Triple RT-PCR method capable of detecting three viruses causing potato tuber necrosis simultaneously and primer combination thereof
A potato block and potato technology, applied in the direction of recombinant DNA technology, biochemical equipment and methods, microbial measurement/testing, etc., can solve the problems of high cost and long time consumption, and achieve improved detection efficiency, high sensitivity, and high specificity Effect
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Embodiment 1 3
[0029] Embodiment 1 Triple RT-PCR detects PVY simultaneously NTN , TSWV, PMTV method establishment
[0030] 1. Primer design
[0031] Due to the need to detect TSWV and PVY at the same time NTN , PMTV these three kinds of viruses, to establish a multiple RT-PCR detection method with the characteristics of many types of viruses detected, simple detection steps, accuracy, and economy. The establishment of this multiplex PCR system has high requirements on primers, which need both specificity and compatibility to ensure that the triplex PCR can work normally and establish an optimal system. According to the nucleocapsid gene sequence of TSWV in Genbank, use Primer5.0 to design primers to design a universal primer pair (forward primer TSWV-F, reverse primer TSWV-R), and the amplified target fragment size is 251bp; according to PVY in Genbank NTN The unique recombination site sequence was designed with Primer5.0 universal primer pair (forward primer PVY NTN -F, reverse prime...
Embodiment 2 3
[0046] Example 2 Optimization of Triple RT-PCR Detection Method and Its Detection Sensitivity (Influence of Different Annealing Temperatures and Different Template Dilution Factors on Triple RT-PCR Detection Effect)
[0047] Since the Tm values of each pair of primers are not the same, it is necessary to select a suitable annealing temperature so that triple RT-PCR can obtain three target fragments and improve detection sensitivity. The annealing temperature is set to 8 temperature gradients of 51.7, 53.6, 55.7, 57.9, 60.1, 62.3, 64.4, and 66.3°C. The electrophoresis results of PCR products are shown in figure 2 . The results showed that the annealing temperature was the most suitable at 57.9°C-62.3°C, and three clear target fragments could be obtained by single-plex and triple-plex RT-PCR.
[0048] In order to test the sensitivity of the triple RT-PCR detection, the initial RNA was diluted 10, 100, 1000 and 10000 times, respectively, that is, the RNA concentration was 10 ...
Embodiment 3 3
[0049] Example 3 triple RT-PCR detection of potato plant samples
[0050] Laboratory samples infected with TSWV and PVY respectively NTN , PMTV potato plants or tubers, a total of 13 samples. After grinding with liquid nitrogen, extract the total RNA of the plant, and use the established triple RT-PCR system to detect the virus infection. The test results are shown in Figure 4 . The results show that the target bands amplified by this system are very clear and specific, and these three viruses can be detected 100%, indicating that the established triple RT-PCR system can be well used in TSWV, PVY NTN , PMTV detection.
[0051] Hunan Agricultural University
[0052] A Triple RT-PCR Method and Primer Combination for Simultaneous Detection of Three Viruses Causing Potato Tuber Necrosis
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[0056] DNA
[0057] Artificial sequence
[0058]
[0059] Description of Artificial Sequences: Artificially Synthesized Sequences
[0060] 1
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