This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Klijn, N.
Right arrow Articles by de Vos, W. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Klijn, N.
Right arrow Articles by de Vos, W. M.
Agricola
Right arrow Articles by Klijn, N.
Right arrow Articles by de Vos, W. M.

 Previous Article  |  Next Article 

Appl. Environ. Microbiol., Jul 1995, 2771-2774, Vol 61, No. 7
Copyright © 1995, American Society for Microbiology

Genetic marking of Lactococcus lactis shows its survival in the human gastrointestinal tract

N Klijn, AH Weerkamp and WM de Vos
Department of Microbiology, Netherlands Institute for Dairy Research (NIZO), Ede.

A human feeding study was performed with Lactococcus lactis TC165.5, which is genetically marked by insertion of the sucrose-nisin conjugative transposon Tn5276 and chromosomal resistance to rifampin and streptomycin. The fate of strain TC165.5 and its nucleic acids was monitored by conventional plating methods and by molecular detection techniques based on specific PCR amplification of the nisin (nisA) gene from DNA extracted from human feces. A method was developed for the efficient extraction of microbial DNA from human feces. The results show that a fraction of viable cells of L. lactis TC165.5 survived passage through the human gastrointestinal tract. Only cells that passed within 3 days of ingestion could be recovered from the feces of the volunteers, and they accounted for approximately 1% of the total number of cells consumed. The presence of nisA in DNA extracted from feces could be detected up to 4 days, when viable cells were no longer present.


This article has been cited by other articles:

  • Boguslawska, J., Zycka-Krzesinska, J., Wilcks, A., Bardowski, J. (2009). Intra- and Interspecies Conjugal Transfer of Tn916-Like Elements from Lactococcus lactis In Vitro and In Vivo. Appl. Environ. Microbiol. 75: 6352-6360 [Abstract] [Full Text]  
  • Cheung, Q. C., Yuan, Z., Dyce, P. W, Wu, D., DeLange, K., Li, J. (2009). Generation of epidermal growth factor-expressing Lactococcus lactis and its enhancement on intestinal development and growth of early-weaned mice. Am. J. Clin. Nutr. 89: 871-879 [Abstract] [Full Text]  
  • de Moreno de LeBlanc, A., LeBlanc, J. G., Perdigon, G., Miyoshi, A., Langella, P., Azevedo, V., Sesma, F. (2008). Oral administration of a catalase-producing Lactococcus lactis can prevent a chemically induced colon cancer in mice. J Med Microbiol 57: 100-105 [Abstract] [Full Text]  
  • Mansfield, L. S., Bell, J. A., Wilson, D. L., Murphy, A. J., Elsheikha, H. M., Rathinam, V. A. K., Fierro, B. R., Linz, J. E., Young, V. B. (2007). C57BL/6 and Congenic Interleukin-10-Deficient Mice Can Serve as Models of Campylobacter jejuni Colonization and Enteritis. Infect. Immun. 75: 1099-1115 [Abstract] [Full Text]  
  • de Jong, P., Vissers, M. M. M., van der Meer, R., Bovee-Oudenhoven, I. M. J. (2007). In Silico Model as a Tool for Interpretation of Intestinal Infection Studies. Appl. Environ. Microbiol. 73: 508-515 [Abstract] [Full Text]  
  • Termont, S., Vandenbroucke, K., Iserentant, D., Neirynck, S., Steidler, L., Remaut, E., Rottiers, P. (2006). Intracellular Accumulation of Trehalose Protects Lactococcus lactis from Freeze-Drying Damage and Bile Toxicity and Increases Gastric Acid Resistance. Appl. Environ. Microbiol. 72: 7694-7700 [Abstract] [Full Text]  
  • Bernbom, N., Licht, T. R., Brogren, C.-H., Jelle, B., Johansen, A. H., Badiola, I., Vogensen, F. K., Norrung, B. (2006). Effects of Lactococcus lactis on Composition of Intestinal Microbiota: Role of Nisin. Appl. Environ. Microbiol. 72: 239-244 [Abstract] [Full Text]  
  • Rochat, T., Gratadoux, J.-J., Corthier, G., Coqueran, B., Nader-Macias, M.-E., Gruss, A., Langella, P. (2005). Lactococcus lactis SpOx Spontaneous Mutants: a Family of Oxidative-Stress-Resistant Dairy Strains. Appl. Environ. Microbiol. 71: 2782-2788 [Abstract] [Full Text]  
  • Oozeer, R., Mater, D. D. G., Goupil-Feuillerat, N., Corthier, G. (2004). Initiation of Protein Synthesis by a Labeled Derivative of the Lactobacillus casei DN-114 001 Strain during Transit from the Stomach to the Cecum in Mice Harboring Human Microbiota. Appl. Environ. Microbiol. 70: 6992-6997 [Abstract] [Full Text]  
  • Beasley, S. S., Saris, P. E. J. (2004). Nisin-Producing Lactococcus lactis Strains Isolated from Human Milk. Appl. Environ. Microbiol. 70: 5051-5053 [Abstract] [Full Text]  
  • Grangette, C., Muller-Alouf, H., Hols, P., Goudercourt, D., Delcour, J., Turneer, M., Mercenier, A. (2004). Enhanced Mucosal Delivery of Antigen with Cell Wall Mutants of Lactic Acid Bacteria. Infect. Immun. 72: 2731-2737 [Abstract] [Full Text]  
  • Fernandez, L., Marin, M. L., Langa, S., Martin, R., Reviriego, C., Fernandez, A., Olivares, M., Xaus, J., Rodriguez, J. M. (2004). A Novel Genetic Label for Detection of Specific Probiotic Lactic Acid Bacteria. Food Science and Technology International 10: 101-108 [Abstract]  
  • Sybesma, W., van den Born, E., Starrenburg, M., Mierau, I., Kleerebezem, M., de Vos, W. M., Hugenholtz, J. (2003). Controlled Modulation of Folate Polyglutamyl Tail Length by Metabolic Engineering of Lactococcus lactis. Appl. Environ. Microbiol. 69: 7101-7107 [Abstract] [Full Text]  
  • Xin, K.-Q., Hoshino, Y., Toda, Y., Igimi, S., Kojima, Y., Jounai, N., Ohba, K., Kushiro, A., Kiwaki, M., Hamajima, K., Klinman, D., Okuda, K. (2003). Immunogenicity and protective efficacy of orally administered recombinant Lactococcus lactis expressing surface-bound HIV Env. Blood 102: 223-228 [Abstract] [Full Text]  
  • Kimoto, H., Ohmomo, S., Okamoto, T. (2002). Cholesterol Removal from Media by Lactococci. J DAIRY SCI 85: 3182-3188 [Abstract] [Full Text]  
  • Bernasconi, E., Germond, J.-E., Delley, M., Fritsche, R., Corthesy, B. (2002). Lactobacillus bulgaricus Proteinase Expressed in Lactococcus lactis Is a Powerful Carrier for Cell Wall-Associated and Secreted Bovine {beta}-Lactoglobulin Fusion Proteins. Appl. Environ. Microbiol. 68: 2917-2923 [Abstract] [Full Text]  
  • Geller, B. L., Wade, N., Gilberts, T. D., Hruby, D. E., Johanson, R., Topisirovic, L. (2001). Surface Expression of the Conserved C Repeat Region of Streptococcal M6 Protein within the Pip Bacteriophage Receptor of Lactococcus lactis. Appl. Environ. Microbiol. 67: 5370-5376 [Abstract] [Full Text]  
  • Lick, S., Drescher, K., Heller, K. J. (2001). Survival of Lactobacillus delbrueckii subsp. bulgaricus and Streptococcus thermophilus in the Terminal Ileum of Fistulated Gottingen Minipigs. Appl. Environ. Microbiol. 67: 4137-4143 [Abstract] [Full Text]  
  • Franks, A. H., Harmsen, H. J. M., Raangs, G. C., Jansen, G. J., Schut, F., Welling, G. W. (1998). Variations of Bacterial Populations in Human Feces Measured by Fluorescent In Situ Hybridization with Group-Specific 16S rRNA-Targeted Oligonucleotide Probes. Appl. Environ. Microbiol. 64: 3336-3345 [Abstract] [Full Text]  
  • Steidler, L., Robinson, K., Chamberlain, L., Schofield, K. M., Remaut, E., Le Page, R. W. F., Wells, J. M. (1998). Mucosal Delivery of Murine Interleukin-2 (IL-2) and IL-6 by Recombinant Strains of Lactococcus lactis Coexpressing Antigen and Cytokine. Infect. Immun. 66: 3183-3189 [Abstract] [Full Text]