RU2378382C1 - Set of synthetic oligonucleotides to detect dna of agent of vegetable desease - gram-negative bacterium xanthomonas campestris pv vesicaroria by polymerase chain reaction - Google Patents

Abstract

FIELD: medicine.

SUBSTANCE: set of synthetic oligonucleotides including primers 5'-5'- Tgg gCA gCg TAT CTT TCA CC -3' and 5'- ATT ggC AgA Agg gTT TgT gTA A -3', and a probe: (BHQl)-5'- CAg ATA TCC gTC C(FdT)g gTC gAA CgT CTC g -3'P is created.

EFFECT: design of polymerase chain reaction with using said set allows detecting reliably DNA of agent of vegetable disease - gram-negative bacterium Xanthomonas campestris pv vesicaroria in a biological material, particularly in a protected ground, seeds, plants, cucumber and tomato fruits.

Description

The invention relates to the field of molecular genetic diagnosis of phytopathogens.

In recent years, various methods have been developed for the molecular genetic diagnosis of phytopathogens, which make it possible to identify DNA sequences that are characteristic of a particular type of infectious disease agent. Thus, the corresponding pathogen is detected and a conclusion is made about its presence in biological material.

The most promising is the use for this purpose of the method of polymerase chain reaction (NDP) - a highly specific and highly sensitive method for detecting bacterial DNA. The principle of the NDP is the multiple copying (amplification) of a specific DNA fragment, which is marker for this type of pathogen.

The invention is known by application No. 2003121605 (published January 27, 2005), which is a kit for the identification of enterohemorrhagic Escherihia coli. This invention involves PCR reactions involving reagents included in this kit. In particular, the following primers are used that are specific for the desired bacteria, which can detect the DNA of this bacterium during PCR:

Rfb for 5'-CAGGTGAAGGTGGAATGGTTG-3 '

Rfb rev 5'-GAGTACATTGGCATGGTGTGG-3 '

stx2 for 5'-ATCAGCAATGTGCTTCCGGAG-3 '

stx2 rev 5'-CTGAGCACTTTGCAGTAACGG-3 '.

As a result, enterohemorrhagic Escherihia coli is detected.

Similar inventions are also known “Method and kit for detecting the DNA of the bacterium of the disease of Lyme borreliosis - borrelia burgdorferi))) (application No. 2004105688, published on 08/10/2005) and the“ Kit of reagents for determining the DNA of periodontopathogenic microbes Prevotella intermedia sensu stricto, Bacteroides forsythus, Treponema denticola, Actinobacillus actinomycetemcomitans, Porphyromonas gingivalis using the multiplex polymerase chain reaction "(application No. 2005136997, published 10.06.2007).

Work on the creation of primers that are used in such sets is usually constructed as follows.

1) Using open and commercial databases of nucleotide sequences of the genomes of microorganisms, or as a result of independent determination of the nucleotide sequence of the studied microorganism, a portion of the genome is selected that is unique to this type of microorganism (or group of species).

2) Based on the selected region of the genome, using special software, the sequence of oligonucleotides used to carry out the PNR reaction is selected (often 2 primers and a sample).

At this stage, the work consists in creating the alignment of many genomic sequences and selecting a portion of the sequence where the number of mutations corresponds to the desired location of the primers.

Alignment of genomic sequences means a comparison of the sequences of many organisms with each other, the search for unique for the desired microorganism sites that have no analogues in other microorganisms.

The search for a correspondence between the number of mutations and the location of primers means that mutations that are possible in a given microorganism (naturally, those data are already in the databases or have already been independently obtained) should not affect the genome region selected for primers, since the substitutions are in the genomic sequence ( mutations) can adversely affect the performance of primers.

3) The manufacture of primers is ordered in a special service center.

4) Using practical experiments, the suitability of the selected sequences for specific purposes is proved (for example, to determine the presence / absence of a given microorganism in a biomaterial).

The present invention allows the detection of the DNA of the phytopathogenic bacterium Xanthomonas campestris pv vesicaroria, which causes black bacterial spotting - one of the most harmful diseases of vegetable crops. The bacterium infects the tomato (Lycopersicum esculentum Mill.) And pepper (Capsicum annum L), causing significant crop losses.

However, similar kits, as well as reaction mixtures, primers and methods for detecting the DNA of this bacterium, are not known.

The technical result, the achievement of which the present invention is directed, is the reliable detection of the indicated bacteria in biological material (protected soil, seeds, plants, fruits of cucumber and tomato).

The specified result is achieved by using a set of synthetic oligonucleotides for the detection of DNA of the causative agent of vegetable diseases, the bacteria Xanthomonas campestris pv vesicaroria, which includes primers:

5'-Tgg gCA gCg TAT CTT TCA CC-3 '

5'-ATT ggC AgA Agg gTT TgT gTA A-3 '

and sample: (BHQl) -5'-CAg ATA TCC gTC C (FdT) g gTC gAA CgT CTC g-3'P, where BHQ1 is a dark fluorescence quencher attached to the 5'-terminal nucleotide, and FdT is a FAM fluorescent dye, attached to nucleotide T.

The specified set of synthetic oligonucleotides is an integral part of the set of the following substances.

1) Test tubes with a reaction mixture sealed with paraffin. This mixture contains the indicated primers and a sample specific for the Xhanthomonas campestris pv vesicaroria DNA site — the Rhs gene, a mixture of four types of deoxyribonucleotide triphosphates, reaction buffer (100 mM Tris-HCl (pH 8.8 at 25 ° С), 500 mM KCl, 0.8% P40 , 20 mM MGCl ₂ ), internal control sample (VK).

Both the primers and the sample are synthetic oligonucleotides. Primers specific for the marker region of the pathogen genome are introduced into the reaction directly for amplification (production) of the product. The sample (also specific to this DNA site) incorporates a fluorescence label, the fluorescence intensity of which indicates the amount of product formed, which in turn depends on the efficiency of the primers, the amount of starting material and other reaction parameters. In other words, the primers provide the reaction, the sample - the manifestation of its results.

An internal control sample (VK) is a DNA sequence introduced into the reaction to evaluate the effectiveness of its course. The accumulation of VC is independent of the production of a specific product using separate primers and samples.

2) Taq polymerase enzyme solution.

3) A positive control sample is the DNA of a recombinant plasmid with a cloned fragment of size 240 bp genome of Xanthomonas campestris pv vesicaroria. It is introduced into the test tube (by analogy with the test samples) in order to be able to compare the results obtained in experimental tubes with how it should be obtained with a "positive reaction". Accordingly, DNA samples added to the remaining tubes are experimental.

4) Negative control sample - a sample that is introduced into the experiment to control possible contamination of reagents with products of previously conducted reactions. A positive result in this sample indicates the need to replace the reagents and rearrange the experiment.

This set is applied as follows.

1) Biological material (protected soil, seeds, plants, fruits of cucumber and tomato) before PCR using the proposed set of reagents is carried out through the sample preparation procedure using another set (a set of reagents for sample preparation is not the subject of this patent); during this procedure, DNA is extracted from the biological material, which in turn is used for PCR.

2) The required number of tubes with the prepared reaction mixture containing specific synthetic oligonucleotide primers and a sample is labeled according to the number of analyzed samples.

3) Taq polymerase solution is added to all labeled tubes without damaging the paraffin layer.

4) All labeled tubes (except K- (negative control sample), K + (positive control sample)) contain DNA isolated according to item 1).

5) A negative control sample is introduced into the tube marked K-,

6) A positive control sample is introduced into the tube labeled K +

7) All tubes are installed in the amplifier unit, amplification is carried out according to the modes prescribed in the instructions for the set. The results are detected automatically by a detecting amplifier during amplification (devices: detecting amplifiers ДТ-322, ДТ-96 (ZAO NPF DNA-Technology).

Analysis of the results is carried out in accordance with the instructions for the device.

In the case of the formation of a specific DNA product, the sample is destroyed, which leads to an increase in the level of fluorescence, which is fixed by special devices - detecting amplifiers.

Claims (1)

A set of synthetic oligonucleotides for detecting DNA of a pathogen of vegetable diseases - bacteria Xanthomonas campestris pv vesicaroria by polymerase chain reaction, characterized in that it includes primers
5'-Tgg gCA gCg TAT CTT TCA CC-3 ';
5'-ATT ggC AgA Agg gTT TgT gTA A-3 ',
and a sample (BHQ1) -5'-CAg ATA TCC gTC C (FdT) g gTC gAA CgT CTC g-3'P, where BHQ1 is a dark fluorescence quencher attached to the 5'-terminal nucleotide, and FdT is a FAM fluorescent dye attached to nucleotide T.