Competitor internal standards for quantitative detection of mycoplasma DNA

• Published in: FEMS microbiology letters 1995-05, Vol.128 (2), p.207-211
• Main Authors: Sidhu, Maninder K., Rashidbaigi, Abbas, Testa, Douglas, Liao, Mei‐June
• Format: Article
• Language: English
• Subjects: Bacteriological methods and techniques used in bacteriology; Bacteriology; Base Sequence; Biological and medical sciences; Cell culture; DNA Primers; DNA, Bacterial - analysis; DNA, Bacterial - isolation & purification; Fundamental and applied biological sciences. Psychology; Microbiology; Molecular Sequence Data; Mycoplasma; Mycoplasma - isolation & purification; Mycoplasma detection; Polymerase Chain Reaction - methods; Quantitative polymerase chain reaction; Reference Standards; RNA, Ribosomal, 16S
• ISSN: 0378-1097; 1574-6968
• DOI: 10.1111/j.1574-6968.1995.tb07524.x

Homologous internal controls were used as competitor DNA in the polymerase chain reaction for the quantitative detection of mycoplasma DNA. PCR primer sets were designed on the basis of the most conserved nucleotide sequences of the 16S rRNA gene of mycoplasma species. Amplification of this gene was examined in five different mycoplasma species: Mycoplasma orale, M. hyorhinus, M. synoviae, M. gallisepticum and M. pneumonias. To evaluate the primers, a number of different cell lines were assayed for the detection of mycoplasma infections. All positive cell lines showed a distinct product on agarose gels while uninfected cells showed no DNA amplification. Neither bacterial nor eukaryotic DNA produced any cross‐reaction with the primers used, thus confirming their specificity. Internal control DNA to be used for quantitation was constructed by modifying the sizes of the wild‐type amplified products and cloning them in plasmid vectors. These controls used the same primer binding sites as the wild‐type and the amplified products were differentiated by a size difference. The detection limits for all the mycoplasma species by competitive quantitative PCR were estimated to range from 4 to 60 genome copies per assay as determined by ethidium bromide‐stained agarose gels. These internal standards also serve as positive controls in PCR‐based detection of mycoplasma DNA, and therefore accidental contamination of test samples with wild‐type positive controls can be eliminated. The quantitative PCR method developed will be useful in monitoring the progression and significance of mycoplasma in the disease process.