Article ID Journal Published Year Pages File Type
5671341 Anaerobe 2017 5 Pages PDF
Abstract

•Developed an absolute qPCR method for quantifying P. histicola from gut samples.•Designed primers for qPCR showed high specificity to16S rDNA gene sequence of P. histicola.•Accuracy in quantification achieved by preparing simulated standards from control gut samples.

We designed species-specific primers and developed a qPCR method for enumerating P. histicola from intestinal samples. The two designed primer sets showed specificity for the target 16S rRNA gene of P. histicola. The absolute qPCR method was sensitive to quantify as few as 103 colony-forming units (CFU) in the gut.

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