In-situ hybridization detection probe of shrimp and crab spiroplasma pathogens, and kit thereof

A detection kit, in situ hybridization technology, applied in the determination/inspection of microorganisms, microorganism-based methods, biochemical equipment and methods, etc. Low, no in situ hybridization detection method and other problems

Inactive Publication Date: 2014-05-21
NANJING NORMAL UNIVERSITY
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Problems solved by technology

At present, ultra-thin section electron microscope observation is the most widely used detection method, but this method requires high operating technology and equipment, and the experimental period is long, so it is difficult to popularize; PCR is also another commonly used detection method[3]. Although this method is relatively simple and highly sensitive, it cannot visually observe and p

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  • In-situ hybridization detection probe of shrimp and crab spiroplasma pathogens, and kit thereof
  • In-situ hybridization detection probe of shrimp and crab spiroplasma pathogens, and kit thereof
  • In-situ hybridization detection probe of shrimp and crab spiroplasma pathogens, and kit thereof

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Embodiment 1

[0027] Procambarus clarkii samples

[0028] The diseased Procambarus clarkii were collected from farms in Jiangsu Province where severe mortality occurred from July to September 2011, with an average weight of 21.7g and carapace length of 42.5mm (sample size n=30). Healthy Procambarus clarkii was collected from Nanjing Procambarus clarkii farm in July 2011, with an average weight of 20.1g and a carapace length of 41.0mm (sample size n=24).

[0029] Healthy Procambarus clarkii was determined to be free of spiroplasma infection through conventional light microscope, electron microscope observation and PCR detection, and was used as a negative control; Procambarus clarkii infected with white spot syndrome virus disease (WSSV) was also used as a negative control; The crayfish were confirmed to be infected with spiroplasma by light microscope, electron microscope observation and PCR detection, and they were used as positive control. Main reagents and materials used for in situ hyb...

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Abstract

The invention relates to an in-situ hybridization detection probe of shrimp and crab spiroplasma pathogens, and a kit thereof. The sequences of the probe are represented by SEQIDNO.1 and SEQIDNO.2 respectively. The above two oligonucleotide probes are labeled with digoxin, the labeled probes are hybridized with spiroplasma 16SrDNA in shrimp and crab tissue slices, signal enlargement is carried out through an antigen-antibody reaction, and then enzyme reaction color development is carried out; the pathogen detection and pathological change can be visually combined; the infection rate and the infection intensity are analyzed on sample slices while spiroplasma is efficiently and accurately detected; the hybridization of the probes and the 16SrDNA is specific, and the signal is amplified step by step, so the probes are more sensitive and accurate than routine dyeing observation; and the slices obtained after the detection result hybridization color development can be preserved for a long term.

Description

technical field [0001] The invention relates to an in situ hybridization detection probe and a detection kit for the pathogen of shrimp and crab spiroplasma. Background technique [0002] Chinese mitten crab (Eriocheir sinensis), commonly known as river crab, is a unique aquaculture treasure in my country. However, with the intensive and large-scale development of aquaculture, various diseases have become an important problem that endangers the crab farming industry. Among the many diseases of river crabs, "shivering disease" is the most common and the most harmful. Since the disease was first discovered in Jiangsu in 1994, it has successively broken out in Shanghai, Zhejiang, Anhui, Jiangxi and other places, and it has been increasing year by year. Later, It has spread to almost all river crab breeding areas in the country. In 2008, the Ministry of Agriculture has listed the disease as the newly revised "List of Types 1, 2, and 3 Animal Diseases". Procambarus clarkii (Pro...

Claims

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Application Information

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IPC IPC(8): C12Q1/68C12N15/11C12R1/01
CPCC12Q1/04C12Q1/6841
Inventor 王文丁正峰孟庆国顾伟任乾
Owner NANJING NORMAL UNIVERSITY
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