Primer combinations and detection kits for identifying 33 serotypes of Streptococcus suis
A detection kit and primer combination technology, applied in the field of molecular biology, can solve the problems of incomplete understanding of information, time-consuming and laborious, molecular typing methods have not been implemented into detection systems, etc., and achieve optimized detection procedures, simplified detection steps, and good market. The effect of the application foreground
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Embodiment 1
[0028] Example 1 Determination of 33 serotype-specific genes of Streptococcus suis and the design of primers
[0029] 1. The 33 reference strains were obtained from the International Reference Laboratory of Streptococcus suis strains (the laboratory of Professor Marcelo Gottschalk, University of Montreal, Canada) for sequencing. The strains were cultured overnight at 37°C on a Columbia plate, and single-clonal colonies were picked and inoculated in THB medium, and cultured with shaking at 37°C for 8 hours.
[0030]2. Whole genome sequencing and interception of cps gene cluster. Genomic DNA was extracted and purified using Wizard Genomic DNA Purification kit (Promega, Madison, USA). After sequencing the strain genome with Illumina Solexa GAIIx (Illumina, San Diego, CA), a paired-end (PE) library with an average insert length of 500bp-2000bp was constructed, and the data was assembled with SOAP denovo (Release1.04). The cps gene clusters of each serotype were intercepted from ...
Embodiment 2
[0038] Embodiment 2 detects the establishment of 33 kinds of serotypes of Streptococcus suis mPCR method
[0039] Using the primers of Example 1, using the genomic DNA of 33 serotype reference bacterial strains of Streptococcus suis in Example 1 as a template, and double-distilled water without nucleic acid as a negative control, first carry out single-plex PCR amplification to each pair of primers, Check its specificity. It was found that in single-plex PCR, the serotypes corresponding to each pair of primers had 100% specificity, and then a multiplex PCR method was established to detect 33 serotypes of Streptococcus suis.
[0040] Considering the practicability and ease of operation, this embodiment divides the multiplex PCR method into three detection systems A, B, and C. System A is used to detect the most common serotypes in clinical isolates, 1-10, 14 and Type 1 / 2; System B detects types 11-21 (except type 14); system C detects types 22-31 and 33. The DNA of 33 referen...
Embodiment 3
[0042] The specificity verification of the mPCR detection method of 33 kinds of serotypes of Streptococcus suis of embodiment 3
[0043] With 33 reference strains of Streptococcus suis as detection objects, the specificity of the mPCR method of the present invention is detected in conjunction with the following strains: Klebsiella pneumoniae (Klebsiella pneumoniae) 46117-3 and other Streptococcus genus including 6 strains of Streptococcus pneumoniae ) ATCC700657, ATCC700670, ATCC700676, ATCC700902, ATCC700906 and ATCC49619, Streptococcus pyogenes 32003, Streptococcus sanguis 32214, Enterococcus faecalis 32221, 3 Streptococcus bovis, 3 Streptococcus bovis Streptococcus bovis ATCC33317, Streptococcus lutetiensis 033 and 2 strains of Streptococcus orisratti originally considered to be Streptococcus suis 32 (strain EA1172.91) and 34 (strain92-2742) types.
[0044] However, there was no non-specific amplification band in the detection of 1 strain of Klebsiella pneumoniae (Klebsiell...
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