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Disparity between Multilocus Enzyme Electrophoresis, Microsatellite Markers and Pulsed-Field Gel Electrophoresis in epidemiological tracking of Candida albicans

dc.contributor.authorGomes Boriollo, Marcelo Fabiano
dc.contributor.authorDias, Ricardo Antunes
dc.contributor.authorFiorini, Joao Evangelista
dc.contributor.authorSilva Oliveira, Nelma de Mello
dc.contributor.authorPalomari Spolidorio, Denise Madalena [UNESP]
dc.contributor.authorBarbosa de Souza, Henrique Marques
dc.contributor.authorde Oliveira Figueira, Antonio Vargas
dc.contributor.authorPizzirani-Kleiner, Aline Aparecida
dc.contributor.institutionUniv Alfenas
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T13:46:14Z
dc.date.available2014-05-20T13:46:14Z
dc.date.issued2010-09-01
dc.description.abstractVarious molecular systems are available for epidemiological, genetic, evolutionary, taxonomic and systematic studies of innumerable fungal infections, especially those caused by the opportunistic pathogen C. albicans. A total of 75 independent oral isolates were selected in order to compare Multilocus Enzyme Electrophoresis (MLEE), Electrophoretic Karyotyping (EK) and Microsatellite Markers (Simple Sequence Repeats - SSRs), in their abilities to differentiate and group C. albicans isolates (discriminatory power), and also, to evaluate the concordance and similarity of the groups of strains determined by cluster analysis for each fingerprinting method. Isoenzyme typing was performed using eleven enzyme systems: Adh, Sdh, M1p, Mdh, Idh, Gdh, G6pdh, Asd, Cat, Po, and Lap (data previously published). The EK method consisted of chromosomal DNA separation by pulsed-field gel electrophoresis using a CHEF system. The microsatellite markers were investigated by PCR using three polymorphic loci: EF3, CDC3, and HIS3. Dendrograms were generated by the SAHN method and UPGMA algorithm based on similarity matrices (S(SM)). The discriminatory power of the three methods was over 95%, however a paired analysis among them showed a parity of 19.7-22.4% in the identification of strains. Weak correlation was also observed among the genetic similarity matrices (S(SM)(MLEE) x S(SM)(EK) x S(SM)(SSRs)). Clustering analyses showed a mean of 9 +/- 12.4 isolates per cluster (3.8 +/- 8 isolates/taxon) for MLEE, 6.2 +/- 4.9 isolates per cluster (4 +/- 4.5 isolates/taxon) for SSRs, and 4.1 +/- 2.3 isolates per cluster (2.6 +/- 2.3 isolates/taxon) for EK. A total of 45 (13%), 39(11.2%), 5 (1.4%) and 3 (0.9%) clusters pairs from 347 showed similarity (Si) of 0.1-10%, 10.1-20%, 20.1-30% and 30.1-40%, respectively. Clinical and molecular epidemiological correlation involving the opportunistic pathogen C. albicans may be attributed dependently of each method of genotyping (i.e., MLEE, EK, and SSRs) supplemented with similarity and grouping analysis. Therefore, the use of genotyping systems that give results which offer minimum disparity, or the combination of the results of these systems, can provide greater security and consistency in the determination of strains and their genetic relationships. (C) 2010 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniv Alfenas, Lab Mol Biol & Genet, Sch Med Sci, Fac Med Sci, BR-37130000 Alfenas, MG, Brazil
dc.description.affiliationUniv Alfenas, Lab Biol & Physiol Microorganisms, Fac Med Sci, BR-37130000 Alfenas, MG, Brazil
dc.description.affiliationState Univ São Paulo, Lab Oral Microbiol, Dept Oral Pathol & Physiol, Fac Ordontol Araraquara, São Paulo, Brazil
dc.description.affiliationUniv São Paulo, Ctr Nucl Energy Agr, Lab Plant Improvement, Piracicaba, SP, Brazil
dc.description.affiliationUniv São Paulo, Dept Genet, Escola Super Agr Luiz Queiroz, Piracicaba, SP, Brazil
dc.description.affiliationUnespState Univ São Paulo, Lab Oral Microbiol, Dept Oral Pathol & Physiol, Fac Ordontol Araraquara, São Paulo, Brazil
dc.format.extent265-281
dc.identifierhttp://dx.doi.org/10.1016/j.mimet.2010.06.012
dc.identifier.citationJournal of Microbiological Methods. Amsterdam: Elsevier B.V., v. 82, n. 3, p. 265-281, 2010.
dc.identifier.doi10.1016/j.mimet.2010.06.012
dc.identifier.issn0167-7012
dc.identifier.urihttp://hdl.handle.net/11449/16339
dc.identifier.wosWOS:000282113000012
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal of Microbiological Methods
dc.relation.ispartofjcr1.701
dc.relation.ispartofsjr0,696
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectCandida albicansen
dc.subjectCluster Analysisen
dc.subjectElectrophoretic Karyotypingen
dc.subjectEpidemiological Trackingen
dc.subjectMicrosatellite Markersen
dc.subjectMultilocus Enzyme Electrophoresisen
dc.titleDisparity between Multilocus Enzyme Electrophoresis, Microsatellite Markers and Pulsed-Field Gel Electrophoresis in epidemiological tracking of Candida albicansen
dc.typeResumopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicationb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isDepartmentOfPublication.latestForDiscoveryb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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