Quantitative Detection of Corynebacterium casei in Cheese by Real-Time PCR

• DOI: 10.1128/aem.01303-06
• Publication Date: 2006-11-06T18:53:46Z
• Authors: Christophe Monnet; Karine Correia; Anne-Sophie Sarthou; Françoise Irlinger
• Keywords: DNA, Bacterial; MICROBIAL FLORA; CORYNEBACTERIUM CASEI; SMEAR-RIPENED CHEESE; Molecular Sequence Data; fromage; Corynebacterium; Diamines; DNA, Ribosomal; Polymerase Chain Reaction; DETECTION; 03 medical and health sciences; Species Specificity; Cheese; RNA, Ribosomal, 16S; MOLECULAR SEQUENCE DATA; Benzothiazoles; REAL-TIME PCR; Organic Chemicals; MICROBIAL FLORA;MOLECULAR SEQUENCE DATA;REAL-TIME PCR;DETECTION;CORYNEBACTERIUM CASEI;SMEAR-RIPENED CHEESE; DNA Primers; 580; [SDV.EE]Life Sciences [q-bio]/Ecology, environment; 2. Zero hunger; 0303 health sciences; microorganisme; Genes, rRNA; Sequence Analysis, DNA; Bacterial Typing Techniques; méthode de détection; [SDV.EE] Life Sciences [q-bio]/Ecology, environment; Quinolines

ABSTRACT

The flora on the surface of smear-ripened cheeses is composed of numerous species of bacteria and yeasts that contribute to the production of the desired organoleptic properties. Due to the absence of selective media, it is very difficult to quantify cheese surface bacteria, and, consequently, the ecology of the cheese surface microflora has not been extensively investigated. We developed a SYBR green I real-time PCR method to quantify Corynebacterium casei , a major species of smear-ripened cheeses, using primers designed to target the 16S rRNA gene. It was possible to recover C. casei genomic DNA from the cheese matrix with nearly the same yield that C. casei genomic DNA is recovered from cells recovered by centrifugation from liquid cultures. Quantification was linear over a range from 10 5 to 10 10 CFU per g of cheese. The specificity of the assay was demonstrated with DNA from species related to C. casei and from other bacteria and yeasts belonging to the cheese flora. Nine commercial cheeses were analyzed by real-time PCR, and six of them were found to contain more than 10 5 CFU equivalents of C. casei per g. In two of them, the proportion of C. casei in the total bacterial flora was nearly 40%. The presence of C. casei in these samples was further confirmed by single-strand conformation polymorphism analysis and by a combined approach consisting of plate counting and 16S rRNA gene sequencing. We concluded that SYBR green I real-time PCR may be used as a reliable species-specific method for quantification of bacteria from the surface of cheeses.