Literature DB >> 16737755

Monitoring the cell number of Lactococcus lactis subsp. cremoris FC in human feces by real-time PCR with strain-specific primers designed using the RAPD technique.

Toshinari Maruo1, Mitsuo Sakamoto, Toshiya Toda, Yoshimi Benno.   

Abstract

Strain-specific PCR primers for Lactococcus lactis subsp. cremoris FC were developed using the randomly amplified polymorphic DNA (RAPD) technique. RAPD was used to generate strain-specific markers. A 1164-bp RAPD marker found to be strain-specific was sequenced, and a primer pair specific for L. lactis subsp. cremoris FC was designed. The specificity of this primer pair was tested with 23 L. lactis subsp. cremoris strains and 20 intestinal bacterial species, and was found to be strain-specific. Subsequently, this primer pair was subjected to the quantification of L. lactis subsp. cremoris FC in the feces of subjects fed fermented milk containing this strain. After administration, L. lactis subsp. cremoris FC was detected in the feces of all 7 subjects, with the maximum number being between 10(5) and 10(9) cells g(-1) of feces. Furthermore, this strain was detected in only one feces sample 2 weeks after administration was stopped. These results suggest that L. lactis subsp. cremoris FC can survive passage through the gastrointestinal tract.

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Year:  2006        PMID: 16737755     DOI: 10.1016/j.ijfoodmicro.2006.01.037

Source DB:  PubMed          Journal:  Int J Food Microbiol        ISSN: 0168-1605            Impact factor:   5.277


  14 in total

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Review 2.  Biodiversity of Intestinal Lactic Acid Bacteria in the Healthy Population.

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3.  Detection of human intestinal catalase-negative, Gram-positive cocci by rRNA-targeted reverse transcription-PCR.

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Journal:  Appl Environ Microbiol       Date:  2010-06-25       Impact factor: 4.792

4.  Quantification of Azospirillum brasilense FP2 Bacteria in Wheat Roots by Strain-Specific Quantitative PCR.

Authors:  Maria Isabel Stets; Sylvia Maria Campbell Alqueres; Emanuel Maltempi Souza; Fábio de Oliveira Pedrosa; Michael Schmid; Anton Hartmann; Leonardo Magalhães Cruz
Journal:  Appl Environ Microbiol       Date:  2015-07-17       Impact factor: 4.792

5.  Development of a sequence-characterized amplified region marker-targeted quantitative PCR assay for strain-specific detection of Oenococcus oeni during wine malolactic fermentation.

Authors:  Lisa Solieri; Paolo Giudici
Journal:  Appl Environ Microbiol       Date:  2010-10-08       Impact factor: 4.792

6.  Quantitative detection of viable Bifidobacterium bifidum BF-1 cells in human feces by using propidium monoazide and strain-specific primers.

Authors:  Junji Fujimoto; Koichi Watanabe
Journal:  Appl Environ Microbiol       Date:  2013-01-25       Impact factor: 4.792

Review 7.  Fluorescent reporter systems for tracking probiotic lactic acid bacteria and bifidobacteria.

Authors:  José M Landete; Margarita Medina; Juan L Arqués
Journal:  World J Microbiol Biotechnol       Date:  2016-06-04       Impact factor: 3.312

8.  Detection of the pediocin gene pedA in strains from human faeces by real-time PCR and characterization of Pediococcus acidilactici UVA1.

Authors:  Sophie Mathys; Ueli von Ah; Christophe Lacroix; Ernö Staub; Raffaella Mini; Tania Cereghetti; Leo Meile
Journal:  BMC Biotechnol       Date:  2007-09-12       Impact factor: 2.563

9.  Use of colony-based bacterial strain typing for tracking the fate of Lactobacillus strains during human consumption.

Authors:  Eshwar Mahenthiralingam; Angela Marchbank; Pavel Drevinek; Iveta Garaiova; Sue Plummer
Journal:  BMC Microbiol       Date:  2009-12-07       Impact factor: 3.605

10.  PCR and real-time PCR primers developed for detection and identification of Bifidobacterium thermophilum in faeces.

Authors:  Sophie Mathys; Christophe Lacroix; Raffaella Mini; Leo Meile
Journal:  BMC Microbiol       Date:  2008-10-10       Impact factor: 3.605

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