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◆ Journal of microbiological methods2026-09-12

Rapid monitoring of sourdough starter and contaminants using a dual-lateral flow immunochromatographic assay.

Sanae Konami, Kyoka Aiki, Tatsuya Tominaga

原始摘要(英文原文)· Original abstract
Sourdough maintenance via daily backslopping faces the persistent risk of starter lactic acid bacteria (LAB) being displaced by competing contaminants. Here, we developed a dual-lateral flow immunochromatographic assay (LFIA) system to simultaneously monitor starter health (Fructilactobacillus sanfranciscensis; Fsanf-LFIA) and contaminant presence (Pediococcus acidilactici; Ped-LFIA). Fsanf-LFIA and Ped-LFIA both exhibited detection limits of 5 log cells/test. Fsanf-LFIA was highly specific to certain strains of F. sanfranciscensis, whereas Ped-LFIA demonstrated a broader detection spectrum, cross-reacting with P. pentosaceus, other LAB (excluding F. sanfranciscensis), Bacillus, and Staphylococcus species. To evaluate practical on-site utility, sourdoughs inoculated with F. sanfranciscensis (9 log cells/g) and P. acidilactici (2 log cells/g) were maintained via daily backslopping at 23 °C, 30 °C, and 37 °C for 4 days. On day 4, conventional monitoring parameters failed to capture any change in sourdough grown at 37 °C, as pH levels dropped below 4.5 and total LAB counts remained virtually identical across all temperatures. However, while Fsanf-LFIA remained positive across all temperatures, Ped-LFIA turned positive exclusively at 37 °C. Amplicon sequencing validated these results, revealing that the abundance of F. sanfranciscensis plummeted to 6.2% at 37 °C, and Pediococcus became the dominant taxon. These findings demonstrate that the developed dual-LFIA system, which requires no specialized equipment, can quickly (within 1 h) detect early microbial displacement via visual-inspection-based binary judgment. This user-friendly system holds strong promise as a versatile quality-control tool for both industrial and artisanal sourdough-manufacturing facilities.
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Rapid monitoring of sourdough starter and contaminants using a dual-lateral flow immunochromatographic assay. — 科研速览 Science Skim