Literature DB >> 26481833

Comparison of culture-dependent and independent approaches to characterize fecal bifidobacteria and lactobacilli.

Andrea Quartieri1, Marta Simone1, Caterina Gozzoli1, Mina Popovic1, Giuseppe D'Auria2, Alberto Amaretti1, Stefano Raimondi1, Maddalena Rossi3.   

Abstract

Different culture-dependent and independent methods were applied to investigate the population of bifidobacteria and lactobacilli in the feces of five healthy subjects. Bacteria were isolated on MRS, a complex medium supporting growth of lactobacilli and bifidobacteria, and on three selective media for bifidobacteria and two for lactobacilli. Taxonomic characterization of the isolates was carried out by RAPD-PCR and partial 16S sequencing. The selectivity of genus-specific media was also investigated by challenging colonies from MRS plates to grow onto each medium. In parallel, a quantitative and qualitative description of bifidobacteria and lactic acid bacteria was obtained by FISH, qPCR, TRFLP, and 16S rRNA gene sequencing. Bifidobacteria did not fail to grow on their specific media and were easily isolated and enumerated, showing comparable quantitative data among culture-dependent and -independent techniques. The Bifidobacterium species identified on plates and those extracted from TRFLP and 16S rRNA gene sequencing were mostly overlapping. Selective media for lactobacilli gave unsuitable results, being too stringent or too permissive. The quantification of lactobacilli through selective plates, qPCR, FISH, and 16S rRNA gene sequencing gave unreliable results. Therefore, unlike bifidobacteria, intestinal lactobacilli are still problematic in terms of quantification and accurate profiling at level of species and possibly of strains by both culture-dependent and culture-independent techniques.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Bifidobacterium; Count; Fecal microbiota; Lactobacillus; Molecular methods; Selective media

Mesh:

Substances:

Year:  2015        PMID: 26481833     DOI: 10.1016/j.anaerobe.2015.10.006

Source DB:  PubMed          Journal:  Anaerobe        ISSN: 1075-9964            Impact factor:   3.331


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