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http://acervodigital.unesp.br/handle/11449/16339
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DC Field | Value | Language |
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dc.contributor.author | Gomes Boriollo, Marcelo Fabiano | - |
dc.contributor.author | Dias, Ricardo Antunes | - |
dc.contributor.author | Fiorini, Joao Evangelista | - |
dc.contributor.author | Silva Oliveira, Nelma de Mello | - |
dc.contributor.author | Palomari Spolidorio, Denise Madalena | - |
dc.contributor.author | Barbosa de Souza, Henrique Marques | - |
dc.contributor.author | de Oliveira Figueira, Antonio Vargas | - |
dc.contributor.author | Pizzirani-Kleiner, Aline Aparecida | - |
dc.date.accessioned | 2014-05-20T13:46:14Z | - |
dc.date.accessioned | 2016-10-25T17:00:01Z | - |
dc.date.available | 2014-05-20T13:46:14Z | - |
dc.date.available | 2016-10-25T17:00:01Z | - |
dc.date.issued | 2010-09-01 | - |
dc.identifier | http://dx.doi.org/10.1016/j.mimet.2010.06.012 | - |
dc.identifier.citation | Journal of Microbiological Methods. Amsterdam: Elsevier B.V., v. 82, n. 3, p. 265-281, 2010. | - |
dc.identifier.issn | 0167-7012 | - |
dc.identifier.uri | http://hdl.handle.net/11449/16339 | - |
dc.identifier.uri | http://acervodigital.unesp.br/handle/11449/16339 | - |
dc.description.abstract | Various 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.format.extent | 265-281 | - |
dc.language.iso | eng | - |
dc.publisher | Elsevier B.V. | - |
dc.source | Web of Science | - |
dc.subject | Candida albicans | en |
dc.subject | Cluster Analysis | en |
dc.subject | Electrophoretic Karyotyping | en |
dc.subject | Epidemiological Tracking | en |
dc.subject | Microsatellite Markers | en |
dc.subject | Multilocus Enzyme Electrophoresis | en |
dc.title | Disparity between Multilocus Enzyme Electrophoresis, Microsatellite Markers and Pulsed-Field Gel Electrophoresis in epidemiological tracking of Candida albicans | en |
dc.type | outro | - |
dc.contributor.institution | Univ Alfenas | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.contributor.institution | Universidade de São Paulo (USP) | - |
dc.description.affiliation | Univ Alfenas, Lab Mol Biol & Genet, Sch Med Sci, Fac Med Sci, BR-37130000 Alfenas, MG, Brazil | - |
dc.description.affiliation | Univ Alfenas, Lab Biol & Physiol Microorganisms, Fac Med Sci, BR-37130000 Alfenas, MG, Brazil | - |
dc.description.affiliation | State Univ São Paulo, Lab Oral Microbiol, Dept Oral Pathol & Physiol, Fac Ordontol Araraquara, São Paulo, Brazil | - |
dc.description.affiliation | Univ São Paulo, Ctr Nucl Energy Agr, Lab Plant Improvement, Piracicaba, SP, Brazil | - |
dc.description.affiliation | Univ São Paulo, Dept Genet, Escola Super Agr Luiz Queiroz, Piracicaba, SP, Brazil | - |
dc.description.affiliationUnesp | State Univ São Paulo, Lab Oral Microbiol, Dept Oral Pathol & Physiol, Fac Ordontol Araraquara, São Paulo, Brazil | - |
dc.identifier.doi | 10.1016/j.mimet.2010.06.012 | - |
dc.identifier.wos | WOS:000282113000012 | - |
dc.rights.accessRights | Acesso restrito | - |
dc.relation.ispartof | Journal of Microbiological Methods | - |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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