CN1178838A - Method for bacterial sensitivity test to medicine - Google Patents
Method for bacterial sensitivity test to medicine Download PDFInfo
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- CN1178838A CN1178838A CN 97107762 CN97107762A CN1178838A CN 1178838 A CN1178838 A CN 1178838A CN 97107762 CN97107762 CN 97107762 CN 97107762 A CN97107762 A CN 97107762A CN 1178838 A CN1178838 A CN 1178838A
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Abstract
By using 5 mg/ml concentration thiazole blue compounded with pH 7.2-7.4 phosphate buffering solution as test reagent, both bacterial suspension and antiseptic solution of standard concentration are maintained at 35-37 deg. c routine condition for 2-5 hr, then bacterial suspension is mixed with the test reagent in the volume ratio of 20 to 1 with the initial concentration of bacterial suspension being not lower than 1,500,000/ml, and the color reation is used to judge the bacterial sensitivity to medicine quality and quantity.
Description
What the present invention relates to is a kind of method of medically bacterium being done drug sensitivity test.Be that malignant bacteria to the live body form carries out the method to the colour developing/colorimetric of drug sensitivity test more specifically.
Various malignant bacterias are different to the susceptibility of antibacterials.Measure the sensitivity of bacterium, select, so that control infection timely and effectively has great importance for the medication in the clinical treatment to different pharmaceutical.Present bacterium can have diffusion process and dilution method two classes to the medicament sensitivity test method.Commonly used in the diffusion process have paper disk method, a paper disk method (with the TTC method of chlorinated triphenyl tetrazole) etc. fast, all is after test solution being done 18～24 hours cultivation, judges by the size of measuring inhibition zone whether bacterium is responsive to medicine.These class methods can only be measured usually qualitatively, are only matching with dilution method, after regression analysis obtains the regression equation of correlationship between its antibacterial circle diameter and MIC (minimal inhibitory concentration) by statistics, just can be used for detection by quantitative.Tube dilution method, trace liquid diluting method etc. are arranged in the dilution method, though can overcome the shortcoming of diffusion process, can make quantitative or semiquantitative MIC measures, but it equally also all will have 18～24 hours culturing process, and be that whether muddiness is come result of determination by observing bacterium liquid, susceptibility is poor, is difficult to find that 10% change is arranged.
The objective of the invention is at above-mentioned situation, provide a kind of energy fast, accurately, convenient and carry out the qualitative and quantitative measuring method of bacterium intuitively to drug sensitivity test.
The method that is used for bacterium to drug sensitivity test of the present invention is that the concentration that is mixed with in the phosphate buffered saline buffer with pH7.2-7.4 is that the tetrazolium bromide of 5 mg/ml is a detection reagent.With the antibiotic of bacteria suspension and normal concentration insulation effect after 2～5 hours under 35 ℃～37 ℃ conventional constant temperatures, by bacteria suspension: the detection reagent volume ratio is that 20: 1 amount is mixed the initial concentration of bacteria suspension 〉=1.5 * 10 with detection reagent
6/ milliliter carries out the qualitative or quantitative judgement of bacterium to drug susceptibility with its color reaction.Concrete decision method can adopt the naked eyes direct observational method, or with the method for its optical density(OD) of spectrophotometric determination (OD) value.
If adopt the method for naked eyes direct viewing, the bacteria suspension Cmin of its used sample can be 1.5 * 10
6/ milliliter after normal concentration antibiotic mixes, in 35～37 ℃ of conventional constant temperature insulations 2～5 hours, adds detection reagent again, places～10 minutes down in room temperature condition, and whether this recombined sample of direct viewing has blue color reaction.Do not show blueness as sample and still remain colourless state, show that wherein not having viable bacteria exists; If show blue, then be judged to be viable bacteria and existed.Because the test orifice plate is white usually, under this background color, the minor variations of this blue color reaction all can very obviously and be easy to observe differentiate.Thereby it not only can be used as simply and intuitively qualitative judgement, can also be easy to according to a conventional method, by the direct viewing blue color reaction of each recombined sample of arranging of antibiotic concentration gradient routinely, to make the quantitative judgement of medicine minimal inhibitory concentration value with this sample that do not develop the color of blue sample institute adjacency.
If adopt instrument to quantitatively judge, the initial concentration of used sample bacteria suspension can be 1 * 10
6/ milliliter.After normal concentration antibiotic mixes, in 35～37 ℃ of conventional constant temperature insulations 2～5 hours, add detection reagent, after 35 ℃～37 ℃ conventional constant temperatures are incubated 30～60 minutes down, by the bacterium liquid measure: the dimethyl sulfoxide (DMSO) volume ratio is to add dimethyl sulfoxide (DMSO) and mixing at 1: 2, surveys 510～530 nanometers, the preferably optical density value of 520 nanometers with spectrophotometer, with the typical curve contrast, can make the quantitative judgement of medicine minimal inhibitory concentration value.
The chemical name of tetrazolium bromide is: 3-(4,5)-two methyl-2-thiazole-(2,5)-phenylbenzene bromination tetrazolium (being called for short MTT) is yellow powder.Now only in the diagnoses and treatment of tumour, be used to the mensuration of aspects such as pair cell poison mensuration, zooblast survival and proliferative response.Thinking at present that its action principle is based on xanchromatic MTT can be by the mitochondrial dehydrogenase in the living mammalian cells, be reduced into blue De Jia Za (Formazan) as succinodehydrogenase and diaphorase etc., and its growing amount is directly proportional with the quantity and the vigor of viable cell, dead cell or red corpuscle do not have this ability, and the activatory cell can produce more first a ceremonial jade-ladle, used in libation than immobilized cell.But thereby carry out determination and analysis by the quantity and the metabolic power thereof of colorimetric analysis method pair cell.Because bacterium and mammiferous cell are the diverse cells of two classes, bacterium does not have the peculiar plastosomes of high eukaryotic cell such as mammalian cell for the low prokaryotic cell prokaryocyte that waits.Thereby the MTT staining of this reflection growth and proliferation of cell and survival condition is considered to always and can only be used for mammiferous cell detection such as the mankind.
The present invention passes through streptococcus aureus, micrococcus scarlatinae, staphylococcus epidermidis, intestinal bacteria, enterobacter cloacae, Klebsiella pneumonia, proteus vulgaris, Pseudomonas aeruginosa, Salmonella typhimurium, ATCC reference cultures such as serratia marcescens, streptococcus aureus, intestinal bacteria, clinical isolates strains such as Pseudomonas aeruginosa, the contaminated bacteria of cell culture fluid, contaminated bacteria in the tumour patient ascites, anerobes such as bifidus bacillus, and multiple common bacteria such as some moulds is tested the back and is found, the bacterium alive of these bacteriums can be dyed blueness by MTT equally, and dead bacterium then can not be colored.The dyed back microscopic examination of viable bacteria, it is blue that thalline is, and it is blue that bacterium liquid also is, and its shade becomes positive correlation with bacterial concentration; Optical density(OD) (OD) value and the bacterial concentration relation of being in line with the spectrophotometer colorimetric analysis.
For further investigating the reliability that aforesaid method of the present invention is measured, tested bacterium liquid sample has been carried out the test of heat treated to the survival rate influence.With meat soup streptococcus aureus (ATCC 25923) and intestinal bacteria (ATCC) all being diluted to concentration is 1 * 10
8Behind/the milliliter, when 60 ℃ of temperature, heat different time respectively, and in 30 minutes with after the differing temps heat treated, again by the bacterium liquid measure: the amount of MTT detection reagent=20: 1 adds above-mentioned detection reagent, effect is 30 minutes under the room temperature, the doubling dose of pressing volume of sample again adds dimethyl sulfoxide (DMSO) and mixing, separately bacteria living rate under two kinds of test conditionss of OD value calculating of 520 nano wave length colorimetrics.Test-results respectively as shown in Table 1 and Table 2.This result demonstrates, the temperature height of the OD value of its blue depth and colorimetric analysis and heating and action time length all become positive correlation.
The bacteria living rate test-results of 60 ℃ of following different heating times of table 1
| Heat-up time (minute) | 0 | ????5 | ????10 | ????15 | ????20 | ????25 | ????30 |
| Streptococcus aureus (survival rate %) | 100 | ????25 | ????21 | ????13 | ????13 | ????11 | ????9 |
| Intestinal bacteria (survival rate %) | 100 | ????91 | ????76 | ????61 | ????63 | ????61 | ????56 |
30 minutes bacteria living rate test-results of heating under table 2 differing temps
| Heating temperature (℃) | 0 | ?50 | ????60 | ????70 | ????80 | ????90 | ????100 |
| Streptococcus aureus (survival rate %) | 100 | ?51 | ????11 | ????8 | ????2 | ????0.1 | ????0.005 |
| Intestinal bacteria (survival rate %) | 100 | ?83 | ????50 | ????47 | ????10 | ????5 | ????0.1 |
Chemostefilant commonly used, when acting on bacterium liquid as formaldehyde, bromogeramine, 75% ethanol, Swashes, Swashes etc., the shade after MTT adds wherein and the OD value of colorimetric analysis are all with the concentration of these sterilizing agents and become positive correlation action time.With the bromogeramine is example, above-mentioned bacterium liquid of the same race was all handled 60 minutes with the bromogeramine of different concns respectively, after all handling different time with 1% bromogeramine, do the processing of adding MTT detection reagent by above-mentioned same procedure after, calculate under two kinds of test conditionss separately bacteria living rate test-results in the OD value of 520 nano wave length colorimetrics, respectively shown in table 3 and table 4.Situation and above-mentioned test when test also shows with ozonize are similar.
Table 3 different concns bromogeramine is handled the bacteria living rate test-results after 60 minutes
| Bromogeramine concentration (%) | ??0 | ????0.1 | ????1 | ????10 |
| Streptococcus aureus (survival rate %) | ??100 | ????100 | ????13 | ????0.002 |
| Intestinal bacteria (survival rate %) | ??100 | ????100 | ????20 | ????0.002 |
The bacteria living rate test-results of 1% bromogeramine different treatment time of table 4
| Treatment time (minute) | ????30 | ????60 | ????90 | ????120 |
| Streptococcus aureus (survival rate %) | ????43 | ????17 | ????6 | ????1 |
Above-mentioned test-results fully shows, as detection reagent, when bacterium is carried out blue dyeing, has only bacterium alive just to be colored with MTT, and dead bacterium then is not colored.Coming to the same thing of this result and present conventional dilution method, thereby this MTT method of the present invention can be applied to bacterium is carried out the mensuration of medicament sensitivity test fully.By revision test repeatedly, the detected result quite stable of the inventive method, the result of revision test is almost completely consistent, and the repetition rate of test-results is 100% substantially.Do to measure the parallel test of M1C with the inventive method and conventional dilution method, the goodness of fit of its MIC that surveys reaches can 95%, the qualitative drug sensitivity test result of shown bacterium (resistance, medium sensitivity, extremely responsive) is then in full accord, and just its MIC is than low 1-2 the extent of dilution of ordinary method.Thereby show that MTT method that the present invention is above-mentioned and present ordinary method can obtain basically identical and identical detection result of determination when bacterium is carried out medicament sensitivity test.Owing to the inventive method is to carry out in the colour developing mode, and the blueness that is shown is obvious and be easy to the observation resolution, can make its diffusion process and dilution method more used than present routine have many-sided superiority.For example, the time that present above-mentioned ordinary method is measured needs 18～24 hours usually, and the above-mentioned MTT method of the present invention then is no more than 5 hours; Above-mentioned conventional dilution method is by whether muddiness realizes to bacterium liquid in each test hole to result's judgement, and is not directly perceived, and the above-mentioned MTT method of the present invention then is to realize by the blue color reaction under each test hole white background; The accuracy of MTT method of the present invention and susceptibility are all very high, are difficult for the test hole of judgement during above-mentioned conventional dilution method is detected, and by adding the MTT detection reagent, whether observation blueness occurs can accurately be decision making.Therefore MT reconnaissance T method of the present invention is compared with present conventional sense method, obviously have more fast, accurately, conveniently and intuitively, particularly the advantage that can make the judgement of quantitative property with direct viewing mode easily has great practical value and meaning aspect medical test.
What below introduce is the example that further describes as to foregoing of the present invention.But this should be interpreted as that the scope of the above-mentioned theme of the present invention only limits to following example.The compound method of used MTT detection reagent is in each example: commercially available MTT is dissolved in the phosphate buffered saline buffer of pH7.2-7.4, is mixed with the solution that concentration is 5 mg/ml, and after millipore filtration (0.22 micron) filters, standby in-20 ℃ of preservations.
Example 1
With the inventive method and conventional micro-dilution method the medicaments insensitive situation of streptococcus aureus reference culture (ATCC 25932) is compared test.
Conventional micro-dilution method adopts " magnificent refreshing susceptibility detection kit " by the development of China refreshing medicine company limited-liability company, by the method operation of its specification sheets regulation.Whether cultivate after 22 hours in the vision slit sample muddy.
It is 1.5 * 10 that the inventive method each Kong Zhongjun of existing normal concentration antibiotic on this drug sensitive plate adds concentration
6The bacterium liquid of/milliliter after 35～37 ℃ of routines are hatched 5 hours, all adds above-mentioned standby MTT detection reagent 5 microlitres respectively and mixes in each hole of test panel, placed 10～30 minutes down in room temperature condition, whether shows blue with sample in the eye direct viewing hole.
The test-results of two kinds of methods and judgement conclusion are as shown in table 5.This experimental result shows, though two kinds of methods slightly little difference on the concrete MIC value of some drugs then is on all four to the medicaments insensitive sex determination conclusion of bacterium.
Example 2
With the inventive method and conventional micro-dilution method the medicaments insensitive situation of enterobacter cloacae reference culture (ATCC 23355) is compared test.
The same example of operation of conventional micro-dilution method is cultivated after 24 hours in the vision slit whether muddiness of sample.
Also the same example of the operation of the inventive method, after cultivating 5 hours and adding detection reagent, whether sample shows blue in the vision slit.
The test-results of two kinds of methods and judgement conclusion are as shown in table 6.This experimental result shows, though two kinds of methods slightly little difference on the concrete MIC value of some drugs equally also is on all four to the medicaments insensitive sex determination conclusion of bacterium.
Two kinds of methods of table 5 are to the drug sensitivity test result of streptococcus aureus
| Trial drug | Ordinary method | The inventive method | ||
| MIC (mg/litre) | Judge conclusion | MIC (mg/litre) | Judge conclusion | |
| Sulfamethoxazole | ????512 | Resistance | ????512 | Resistance |
| Fortum | ????16 | Medium sensitivity | ????16 | Medium sensitivity |
| Cephradine | ????2 | Extremely responsive | ????8 | Extremely responsive |
| Norvancomycin | ????1 | Extremely responsive | ????＜0.5 | Extremely responsive |
| U-10149 | ????0.5 | Extremely responsive | ????＜0.25 | Extremely responsive |
Two kinds of methods of table 6 are to the drug sensitivity test result of enterobacter cloacae
| Trial drug | Ordinary method | The inventive method | ||
| MIC (mg/litre) | Judge conclusion | MIC (mg/litre) | Judge conclusion | |
| To acillin | ????8 | Extremely responsive | ????4 | Extremely responsive |
| To Pipril | ????16 | Extremely responsive | ????8 | Extremely responsive |
Claims (5)
1. method that is used for bacterium to drug sensitivity test, it is characterized in that the concentration that is mixed with in the phosphate buffered saline buffer with pH7.2-7.4 is that the tetrazolium bromide of 5 mg/ml is a detection reagent, with the antibiotic of bacteria suspension and normal concentration insulation effect after 2～5 hours under 35 ℃～37 ℃ conventional constant temperatures, by bacteria suspension: the detection reagent volume ratio is that 20: 1 amount is mixed the initial concentration of bacteria suspension 〉=1.5 * 10 with detection reagent
6/ milliliter carries out the judgement of bacterium to drug susceptibility with its color reaction.
2. bacterium as claimed in claim 1 is characterized in that to the method for drug sensitivity test said bacteria suspension initial concentration is 1.5 * 10
6/ milliliter, be mixed in 35～37 ℃ of conventional constant temperature insulations 2～5 hours with normal concentration antibiotic, add detection reagent again after room temperature condition is placed～10 minutes down, each recombined sample of direct viewing is to have blue color reaction as the qualitative judgement that has viable bacteria to exist.
3. bacterium as claimed in claim 2 is characterized in that to the method for drug sensitivity test said bacteria suspension concentration is 1.5 * 10
6/ milliliter, be mixed in 35～37 ℃ of conventional constant temperature insulations 2～5 hours with normal concentration antibiotic, add detection reagent again after room temperature condition is placed～10 minutes down, direct viewing is the blue color reaction of each recombined sample of arranging of standard antibiotic concentration gradient routinely, to do the quantitative judgement of medicine minimal inhibitory concentration value with this sample that do not develop the color of blueness colour developing sample institute adjacency.
4. bacterium as claimed in claim 1 is characterized in that to the method for drug sensitivity test said bacteria suspension concentration is 1 * 10
6/ milliliter, be mixed in 35～37 ℃ of conventional constant temperature insulations 2～5 hours with normal concentration antibiotic, add detection reagent again and continue insulation after 30～60 minutes, by the bacterium liquid measure: the dimethyl sulfoxide (DMSO) volume ratio is to add dimethyl sulfoxide (DMSO) and mixing at 1: 2, does the quantitative judgement of medicine minimal inhibitory concentration value with the optical density value of spectrophotometer 510～530 nanometers.
5. bacterium as claimed in claim 4 is to the method for drug sensitivity test, it is characterized in that doing with the optical density value of 520 nanometers of said spectrophotometer the quantitative judgement of medicine minimal inhibitory concentration value.
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| Application Number | Priority Date | Filing Date | Title |
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| CN97107762A CN1065918C (en) | 1997-11-05 | 1997-11-05 | Method for bacterial sensitivity test to medicine |
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| CN97107762A CN1065918C (en) | 1997-11-05 | 1997-11-05 | Method for bacterial sensitivity test to medicine |
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| CN1178838A true CN1178838A (en) | 1998-04-15 |
| CN1065918C CN1065918C (en) | 2001-05-16 |
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101852765A (en) * | 2010-05-06 | 2010-10-06 | 解宇 | Device and method for judging bacterium drug susceptibility by utilizing oxidation reaction of bacterium |
| CN101200755B (en) * | 2007-12-05 | 2011-06-22 | 华南农业大学 | Bacterium identification reagent kit as well as preparation method and uses thereof |
| CN102507567A (en) * | 2011-11-22 | 2012-06-20 | 鲁东大学 | Bacterial quantitative colorimetric card as well as preparation method and application method thereof |
| CN102519954A (en) * | 2011-11-22 | 2012-06-27 | 鲁东大学 | Bacteria quantitative colorimeter and preparation and application method thereof |
| CN101760502B (en) * | 2010-01-28 | 2013-04-24 | 中国检验检疫科学研究院 | Method for rapidly determining drug tolerance of strain |
| CN103760159A (en) * | 2014-01-24 | 2014-04-30 | 山东鑫科生物科技股份有限公司 | Method and system for identifying bacteria and analyzing drug sensitivity |
| CN106282299A (en) * | 2015-05-14 | 2017-01-04 | 北京中医药大学 | A kind of method of external artificial acquisition bacterial resistance bacterial strain |
| WO2019063990A1 (en) * | 2017-09-28 | 2019-04-04 | Microbiosensor Limited | Devices and methods for detection of microorganisms |
| US10689226B2 (en) | 2015-02-04 | 2020-06-23 | Otis Elevator Company | Position determining system for multicar ropeless elevator system |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN2156509Y (en) * | 1993-04-22 | 1994-02-16 | 金华钧 | Plate chip for testing sensitivity of bacteria to medicine |
-
1997
- 1997-11-05 CN CN97107762A patent/CN1065918C/en not_active Expired - Fee Related
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101200755B (en) * | 2007-12-05 | 2011-06-22 | 华南农业大学 | Bacterium identification reagent kit as well as preparation method and uses thereof |
| CN101760502B (en) * | 2010-01-28 | 2013-04-24 | 中国检验检疫科学研究院 | Method for rapidly determining drug tolerance of strain |
| CN101852765A (en) * | 2010-05-06 | 2010-10-06 | 解宇 | Device and method for judging bacterium drug susceptibility by utilizing oxidation reaction of bacterium |
| CN102507567A (en) * | 2011-11-22 | 2012-06-20 | 鲁东大学 | Bacterial quantitative colorimetric card as well as preparation method and application method thereof |
| CN102519954A (en) * | 2011-11-22 | 2012-06-27 | 鲁东大学 | Bacteria quantitative colorimeter and preparation and application method thereof |
| CN102519954B (en) * | 2011-11-22 | 2015-07-22 | 鲁东大学 | Bacteria quantitative colorimeter and preparation and application method thereof |
| CN102507567B (en) * | 2011-11-22 | 2016-01-20 | 鲁东大学 | Bacteria quantified colorimetric card and preparation thereof, using method |
| CN103760159A (en) * | 2014-01-24 | 2014-04-30 | 山东鑫科生物科技股份有限公司 | Method and system for identifying bacteria and analyzing drug sensitivity |
| US10689226B2 (en) | 2015-02-04 | 2020-06-23 | Otis Elevator Company | Position determining system for multicar ropeless elevator system |
| CN106282299A (en) * | 2015-05-14 | 2017-01-04 | 北京中医药大学 | A kind of method of external artificial acquisition bacterial resistance bacterial strain |
| WO2019063990A1 (en) * | 2017-09-28 | 2019-04-04 | Microbiosensor Limited | Devices and methods for detection of microorganisms |
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|---|---|
| CN1065918C (en) | 2001-05-16 |
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