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HomePathogen & Spoilage TestingHybriScan® Rapid Microbial Test System

HybriScan® Rapid Microbial Test System

The routine control of microbial contamination in food production, from raw materials to finished goods, conventional standard cultivation-based methods are time consuming and often take from 2 to 15 days to get results. Our HybriScan® assays provides fast and accurate molecular detection of spoilage organisms and pathogens, without the need to use expensive PCR methods. HybriScan® Molecular Screening System is suitable for the safety and quality control of beverages, water, and food.

Rapid Microbiological Method: Sandwich Hybridization

The HybriScan® system is based on the detection of microbe-specific rRNA using sandwich hybridization. The method simply needs a centrifuge, a thermal mixer, and an optional microplate reader. The complete analysis can be achieved in 2 hours for the HybriScan®D kit (quantitative kits) and about 1 hour for the HybriScan®I kit (identification kits). Qualitative results can be determined by eye or, for quantitative measurement, used with a microplate reader.

HybriScan® system screening workflow includes pre-cultivation of the sample in enrichment broth. After centrifugation, the sample is incubated, immobilized, purified, and finally detected with a read out available in less than 10 min. The total analysis time takes up to 2–2.5 hours.

Figure 1.HybriScan® system screening workflow with an analysis time of approx. 2–2.5 hours.

Sensitivity, Specificity and Flexibility of Sandwich Hybridization

Sandwich hybridization is very sensitive and can detect attomoles of the target rRNA molecules in yeast or bacteria.1-3 These types of cells comprise a large number of rRNA-containing ribosomes; a single cell therefore contains several thousand copies of rRNA but only one DNA copy. Sandwich hybridization provides sensitivity in crude biological samples because it is not susceptible to matrix interference. By using specific probes, the HybriScan® system allows both genus or species-specific detection and it is therefore applicable to many analytical fields, including monitoring the microbial content of beer, wine, non-alcoholic beverages, drinking water, a wide variety of foods and wastewater.

HybriScan®kits for detection and identification of microorganisms

Figure 2.HybriScan® technology

  • Detects viable microorganisms only—minimizes false-positive results from dead bacteria
  • Not sensitive to sample matrix
  • Genus- and species-specific detection
  • Results in just 2 hours after enrichment
  • Broad application range: beer, wine, non-alcoholic beverages, drinking water, food and wastewater
  • Can be used to detect non-culturable microbes

Advantages of HybriScan® technology over other microbial detection techniques

Detection TechnologyAdvantageDisadvantage
HybriScan® system
  • Detects only living cells 
  • Minimal interference by sample matrix
  • High specificity
  • Low cross-reactivity
  • Easy handling
  • Cost-efficient read-out
  • Quantitative and qualitative
  • High sample throughput (96-microwell plates)
  • Detects of non-culturable microbes
  • No differentiation of serotypes or subspecies
  • Limited probe design (rRNA target)
PCR
  • High sample throughput
  • Sensitive
  • Quantitative
  • No live/dead cell differentiation
  • Sensitive to matrix interference (high extraction effort)
  • Susceptible to polymerase inhibition
ELISA
  • Differentiation of serotypes or subspecies
  • High sample throughput (96-microwell plates)
  • Quantitative and qualitative
  • Low sensitivity
  • Low specificity, higher cross-reactivity
  • Slow and expensive assay development
Conventional cultivation-based methods
  • Relatively inexpensive
  • Simple
  • Specific
  • Widely accepted method
  • Time-consuming (up to 10 days)
  • No detection of non-culturable microbes
  • Low sample throughput
  • Laborious

HybriScan® Wastewater Bacterial Count Calculator

For our Wastewater Kits - (HybriScan®D Waste Water Microthrix parvicella and  HybriScan®D Waste Water Total Bacterial Count), we are providing an excel sheet (below) for calculation of total bacterial count, Microthrix count, and the ratio of Microthrix: Total Bacterial Count.

HybriScan® I (Identification) Kits
Product NumberProduct NameProduct DescriptionPricing
39851HybriScanI Alicyclobacillussuitable for microbiology
79742HybriScanI Brettanomycessuitable for food and beverages, microbiology, suitable for microbe id | in situ hybriziation
19503HybriScan I Candida albicanssuitable for microbiology
76545HybriScanI E. colisuitable for microbiology
75724HybriScanI Lactobacillus brevissuitable for food and beverages, microbiology, suitable for microbe id | in situ hybriziation
49417HybriScanI Legionella pneumophilasuitable for environmental, microbiology, suitable for microbe id | in situ hybriziation
77007HybriScanI Leuconostocsuitable for food and beverages, microbiology, suitable for microbe id | in situ hybriziation
49712HybriScanI Listeria monocytogenessuitable for food and beverages, microbiology, suitable for microbe id | in situ hybriziation
42875HybriScanI Megasphaerasuitable for environmental, microbiology, suitable for microbe id | in situ hybriziation
89384HybriScanI Pectinatus cerevisiiphilussuitable for food and beverages, microbiology, suitable for microbe id | in situ hybriziation
73582HybriScanI Pectinatus frisingensissuitable for food and beverages, microbiology, suitable for microbe id | in situ hybriziation
67289HybriScanI Pediococcus damnosussuitable for food and beverages, microbiology, suitable for microbe id | in situ hybriziation

References

1.
Huhtamella S, Leinonen M, Nieminen T, Fahnert B, Myllykoski L, Breitenstein A, Neubauer P. 2007. RNA-based sandwich hybridisation method for detection of lactic acid bacteria in brewery samples. Journal of Microbiological Methods. 68(3):543-553. https://doi.org/10.1016/j.mimet.2006.10.009
2.
Leskelä T, Tilsala-Timisjärvi A, Kusnetsov J, Neubauer P, Breitenstein A. 2005. Sensitive genus-specific detection of Legionella by a 16S rRNA based sandwich hybridization assay. Journal of Microbiological Methods. 62(2):167-179. https://doi.org/10.1016/j.mimet.2005.02.008
3.
Rautio J, Barken K, Lahdenperä J, Breitenstein A, Molin S, Neubauer P. 2003. Microb Cell Fact. 2(1):4. https://doi.org/10.1186/1475-2859-2-4
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