Sodium Deoxycholate-Propidium Monoazide Droplet Digital PCR for Rapid and Quantitative Detection of Viable Lacticaseibacillus rhamnosus HN001 in Compound Probiotic Products

Author:

Wang Ping1,Liang Lijiao12,Peng Xinkai13,Qu Tianming14,Zhao Xiaomei1,Ji Qinglong1ORCID,Chen Ying1

Affiliation:

1. Chinese Academy of Inspection and Quarantine, Beijing 100176, China

2. College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou 310058, China

3. College of Food Science and Pharmacy, Xinjiang Agricultural University, Urumqi 830052, China

4. College of Food Science and Engineering, Jilin Agricultural University, Changchun 130118, China

Abstract

As a famous probiotic, Lacticaseibacillus rhamnosus HN001 is widely added to probiotic products. Different L. rhamnosus strains have different probiotic effects, and the active HN001 strain is the key to exerting probiotic effects, so it is of great practical significance for realising the detection of L. rhamnosus HN001 at the strain level in probiotic products. In this study, strain-specific primer pairs and probes were designed. A combined treatment of sodium deoxycholate (SD) and propidium monoazide (PMA) inhibited the amplification of dead bacterial DNA, establishing a SD-PMA-ddPCR system and conditions for detecting live L. rhamnosus HN001 in probiotic powders. Specificity was confirmed using type strains and commercial strains. Sensitivity tests with spiked samples showed a detection limit of 10⁵ CFU/g and a linear quantification range of 1.42 × 10⁵–1.42 × 10⁹ CFU/g. Actual sample testing demonstrated the method’s efficiency in quantifying HN001 in compound probiotic products. This method offers a reliable tool for the rapid and precise quantification of viable L. rhamnosus HN001, crucial for the quality monitoring of probiotic products.

Funder

National Key Research and Development Program of China

Fundamental Research Funds for the Public Research Institutes of the Chinese Academy of Inspection and Quarantine

Publisher

MDPI AG

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