Detection and vitality of Lactococcus lactis in cheese

Detection and vitality of Lactococcus lactis in cheese ripening Marianna Ruggirello (marianna. ruggirello@unito. it) DISAFA - Dept. of Agricultural, Forest and Food Sciences, University of Turin, Italy Tutor: Dott. ssa Paola Dolci The objective of my Ph. D project is to assess the presence of metabolically active populations of Lactococcus lactis in ripened cheeses and to understand the possible contribute of this microorganism in the development of unique chemical and sensory characteristics of the final product. ACTIVITIES and MATHERIALS AND METHODS: A 1) Optimization of q. PCR protocols for L. lactis detection and viability determination: the housekeeping gene tuf (Ulve et al. 2008) was chosen as target and the primers Tuf 2 f and Tuf 2 r were used on both target (L. lactis subsp. lactis and L. lactis subsp. cremoris) and non-target lactic acid bacteria commonly found in dairy products. Different primer concentrations and annealing temperatures were tested in q. PCR and RT-q. PCR experiments to determine the most selective and efficient amplification conditions. Standard curves were constructed by plotting the Ct values against the colony forming units (CFU)/m. L and CFU/g, respectively, of the pure culture and the grated cheese inoculated with L. lactis subsp. lactis, evaluated by traditional plating on M 17 agar. Correlation coefficients (R 2) and the efficiency (E) parameters were calculated according to Rutledge & Coté (2003). A 2) Application of the q. PCR protocols for the analysis of ripened commercial cheeses to detect metabolically active populations of L. lactis: thirty-three ripened commercial cheeses were analyzed by both q. PCR and RT-q. PCR and traditional plating. The identification of L. lactis isolates obtained on M 17 plates was carried out by L. lactis specific PCR (His-PCR)(Corroler et al. 1998). Culture-independent and –dependent results were compared. A 3) Manufacturing and ripening of miniature cheeses to follow L. lactis persistence: miniature cheeses produced according to the protocol described by Shakeel-Ur-Rehman et al. (1998) were inoculated with 8 L. lactis commercial starters, ripened at 8°C vacuum for 180 days and analyzed by both q. PCR and RT-q. PCR and traditional plating. The plates obtained from the cheese sample 10 -1 dilution were used for bulk formation (Ercolini et al. , 2001). One millilitre of bulk cell suspension was collected and submitted to DNA extraction and q. PCR for the detection of L. lactis. Table 2 a, 2 b, 2 c, 2 d. Detection of alive cells of L. lactis throughout manufacturing and ripening of miniature cheeses: comparison of the results obtained by culture-independent and -dependent approaches. RESULTS: starters Fig. 1: q. PCR and RT-q. PCR protocols. Figure 2. Standard curves for L. lactis inoculated in cheese matrix [DNA (A) and RNA (B)] and L. lactis pure culture [DNA (C) and RNA (D)]. The fluorescence signal was detected for the subspecies L. lactis subsp. lactis and subsp. cremoris at Ct values of 14. 37 ( 0. 12) and 15. 69 ( 0. 31), respectively; the other lactic acid bacteria species were not amplified within the 40 cycles set in the amplification protocol. The melting curve showed a single peak confirming the high specificity of the protocol optimized. Y HISBULK** PCR RNA (CFU/g) *** Step RNA analysis (CFU/g)* Plate counts Log CFU/g milk 3, 87 7, 60 + 10 curd 4, 98 8, 59 + dry 5, 34 9, 41 salt 6, 70 7 d B Plate counts Log CFU/g BULK HIS-PCR 6, 99 8, 01 + 10 10 7, 87 8, 82 + 10 7, 99 9, 46 + 10 10, 60 + 10 8, 24 9, 69 + 10 7, 00 8, 46 + 10 7, 27 9, 18 + 10 Toma di capra 8, 47 8, 59 0 15 d 6, 98 8, 45 + 10 6, 33 9, 02 + 10 Toma piemontese 7, 68 8, 95 1 30 d 6, 78 7, 78 + 10 4, 96 8, 75 + 7 60 d 7, 58 6, 51 0 7, 00 + 9 4, 81 8, 66 + 5 Pecorino Toscano PDO 4, 55 90 d 3, 07 7, 41 + 9 4, 81 8, 48 + 5 Pecorino fioretto 7, 48 7, 79 7 120 d 2, 39 5, 78 + 9 4, 75 8, 81 + 0 150 d 1, 44 3, 90 + 8 4, 67 7, 90 - 0 Toma stagionata 7, 40 7, 45 0 180 d 1, 40 4, 08 - 0 3, 81 7, 76 - 0 Asiago PDO 7, 13 6, 94 2 Toma di Lanzo 7, 06 8, 15 0 Toma di Lanzo 7, 03 8, 60 0 Pecorino di Gallura 6, 97 9, 48 0 Pecorino Fiore Sardo 6, 29 7, 57 0 Castelmagno PDO 6, 16 5, 40 0 Ripening 40 cycles HIS ** Table 2 b. starters Manufacturing 95°C 5'' 68. 7°C 30'' Plate counts Log CFU/g J C Step RNA (CFU/g) Plate counts Log CFU/g BULK milk 5, 91 8, 06 + 10 6, 14 7, 85 + 10 curd 6, 99 9, 38 + 10 6, 37 8, 66 + 10 dry 7, 12 9, 78 + 10 6, 52 9, 51 + 10 salt 6, 40 9, 95 + 10 7, 00 9, 78 + 10 7 d 5, 99 9, 29 + 10 7, 08 9, 43 + 10 HIS-PCR RNA (CFU/g) Plate counts Log CFU/g BULK HIS-PCR Fontina d’ Aosta PDO 6, 11 8, 59 0 15 d 5, 70 9, 04 + 10 7, 87 9, 47 + 10 Pecorino romano 5, 56 6, 88 0 30 d 5, 65 7, 70 + 8 8, 15 8, 93 + 10 Fontina d’Aosta PDO 5, 50 7, 33 0 60 d 5, 42 6, 30 + 8 6, 78 7, 57 + 10 90 d 4, 99 4, 48 + 6 5, 37 5, 85 + 7 Fontina d’ Aosta PDO 5, 39 8, 36 0 120 d 4, 58 <1000 + 0 2, 52 7, 51 + 4 150 d 5, 34 6, 58 1 4, 15 + 0 Castelmagno 3, 41 2, 31 7, 00 + 0 180 d 3, 38 5, 95 - 0 1, 71 4, 30 + 0 Raschera PDO 5, 24 8, 01 0 Fontal 5, 05 5, 48 0 Pecorino sardo PDO 4, 96 7, 76 0 Toma di Lanzo 4, 82 8, 92 6 Toma di Lanzo 4, 55 8, 88 0 Fontina d'Aosta PDO 3, 82 6, 86 1 Fontina PDO 3, 78 6, 38 0 Raschera PDO 3, 76 6, 40 0 Toma piemontese PDO 3, 72 8, 38 3 Asiago d'Allevo 0, 00 8, 32 0 Bra tenero PDO 0, 00 8, 41 0 Pecorino pastore 0, 00 5, 70 0 Raschera 0, 00 8, 23 0 Raschera PDO 0, 00 9, 52 0 Toma di Bra 0, 00 7, 77 0 Toma d'Oropa 0, 00 9, 16 3 Toma Piemontese 0, 00 9, 19 0 *The values, expressed as microbial loads, have been extrapolated from standard curves. ** Number of isolates found belonging to L. lactis species on a total of 12 colonies. Twenty-five samples, on a total of thirty-three, resulted positive for the presence of metabolically active cells of L. lactis, as detected by RT-q. PCR. The L. lactis loads ranged from 103 to 108 CFU/g for RNA analysis. The highest values were obtained for some of the Toma, Pecorino and Asiago cheese type samples. On the contrary, eight samples belonging to Asiago, Bra, Pecorino, Raschera and Toma cheese type were negative for L. lactis. The total viable counts on M 17 medium ranged from 105 to 109 CFU/g but only 24 isolates, spread among eight cheese samples, resulted to belong to L. lactis species. The absence or low abundance of L. lactis isolates on M 17 could be interpreted as a lack of selectivity of the medium where colony growth is not always related to lactococcal species. Ripening Tuf 2 f 0, 4 μM Tuf 2 r 0, 05 μM RNA (CFU/g)* Table 2 c. Starters Manufacturing 98°C 2' Sample Ripening Sso. Advanced. TM SYBR@ Green Supermix 1 X (Biorad) commercial cheeses: comparison of the results obtained by culture-independent and -dependent approach. K W Plate counts Log CFU/g Step RNA (CFU/g) Plate counts Log CFU/g BULK milk 3, 27 7, 70 + 10 3, 17 8, 40 + 10 curd 4, 30 9, 27 + 10 4, 29 8, 93 + 10 dry 6, 80 9, 61 + 10 4, 57 9, 46 + 10 salt 6, 91 9, 52 + 10 4, 60 9, 77 + 10 7 d 7, 05 9, 20 + 10 4, 46 9, 52 + 10 15 d 7, 19 8, 26 + 10 4, 42 8, 41 + 10 30 d 4, 09 8, 45 + 8 4, 35 8, 28 + 10 60 d 3, 26 8, 15 + 6 3, 90 7, 95 + 10 90 d 2, 76 7, 48 + 6 3, 78 6, 00 + 10 120 d 2, 71 8, 25 - 0 3, 54 5, 00 + 10 150 d 2, 63 8, 68 - 0 3, 41 4, 90 + 10 180 d 2, 60 8, 20 - 0 2, 55 2, 90 + 10 HIS-PCR RNA (CFU/g) BULK HIS-PCR Table 2 d. starters Manufacturing Amplification Cycle Ripening Amplification conditions Manufacturing A 1) A 2) A 3) Table 1. Detection of alive cells of L. lactis in ripened M X Step RNA (CFU/g) Plate counts Log CFU/g BULK milk 3, 20 8, 57 + 10 6, 13 6, 70 + 10 curd 4, 45 8, 99 + 10 7, 24 7, 90 + 10 dry 8, 17 9, 45 + 10 7, 76 9, 13 + 10 salt 8, 23 9, 43 + 10 6, 40 8, 72 + 10 7 d 8, 00 9, 33 + 10 5, 28 8, 18 + 10 15 d 7, 99 8, 48 + 10 3, 92 8, 00 + 10 30 d 7, 54 7, 66 + 10 3, 33 7, 63 + 10 60 d 7, 41 7, 49 + 10 3, 27 7, 00 + 10 90 d 6, 98 8, 51 + 10 3, 25 7, 56 + 10 120 d 6, 04 8, 60 + 10 2, 73 4, 90 + 10 150 d 4, 646 7, 20 + 9 2, 65 3, 95 + 10 180 d 2, 80 8, 40 + 2 2, 44 2, 36 + 10 HIS-PCR RNA (CFU/g) Plate counts Log CFU/g BULK HIS-PCR *The values, expressed as microbial loads, have been extrapolated from standard curves. ** “+”: L. lactis was detected; “-”: L. lactis was not detected. *** Number of isolates found belonging to L. lactis species on a total of 10 colonies. On the basis of RNA analysis, L. lactis was found with loads up to 104 CFU/g until the sixth month of ripening. Conversely, in a few late ripened cheese samples, L. lactis was not found on M 17 plates. These preliminary data could support thesis hypothesized by other authors (Ganesan et al. , 2007) that L. lactis starter populations are mainly present in viable but not culturable state during cheese ripening and, for this reason, culture-dependent methods are not able to detect their presence and have to be complemented by direct analysis. Selected References Corroler, D, I Mangin, N Desmasures, and M Gueguen. 1998. “An Ecological Study of Lactococci Isolated from Raw Milk in the Camembert Cheese Registered Designation of Origin Area. ” Applied and Environmental Microbiology 64 (12): 4729– 35. Ercolini D, Moschetti G, Blaiotta G, Coppola S (2001) The Potential of a Polyphasic PCR-DGGE Approach in Evaluating Microbial Diversity of Natural Whey Cultures for Water-Buffalo Mozzarella Cheese Production: Bias of Culture-Dependent and Culture-Independent Analyses. System. Appl. Microbiol. 24, 610– 617 Ganesan B, Stuart MR, Weimer BC (2007) Carbohydrate starvation causes a metabolically active but nonculturable state in Lactococcus lactis. Appl Environ Microbiol 73: 2498– 2512. Shakeel-Ur-Rehman, Mc. Sweeney P. I. H. , Fox P. F. 1998. "Protocol for the manufacture of miniature cheeses". Lait 78 (6): 607 -620. Ulve, V M, C Monnet, F Valence, J Fauquant, H Falentin, and S Lortal. 2008. “RNA Extraction from Cheese for Analysis of in Situ Gene Expression of Lactococcus Lactis. ” Journal of Applied Microbiology 105 (5): 1327– 33. XIX WORKSHOP ON THE DEVELOPMENTS IN THE ITALIAN PHD RESEARCH ON FOOD SCIENCE TECHNOLOGY AND BIOTECHNOLOGY Bari, September 24 th-26 th, 2014