• 云顶集团3118(中国)

    Canine Respiratory Pathogen Detection Assays

    Come J Thieulent, Mariano Carossino, Laura Peak, Udeni B. R. Balasuriya

    Published: 2023-10-24 DOI: 10.17504/protocols.io.kxygx9x7zg8j/v1
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    Disclaimer

    Reference to any commercial materials, equipment, or processes do not in any way constitute approval, endorsement, or recommendation by the Food and Drug Administration.

    Abstract

    The Canine Respiratory Pathogen (CRP) Detection Assays is intended as an in vitro veterinary reagent set, based on Reverse Transcription quantitative PCR (RT-qPCR), for the detection of canine adenovirus-2 (CAdV-2), canine distemper (CDV), canine herpesvirus type 1 (CHV-1), canine influenza A virus (CIV), canine parainfluenza (CPiV), canine pneumovirus (CPnV), canine respiratory coronavirus (CRCoV), SARS-CoV-2, Bordetella bronchiseptica , Streptococcus equi subsp. zooepidemicus , Mycoplasma cynos and Mycoplasma canis in nasal and pharyngeal swab samples.

    Steps

    Reaction Setup

    1.

    Thaw all reagents on ice.

    2.

    Centrifuge all reagents on a benchtop centrifuge to ensure no liquid is in cap and keep on ice

    Note
    The CRP Detection Reagents do not include an internal control, but positive controls are provided for each of the three assays (CRA_1, CRA_2 and CRA_3). A positive and a negative control should be run simultaneously with each sample setup.

    3.

    Setup the Master Mix according to the following table 1:

    Table 1.
    Table 1.

    Programming the Thermocycler

    4.

    The following fluorescence channels should be selected: ABYTM, FAMTM, JUNTM, and VICTM.

    5.

    ROXTM should be used as a passive reference dye.

    6.

    The standard mode should be selected. Setup cycling condition following table 2:

    ABCD
    StepNumber of cyclesTemp. (°C)Time (min:sec)
    Reverse transcriptase15020:00
    Initial activation19515:00
    Denaturation409400:45
    Annealing/extension6000:75

    Table 2. Thermal profile. The data acquisition is performed during the annealing/extension step.

    Results interpretation

    7.

    Before results analysis, the threshold value of each fluorescent dye must be manually set in the region of exponential amplification, typically 0.1 × ΔRn value at the plateau phase.

    8.

    Each assay is considered valid if the following criteria are met:

    Table 3. Assays criteria
    Table 3. Assays criteria
    9.

    The results are qualitative (Positive or Negative). A specimen is considered positive if the Ct value obtained is below the following Ct cut-off values:

    Table 4. Ct cut-off values
    Table 4. Ct cut-off values

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