Diagnóstico e tratamento de células hep-2 contaminadas por micoplasma

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T10:22:47Z
dc.date.accessioned2022-12-19T22:10:11Z
dc.date.available2021-06-25T10:22:47Z
dc.date.available2022-12-19T22:10:11Z
dc.date.created2021-06-25T10:22:47Z
dc.date.issued2021-02-01
dc.identifierBrazilian Journal of Biology, v. 81, n. 1, p. 37-43, 2021.
dc.identifier1678-4375
dc.identifier1519-6984
dc.identifierhttp://hdl.handle.net/11449/205878
dc.identifier10.1590/1519-6984.215721
dc.identifierS1519-69842021000100037
dc.identifier2-s2.0-85100847017
dc.identifierS1519-69842021000100037.pdf
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/5386475
dc.description.abstractContamination of primary and cell cultures by mycoplasmas is one of the main economic and biological pitfalls in basic research, diagnosis and manufacture of biotechnological products. It is a common issue which may be difficult to conduct surveillance on. Mycoplasma presence may affect several physiological parameters of the cell, besides being considered an important source of inaccurate and/or non-reproducible scientific results. Each cell type presents characteristical symptoms, mainly morphological, that indicate a contamination by mycoplasma. HEp-2 cells originate from carcinoma of the larynx and are, therefore, part of the respiratory tract, which is one of mycoplasma habitats. Despite the importance these cells in several biological research (evaluation of cell proliferation and migration, apoptosis, antiviral and antitumor compounds), the alterations induced by mycoplasma contamination in HEp-2 cells have not yet been described. Here, we describe the progressive morphological alterations in culture of HEp-2 cells infected with mycoplasma, as well as the-diagnosis of the infection and its treatment. Mycoplasma contamination described within this work led to cytoplasm elongation, cell-to-cell spacing, thin plasma membrane projections, cytoplasmic vacuoles, fusion with neighboring cells, and, finally, cell death. Contamination was detected by fluorescence imaging (DAPI) and PCR reactions. The cultures were treated with BM-Cyclin antibiotic to eliminate contamination. The data presented here will be of relevance to researchers whose investigations involve cell culture, especially respiratory and HEp-2 cells.
dc.languageeng
dc.relationBrazilian Journal of Biology
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectCell culture
dc.subjectContamination
dc.subjectHEp-2 cells
dc.subjectMycoplasma
dc.subjectTreatment
dc.titleDiagnosis and treatment of hep-2 cells contaminated with mycoplasma
dc.titleDiagnóstico e tratamento de células hep-2 contaminadas por micoplasma
dc.typeArtículos de revistas


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