Improved Quantitative Real-Time PCR Protocol for Detection and Quantification of Methanogenic Archaea in Stool Samples

• Published in: Microorganisms (Basel) Vol. 11; no. 3; p. 660
• Main Authors: Cisek, Agata Anna, Bąk, Iwona, Cukrowska, Bożena
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 05.03.2023; MDPI
• Subjects: Annealing; Archaea; Biotechnology; chickens; Copy number; Dimerization; genes; Genomes; Health aspects; humans; Identification and classification; Intestinal microflora; intestinal microorganisms; Life sciences; Linearity; mcrA; Methanobacteriaceae; Methanobrevibacter; Methanogenic archaea; Methanogenic bacteria; methanogens; Microbiota; Microbiota (Symbiotic organisms); Polymerase chain reaction; Poultry; qPCR; quantitative polymerase chain reaction; Real time; real-time PCR; Veterinary medicine; Poland; United States > US; qPCR; real-time PCR; methanogens; mcrA; Methanobrevibacter; archaea
• ISSN: 2076-2607; 2076-2607
• DOI: 10.3390/microorganisms11030660

Methanogenic archaea are an important component of the human and animal intestinal microbiota, and yet their presence is rarely reported in publications describing the subject. One of the methods of quantifying the prevalence of methanogens is quantitative real-time PCR (qPCR) of the methanogen-specific mcrA gene, and one of the possible reasons for detection failure is usually a methodology bias. Here, we refined the existing protocol by changing one of the primers and improving the conditions of the qPCR reaction. As a result, at the expense of a slightly lower yet acceptable PCR efficiency, the new assay was characterized by increased specificity and sensitivity and a wider linear detection range of 7 orders of magnitude. The lowest copy number of mcrA quantified at a frequency of 100% was 21 copies per reaction. The other validation parameters tested, such as reproducibility and linearity, also gave satisfactory results. Overall, we were able to minimize the negative impacts of primer dimerization and other cross-reactions on qPCR and increase the number of not only detectable but also quantifiable stool samples—or in this case, chicken droppings.