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Pseudomonas aeruginosa chromogenic culture medium and method for quick detection by same

A technology of Pseudomonas aeruginosa and chromogenic culture medium, which is applied in the directions of microorganism-based methods, biochemical equipment and methods, measuring devices, etc., and can solve the problems of missed judgment, misjudgment, time-consuming and laborious, judgment, etc.

Pending Publication Date: 2019-08-16
上海源本食品质量检验有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] There may be Pseudomonas aeruginosa or other interfering interfering bacteria in the water sample. Therefore, after the above method is used to filter and culture the water sample for 24h to 48h, interfering colonies will usually appear, that is, fluorescent (non-blue / green) colonies or red colonies will appear. For brown colonies, it takes at least 1-5 days for further biochemical experiments to determine whether these colonies are Pseudomonas aeruginosa. The comprehensive detection time takes about 5-7 days, which is very time-consuming and laborious; and in After culture, the colonies of Pseudomonas aeruginosa and other interfering bacteria need to be judged by the naked eye of a professional experimenter on the color and shape of the colony. Colony fusion may occur if the colony is overgrown, which is a test of whether the experimenter has rich work experience. When Pseudomonas aeruginosa mutates, the shape and color of the colony change, it is difficult to judge from the color and shape of the colony, and it is easy to cause missed judgments and misjudgments

Method used

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  • Pseudomonas aeruginosa chromogenic culture medium and method for quick detection by same
  • Pseudomonas aeruginosa chromogenic culture medium and method for quick detection by same
  • Pseudomonas aeruginosa chromogenic culture medium and method for quick detection by same

Examples

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Effect test

Embodiment 1

[0072] Embodiment 1: A kind of Pseudomonas aeruginosa chromogenic culture medium, its preparation method is: add basal medium formula, with peptone 15.0g; Yeast extract 8.0g; Potassium sulfate 10.0g, magnesium chloride 1.4g, directly add distilled water Dilute to 1L, heat slightly to dissolve completely; then add 0.5g of chromogenic substrate 2,3,5-phenyltetrazolium chloride, add chromogenic substrate 4-methylumbelliferone-D-glucose Add aldoside 0.01g, add bacteriostatic agent nalidixic acid 0.015g, adjust pH=7.2±0.2 at 25°C after mixing, finally add agar 15.0g, boil to dissolve completely, cool to about 50°C and pour plate, Prepare Pseudomonas aeruginosa chromogenic medium, recover Pseudomonas aeruginosa (ATCC 9027) overnight in nutrient broth, prepare 10 5 The CFU bacterial suspension was transferred to Pseudomonas aeruginosa chromogenic medium, cultivated in an incubator at 36±1°C for 24 hours, and observed.

Embodiment 2-7

[0073] Embodiment 2-7: A chromogenic medium for Pseudomonas aeruginosa, the difference from Example 1 lies in that the strains inoculated on the chromogenic medium for Pseudomonas aeruginosa are different. See Table 1 for details, where "+" means added, and "-" means not added.

[0074] Table 1 embodiment 2-7 bacterial species specificity test

[0075]

[0076]

Embodiment 8

[0077] Example 8: A chromogenic medium for Pseudomonas aeruginosa, the difference from Example 1 is that no chromogenic substrate 4-methylumbelliferone-D-glucuronide is added.

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PUM

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Abstract

The invention relates to the technical field of pseudomonas aeruginosa detection and discloses a pseudomonas aeruginosa chromogenic culture medium and a method for quick detection by the same. The pseudomonas aeruginosa chromogenic culture medium comprises a basic medium, a chromogenic substrate and an antibacterial agent. The chromogenic substrate comprises 2,3,5-phenyl tetrazolium chloride, 4-methyl umbelliferone-D-glucuronide, and the antibacterial agent comprises nalidixic acid, cycloserine and bile salt. 2,3,5-phenyl tetrazolium chloride acts on a pseudomonas aeruginosa metabolite to showa red color; 4-methyl umbelliferone-D-glucuronide acts on pseudomonas aeruginosa to show fluorescence under a 366nm ultraviolet lamp; by joint action of 2,3,5-phenyl tetrazolium chloride and the antibacterial agent, growth of common disturbance bacteria can be inhibited, and false positive results are avoided. By adoption of the pseudomonas aeruginosa quick detection method, detection and count of pseudomonas aeruginosa can be finished in 24h, and time saving, labor saving, stability, reliability and high sensitivity are realized.

Description

technical field [0001] The invention relates to the technical field of Pseudomonas aeruginosa detection, more specifically, it relates to a chromogenic culture medium for Pseudomonas aeruginosa and a method for rapid detection thereof. Background technique [0002] Pseudomonas aeruginosa (Pseudomonas aeruginosa) belongs to the genus Pseudomonas, is widely distributed in nature, can survive in water for a long time, and is considered to be a water-borne conditional pathogen; Pseudomonas aeruginosa can cause Diarrhea and other diseases in normal people, patients with metabolic diseases, blood diseases and malignant tumors, as well as postoperative patients or patients after certain treatments are susceptible to infection with this bacteria; this bacteria often causes postoperative wound infections, and can also cause bedsores, abscesses, suppuration Infection lesions caused by this bacterium can lead to hematogenous dissemination, resulting in bacteremia and sepsis. Infection ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/04C12Q1/06C12R1/385
CPCC12Q1/045C12Q1/06G01N2333/21
Inventor 蒋曙光薛亮曹琥靓陈李帆张晨俍陈昌经
Owner 上海源本食品质量检验有限公司
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