacterial populations by promoting adaptation to selective environments, including resistance to antibiotics. Five hundred Haernophilus influenzae isolates were screened for an increased frequency of mutation to resistance to rifampicin, nalidixic acid and spectinomycin: of the 14 hypermutable isolates identified, 12 were isolated from cystic fibrosis (CF) sputum. Analysis by enterobacterial repetitive intergenic consensus (ERIC)-PCR and ribotyping identified eight distinct genetic fingerprints. The hypermutable phenotype of seven of the eight unique isolates was associated with polymorphisms in conserved sites of mutS. Four of the mutant mutS alleles were cloned and failed to complement the mutator phenotype of a mutS::TSTE mutant of H. influenzae strain Rd KW20. Antibiotic susceptibility testing of the hypermutators identified one beta-lactamase-negative ampicillin-resistant (BLNAR) isolate with two isolates producing beta-lactamase. Six isolates from the same patient with CF, with the same genetic fingerprint, were clonal by multilocus sequence typing (MLST). In this clone, there was an evolution to higher MIC values for the antibiotics administered to the patient during the period in which the strains were isolated. Hypermutable H. influenzae with mutations in mutS are prevalent, particularly in the CF lung environment, and may be selected for and maintained by antibiotic pressure.