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Identification of genomic groups in the genus Stenotrophomonas using gyrB RFLP analysis

dc.contributor.authorCoenye, Tomen_US
dc.contributor.authorVanlaere, Elkeen_US
dc.contributor.authorLiPuma, John J.en_US
dc.contributor.authorVandamme, Peteren_US
dc.date.accessioned2010-06-01T19:11:36Z
dc.date.available2010-06-01T19:11:36Z
dc.date.issued2004-04en_US
dc.identifier.citationCoenye, Tom; Vanlaere, Elke; LiPuma, John J; Vandamme, Peter (2004). "Identification of genomic groups in the genus Stenotrophomonas using gyrB RFLP analysis." FEMS Immunology & Medical Microbiology 40(3): 181-185. <http://hdl.handle.net/2027.42/72378>en_US
dc.identifier.issn0928-8244en_US
dc.identifier.issn1574-695Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/72378
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=15039092&dopt=citationen_US
dc.description.abstractStenotrophomonas maltophilia isolates have been recovered from various clinical samples, including the respiratory tract of cystic fibrosis (CF) patients, but this organism is also widespread in nature. Previously it has been shown that there is a considerable genomic diversity within S. maltophilia . The aims of our study were to determine the taxonomic resolution of restriction fragment length polymorphism (RFLP) analysis of the polymerase chain reaction-amplified gyrB gene for the genus Stenotrophomonas . Subsequently, we wanted to use this technique to screen a set of S. maltophilia isolates (with emphasis on a specific subset, isolates recovered from CF patients), to assess the genomic diversity within this group. In this study we investigated 191 Stenotrophomonas sp. isolates (including 40 isolates recovered from CF patients) by means of gyrB RFLP. The taxonomic resolution of gyrB RFLP, and hence its potential as an identification tool, was confirmed by comparison with results from published and novel DNA–DNA hybridisation experiments. Our data also indicate that the majority of CF isolates grouped in two clusters. This may indicate that isolates from specific genomic groups have an increased potential for colonisation of the respiratory tract of CF patients.en_US
dc.format.extent286998 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights2004 Federation of European Microbiological Societiesen_US
dc.subject.otherStenotrophomonas Maltophiliaen_US
dc.subject.otherIdentificationen_US
dc.subject.otherCystic Fibrosisen_US
dc.subject.otherGyrB Restriction Fragment Length Polymorphismen_US
dc.titleIdentification of genomic groups in the genus Stenotrophomonas using gyrB RFLP analysisen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMicrobiology and Immunologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherLaboratorium voor Microbiologie, Universiteit Gent, K.L. Ledeganckstraat 35, B-9000 Gent, Belgiumen_US
dc.identifier.pmid15039092en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/72378/1/S0928-8244_03_00307-9.pdf
dc.identifier.doi10.1016/S0928-8244(03)00307-9en_US
dc.identifier.sourceFEMS Immunology & Medical Microbiologyen_US
dc.identifier.citedreferenceDenton, M., Kerr, K.G. ( 1998 ) Microbiological and clinical aspects of infection associated with Stenotrophomonas maltophilia. Clin. Microbiol. Rev. 11, 57 – 80.en_US
dc.identifier.citedreferenceBerg, G., Balling, G. ( 1994 ) Bacterial antagonists to Verticillium dahliae. J. Phytopathol. 141, 99 – 110.en_US
dc.identifier.citedreferenceNakayama, T., Homma, Y., Hashidoko, Y., Mizutani, J., Tahara, S. ( 1999 ) Possible role of xanthobaccins produced by Stenotrophomonas sp. strain SB-K88 in suppression of sugar beet damping-off disease. Appl. Environ. Microbiol. 65, 4334 – 4339.en_US
dc.identifier.citedreferenceBinks, P.R., Nicklin, S., Bruce, N.C. ( 1995 ) Degradation of hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) by Stenotrophomonas maltophilia PB1. Appl. Environ. Microbiol. 61, 1318 – 1322.en_US
dc.identifier.citedreferenceBurns, J.L., Emerson, J., Stapp, J.R., Yim, D.L., Krzewinski, J., Louden, L., Ramsey, B.W., Clausen, C.R. ( 1998 ) Microbiology of sputum from patients at cystic fibrosis centers in the United States. Clin. Infect. Dis. 27, 158 – 163.en_US
dc.identifier.citedreferenceValdezate, S., Vindel, A., Maiz, L., Baquero, F., Escobar, H., Canton, R. ( 2001 ) Persistence and variability of Stenotrophomonas maltophilia in cystic fibrosis patients, Madrid, 1991–1998. Emerg. Infect. Dis. 7, 113 – 122.en_US
dc.identifier.citedreferenceTalmaciu, I., Varlotta, L., Mortensen, J., Schidlow, D.V. ( 2000 ) Risk factors for emergence of Stenotrophomonas maltophilia in cystic fibrosis. Pediatr. Pulmonol. 30, 10 – 15.en_US
dc.identifier.citedreferenceGoss, C.H., Otto, K., Aitken, M.L., Rubenfeld, G.D. ( 2002 ) Detecting Stenotrophomonas maltophilia does not reduce survival of patients with cystic fibrosis. Am. J. Respir. Crit. Care Med. 166, 356 – 361.en_US
dc.identifier.citedreferenceGraff, G.R., Burns, J.L. ( 2002 ) Factors affecting the incidence of Stenotrophomonas maltophilia isolation in cystic fibrosis. Chest 121, 1754 – 1760.en_US
dc.identifier.citedreferenceDenton, M., Todd, N.J., Kerr, K.G., Kawkey, P.M., Littlewood, J.M. ( 1998 ) Molecular epidemiology of Stenotrophomonas maltophilia isolated from clinical specimens from patients with cystic fibrosis and associated environmental samples. J. Clin. Microbiol. 36, 1953 – 1958.en_US
dc.identifier.citedreferenceKrzewisnki, J.W., Nguyen, C.D., Foster, J.M., Burns, J.L. ( 2001 ) Use of random amplified polymorphic DNA PCR to examine epidemiology of Stenoptrophomonas maltophilia and Achromobacter ( Alcaligenes ) xylosoxidans from patients with cystic fibrosis. J. Clin. microbiol. 39, 3597 – 3602.en_US
dc.identifier.citedreferenceHauben, L., Vauterin, L., Moore, E.R.B., Hoste, B., Swings, J. ( 1999 ) Genomic diversity of the genus Stenotrophomonas. Int. J. Syst. Bacteriol. 49, 1749 – 1760.en_US
dc.identifier.citedreferenceDrancourt, M., Bollet, C., Raoult, D. ( 1997 ) Stenotrophomonas africana sp. nov., an opportunistic human pathogen in Africa. Int. J. Syst. Bacteriol. 47, 160 – 163.en_US
dc.identifier.citedreferenceFinkmann, W., Altendorf, K., Stackebrandt, E., Lipski, A. ( 2000 ) Characterisation of N2O-producing Xanthomonas -like isolates from biofilters as Stenotrophomonas nitritireducens sp. nov., Luteimonas meohitis gen. nov., sp. nov. and Pseudoxanthomonas broegbernensis gen. nov., sp. nov. Int. J. Syst. Evol. Microbiol. 50, 273 – 282.en_US
dc.identifier.citedreferenceAssih, E.A., Ouattara, A.S., Thierry, S., Cayol, J.L., Labat, M., Macarie, H. ( 2002 ) Stenotrophomonas acidaminiphila sp. nov., a strictly aerobic bacterium isolated from an upflow anaerobic sludge blanket (UASB) reactor. Int. J. Syst. Evol. Microbiol. 52, 559 – 568.en_US
dc.identifier.citedreferenceWolf, A., Fritze, A., Hagemann, M., Berg, G. ( 2002 ) Stenotrophomonas rhizophila sp. nov., a novel plant-associated bacterium with antifungal properties. Int. J. Syst. Evol. Microbiol. 52, 1937 – 1944.en_US
dc.identifier.citedreferenceCoenye, T., LiPuma, J.J. ( 2002 ) Use of the gyrB gene for the identification of Pandoraea species. FEMS Microbiol. Lett. 208, 15 – 19.en_US
dc.identifier.citedreferencePitcher, D.G., Saunders, N.A., Owen, R.J. ( 1989 ) Rapid extraction of bacterial genomic DNA with guanidium thiocyanate. Lett. Appl. Microbiol. 8, 109 – 114.en_US
dc.identifier.citedreferenceEzaki, T., Hashimoto, Y., Yabuuchi, E. ( 1989 ) Fluorometric deoxyribonucleic acid-deoxyribonucleic acid hybridisation in microdilution wells as an alternative to membrane filter hybridisation in which radioisotopes are used to determine genetic relatedness among bacterial strains. Int. J. Syst. Bacteriol. 39, 224 – 229.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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