用于鉴定铜绿假单胞菌的分子靶标及其定量检测方法

By using novel molecular targets and their primer sets for PCR and qPCR methods, the problems of long testing cycles and inaccurate results in the detection of Pseudomonas aeruginosa have been solved, enabling rapid and accurate identification and quantification of Pseudomonas aeruginosa, thus improving detection efficiency and accuracy.

CN117327817BActive Publication Date: 2026-07-17GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY +1

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY
Filing Date
2021-12-20
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing technologies for detecting Pseudomonas aeruginosa suffer from problems such as long testing cycles, inaccurate results, and poor specificity, making it difficult to quickly and accurately identify and quantify Pseudomonas aeruginosa.

Method used

Novel and highly specific molecular targets and their corresponding PCR and qPCR methods were used to screen molecular targets of SEQ ID NO.1 to SEQ ID NO.4 through pan-genome analysis, and corresponding primer sets were designed for the identification and quantitative detection of Pseudomonas aeruginosa.

Benefits of technology

It enables rapid and accurate detection of Pseudomonas aeruginosa with a coverage rate of up to 100%. The detection time is short, the cost is low, the results are easy to interpret, the specificity is high, the stability is good, and the detection time is shortened from 3 to 5 days in traditional methods to about 15 hours.

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Abstract

本发明公开了用于铜绿假单胞菌鉴定的分子靶标及其检测方法,属于微生物技术领域。本发明的用于铜绿假单胞菌鉴定的分子靶标,所述分子靶标的序列如SEQ ID NO.1~SEQ ID NO.4任一项所示。本发明的分子靶标可检测到更多的铜绿假单胞菌,铜绿假单胞菌覆盖率更大,增强了实用性;本发明的检测方法针对铜绿假单胞菌检测具有操作简单、结果判定易、检测时间短、特异性强、成本低、稳定性好的优点。
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