Open AccessDevelopment of a Standard Curve to Account for Viable Loads of Bifidobacterium animalis subsp. lactis HN019 Using RNA by Real-Time PCR
Author(s) -
M. A. Ali,
Hui Wang,
Guangen Lin,
Fang F Dang,
Shuang Wu,
Chaoxin Man,
Yujun Jiang
Publication year - 2019
Publication title -
journal of aoac international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.432
H-Index - 87
eISSN - 1944-7922
pISSN - 1060-3271
DOI - 10.5740/jaoacint.18-0216
Subject(s) - bifidobacterium animalis , enumeration , standard curve , growth curve (statistics) , strain (injury) , biology , probiotic , chromatography , food science , mathematics , bifidobacterium , chemistry , statistics , bacteria , lactobacillus , anatomy , combinatorics , genetics , fermentation
Background: Bifidobacterium animalis subsp. lactis HN019 is widely used as a probiotic in various dairy preparations. To ensure optimal health benefits, an adequate number of probiotics should be viable in products, but the culture-based methods require longer periods to account for the strain. Objective: Develop a standard curve to account viable loadof B. animalis subsp. lactis HN019 by real-time PCR. Methods: The growth curve was developed accordingto plate count method, and cycle threshold (CT) curve was prepared using CT values. These two curves were then combined to construct the standard curve. To validate the method, the strain was proliferated in whole milk, and viable loads were enumerated by plate counting and relativePCR counting followed by determining the SEM betweenthe two counts. Results: The growth curve and CT curve, respectively, showed the highest viable load (2.13 × 108 CFU/mL) and lowest CT value (18.29) after 18 h, and during the entire growth phase (0–18 h), viable loads are inversely proportional to the CT values. The standard curverevealed the model y = 2E + 18e−1.233x (y = cells/mL, x = CT value; R2 = 0.992). In validation, the highest SEM (± 0.70 × 108) was found between the plate count (1.15 × 108 cells/mL) and relative PCR count (1.29 × 108 cells/mL) after cultivating for 14 h. Conclusions: The method could be readilyused in dairy industries to quantify viable B. animalis subsp. lactis HN019 by a shorter period. Highlights: Culture-independent enumeration of viable B. animalis subsp. lactis HN019 by real-time PCR.