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77 results about "Salmonella frintrop" patented technology

Vectors for the diagnosis and treatment of solid tumors including melanoma

The present invention is directed to the isolation and use of super-infective, tumor-specific vectors that are strains of parasites including, but not limited to bacteria, fungi and protists. In certain embodiments the parasites include, but are not limited to, the bacterium Salmonella spp., such as Salmonella typhimurium, the bacterium Mycobacterium avium and the protozoan Leishmania amazonensis. In other embodiments, the present invention is concerned with the isolation of super-infective, tumor-specific, suicide gene-containing strains of parasites for use in treatment of solid tumors.
Owner:YALE UNIV

Genetically modified tumor-targeted bacteria with reduced virulence

The present invention is directed to mutant Salmonella sp. having a genetically modified msbB gene in which the mutant Salmonella is capable of targeting solid tumors. The invention is also directed to Salmonella sp. containing a genetically modified msbB gene as well as an genetic modification in a biosynthetic pathway gene such as the purl gene. The present invention further relates to the therapeutic use of the mutant Salmonella for growth inhibition and / or reduction in volume of solid tumors.
Owner:YALE UNIV +1

Visual detection method for mouse typhus salmonella based on aptamer recognition

The invention provides a visual detection method for mouse typhus salmonella based on aptamer recognition. The basic principle of the method is that the surface of a microwell plate is coated with avidin, sulfhydrylation salmonella aptamer which is marked by biotinylation salmonella aptamer and nanogold is adopted to recognize targeted salmonella, and on the basis, a silver enhancement technique is utilized to further amplify a detection signal, so that the visual detection is achieved. The visual detection method for the mouse typhus salmonella based on the aptamer recognition has the advantages of high specificity, strong sensitivity, simplification and rapidness, thereby providing the possibility for rapidly detecting the mouse typhus salmonella in an environment.
Owner:JIANGNAN UNIV +1

Fluorescence quantitative PCR (polymerase chain reaction) detection kit for salmonella and detection method thereof

The invention relates to a fluorescence quantitative PCR (polymerase chain reaction) detection kit for salmonella, comprising a salmonella PCR reaction liquid, a Taq enzyme, a positive control and a negative control. The sequences of the specific primers of the fluorescence quantitative PCR detection kit for salmonella are as follows: the upstream primer is 5'-TGCGCCTGCCGTTATCAC-3'; the downstream primer is 5'-ATTTGAGCTGTTGGTTCAGTAACTC-3'; and the fluorescence probe sequence is 5'-CCAACGCCGCAGATATTTGATCGCC-3'. The detection for salmonella in a clinical excrement by using the kit disclosed by the invention has great specificity, sensitivity and stability, the whole detection process can be finished in 2-3 hours, and salmonella in foods or other cultures also can be rapidly and accurately detected.
Owner:广州华银医学检验中心有限公司

Aptamer based salmonella typhimurium detection biosensor and preparation method thereof

The invention relates to an aptamer based salmonella typhimurium detection biosensor and a preparation method thereof. Signal amplification is realized by continuous generation and cyclic utilization of Primer, and consequently high-sensitivity detection of salmonella typhimurium is realized, and lower detection limit can be acquired. The aptamer based salmonella typhimurium detection biosensor is high in specificity and sensitivity, low in cost and quick in detection. By the detection method, a salmonella typhimurium detection limit is 5-15cfu / mL, and a detection range is 1*10-1*107cfu / mL.
Owner:UNIV OF JINAN

RPA primer, probe and detection method for detecting salmonella

The invention provides a RPA primer, probe and detection method for detecting salmonella. A primer sequence of the RPA primer is as follows: for an iroB gene: an upstream primer SEQ ID No.1:5'-GGAATGTCATACTTAGCGGGTTTGACACGAGC-3', and a downstream primer SEQ ID No.2:5'-GGTGGTATTTGACGCTGGCGGTGCAAACCT-3'. According to the invention, an RPA technology is combined with fluorescence detection, the salmonella can be quickly and accurately detected. By adopting the method, the salmonella can be specifically detected from common pathogenic bacteria, thereby providing a technical support for rapid detection of the salmonella, and at the same time, the investment of expensive instruments can be eliminated, and the method is convenient for popularization and use at the grassroots level.
Owner:深圳市计量质量检测研究院(国家高新技术计量站国家数字电子产品质量监督检验中心)

Salmonella enterica presenting c. jejuni n-glycan or derivatives thereof

The present invention relates to Salmonella enterica comprising at least one pgl operon of Campylobacter jejuni or a functional derivative thereof and presenting at least one N-glycan of Campylobacter jejuni or N-glycan derivative thereof on its cell surface. In addition, it is directed to medical uses and pharmaceutical compositions thereof as well as methods for treating and / or preventing Campylobacter and optionally Salmonella infections and methods for producing these Salmonella strains.
Owner:ETH ZZURICH

Method for rapidly detecting quinolone-resistant Salmonella spp. and the probes and primers utilized therein

The present invention relates to a method for rapidly detecting quinolone-resistant Salmonella spp. The invention also relates to the oligonucleotide primers and probes utilized in the method, which can differentiate mutant strains having one or two single point mutations in gyrA gene or single point mutation in parC gene from wild type strains, respectively. Said primers and probes can be effectively used for detection of nalidixic acid-resistant and / or ciprofloxacin-resistant Salmonella strains.
Owner:BUREAU FOOD & DRUG ANALYSIS DEPT HEALTH EXECUTIVE YUAN TAIWAN R O C

Multiple fluorescence quantitative PCR method for simultaneous and fast detecting three types of pathogenic bacteria in food

The invention belongs to the technical field of food quality safety detection, and particularly relates to a method in which the processes of fast extraction of co-enrichment and bacterium gene groups and multiple Taqman fluorescence quantitative PCR are used to carry out simultaneous and fast detection on salmonella, staphylococcus aureus and shigella in food and a recombined positive internal reference DNA is designed to monitor PCR reaction so as to guarantee the accuracy of a detected result. The result proves that the method has good specificity for target pathogenic bacteria, the detection limit can reach 101cfu / PCR, and all components of a reaction system do not generate cross interference. Blind sample detection on artificially contaminated foods verifies the practicability of the method. Positive internal reference DNA effectively guarantees the reliability of detection, and avoids the occurrence of false negative results. In conclusion, the invention establishes a multiple fluorescence quantitative PCR method for simultaneous and fast detecting staphylococcus aureus, salmonella and shigella in the food, and provides a new method for high-throughput detection of food origin diseases.
Owner:NANJING INST OF PROD QUALITY INSPECTION

Fowl salmonella gallinarum attenuated isolated strain and application thereof

The invention relates to a fowl salmonella gallinarum attenuated isolated strain and application thereof. The isolated strain is preserved in the China General Microbiological Culture Collection Center, Beijing, China, on July 2, 2018, has a preservation number of CGMCC No.16049, and is classified and named as Salmonella Gallinarum. The strain is attenuated to chicken of different ages, is apathogenic, and can be used as a strain vector for preventing livestock salmonella gallinarum infection and preventing infectious diseases of livestock (chicken). The fowl salmonella gallinarum attenuated isolated strain provides data reference to evaluating the toxicity of salmonella attenuated vaccine strains and potential as the strain vector of livestock (chicken) live vaccines.
Owner:YANGZHOU UNIV

Salmonella typhimurium bacteriophage T156 and application thereof

ActiveCN111944766AOvercoming the disadvantages of isotype specificityImprove the bactericidal effectBiocideMicroorganism based processesSalmonella frintropBacteriophage
The invention discloses a salmonella typhimurium bacteriophage T156 and application thereof. The bacteriophage is a broad-spectrum type, can split salmonella and a drug-resistant strain thereof, and is identified as a caudal bacteriophage long-tail bacteriophage family; and the bacteriophage T156 has stable titer with the pH of 3-12 and the temperature of 30-50 DEG C. The bacteriophage provided bythe invention can be used for effectively controlling salmonella typhimurium ATCC 13311 in a food sample, and has the characteristics of high specificity, no residue and safety compared with antibiotics and chemical preservatives.
Owner:HUAZHONG AGRI UNIV

Methods and kits for testing mutagenicity

In one aspect, methods and kits for determining the mutagenic potential of a test substance. The method includes exposing a tester strain (such as Salmonella typhimurium) to the substance, wherein the tester strain includes a gene (such as the histidine gene) having a preexisting mutation conferring auxotrophy, and the mutation is located at a pre-determined position in the gene, growing the tester strain in growth media lacking histidine, and detecting the presence of a back-mutation at the position by analysis of the nucleic acid. The tester strain can be selected from TA98, TA100, TA102 TA1535, TA1537, TA1538, and TA97. The test substance can be any of a wide variety of compounds such as petroleum extracts, pesticides, cosmetics, adhesives, herbicides, hair dyes, and pharmaceuticals. The detecting step can include one or more conventional mutation detection methods. Also provided are kits for conducting the method. The kits can include one or more tester strains, PCR primers, positive control compounds, and DNA polymerase.
Owner:TRANSGENOMIC

Construction and application of engineering bacterium LZ-17

The present invention relates to the construction and application of engineering bacterium LZ-17, and belongs to the field of bioengineering and gene engineering technology. By means of molecular cloning technology, the luminous gene of Qinghai vibrio is introduced into Salmonella typhimurium TA97 to constitute engineering bacterium LZ-17. The engineering bacterium can produce bacterioleuciferinase, can glow with visible light of 440-640 nm wavelength after decanol is added, and has the Ames test relevant characters the same as Salmonella typhimurium TA97. The engineering bacterium is applied in Ames test as testee life form for determining the number of back varying bacterium. The engineering bacterium is especially suitable for detection of mutagenicity of the testee sample.
Owner:EAST CHINA NORMAL UNIVERSITY +1

Traditional Chinese medicine preparation for controlling pullorosis salmonellosis and preparation method thereof

The invention provides a traditional Chinese medicine preparation for controlling pullorosis salmonellosis. The traditional Chinese medicine preparation is characterized by being prepared from the following extracts in parts by weight: 3 to 5 parts of polygonum cuspidatum extract, 1 to 2 parts of fructus chebulae extract, and 1 to 2 parts of herba violae extract. The prepared traditional Chinese medicine compound particles are uniform in size, consistent in color and luster, and free of moisture adsorption, caking, deliquescence and other phenomena, meet the requirements of Chinese Pharmacopoeia, and are controllable in quality. The pharmacodynamics study shows that the traditional Chinese medicine preparation can be used for preventing and treating pullorosis salmonellosis.
Owner:SICHUAN AGRI UNIV

Detection of salmonella by real-time multiplex PCR

The invention relates to the detection of Salmonella by nucleic acid amplification. The invention provides primer and probe oligonucleotides that can be used in multiplex to detect Salmonella in real-time amplification. The oligonucleotides of the invention detect all group I serovars, and have an increased Salmonella detection range: they enable to cover the seven Salmonella groups. They also have an increased sensitivity, without loss in specificity.
Owner:BIO RAD EURO GMBH

Compound microecological preparation as well as preparation and application thereof

InactiveCN109022331AExcellent in vitro antibacterial propertiesGood preventive effectAntibacterial agentsBacteriaChemistryFreeze dry
The invention provides a compound microecological preparation as well as preparation and application thereof. A preparation method of the compound microecological preparation comprises the steps of fermenting and culturing lactobacillus plantarum subspecies Zhang-LL and lactobacillus paracasei KL1 to obtain fermentation liquor, and separately centrifuging the fermentation liquor to obtain bacterial mud; separately mixing the two types of bacterial mud with a freeze-drying protective additive, then carrying out freeze-drying treatment, and compounding to obtain the compound microecological preparation. The compound microecological preparation provided by the invention has a strong in-vitro salmonella inhibition effect, has an excellent preventive effect on salmonella pullorum disease, can inhibit the growth of salmonella enterica, maintains the intestinal micro-ecological balance of chicks, and has a good repair effect for the diseased tissues of the infected chicks; the compound microecological preparation can improve the growth performance of the chicks infected with the salmonella pullorum disease, improves the immunity of the chicks, and improves the anti-stress ability and antioxidant capacity of the organism; an effective method is provided for preventing the occurrence of chicken salmonellosis, and a thought is also provided for the development of a novel biological feedadditive.
Owner:BEIJING UNIV OF AGRI

Salmonella constant-temperature fluorescent detection primer combination capable of avoiding false negative, reagent kit and detection method

The invention discloses a salmonella constant-temperature fluorescent detection primer combination capable of avoiding false negative, a reagent kit and a detection method. The salmonella constant-temperature fluorescent detection primer comprises a detection primer group and an internal standard primer group, wherein the detection primer group is designed according to a salmonella SPI gene, and a sequence of the detection primer group is as shown in SEQ ID NO.1 to 6; the internal standard primer group is designed according to a salmonella SPF gene, and a sequence of the internal standard group is as shown in SEQ ID NO.7 to 12. Besides the primer groups, the salmonella constant-temperature detection reagent kit also comprises a DNA polymerase, reaction liquid, an internal standard target fragment, a positive reference and a negative reference. The detection primer, the reagent kit and the detection method have advantages of rapidness, high efficiency, simplicity in operation, high specificity, high sensitivity, suitability for the on-site detection and the like, can effectively prevent the occurrence of false negative and are suitable for being popularized to use.
Owner:GUANGDONG NO 2 PROVINCIAL PEOPLES HOSPITAL +1

Salmonella pullorum and mycoplasma synoviae double-plate agglutination antigen as well as preparation method and application thereof

The invention discloses a salmonella pullorum and mycoplasma synoviae double-plate agglutination antigen as well as a preparation method and application thereof, and the preparation method comprises the following steps: respectively carrying out resuscitation passage on salmonella pullorum C79-1 and mycoplasma synoviae GX11-T to prepare seed bacterial liquid, inoculating the seed bacterial liquid into a corresponding culture medium, carrying out enlarged culture, harvesting, respectively inactivating by a formaldehyde solution, concentrating, mixing the two bacterial liquids according to a certain volume ratio, adding a crystal violet solution with the final concentration of 3% by mass fraction for dyeing and glycerol with the volume fraction of 10%, uniformly mixing, and subpackaging, thereby obtaining the product. The technological method is simple and reasonable, low in cost and good in stability, the prepared double-plate agglutination antigen can detect two epidemic disease antibodies at the same time through one-time reaction, the advantages of being high in sensitivity, rapid in diagnosis, high in specificity, easy to observe the agglutination effect and the like are achieved, the detection time and the detection cost are remarkably saved, and the detection efficiency is improved. The product can be clinically used for rapidly detecting the two antibodies of the pullorum disease and the mycoplasma synoviae, diseased chickens are eliminated, and disease purification is achieved.
Owner:SHANDONG BINZHOU ANIMAL SCI & VETERINARY MEDICINE ACADEMY

Trace element premix capable of reducing propagation and invasion of Salmonella Enteritidis phage type 4 in laying hen and preparation method thereof

The invention discloses a premix capable of reducing propagation and invasion of Salmonella Enteritidis phage type 4 in a laying hen. The premix comprises, by mass, ferrous fumarate, ferrous lactate, zinc methionine chelate, zinc propionate, manganese methionine chelate, copper sulphate, cobalt acetate, a sodium selenite premix, a potassium iodide premix, magnesium sulfate and calcium carbonate. The invention also discloses a preparation method for the premix capable of reducing propagation and invasion of Salmonella Enteritidis phage type 4 in the laying hen. The additive premix can provide trace element nutritional components needed by the laying hen and reduce the positive rate of almonella Enteritidis phage type 4 in laying hens of common chicken flocks; and the proportion of salmonella-positive eggs is reduced by 20 to 30%, and the course that the excrement of the laying hen carries Salmonella Enteritidis phage type 4 is shorted by 7 to 14 d.
Owner:SICHUAN AGRI UNIV

Method for detecting salmonella

The invention provides a method for detecting salmonella. The method comprises the following steps: (1) taking nucleic acid of a sample to be detected as a template, and carrying out amplification bya loop-mediated isothermal amplification technique by using specific primers of the salmonella, so as to obtain an amplified product; (2) under mediation of specific crRNA, subjecting the amplified product obtained in the step (1) to a cracking reaction by using a CRISPR system, so as to obtain a cracked product; and (3) carrying out chromogenic detection on the cracked product obtained in the step (2) by using a colloidal gold test paper strip. The method has very good sensitivity and accuracy.
Owner:FOSHAN UNIVERSITY

Preparation method and test method of bacteriophage mixed preparation for killing salmonella

The invention discloses a preparation method and a test method of a bacteriophage mixed preparation for killing salmonella, and relates to the technical field of veterinary sterilization preparations.The preparation method disclosed by the invention comprises the following steps: s01, performing induction and identification of mild salmonella bacteriophage; s02, purifying the salmonella bacteriophage; s03, storing the suspension; and s04, preparing phage cocktail; the test method comprises the following steps: t1, preparing a liquid culture medium; t2, diluting a bacterial liquid; t3, performing mixing preparation; and t4, performing reference test. For the salmonella with different concentrations, the preparation has a good bactericidal effect, can improve the bactericidal ability of thesalmonella compared with antibiotics and reduce the generation of bacterial resistance, and is a mixed preparation applied to environmental sterilization instead of the antibiotics.
Owner:NANJING AGRICULTURAL UNIVERSITY

Classification method of salmonella strains by using whole-cell fatty acid

The invention relates to a classification method of salmonella strains by using whole-cell fatty acid, which belongs to the bioengineering technical field. The method comprises the following steps: respectively culturing a plurality of salmonella strains, extracting strain cells, acquiring types and content of aliphatic acid in strain cells, drafting an aliphatic acid system dendrogram of salmonella strains according to types and content of aliphatic acid of salmonella; employing the above method to obtain the types and content of aliphatic acid of salmonella strains to be measured, comparing the types and content with the aliphatic acid system dendrogram of salmonella strains, and then classifying the salmonella strains to be measured. The method provided in the invention has the advantages of precise classification for salmonella strains, faster classification speed and low application cost.
Owner:中华人民共和国陕西出入境检验检疫局

A kind of Salmonella pullorum sp9905 and its application

ActiveCN104774791BHigh bacterial countFreeze-drying has a low mortality rateAntibacterial agentsBacteriaSalmonella urbanaFreeze-drying
The invention discloses Salmonella pullorum sp9905, which has been preserved. The preservation unit: China Typical Culture Collection Center; address: Wuhan University; preservation date: October 15, 2014; collection number: CCTCC NO.M 2014478 . The invention also provides the application of the Salmonella pullorum pullorum in the preparation of live vaccines. The vaccine prepared by the present invention has the advantages of high number of viable bacteria and low freeze-drying mortality rate, and the product is safe and reliable. The immune protection can produce a strong protective force on the 14th day, and the immune protection rate reaches 100%. It is also resistant to other serotypes of Salmonella (Salmonella enteritidis, Salmonella gallinarum typhi) also has a good protection ability (80%~100%).
Owner:JIANGSU INST OF POULTRY SCI

Enterococcus faecium YQH2 and application thereof

The invention discloses an enterococcus faecium YQH2, and further discloses a probiotic preparation. The probiotic preparation comprises the enterococcus faecium YQH2. The invention also discloses application of the enterococcus faecium YQH2 or the probiotic preparation in breeding of poultry animals. The invention also discloses application of the enterococcus faecium YQH2 or the probiotic preparation in preparation of medicines for repairing intestinal injury or enhancing intestinal immunity. The invention further discloses application of the enterococcus faecium YQH2 or the probiotic preparation in preparation of amedicines for inhibiting salmonella typhimurium infection. The enterococcus faecium YQH2 disclosed by the invention can inhibit the growth of pathogenic bacteria. The enterococcus faecium YQH2 can improve the crypt depth of salmonella infection and increase of an inflammatory factor level, stimulates proliferation of intestinal mucosa epithelial cells and has the potential of maintaining intestinal mucosa barriers.
Owner:NANJING AGRICULTURAL UNIVERSITY
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