Literature DB >> 25742733

Real-time PCR assay is superior to other methods for the detection of mycoplasma contamination in the cell lines of the National Cell Bank of Iran.

Vahid Molla Kazemiha1, Shahin Bonakdar1, Amir Amanzadeh1, Shahram Azari1, Arash Memarnejadian2, Shirin Shahbazi3, Mohammad Ali Shokrgozar4, Reza Mahdian5.   

Abstract

Mycoplasmas are the most important contaminants of cell cultures throughout the world. They are considered as a major problem in biological studies and biopharmaceutical economic issues. In this study, our aim was to find the best standard technique as a rapid method with high sensitivity, specificity and accuracy for the detection of mycoplasma contamination in the cell lines of the National Cell Bank of Iran. Thirty cell lines suspected to mycoplasma contamination were evaluated by five different techniques including microbial culture, indirect DNA DAPI staining, enzymatic mycoalert(®) assay, conventional PCR and real-time PCR. Five mycoplasma-contaminated cell lines were assigned as positive controls and five mycoplasma-free cell lines as negative controls. The enzymatic method was performed using the mycoalert(®) mycoplasma detection kit. Real-time PCR technique was conducted by PromoKine diagnostic kits. In the conventional PCR method, mycoplasma genus-specific primers were designed to analyze the sequences based on a fixed and common region on 16S ribosomal RNA with PCR product size of 425 bp. Mycoplasma contamination was observed in 60, 56.66, 53.33, 46.66 and 33.33 % of 30 different cell cultures by real-time PCR, PCR, enzymatic mycoalert(®), indirect DNA DAPI staining and microbial culture methods, respectively. The analysis of the results of the different methods showed that the real-time PCR assay was superior the other methods with the sensitivity, specificity, accuracy, predictive value of positive and negative results of 100 %. These values were 94.44, 100, 96.77, 100 and 92.85 % for the conventional PCR method, respectively. Therefore, this study showed that real-time PCR and PCR assays based on the common sequences in the 16S ribosomal RNA are reliable methods with high sensitivity, specificity and accuracy for detection of mycoplasma contamination in cell cultures and other biological products.

Entities:  

Keywords:  Cell culture; DAPI staining; Mycoplasma contamination; PCR; Real-time PCR

Year:  2015        PMID: 25742733      PMCID: PMC4960155          DOI: 10.1007/s10616-015-9862-0

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  39 in total

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Journal:  Angew Chem Int Ed Engl       Date:  2013-07-10       Impact factor: 15.336

5.  Sensitivity of biochemical test in comparison with other methods for the detection of mycoplasma contamination in human and animal cell lines stored in the National Cell Bank of Iran.

Authors:  Vahid Molla Kazemiha; Amir Amanzadeh; Arash Memarnejadian; Shahram Azari; Mohammad Ali Shokrgozar; Reza Mahdian; Shahin Bonakdar
Journal:  Cytotechnology       Date:  2014-02-04       Impact factor: 2.058

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2.  Effectiveness of Plasmocure™ in Elimination of Mycoplasma Species from Contaminated Cell Cultures: A Comparative Study versus other Antibiotics.

Authors:  Vahid Molla Kazemiha; Shahram Azari; Mahdi Habibi-Anbouhi; Amir Amanzadeh; Shahin Bonakdar; Mohammad Ali Shokrgozar; Reza Mahdian
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7.  Detection of Mycoplasma Contamination of Cell Culture by A Loop-Mediated Isothermal Amplification Method.

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