Method and special kit thereof for detecting babesia

A technology for Babesia and Babesia deer, which is applied in the biological field to achieve the effects of improving specificity and improving sensitivity

Inactive Publication Date: 2016-01-06
MICROBE EPIDEMIC DISEASE INST OF PLA MILITARY MEDICAL ACAD OF SCI
View PDF0 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

heavily restricted

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method and special kit thereof for detecting babesia
  • Method and special kit thereof for detecting babesia
  • Method and special kit thereof for detecting babesia

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0046] The design of embodiment 1, primer and probe

[0047] 1. There are three main hypervariable regions in the 18srRNA gene of Babesia, the first is located at the 100-200nt position from the 5' end, the second is located at the 550-660nt position, and the third is located at the 1250- 1300nt position. The difference between different species of Babesia is between 0.0% and 11.2%, and the corresponding positions of the 18srRNA gene of rodent and human origin are close to 30%.

[0048] According to the principle of primer design, a 406bp gene region (SEQ ID No.1) containing the second hypervariable region (550-660 nucleotides from the 5' end) of the 18srRNA gene of Babesia (the sequence was derived from divergence Babesia divergens (Babesia divergens, sequence accession number GU057385 in GenBank) was further analyzed, wherein the bold part is the variation region of different Babesia species.

[0049] SEQ ID No. 1:

[0050] 5’-AATTACCCAATCCTGACACAGGGAGGTAGTGACAAGAAATAACAA...

Embodiment 2

[0059] Embodiment 2, common PCR amplification verification

[0060] 1. Synthesize the fragment shown in SEQIDNo.1 and insert it into the plasmid vector pMD18-T to obtain a recombinant plasmid, which is named pBabesi406. The recombinant plasmid pBabesi406 was sent for sequencing, and the result was correct.

[0061] Two, with the recombinant plasmid pBabesi406 of different gradient dilutions as a template, with SEQIDNo.2 and SEQIDNo.3 (y=t / c, s=g / c, the equal concentration mixture of four kinds of primers) as primers, carry out common PCR amplification Each PCR amplification product was obtained, and the agarose gel electrophoresis results of each PCR amplification product were as follows: figure 1 shown.

[0062] figure 1 Among them, 1-5 are PCR amplification products; M is DNAmarker.

[0063] figure 1 It shows that the target band of about 120bp can be obtained by PCR amplification, and the target band is sequenced, and the result is consistent with the sequence of SEQID...

Embodiment 3

[0064] Embodiment 3, real-time fluorescent quantitative PCR verification

[0065] 1. Insert the DNA fragment shown in SEQIDNo.5 into pMD18-T to obtain a recombinant plasmid, which is named pBabesi116. The pBabesi116 was sent for sequencing, and the result was correct.

[0066] Two, according to the base number (2692+116=2808bp) of the recombinant plasmid pBabesi116, calculate the molecular weight (MW=2808×660=1853280Daltons), that is, 1mol=1.85328×10 6 g.

[0067] The actual nucleic acid concentration of pBabesi116 was measured and repeated three times. The results were 147, 133, and 127 (ng / uL) respectively, and the average value was 135.7 ng / μL, which was used as a standard.

[0068] Calculate standard copy number: (6.02x10 23 copy number / mole)x(1357x10 -10 g / μl) / (1.85328x10 6 g / mol)=4.4x10 10 copies / μL, dilute the standard in different gradients, and calculate the corresponding concentration at the same time, as shown in Table 1.

[0069] 3. PCR detection was perform...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a method and a special kit thereof for detecting babesia. The invention discloses a group of DNA molecules which include DNA molecules as shown in (1)-(3): (1) a DNA molecule as shown in SEQ ID No.2; (2) a DNA molecule as shown in SEQ ID No.3; and (3) a DNA molecule as shown in SEQ ID No.4. The method disclosed by the invention, compared with morphological and immunofluorescent methods adopted in clinical field in the past, can greatly improve the sensitivity of detecting babesia, and the method has the characteristics of being rapid and convenient; and the method and the special kit thereof are suitable for basic hospitals and suitable for monitoring babesia propagation media and animal hosts.

Description

technical field [0001] The invention relates to a method for detecting Babesia and a special kit thereof, belonging to the field of biotechnology. Background technique [0002] The main clinical symptoms of Babesiosis are high fever, hemolytic anemia, jaundice and hemoglobinuria. Zoonoses. In recent years, there have been continuous occurrences of human infection cases around the world, and even outbreaks in several states in the United States. Confirmed / suspected cases of Babesia have continued to occur in Shandong, Zhejiang, Xinjiang, Yunnan, Beijing and other places in my country. "New health threats". At present, more than 100 species of Babesia parasitic in vertebrates have been reported in the world. Babesia that infects humans mainly includes Babesia parvum, Babesia dunnai, Babesia divergentis, Babesia orioni, and Babesia KO1 strain. Due to the presence of a considerable proportion of recessive or subclinical infections in the disease, clinical misdiagnosis and mis...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): C12Q1/68C12Q1/04C12N15/11C12R1/90
Inventor 江佳富曹务春蒋宝贵张圆孙毅江瑞若
Owner MICROBE EPIDEMIC DISEASE INST OF PLA MILITARY MEDICAL ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap