V Cleusix1, C Lacroix, G Dasen, M Leo, G Le Blay. 1. Institute of Food Science and Nutrition, Swiss Federal Institute of Technology, Zentrum, Zürich, Switzerland.
Abstract
AIMS: To detect and enumerate bifidobacteria in faeces with a new quantitative multiplex real-time PCR (qPCR) method and to compare the results obtained with fluorescence in situ hybridization (FISH) methods. METHODS AND RESULTS: A multiplex qPCR assay was developed, which enabled the enumeration of Bifidobacterium spp. by targeting the bifidobacterial xylulose-5-phosphate/fructose-6-phosphate phosphoketolase gene (xfp) and total bacteria using universal Eub-primers targeting 16S rRNA gene from the domain bacteria. The qPCR assay showed high sensitivity and specificity and a low detection limit of about 2.5 x 10(3) bifidobacterial cells per gram of faeces. The qPCR results were compared with FISH combined with microscopy or flow cytometry (FCM). No statistical differences among bifidobacterial counts averages measured in adult faeces with the three methods were observed. Total bacterial count averages were higher with the FISH method coupled with microscopic analyses compared to FISH with FCM, whereas total cell numbers estimated by qPCR were intermediate between the two FISH methods. CONCLUSIONS: The new qPCR assay was shown to be sensitive, rapid and accurate for enumerating bifidobacteria in faeces. SIGNIFICANCE AND IMPACT OF THE STUDY: This method is a valuable alternative for other molecular methods for detecting faecal bifidobacteria, especially when their counts are below the detection limit of the FISH methods.
AIMS: To detect and enumerate bifidobacteria in faeces with a new quantitative multiplex real-time PCR (qPCR) method and to compare the results obtained with fluorescence in situ hybridization (FISH) methods. METHODS AND RESULTS: A multiplex qPCR assay was developed, which enabled the enumeration of Bifidobacterium spp. by targeting the bifidobacterial xylulose-5-phosphate/fructose-6-phosphate phosphoketolase gene (xfp) and total bacteria using universal Eub-primers targeting 16S rRNA gene from the domain bacteria. The qPCR assay showed high sensitivity and specificity and a low detection limit of about 2.5 x 10(3) bifidobacterial cells per gram of faeces. The qPCR results were compared with FISH combined with microscopy or flow cytometry (FCM). No statistical differences among bifidobacterial counts averages measured in adult faeces with the three methods were observed. Total bacterial count averages were higher with the FISH method coupled with microscopic analyses compared to FISH with FCM, whereas total cell numbers estimated by qPCR were intermediate between the two FISH methods. CONCLUSIONS: The new qPCR assay was shown to be sensitive, rapid and accurate for enumerating bifidobacteria in faeces. SIGNIFICANCE AND IMPACT OF THE STUDY: This method is a valuable alternative for other molecular methods for detecting faecal bifidobacteria, especially when their counts are below the detection limit of the FISH methods.
Authors: Antti E Seppo; Kevin Bu; Madina Jumabaeva; Juilee Thakar; Rakin A Choudhury; Chloe Yonemitsu; Lars Bode; Camille A Martina; Maria Allen; Sabrina Tamburini; Enrica Piras; David S Wallach; R John Looney; Jose C Clemente; Kirsi M Järvinen Journal: Allergy Date: 2021-05-14 Impact factor: 14.710