I think the best alternative to using real time PCR in quantitation of a particular bateria in a human stool sample is deep sequencing of 16S rRNA gene(V3-V4 or V4 region) amplicon via Illumina Hiseq or Miseq platform.
You could deploy the traditional bacteriological technique of dilution plate counting, particularly if you have a selective medium or antibiotic available for your target. Good luck!
Thank you so much for your answer. I have another question . If I use the conventinal method , which would give better results, pour plate method or spread method? ?
Hi Heba. I would do triplicate plates using the spread method, ensuring you dilute to extinction. This will give you the viable cell count which might vary from the qPCR count. Good luck with it!