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1.
Biosens Bioelectron ; 152: 112007, 2020 Mar 15.
Article in English | MEDLINE | ID: mdl-31941616

ABSTRACT

Rapid, sensitive and accurate point-of-care-testing (POCT) of bacterial load from a variety of samples can help prevent human infections caused by pathogenic bacteria and mitigate their spreading. However, there is an unmet demand for a POCT device that can detect extremely low concentrations of bacteria in raw samples. Herein, we introduce the 'count-on-a-cartridge' (COC) platform for quantitation of the food-borne pathogenic bacteria Staphylococcus aureus. The system comprised of magnetic concentrator, sensing cartridge and fluorescent image reader with a built-in counting algorithm facilitated fluorescent microscopic bacterial enumeration in user-convenient manner with high sensitivity and accuracy within a couple of hours. The analytical performance of this assay is comparable to that of a standard plate count. The COC assay shows a sensitivity of 92.9% and specificity of 100% performed according to global microbiological criteria for S. aureus which is acceptable below 100 CFU/g in the food matrix. This culture-independent, rapid, ultrasensitive and highly accurate COC assay has great potential for places where prompt bacteria surveillance is in high demand.


Subject(s)
Bacterial Load/instrumentation , Food Microbiology , Optical Imaging/instrumentation , Staphylococcus aureus/isolation & purification , Bacterial Load/economics , Biosensing Techniques/economics , Biosensing Techniques/instrumentation , Equipment Design , Foodborne Diseases/microbiology , Humans , Optical Imaging/economics , Staphylococcal Infections/microbiology , Time Factors
2.
Biomed Microdevices ; 21(3): 49, 2019 06 14.
Article in English | MEDLINE | ID: mdl-31201569

ABSTRACT

Microfluidics systems that have been emerged in the last 20 years and used for processing the fluid in a microchannel structure at microliter levels are alternative to the conventional methods. The objective of the study is to develop a microfluidic platform for determination of the microbial load and the number of somatic cells in milk. For this purpose, a polydimethylsiloxane (PDMS) chip with a channel size of 300 µm × 60 µm was produced. Cells/bacteria labeled with fluorescent stain in milk were counted with the proposed microfluidic platform and the results were compared with the reference cell concentration/the bacterial counts by conventional method. It was found that our platform could count somatic and bacterial cells with an accuracy above 80% in 20 min run for each analysis. The portable overall platform has an overall dimension of 25x25x25 cm and weighs approximately 9 kg.


Subject(s)
Bacterial Load/instrumentation , Cell Count/instrumentation , Food Microbiology/instrumentation , Lab-On-A-Chip Devices , Milk/microbiology , Animals , Bacterial Load/economics , Cell Count/economics , Costs and Cost Analysis , Dimethylpolysiloxanes , Food Microbiology/economics , Lab-On-A-Chip Devices/economics , Nylons , Time Factors
3.
Prev Vet Med ; 113(4): 620-4, 2014 Mar 01.
Article in English | MEDLINE | ID: mdl-24382427

ABSTRACT

Clinical mastitis is one of the most common and expensive diseases of dairy cattle. To make an informed treatment decision, it is important to know the causative pathogen. However, no detection of bacterial growth can be made in approximately 30% of all clinical cases of mastitis. Before selecting the treatment regimen, it is important to know whether the mastitis-causing pathogen (MCP) is Gram-positive or Gram-negative. The aim of this field study was to investigate whether using two 3M Petrifilm™ products on-farm (which conveys a higher degree of sample freshness but also bears a higher risk for contamination than working in a lab) as 24-h rapid diagnostic of clinical mastitis achieved results that were comparable to the conventional microbiological diagnostic method. AerobicCount (AC)-Petrifilm™ and ColiformCount (CC)-Petrifilm™ were used to identify the total bacterial counts and Gram-negative bacteria in samples from clinical mastitis cases, respectively. Missing growth on both plates was classified as no bacterial detection. Growth only on the AC-Petrifilm™ was assessed as Gram-positive, and growth on both Petrifilm™ plates was assessed as Gram-negative bacterial growth. Additionally, milk samples were analysed by conventional microbiological diagnostic method on aesculin blood agar as a reference method. Overall, 616 samples from clinical mastitis cases were analysed. Using the reference method, Gram-positive and Gram-negative bacteria, mixed bacterial growth, contaminated samples and yeast were determined in 32.6%, 20.0%, 2.5%, 14.1% and 1.1% of the samples, respectively. In 29.7% of the samples, microbiological growth could not be identified. Using the Petrifilm™ concept, bacterial growth was detected in 59% of the culture-negative samples. The sensitivity of the Petrifilm™ for Gram-positive and Gram-negative MCP was 85.2% and 89.9%, respectively. The specificity was 75.4% for Gram-positive and 88.4% for Gram-negative MCP. For the culture-negative samples, sensitivity was 41.0% and specificity was 91.0%. The results indicate that the Petrifilm™ concept is suitable for therapeutic decision-making at the farm level or in veterinary practice. As this concept does not allow any statement about the genus or species of microorganisms, relevant MCP should be assessed periodically at the herd level with conventional microbiological diagnostics.


Subject(s)
Bacterial Load/veterinary , Diagnostic Tests, Routine/veterinary , Mastitis, Bovine/diagnosis , Animals , Bacterial Load/economics , Bacterial Load/instrumentation , Cattle , Cost-Benefit Analysis , Diagnostic Tests, Routine/economics , Diagnostic Tests, Routine/instrumentation , Environment , Female , Mastitis, Bovine/microbiology , Sensitivity and Specificity
4.
J Microbiol Methods ; 93(1): 12-9, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23384829

ABSTRACT

A novel miniaturized most probable number (mMPN) method was developed for the enumeration of thermophilic Campylobacter spp. using a modification of blood-free Bolton broth (supplemented with 25mg/l of sulfamethoxazole) and CampyFood ID agar. The mMPN was evaluated by comparison with direct plating (modified ISO/TS, 10272-2:2006) for the analysis of samples (n=149) representing various poultry matrices (carcases, broiler ceca and feces, scald tank water and feed). A sensitivity of 95%, specificity of 90% and Cohen KAPPA agreement of 0.84 was determined for the mMPN method compared to direct plating. Quantitative comparison found 83% of enumerations to be less than ±1log10 different (Student's t-test P<0.001). Financial analysis showed that the mMPN required 51% less media and 60% less labor than the direct plating protocol. The mMPN provides a method that can be used for complete through-chain analysis that has a single enrichment step and multiple dilutions to extinction for a variety of samples (containing low, medium and high populations).


Subject(s)
Bacterial Load/methods , Campylobacter/isolation & purification , Environmental Microbiology , Poultry/microbiology , Animals , Bacterial Load/economics , Culture Media/chemistry , Sensitivity and Specificity
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