RU2819044C1 - Test system for detecting dna of causative agent of moraxellosis kpc (moraxella bovis) in biological material of animals and feed using polymerase chain reaction in real time - Google Patents

Abstract

FIELD: veterinary microbiology.

SUBSTANCE: test system for detecting the DNA of the causative agent of bovine moraxellosis (Moraxella bovis) in animal biological material and feed using real-time polymerase chain reaction is described. The test system includes a buffer for carrying out a polymerase chain reaction, a mixture for carrying it out, consisting of deoxynucleoside triphosphates, oligonucleotide primers and fluorescent probes specific for a region of the animal's genome and for an internal control sample; a mixture of enzymes from DNA polymerase with antibodies that inhibit enzyme activity, TAQ POLYMERASE, an internal control sample in the form of a suspension of bacteriophage T4 with a concentration of 5×10³ phage particles per 1 µl, negative control sample, which is a mixture of recombinant plasmid DNA containing a fragment of the animal genome and a fragment of the genome of bacteriophage T4 with the following nucleotide sequence: T4F: 5'-TACATATAAATCACGCAAAGC-3' is direct primer; T4R: 5'-TAGTATGGCTAATCTTATTGG-3' is reverse primer; Т4Р: SU5-5' - ACATTGGCACTGACCGAGTTC-3'-BHQ1 is a probe taken in a volumetric ratio of 1:1. For a positive control sample, a fragment of the genome of the causative agent of bovine moraxellosis (Moraxella bovis) with the following nucleotide sequence was used (5'-3''):

Morab-F GATTTACTCGATGGTGGTGC; Morab-R CCATCGAGTGGGTCATCGC; Morab-P R6G-ACCGCTTGTTTGGTGGTAAAGGCAAC-BHQ1, and for the DNA of the causative agent of bovine moraxellosis (Moraxella bovis), the fluorescent dye HEX/Yellow was used.

EFFECT: invention is used to expand functionality and increase accuracy in identifying the causative agent of bovine moraxellosis (Moraxella bovis).

1 cl, 4 tbl, 1 ex

Description

The invention relates to veterinary microbiology, in particular to laboratory diagnostics of pathogens of infectious diseases, namely to means for diagnosing infection in animals using polymerase chain reaction.

It is known in medicine to diagnose moraxellosis with the help of drugs through histological examination of a biopsy specimen, additional fixation of sections with methanol, exposure to carbol fuchsin staining is carried out for 5-10 minutes, and 5% sulfuric acid is used as a declorizer. The known technical solution provides a positive effect in the form of identifying objective criteria for the diagnosis of moraxellosis, providing treatment tactics (RF patent No. 2229128, class G01N 1/30, 2004).

The closest in technical essence is the invention according to patent RU No. 2726242, class. C12Q 1/68, 2020, including a buffer for carrying out a polymerase chain reaction, a mixture for carrying it out, consisting of deoxynucleoside triphosphates, oligonucleotide primers and fluorescent probes specific for a region of the animal’s genome and for an internal control sample; a mixture of enzymes from DNA polymerase with antibodies that inhibit enzyme activity, TAQ POLYMERASE, an internal control sample in the form of a suspension of bacteriophage T4 with a concentration of 5 × 10 ³ phage particles per 1 μl, a negative control sample, which is a mixture of recombinant plasmid DNA containing a fragment of the animal genome and a fragment of the genome of bacteriophage T4 with the nucleotide sequence:

T4F: 5'- TACATATAAATCACGCAAAGC -3' - forward primer

T4R: 5'- TAGTATGGCTAATCTTATTGG -3' - reverse primer

T4P: SU5-5'-ACATTGGCACTGACCGAGTTC -3'-BHQ1 - probe, taken in a volumetric ratio of 1:1.

The disadvantage of the known technical solution is the inability to detect DNA of the causative agent of bovine moraxellosis (Moraxella bovis) in animal biological material.

The technical result is to expand the functionality and increase the accuracy in identifying the causative agent of bovine moraxellosis (Moraxella bovis).

The technical result is achieved by the fact that in the test system for identifying the DNA of the causative agent of bovine moraxellosis (Moraxella bovis) in animal biological material and feed using a real-time polymerase chain reaction, including a buffer for carrying out the polymerase chain reaction, a mixture for its implementation, consisting from deoxynucleoside triphosphates, oligonucleotide primers and fluorescent probes specific to the animal genome region and to the internal control sample; a mixture of enzymes from DNA polymerase with antibodies that inhibit enzyme activity, TAQ POLYMERASE, an internal control sample in the form of a suspension of bacteriophage T4 with a concentration of 5 × 10 ³ phage particles per 1 μl, a negative control sample, which is a mixture of recombinant plasmid DNA containing a fragment of the animal genome and a fragment of the genome of bacteriophage T4 with the nucleotide sequence:

T4F: 5'- TACATATAAATCACGCAAAGC -3' - forward primer

T4R: 5'- TAGTATGGCTAATCTTATTGG -3' - reverse primer

T4P: SU5-5'- ACATTGGCACTGACCGAGTTC -3'-BHQ1 - probe, taken in a volume ratio of 1:1, according to the invention, a fragment of the genome of the causative agent of bovine moraxellosis (Moraxella bovis) with the following nucleotide sequence (5'-3') was used for the positive control sample ):

Morab-F GATTTACTCGATGGTGGTGC

Morab-R CCATCGAGTGGGTCATCGC

Morab-P R6G-ACCGCTTGTTTGGTGGTAAAGGCAAC-BHQ1,

and for the DNA of the causative agent of bovine moraxellosis (Moraxella bovis), the fluorescent dye HEX/Yellow was used.

The novelty of the proposed test system consists in identifying the DNA of the causative agent of bovine moraxellosis (Moraxella bovis) using polymerase chain reaction (PCR) with fluorescent detection in real time using oligonucleotide primers specific to the genome region of a fluorescent-labeled probe. This real-time PCR shortens and simplifies the analysis procedure and reduces the risk of contamination. In addition, fluorescent detection of amplification products is carried out using the principle of cleavage of a fluorescent label at the 5' end of the oligonucleotide probe.

The features that distinguish the claimed technical solution from the prototype are aimed at achieving a technical result and have not been identified in the study of this and related fields of science and technology and, therefore, meet the criterion of “inventive step”.

The claimed test system is recommended for use in specialized veterinary, sanitary-epidemiological, livestock, and agricultural enterprises, which meets the criterion of “industrial applicability.”

A test system for detecting DNA of the causative agent of bovine moraxellosis (Moraxella bovis) in biological material of animals using polymerase chain reaction in real time is used as follows.

DNA is first isolated from animal biological material using the sorption method. The following can be used as biological material: parenchymal organs, intestines and small intestines, meat.

A polymerase chain reaction with fluorescent detection is carried out with 40 cycles of amplification in real time using oligonucleotide primers, probes, and fluorescent dyes specific to the DNA region of the DNA of the causative agent of bovine moraxellosis (Moraxella bovis): for a specific signal for the DNA of the causative agent of bovine moraxellosis (Moraxella bovis) fluorescent dye - HEX/Yellow and for the internal control sample, bacteriophage T4 with a concentration of 5×10 ³ phage particles per 1 μl - FAM/Green. For a positive control sample, a mixture was used containing in the same volume ratio fragments of the genomes of the causative agent of bovine moraxellosis (Moraxella bovis) and bacteriophage T4 with the following nucleotide sequences (5'-3'):

Morab-F GATTTACTCGATGGTGGTGC

Morab-R CCATCGAGTGGGTCATCGC

Morab-P R6G-ACCGCTTGTTTGGTGGTAAAGGCAAC-BHQ1

T4-F TACATATAAATCACGCAAAGC

T4-R TAGTATGGCTAATCTTATTGG

T4-P FAM-CATTGGCACTGACCGAGTTC - BHQ1.

Then the accumulation of fluorescent signals is measured through the channels of the corresponding fluorescent dyes, the results are interpreted based on the presence or absence of intersection of the fluorescence curve with the threshold line, if the accumulation curves of the fluorescent signal appear before the 35th cycle, then the reaction result is considered positive, and if the curves do not cross the threshold line or cross it after the 35th cycle, then the result of the reaction is negative.

To increase the accuracy of identification of the causative agent of bovine moraxellosis (Moraxella bovis), bacteriophage T4 with a concentration of 5 × 10 ³ phage particles per 1 μl is used for the internal control sample; if the concentration of phage particles deviates upward or downward, then duplicates of doubtful samples are observed. For a positive control sample, use a mixture containing fragments of the genomes of the native bacteriophage T4 and DNA of the causative agent of bovine moraxellosis (Moraxella bovis) taken in a 1:1 ratio, with the following nucleotide sequences (5'-3'):

Morab-F GATTTACTCGATGGTGGTGC

Morab-R CCATCGAGTGGGTCATCGC

Morab-P R6G-ACCGCTTGTTTGGTGGTAAAGGCAAC-BHQ1,

T4F: 5'- TACATATAAATCACGCAAAGC -3' - forward primer

T4R: 5'- TAGTATGGCTAATCTTATTGG -3' - reverse primer

Т4Р: FAM-5'- ACATTGGCACTGACCGAGTTC -3'-BHQ1 - probe.

When designing primers and probes, the main requirements were: degree of homology (complementarity) with the selected gene region; the absence of self-complementary regions within oligonucleotides and complementarity to each other, in order to prevent the formation of stable secondary structures (dimers); proximity of primer annealing temperatures.

The design of specific primers and a probe was carried out using computer programs based on the analysis of nucleotide sequences of reference strains and isolates published on the GenBank resource and the selection of conditions for real-time PCR using the developed primers and probe carrying a fluorophore and quencher, and complementary to part of the amplified substance. specific fragment primers.

Primers were designed using Primer Express Software v3.0 (Applied Biosystems) and examined using BLAST to confirm their specificity. To detect amplification products, an oligonucleotide fluorescently labeled probe Morab-P (complementary to the region of the nucleotide sequence limited by the annealing positions of primers Morab-F and Morab-R) was selected. The fluorescent dye 6-Carboxyrhodamine (R6G) is placed at the 5' end of the oligonucleotide probe.

Morab-F GATTTACTCGATGGTGGTGC

Morab-R CCATCGAGTGGGTCATCGC

Morab-P R6G-ACCGCTTGTTTGGTGGTAAAGGCAAC-BHQ1,

Using the "Oligo 6.0" program, the main properties of the calculated oligonucleotides are described, which determine the possibility of their use in PCR as primers and probes. None of the selected sequences were found in the genomes of other representatives of the coccidia group of protozoa, or in the genomes of any species of animals or humans.

To detect amplification products, an oligonucleotide fluorescently labeled probe T4P was selected, complementary to the region of the nucleotide sequence limited by the annealing positions of primers T4F and T4R. The probe was labeled with FAM dye (Carboxyfluorescein - excitation wavelength - 490 nm, fluorescence wavelength - 520 nm). Using the "Oligo 6.0" program, the main properties of the calculated oligonucleotides are described, which determine the possibility of their use in PCR. The 3' end of the oligonucleotide probe was labeled with the fluorescent dye HEX, and the 5' end of the probe contained the fluorescence quencher BHQ1:

Using the "Oligo 6.0" program, the main properties of the calculated oligonucleotides are described, which determine the possibility of their use in PCR as primers and probes. None of the selected sequences were found in the genomes of other representatives of the coccidia group of protozoa, or in the genomes of any species of animals or humans.

T4F TACATATAAATCACGCAAAGC direct primer

T4R TAGTATGGCTAATCTTATTGG reverse primer

T4P FAM-5'- ACATTGGCACTGACCGAGTTC probe.

An example of a specific use of a test system for detecting DNA of the causative agent of bovine moraxellosis (Moraxella bovis) using real-time polymerase chain reaction (RT-PCR)

The example includes the following steps:

1. Selection of material for research

The following material is used for the study:

• Swabs and scrapings of the nasal mucous membranes. Removed using a sterile probe, the probe is placed in a 1.5 ml plastic microtube with 0.5 ml of sterile saline;

• Fragments of parenchymal organs (fragments of the liver, lungs, spleen, as well as tonsils, lymph nodes, etc.). Collect in a sterile container.

• Whole blood. Blood is taken into a test tube with 6% EDTA at the rate of 50 μl of EDTA solution per 1 ml of blood, the closed tube with blood is inverted several times.

• Milk is taken in a volume of 10-30 ml into a sterile container.

• The selection of test samples of feed/raw materials is carried out according to national standards that establish the procedure for sampling for homogeneous groups of raw materials, food products and feed.

2. Preparation of the test material

Smears and scrapings from the mucous membranes of the conjunctiva in saline are examined without prior preparation.

Tissue and organ samples and animal product samples are homogenized using sterile porcelain mortars and pestles, then usually prepared as a 10% suspension in sterile saline or phosphate buffer. The suspension is transferred into a 1.5 ml test tube and centrifuged at 10-12 thousand rpm for 2 minutes. The supernatant is used for NC extraction. In some cases, the resulting suspension is not centrifuged, but left at room temperature for 5 minutes, then the upper phase of 0.4-0.5 ml is transferred with a Pasteur pipette (or a tip with an aerosol barrier) into 1.5 ml tubes, and into an amount of 0.1 ml is used to isolate nucleic acid (NA).

Milk in a volume of up to 10 ml is disinfected and centrifuged at 3 thousand rpm for 10-15 minutes. The supernatant is carefully removed, leaving approximately 0.2 ml of liquid above the sediment. The pellet is resuspended in the remaining supernatant and 0.1 ml of the suspension is used for DNA extraction.

From feed/raw materials with a dense consistency, a total sample weighing 10-50 g is taken for research. Granulated or canned feed/raw materials (10-20 g) are ground in a mortar until homogeneous before testing. Laboratory samples (20-40 mg) are collected in disposable micro-tubes with a capacity of 1.5 ml and sent for NK isolation.

3. Conducting analysis

The study was carried out using a set of reagents “PCR-MORAXELLOSIS-FACTOR” to detect the DNA of the causative agent of moraxellosis (Moraxella bovis). The kit consists of a set of reagents for multiplex PCR (Table 1, kit No. 1) and a set of control samples (Table 2, kit No. 2). The set is available in two versions:

1) For analysis of 55 samples (including control samples)

2) For analysis of 110 samples (including control samples).

The kits are used in accordance with the instructions for use of the PCR-MORAXELLOSIS-FACTOR reagent kit to detect the DNA of the causative agent of moraxellosis (Moraxella bovis) in biological material using the polymerase chain reaction (PCR) method with fluorescent detection in real time, 10.21.60-221- 51062356-2020 For in vitro diagnostics, http://www.vetfaktor.ru

The study using the “PCR-MORAXELLOSIS-FACTOR” reagent kit consists of three cycles:

• DNA extraction;

• carrying out RT-PCR;

• taking into account the results of the analysis.

4. Extraction (isolation) of NA from clinical material

Select the required number of 1.5 ml disposable tubes, including the negative isolation control. Add 10 µl of VKO MORO to all test tubes with test samples, including the test tube for OCO.

Add the test samples in the volume according to the instructions for the DNA extraction kit; add OKO instead of the test sample into the negative control tube (designate the test tube as VK-).

Extract DNA from test and control samples according to the DNA extraction kit manufacturer's instructions.

The isolated DNA can be stored for one week at a temperature of 2°C to 8°C or for a year at a temperature not exceeding minus 16°C.

5. Preparation of samples for PCR

The total volume of the reaction mixture is 25 μl, the volume of DNA sample is 10 μl.

The successful completion of the reaction is monitored using PKO MORO, VKO MORO and DNA buffer.

In a separate tube, mix the components of the kit based on each PCR reaction:

• 5 µl PCR MIX MORO

• 10 µl PCR BUFFER MORO

• 0.5 µl TAQ POLYMERASE

Mix the mixture by vortex and discard the drops by short-term centrifugation.

Select the required number of tubes for DNA amplification of test and control samples. Add 15 µl of the prepared reaction mixture.

Using tips with a filter, add the following to the prepared test tubes:

a) 10 µl of DNA buffer into a negative control PCR tube (K-);

b) into a row of test tubes for the test samples - add 10 µl of DNA from the corresponding sample obtained according to clause 7.1 (including the BK- sample) into each tube;

c) 10 µl of PCO MORO into the test tube (K+) positive control.

6. Carrying out RT-PCR reaction with fluorescent detection

Place the tubes prepared for PCR into the cells of the Rotor-Gene Q device. The parameters of the temperature-time regime of amplification on the Rotor-Gene Q device are shown in Table 3.

Place the tubes prepared for PCR into the cells of the amplifier.

7. Interpretation of analysis results

The obtained data - fluorescent signal accumulation curves are analyzed using the software of the device used to carry out PCR in real time in accordance with the manufacturer's instructions for the device and in accordance with Appendices 1, 2 and 3 to the Instructions.

The results of PCR analysis are taken into account by the presence or absence of intersection of the fluorescence curve with the threshold line set at the appropriate level (which corresponds to the presence or absence of the threshold cycle “Ct” value for the test sample).

The result is considered reliable if the positive and negative controls for amplification and DNA extraction are correctly passed in accordance with Table 4.

The appearance of any Ct value in the results table for the negative control of the extraction step BK- (on the HEX/Yellow channel) and for the negative control of the PCR step K- (on any of the channels) indicates the presence of contamination of the reagents or samples. In this case, the analysis results for all samples are considered invalid. It is necessary to repeat the analysis of all samples, as well as take measures to identify and eliminate the source of contamination.

Samples for which there is no Ct value according to the FAM/Green channel or exceeds cycle 35 (and at the same time there is no Ct value according to the HEX/Yellow channel) require repeat testing from the PCR stage. A delay in threshold cycle values for test samples on the FAM/Green channel indicates the presence of inhibitors in the sample(s) or errors in DNA extraction or reaction setup. It is required to conduct research starting from the DNA extraction stage.

A sample is considered positive (DNA of the causative agent of bovine moraxellosis (Moraxella bovis) is present) if an exponential increase in the signal on the HEX/Yellow channel is observed, while the Ct values of control samples are within the normal range (Table 4). If the Ct value for the test sample via the HEX/Yellow channel is determined later than cycle 35 with the correct passage of positive and negative controls, it is considered controversial and is re-tested from the stage of DNA extraction. If, upon repeated testing, a similar result is observed (Ct on the HEX/Yellow channel is more than 35), repeated collection of material from the same animal is required for PCR testing and (or) the use of alternative diagnostic methods. If a Ct value on the HEX/Yellow channel is less than 35 when examining material repeatedly taken from an animal, the sample is considered positive.

A sample is considered negative (no bovine moraxellosis DNA (Moraxella bovis)) if there is no increase in the fluorescence signal on the HEX/Yellow channel, while the Ct values of control samples are within the normal range (see Table 4).

Claims (8)

Test system for detecting the DNA of the causative agent of bovine moraxellosis (Moraxella bovis) in biological material of animals and feed using a polymerase chain reaction in real time, including a buffer for carrying out the polymerase chain reaction, a mixture for its implementation, consisting of deoxynucleoside triphosphates, oligonucleotide primers and fluorescent probes specific for a region of the animal's genome and for an internal control sample; a mixture of enzymes from DNA polymerase with antibodies that inhibit enzyme activity, TAQ POLYMERASE, an internal control sample in the form of a suspension of bacteriophage T4 with a concentration of 5 × 10 ³ phage particles per 1 μl, a negative control sample, which is a mixture of recombinant plasmid DNA containing a fragment of the pathogen genome and a fragment of the genome of bacteriophage T4 with the nucleotide sequence: T4F: 5-TACATATAAATCACGCAAAGC-3' - forward primer, T4R: 5'-TAGTATGGCTAATCTTATTGG-3' - reverse primer, T4P: SU5-5'-ACATTGGCACTGACCGAGTTC-3-BHQ1 - probe taken in a volume ratio of 1:1, characterized in that a fragment of the genome of the causative agent of bovine moraxellosis (Moraxella bovis) with the following nucleotide sequence (5'-3) is used for the positive control sample '): Morab-F GATTTACTCGATGGTGGTGC, Morab-R CCATCGAGTGGGTCATCGC, Morab-P R6G-ACCGCTTGTTTGGTGGTAAAGGCAAC-BHQ1, and for the DNA of the causative agent of bovine moraxellosis (Moraxella bovis), a fluorescent dye was used - HEX/Yellow.