Understanding the genetic defects underlying cystic fibrosis is only half the battle. Identifying the specific bacterium infecting CF patients is just as important (pages 661–666).
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References
The CF Genotype-Phenotype Consortium. Correlation between genotype and phenotype in patients with cystic fibrosis. New Engl. J. Med. 329, 1308–1312 (1993).
Rosenstein, B.J. Genotype-phenotype correlations in cystic fibrosis [Commentary]. Lancet 343, 746–747 (1994).
Marshall, E. Varmus orders up a review of the science of gene therapy [News]. Science 267, 1588 (1995).
Sun, L. et al. The emergence of a highly transmissible lineage of cbl+ Pseudomonas (Burkholderia) cepacia causing CF centre epidemics in North America and Britain. Nature Med. 1, 661–666 (1995).
LiPuma, J., Dansen, S., Nielson, D., Stern, R. & Stull, T. Person-to-person transmission of P. cepacia between patients with cystic fibrosis. Lancet 336, 1094–1096 (1990).
Govan, J.R.W. et al. Evidence for transmission of Pseudomonas cepacia by social contact in cystic fibrosis. Lancet 342, 15–19 (1993).
Govan, J.R.W. & Nelson, W. Microbiology of cystic fibrosis lung infections: Themes and issues. Archs. Dis. Childh. 59, 1131–1134 (1984).
Walters, S. & Smith, E.G. [commentary]. Pseudomonas cepacia in cystic fibrosis: Transmissibility and its implications. Lancet 342, 3–4 (1993).
Steinbach, S. et al. Transmissibility of Pseudomonas cepacia infection in clinic patients and lung-transplant recipients with cystic fibrosis. New Engl. J. Med. 331, 981–987 (1994).
Sajjan, U., Brockhausen, I., Reisman, J., Corey, M. & Forstner, J.P. P. cepacia binding to mucins and buccal epithelial cells. Glycoconjugate J. 8, 209–210 (1991).
Sajjan, U. & Forstner, J. Identification of the mucin-binding adhesin of P. cepacia isolated from patients with cystic fibrosis. Infect. Immun. 60, 1434–1440 (1992).
Sajjan, U., Corey, M., Karmali, M. & Forstner, J. Binding of Pseudomonas cepacia to normal human intestinal mucin and respiratory mucin from patients with cystic fibrosis. J. clin. Invest. 89, 648–656 (1992).
Sajjan, U. & Forstner, J. Role of a 22-kilodalton pilin protein in binding of Pseudomonas cepacia to buccal epithelial cells. Infect. Immun. 61, 3156–3163 (1993).
Sajjan, U., Sun, L., Goldstein, R. & Forstner, J. Cable (Cbl) type II pili of cystic fibrosis-associated Burkholderia (Pseudomonas) cepacia: nucleotide sequence of the cbl A major subunit pilin gene and novel morphology of the assembled appendage fibers. J. Bacteriol. 177, 10301038 (1995).
Goldstein, R., Sun, L., Jiang, R.-Z., Sajjan, U., Forstner, J. & Campanelli, C. Structurally variant classes of pilus appendage fibers coexpressed from Burkholderia (Pseudomonas) cepacia. J. Bacteriol 177, 1039–1052 (1995).
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Hearst, J., Elliott, K. Identifying the killer in cystic fibrosis. Nat Med 1, 626–627 (1995). https://doi.org/10.1038/nm0795-626
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DOI: https://doi.org/10.1038/nm0795-626
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