Lysing bacteriophage and application thereof in prevention and control of tobacco soil-borne bacterial wilt

A technology of bacteriophage and bacterial wilt, applied in the field of microorganisms, can solve problems such as polluting the environment, destroying the stability of soil microorganisms, affecting the quality of tobacco, and achieving the effect of reducing disturbance and inhibiting the occurrence of bacterial wilt

Active Publication Date: 2021-05-25
NANJING AGRICULTURAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the above methods are easy to induce the drug resistance of pathogenic bacteria, and will kill the indigenous microorganisms in the soil, destroy the homeostasis of soil microorganisms, pollute the environment and affect the quality of tobacco

Method used

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  • Lysing bacteriophage and application thereof in prevention and control of tobacco soil-borne bacterial wilt
  • Lysing bacteriophage and application thereof in prevention and control of tobacco soil-borne bacterial wilt
  • Lysing bacteriophage and application thereof in prevention and control of tobacco soil-borne bacterial wilt

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] Isolation of Ralstonia solanacearum

[0035] Take 1 g of tobacco plant rhizosphere soil sample collected from the bacterial wilt disease incidence area in Yunnan Province, and put it into a sterilized 50 mL conical flask containing 9 mL of deionized water (water-soil ratio 1:9). Put the Erlenmeyer flask into a shaker at 30°C and 150-180 rpm for 30-60 min to obtain a soil suspension. Take the soil suspension for gradient dilution. The specific method is: take 100 μL of soil suspension, add it to a centrifuge tube containing 900 μL of sterile water, and vortex; the dilution gradient is 10 -1 of soil suspension, repeat this step for gradient dilution to obtain a dilution gradient of 10 -2 , 10 -3 , 10 -4 soil suspension. Take 100 μL of the soil suspension of each dilution gradient and apply it to the semi-selective M-SMSA solid medium of R. solanacearum. Three replicates were set for each dilution gradient. The plate was placed upside down in a constant temperature i...

Embodiment 2

[0054] Phage electron microscope observation

[0055] 1. Select the phage FQ44 to be observed and the corresponding host R. solanacearum YNYC-23.

[0056] 2. Prepare a double-layer plate of R. solanacearum according to the method in Example 1, drop 150 μL of phage suspension on the plate, and place it in a 30°C constant temperature incubator for 12-24 hours until plaques appear.

[0057] 3. Add a small amount of sterile ddH to the place where plaques appear 2 O (500 ~ 1000μL), let stand for about 1h, during which it should be shaken gently for many times, so that the phage floats from the agar to the water surface.

[0058] 4. Take an appropriate amount of phage suspension, negatively stain with 2% phosphotungstic acid dye solution, take out from the dye solution after about 90s of staining, and air dry naturally at room temperature.

[0059] 5. Use transmission electron microscope to observe the morphology of phage.

[0060] Depend on figure 2 It can be seen that the hea...

Embodiment 3

[0062] Phage optimal multiplicity of infection determination

[0063] The multiplicity of infection (MOI) refers to the ratio of the number of phage to the host bacteria before the phage adsorbs and infects the host bacteria. The optimal multiplicity of infection is the MOI that yields the highest progeny phage yield.

[0064] With reference to the method in Example 1, the bacterial liquid of R. solanacearum YNYC-23 in logarithmic growth phase was obtained, and the bacterial liquid of R. solanacearum was OD with sterile water. 600 The value is adjusted to 0.5. The phage suspension purified in Example 1 was added dropwise to the NA liquid medium containing Ralstonia solanacearum, and incubated at 30°C with shaking at 170 rpm for 12 hours; the culture medium was centrifuged at 13,000 rpm for 3 minutes at room temperature, and the supernatant was taken and filtered with a 0.22 μm membrane. Filter to obtain a phage suspension; adjust the titer of the phage suspension to 1×10 wit...

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PUM

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Abstract

The invention discloses a lytic bacteriophage FQ44, which is classified and named as a lauraceae bacteriophage, and is preserved in the China Center for Type Culture Collection on September 29, 2020, and the preservation number of the bacteriophage is CCTCC (China Center for Type Culture Collection) NO: M2020560. The invention also discloses an application of the bacteriophage FQ44 in prevention and control of tobacco soil-borne bacterial wilt, and the bacteriophage is applied into soil by adopting a root irrigation method. According to the invention, the ralstonia solanacearum obligate bacteriophage is used for inhibiting tobacco soil-borne bacterial wilt, so that damage to common microbial communities in soil is avoided while the soil-borne bacterial wilt is prevented and controlled. Indoor related experiments show that the bacteriophage FQ44 belongs to muscular tail bacteriophage, can effectively inhibit the growth of part of tobacco ralstonia solanacearum, and has the best effect when being applied according to the optimal infection complex number (MOI 1-10); and field experiment results show that the bacterial wilt can be effectively inhibited, and the bacterial wilt inhibitor has a wide prospect.

Description

technical field [0001] The invention belongs to the technical field of microorganisms, and relates to a bacteriophage and its application in preventing and controlling tobacco bacterial wilt, in particular to a lytic bacteriophage FQ44 and its application in preventing and controlling tobacco soil-borne bacterial wilt. Background technique [0002] Tobacco bacterial wilt is a soil-borne disease caused by Ralstonia solanacearum (Ralstonia solanacearum, referred to as Ralstonia solanacearum). , restricting the development of the tobacco economy. Traditional methods such as application of pesticides or fumigation can kill the soil-borne R. solanacearum in a short time, effectively slowing down the occurrence of the disease. However, the above methods are easy to induce drug resistance of pathogenic bacteria, and will kill indigenous microorganisms in soil, destroy soil microbial homeostasis, pollute the environment and affect the quality of tobacco. [0003] Bacteriophages ar...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N7/00A01N63/40A01P1/00C12N1/20A01G22/45A01G7/06C12R1/92C12R1/01
CPCC12N7/00A01N63/40A01G22/45A01G7/06C12N2795/10121C12N2795/10131C12N2795/10151Y02A50/30
Inventor 韦中王硕杨天杰王孝芳王佳宁徐阳春沈其荣
Owner NANJING AGRICULTURAL UNIVERSITY
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