language English
Article 2025 · 2 atıf

Sample-to-answer microfluidic device towards the point-of-need detection of <i>Staphylococcus aureus</i> enterotoxin genes in ruminant milk

Shalaby, Maha, Busin, Valentina, Yan, Xiaoxiang, Cengiz, Seyda, Adiguzel, Mehmet Cemal, Cooper, Jonathan M., Forde, Taya, Reboud, Julien

Özet

Milk is commonly screened both for indicators of animal disease and health, but also for foodborne hazards. Included in these analyses is the detection of Staphylococcus aureus, that can produce an enterotoxin, causing staphylococcal food poisoning (SFP), which often leads to sudden onset of significant gastrointestinal symptoms in humans. Epidemiological data on SFP are limited, particularly in low- and middle-income countries. Many conventional assays for the detection of staphylococcal enterotoxins rely on the detection of the genes coding for them, either directly in food samples or after bacterial culture. Currently, many of the nucleic acid-based methods used require specific expertise and equipment, whilst bacterial culture takes 24-48 hours; both are contributory factors that limit efforts either during food safety emergencies or routine screening. Here we present the development of a "sample-to-answer" isothermal nucleic acid loop-mediated amplification (LAMP) assay in a microfluidic device for the detection of Staphylococcus aureus enterotoxin genes in ruminant milk. A multiplex LAMP assay targeting two of the most prevalent S. aureus enterotoxin-encoding genes (A and B) was integrated into a microfluidic device combining simple 1 : 10 dilution for sample preparation and a lateral flow assay for easy readout. We achieved a limit of detection of 104 colony forming units per ml in spiked cow and goat milk samples, an order of magnitude more sensitive than the European recommendation for the maximum allowable presence of coagulase-positive staphylococci in raw milk. The assay showed no cross-reactivity in detecting other tested non-enterotoxigenic S. aureus strains or associated foodborne pathogens. The test integrated the simplicity of use of microfluidic devices with the sensitivity, specificity and rapidity of a nucleic acid-based assay, and a simple lateral flow readout to provide an appropriate device to ensure the safety of milk for human consumption. To illustrate its potential for point-of-need practical applications, the test was performed in agricultural settings in rural Turkey in a limited feasibility exercise.

Anahtar Kelimeler
MEDIATED ISOTHERMAL AMPLIFICATION DNA EXTRACTION METHOD MULTIPLEX PCR MASTITIS PATHOGENS RAPID DETECTION OUTBREAK IDENTIFICATION PREVALENCE TOXINS BLOOD
WoS Kategorileri
Biochemical Research Methods Chemistry, Multidisciplinary Chemistry, Analytical Nanoscience & Nanotechnology Instruments & Instrumentation
Sürdürülebilir Kalkınma Amaçları
Künye
Dergi
LAB ON A CHIP
Yıl
2025
Cilt
25
Sayı
4
Sayfa
524-535
ISSN
1473-0197
eISSN
1473-0189
DOI
10.1039/d4lc00907j
WoS UID
WOS:001391213100001
Yayını aç (DOI)