Pseudomonas plecoglossicida tonB gene silencing strain and application thereof
A Pseudomonas mutans, gene silencing technology, applied in the field of microorganisms
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Embodiment 1
[0029] Pseudomonas mutans ton B A method for constructing a gene stable silencing strain, comprising the following steps:
[0030] Step 1: Using comparative transcriptomics technology to analyze the gene expression of Pseudomonas mutans in the spleen of grouper, it was found that ton B Gene-specific high expression will lock the target ton B Gene; ton B The gene sequence is shown in SEQ ID NO.1;
[0031] Step 2: For ton B Gene sequence using online shRNA design tool from Thermo-fisher Scientific , using the online shRNA design tool to design and synthesize 4 pairs of shRNA primers, which were respectively connected into pCM130 / tac to construct recombinant vectors, and then each recombinant vector was electroporated into Pseudomonas mutans competent cells, and Pseudomonas mutans was successfully constructed ton B Stable gene silencing strains; using qRT-PCR technology, the primers are (F: 5'-GTGGACACGCCGCCAAGCAA-3'; R: 5'- GCCAGGTGACGCAGCAAATCG-3') to test the silencing e...
Embodiment 2
[0047] Using artificial infection experiments, the wild strains of Pseudomonas mutans and ton B The virulence of gene stable and efficient silenced strains was compared.
[0048] ton B The gene stable and efficient silencing strain and the wild strain of Pseudomonas mutans came from our research group, were isolated and identified by Hu Jiao et al. Large yellow croaker ( Pseudosciaena crocea ) Pathogen isolation and identification of visceral white spot disease and its pathogenicity[J]. Ocean and Limnology, 2014, 45(02): 409-417. 2 HPO 4 0.36g, KH 2 PO 4 0.024g, H 2 O 1L, PH 7.0) were used to infect the three groups of grouper by intrathoracic injection, and the infection concentration of the strain was 5 10 4 cfu / tail, each fish was injected with 0.2 mL, 20 fish in each group, and then continued to be raised normally (under non-pathogenic laboratory conditions, water temperature 18 ± 2°C), and the survival status of each group of fish was recorded every day .
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Embodiment 3
[0051] Using RNA-seq technology to ton B Transcriptome sequencing and comparative analysis of spleens from gene-silenced and wild-type Pseudomonas mutans infection ton B Effects of gene silencing on gene expression in Pseudomonas metamorphans and grouper.
[0052] The results of RNA-seq analysis showed that at the mRNA level, according to statistical criteria (|log2 fold change| ≥1, padj ≤0.05), a total of 375 differentially expressed genes were identified in the grouper on the third day of infection. In these differentially expressed genes, compared with infected wild-type strains, infection ton B -84 of the RNAi strain group were significantly down-regulated, and 291 were significantly up-regulated ( image 3 ). GO classification and KEGG pathway analysis to determine the biological functions of the differentially expressed genes of the host grouper. The results of KEGG enrichment analysis also showed that DEMs (Differential Expression mRNAs) are highly related to immuni...
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