Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells

Background and Objectives: Contamination of cell lines and biological products is one of the major problems of cell culture techniques. Rapid detection of mycoplasma contamination in cell culture is an important part of quality control standards in related laboratories. The aim of this study was to...

Full description

Bibliographic Details
Main Authors: Reza Tabatabaei-Qomi, Mohsen Sheykh-Hasan, Hoda Fazaely, Naser Kalhor, Mahdieh Ghiasi
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2014-08-01
Series:Iranian Journal of Microbiology
Subjects:
PCR
Online Access:https://ijm.tums.ac.ir/index.php/ijm/article/view/387
id doaj-eda08dc4595f48e891a4182e84335afa
record_format Article
spelling doaj-eda08dc4595f48e891a4182e84335afa2020-12-02T05:59:36ZengTehran University of Medical SciencesIranian Journal of Microbiology2008-32892008-44472014-08-0164Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cellsReza Tabatabaei-Qomi0Mohsen Sheykh-Hasan1Hoda Fazaely2Naser Kalhor3Mahdieh Ghiasi4Jihad Daneshgahi Infertility Treatment Center, Stem Cell laboratory, Qom, Iran.Jihad Daneshgahi Infertility Treatment Center, Stem Cell laboratory, Qom, Iran.Jihad Daneshgahi Infertility Treatment Center, Stem Cell laboratory, Qom, Iran.Jihad Daneshgahi Infertility Treatment Center, Stem Cell laboratory, Qom, Iran.Jihad Daneshgahi Infertility Treatment Center, Stem Cell laboratory, Qom, Iran. Background and Objectives: Contamination of cell lines and biological products is one of the major problems of cell culture techniques. Rapid detection of mycoplasma contamination in cell culture is an important part of quality control standards in related laboratories. The aim of this study was to evaluate the efficacy of PCR in detection of myroplasma as contaminants in cell cultures and other biological products. Method: PCR assays were optimized for 16 S rRNA target gene. Also the utilized PCR method was evaluated in terms of sensitivity and specificity. Finally, a simple DNA extraction and PCR analysis of 164 cell culture of adipose tissue derived mesenchymal stem cells were performed. Results: A 715 bp product was amplified and subsequently was confirmed by sequencing. The technique could detect 10 copies of the target DNA. No cross-reactivity with genomic DNA of other microorganisms was observed. Conclusions: The PCR technique in this study was based on 16S rRNA gene. It was highly sensitive and specific since it was able to detected Mycoplasma contamination in cell cultures https://ijm.tums.ac.ir/index.php/ijm/article/view/387MycoplasmaPCRcell culturecontaminationmolecular detection
collection DOAJ
language English
format Article
sources DOAJ
author Reza Tabatabaei-Qomi
Mohsen Sheykh-Hasan
Hoda Fazaely
Naser Kalhor
Mahdieh Ghiasi
spellingShingle Reza Tabatabaei-Qomi
Mohsen Sheykh-Hasan
Hoda Fazaely
Naser Kalhor
Mahdieh Ghiasi
Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells
Iranian Journal of Microbiology
Mycoplasma
PCR
cell culture
contamination
molecular detection
author_facet Reza Tabatabaei-Qomi
Mohsen Sheykh-Hasan
Hoda Fazaely
Naser Kalhor
Mahdieh Ghiasi
author_sort Reza Tabatabaei-Qomi
title Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells
title_short Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells
title_full Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells
title_fullStr Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells
title_full_unstemmed Development of a PCR assay to detect mycoplasma contamination in cord blood hematopoietic stem cells
title_sort development of a pcr assay to detect mycoplasma contamination in cord blood hematopoietic stem cells
publisher Tehran University of Medical Sciences
series Iranian Journal of Microbiology
issn 2008-3289
2008-4447
publishDate 2014-08-01
description Background and Objectives: Contamination of cell lines and biological products is one of the major problems of cell culture techniques. Rapid detection of mycoplasma contamination in cell culture is an important part of quality control standards in related laboratories. The aim of this study was to evaluate the efficacy of PCR in detection of myroplasma as contaminants in cell cultures and other biological products. Method: PCR assays were optimized for 16 S rRNA target gene. Also the utilized PCR method was evaluated in terms of sensitivity and specificity. Finally, a simple DNA extraction and PCR analysis of 164 cell culture of adipose tissue derived mesenchymal stem cells were performed. Results: A 715 bp product was amplified and subsequently was confirmed by sequencing. The technique could detect 10 copies of the target DNA. No cross-reactivity with genomic DNA of other microorganisms was observed. Conclusions: The PCR technique in this study was based on 16S rRNA gene. It was highly sensitive and specific since it was able to detected Mycoplasma contamination in cell cultures
topic Mycoplasma
PCR
cell culture
contamination
molecular detection
url https://ijm.tums.ac.ir/index.php/ijm/article/view/387
work_keys_str_mv AT rezatabatabaeiqomi developmentofapcrassaytodetectmycoplasmacontaminationincordbloodhematopoieticstemcells
AT mohsensheykhhasan developmentofapcrassaytodetectmycoplasmacontaminationincordbloodhematopoieticstemcells
AT hodafazaely developmentofapcrassaytodetectmycoplasmacontaminationincordbloodhematopoieticstemcells
AT naserkalhor developmentofapcrassaytodetectmycoplasmacontaminationincordbloodhematopoieticstemcells
AT mahdiehghiasi developmentofapcrassaytodetectmycoplasmacontaminationincordbloodhematopoieticstemcells
_version_ 1724408960759365632