Evidence map›Paper›PMID 40905700›Full record

ArticleJournal of AOAC International2025

A Novel Loop-Mediated Isothermal Amplification (LAMP) Assay for Detecting Salmonella Ser. Typhimurium in Egg Products.

Lijun Hu, Guodong Zhang

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Article in Journal of AOAC International, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Lijun HuHuman Foods Program, U.S. Food and Drug Administration, Office of Laboratory Operations and Applied Science, College Park, MD, USA.ORCID 0009-0003-3660-1983
Guodong ZhangHuman Foods Program, U.S. Food and Drug Administration, Office of Laboratory Operations and Applied Science, College Park, MD, USA.ORCID 0000-0001-8808-7435

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs a leading cause of foodborne illness worldwide, detection of Salmonella enterica subsp. enterica serovar Typhimurium is essential for food safety and public health.

objectiveThis study aimed to develop a loop-mediated isothermal amplification (LAMP) assay for the rapid and sensitive detection of Salmonella ser. Typhimurium in egg products.

methodsThe primer set targeting the open reading frame STM3845 of Salmonella ser. Typhimurium was designed using PrimerExplorer v.4. The LAMP assay was optimized by adjusting reagent concentrations, reaction temperature, and incubation time, achieving the highest amplification/fluorescence in a 25.0 µL reaction at 65°C for 30 min.

resultsResults indicated that the newly designed assay could successfully detect and differentiate Salmonella ser. Typhimurium from other Salmonella serotypes and non-Salmonella bacterial pathogens except for Salmonella serotypes Montevideo, Michigan, and Senftenberg after testing 73 Salmonella ser. Typhimurium, 100 non-Typhimurium Salmonella, and 35 non-Salmonella bacterial pathogens of pure cultures. The LAMP assay was further compared with a commercial real-time PCR and FDA BAM culture method by testing pure culture and 200 inoculated (1-5 CFU/25g) egg and egg product samples, and proved to be comparable to the FDA BAM culture method; it also demonstrated 100 times more sensitivity than the real-time PCR assay in pure culture testing, with a detection limit of 0.56 log CFU/mL.

conclusionsThe newly developed LAMP assay offers a rapid, specific, and sensitive method for detecting Salmonella ser. Typhimurium in egg products. Its simplicity, speed, and sensitivity position it as a powerful tool for routine monitoring, outbreak investigation, and on-site testing in the food industry. HIGHLIGHTS: Developed a LAMP assay for specific detection Salmonella ser. Typhimurium in egg products. The newly developed LAMP assay was 100 times more sensitive than the real-time PCR assay. Our new LAMP assay was validated with hundreds of pure isolates and food samples.

Indexed as

EggsMolecular Diagnostic TechniquesNucleic Acid Amplification TechniquesSalmonella typhimuriumFood ContaminationFood MicrobiologyLimit of DetectionSensitivity and Specificity

Identifiers

PMID40905700
PMCPMC12579537

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