Method for quickly concentrating viruses in water body
A water and virus technology, applied in the field of environmental virology and environmental monitoring, can solve the problems of limited promotion and application, high requirements, complex operation, etc., and achieve the effects of low equipment requirements, high recovery efficiency and simple operation.
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Embodiment 1
[0021] An outbreak of diarrhea occurred in a company. First, norovirus was detected positive in the stool samples of two cases. Epidemiological investigations showed that the attack rate of people who drank the company's direct drinking water was higher than that of people who drank other types of water. Norovirus detection was performed on 9 water samples, and norovirus was detected from 3 samples. The specific method is as follows:
[0022] Carry out virus concentration with the method of the present invention respectively to every part of water sample, the steps are as follows:
[0023] 1. Pretreatment of virus-contaminated water samples
[0024] Take 1 L of water sample, add MgCl2 solution to make the final concentration 0.05 mol / L, then adjust the pH of the solution to 3.5 with 1 mol / L hydrochloric acid, stir and mix evenly on a magnetic stirrer.
[0025] 2. Filter
[0026] Use Millipore's microbial filtration system or Milliflex automatic biological filtration system ...
Embodiment 2
[0037] To monitor enteroviruses in environmental water, river water was randomly selected, a total of 6 water samples, 1000ml / point, and enteroviruses were detected from 1 sample. The specific method is as follows:
[0038] Carry out virus concentration to each part of water sample respectively, the concentration step is the same as embodiment 1.
[0039] Take 200 μl of the resuspended water virus concentrate and extract RNA.
[0040]RT-PCR detection, including: use the extracted viral RNA as a template, apply random primers to obtain viral genome cDNA by reverse transcription under the action of M-MLV reverse transcriptase, the reaction condition is 65°C for 5min, and incubate at 25°C after adding reverse transcriptase 10min, 42°C extension for 1h, 70°C denaturation for 10min. Using viral cDNA as a template, human enterovirus nucleic acid detection universal primer sequence: 5'-TCC GGC CCC TGA ATG CGGCTA ATC C-3'PE1 (downstream): 5'-ACA CGG ACA CCC AAA GTA GTC GGT CC-3 'Am...
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