| Title | PCR-Based Detection of Mycoplasma Species |
|---|---|
| Author | Hyeran Sung, Seung Hye Kang, Yoon jin Bae, Jin Tae Hong, Youn Bok Chung, Chong-Kil Lee, and Sukgil Song* |
| Address | College of Pharmacy, Chungbuk National University, 12 Gaeshindong, Cheongju, Chungbuk, Republic of Korea |
| Bibliography | Journal of Microbiology, 44(1),42-49, 2006, |
| DOI | |
| Key Words | Mycoplasma, molecular diagnosis, nested PCR, rDNA |
| Abstract | In this study, we describe our newly-developed sensitive two-stage PCR procedure for the detection of 13 common mycoplasmal contaminants (M. arthritidis, M. bovis, M. fermentans, M. genitalium, M. hominis, M. hyorhinis, M. neurolyticum, M. orale, M. pirum, M. pneumoniae, M. pulmonis, M. salivarium, U. urealyticum). For primary amplification, the DNA regions encompassing the 16S and 23S rRNA genes of 13 species were targeted using general mycoplasma primers. The primary PCR products were then subjected to secondary nested PCR, using two different primer pair sets, designed via the multiple alignment of nucleotide sequences obtained from the 13 mycoplasmal species. The nested PCR, which generated DNA fragments of 165-353 bp, was found to be able to detect 1-2 copies of the target DNA, and evidenced no cross-reactivity with the genomic DNA of related microorganisms or of human cell lines, thereby confirming the sensitivity and specificity of the primers used. The identification of contaminated species was achieved via the performance of restriction fragment length polymorphism (RFLP) coupled with Sau3AI digestion. The results obtained in this study furnish evidence suggesting that the employed assay system constitutes an effective tool for the disagnosis of mycoplasmal contamination in cell culture systems. |
| Download PDF | 07 JM2005-137.pdf |