• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
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    • 专利摘要:
    A liquid detergent composition comprising a bacterium capable of interacting with the growth of pathogenic or undesirable microorganisms and uses thereof.
    公开号:BE1025484B1
    申请号:E2018/5504
    申请日:2018-07-12
    公开日:2019-03-15
    发明作者:Abdelhamid Jabrane
    申请人:Ets Pollet Sa；
    IPC主号:
    专利说明:

    Detergent composition
    Technical field of the invention invention
    The present invention relates to detergent compositions having the property of specific inhibition of the growth of pathogens or undesirable.
    Technological background of the invention
    Pathogenic bacteria are a health hazard. This danger, due to their pathogenic power, is amplified by their multi resistance to antibiotics. Indeed, the use, even overuse, of antibiotics has led to the emergence of multi-resistant pathogenic strains.
    There is therefore a need for compositions capable of limiting the emergence of bacteria resistant to antibiotics. Disinfectants can present a solution but with toxicological and ecotoxicological risks that these disinfectants present.
    Patent application WO 2014/079938 describes the addition of enzymes to detergent compositions for the treatment of biofilms resistant to conventional disinfectants and / or biocides.
    The patent application US 2008/0233093 describes the use of very particulate strains of Bacillus ssp to reduce the formation of biofilms.
    No document of the prior art describes the addition of bacteria to detergent compositions further comprising a preservative for the purpose of interacting specifically with pathogens.
    BE2018 / 5504
    Brief description of the invention
    The present invention relates to a method for the identification of a bacterium capable of interacting with the growth of pathogenic or undesirable microorganisms comprising the following successive stages: a bacterium to be tested is sampled;
    one or more pathogenic or undesirable microorganism (s) is removed;
    the culture conditions allowing the growth of both said pathogenic or undesirable microorganism (s) and said bacterium (to be tested) are determined and / or a culture supernatant of said bacteria (to be tested) is taken;
    the growth of said micro-micro-organism (s) is determined
    organization (s) pathogen (s) or undesirable (s) (I) in the absence of said bacterium (to test) and (Ü) in presence of said bacterium (to test) or said supernatant of culture of said bacteria (to test);we identify trust one bacterium causing a reduction specific of the growth at least a said or
    said pathogenic or undesirable microorganism (s).
    Preferably, in the method, the pathogen (s) is (are) selected from Gram- bacteria, Gram + bacteria, molds and yeasts.
    Advantageously, at least 2, 3, 4 or 5 pathogenic or undesirable microorganisms are selected.
    Preferably, the pathogenic or undesirable microorganism (s) include Escherichia coli, Staphyloccocus aureus (ex. MRSA), and another pathogen
    BE2018 / 5504 chosen from Pseudomonas aeruginosa, a yeast and a fungus, preferably where one, 2, or each of said pathogens is (are) resistant to antibiotic treatment.
    Advantageously, pathogens are known to cause diseases, for example nosocomial diseases.
    Preferably, the bacteria (to be tested) is from the Bacillus amyloliquefaciens group.
    Preferably at least 100 contiguous nucleotides of the genome of the bacterium (to be tested) has at least 75% identity with at least 100 contiguous nucleotides of SEQ.ID.NO: 1, SEQ.ID.NO: 3, SEQ. ID.NO: 4 and / or SEQ.ID.NO: 5.
    A related aspect of the invention relates to the use of the bacterium capable of being obtained by the above method (in particular a bacterium of the Bacillus amyloliquefaciens group and / or a bacterium having at least 75% identity with at least 100 contiguous nucleotides of SEQ.ID.NO: 1, SEQ.ID.NO: 3, SEQ.ID.NO: 4 and / or of SEQ.ID.NO: 5), in a detergent composition, preferably intended cleaning surfaces and / or floors and / or contact points.
    Such use is advantageous for communities, such as hospitals, nurseries for young children, nursing homes for the elderly or revalidation, department stores, canteens and kitchens.
    Another associated aspect of the present invention is the use of a liquid detergent composition of pH between 2.5 and 11.5 comprising (i) a bacterium, (ii) one or more molecule (s) having properties of surface and / or surfactant and / or amphiphilic and (iii) a preservative for the reduction of pathogenic bacteria
    BE2018 / 5504 and / or nosocomiales present on a surface and / or contact points.
    For this use, preferably, the bacteria is capable of being obtained by the method described above (in particular bacteria of the Bacillus amyloliquefaciens group and / or those having at least 75% identity with at least 100 contiguous nucleotides of SEQ .ID.NO: 1, SEQ.ID.NO: 3, SEQ.ID.NO: 4 and / or SEQ.ID.NO: 5).
    For this use, preferably, the preservative is chosen from the group consisting of isothiazolinone, formaldehyde and its liberators, preservatives with an amine function, preservatives with an alcohol function, benzoate and its derivatives, parabens and derivatives, methyldibromoglutaronitrile, Sodium hydroxy methyl glycinate, triclosan and Sorbate (and / or sorbic acid).
    Another associated aspect of the present invention is a liquid detergent composition comprising one or more molecule (s) having surface and / or surfactant and / or amphiphilic properties in an amount by weight of between 1% and 30%; one or more preservative (s) in a quantity by weight of between 0.001% and 10% and a bacterium capable of being obtained by the method described above (in particular a bacterium of the Bacillus amyloliquefaciens group and / or a bacteria with at least 75% identity with at least 100 contiguous nucleotides of SEQ.ID.NO: 1, SEQ.ID.NO: 3, SEQ.ID.NO: 4 and / or SEQ.ID.NO : 5).
    Preferably, the preservative of the detergent composition is chosen from the group consisting of isothiazolinone, formaldehyde and its liberators,
    BE2018 / 5504 preservatives with an amine function, preservatives with an alcohol function, benzoate and its derivatives, parabens and derivatives, quaternary ammoniums, methyldibromoglutaronitrile, Sodium hydroxy methyl glycinate, triclosan and Sorbate (and / or sorbic acid).
    Preferably, in the detergent composition, the bacteria is present at a concentration of at least 200,000 cfu / ml, preferably at least 1,000,000 cfu / ml, even more preferably at a concentration of at least 10,000,000 cfu / ml.
    Advantageously, the detergent composition further comprises one or more compound (s) chosen from (mono-) nucleotides (or nucleosides), a phytohormone, mineral nitrogen and a carbon source.
    Another related aspect of the present invention is a liquid composition comprising at least 200,000 cfu / ml, preferably at least 1,000,000 cfu / ml, even more preferably at least 10,000,000 cfu / ml of a bacterium including at least 100 contiguous nucleotides of its genome has at least 75% identity with at least 100 contiguous nucleotides of SEQ.ID. NO: 1 or SEQ.ID.NO: 3 and / or SEQ.ID.NO: 4 and / or SEQ.ID.NO: 5.
    Advantageously, this liquid composition also comprises a preservative (chosen from the group consisting of isothiazolinone, formaldehyde and its liberators, preservatives with an amine function, preservatives with an alcohol function, benzoate and its derivatives, parabens and derivatives, quaternary ammoniums, methyldibromoglutaronitrile, Sodium hydroxy methyl glycinate, triclosan and Sorbate (and / or sorbic acid)) and / or one or more
    BE2018 / 5504 compound (s) chosen from nucleotides, a phytohormone, mineral nitrogen and a carbon source.
    Brief description of the figures
    Figure 1 describes the interaction between the bacteria of the invention (BS) and Candida albicans (CA) in liquid culture.
    Figure 2 describes the interaction between the bacteria of the invention (BS) and Staphylococcus aureus (methicillin resistant strain; MRSA) in liquid culture.
    Figure 3 describes the interaction between the bacteria of the invention (BS) and Escherichia coli (EC) in liquid culture.
    Detailed description of the invention
    The inventor has noticed, surprisingly, that the enrichment of bacteria specific to a detergent composition intended to be applied to a surface reduces the amount of pathogens on this surface without there being an overall biocidal or disinfectant effect.
    In addition, the inventor has succeeded in introducing this bacterium into detergent compositions, which, both in their concentrated and diluted forms, are compatible with the metabolism of these bacteria.
    A first aspect of the invention is therefore a method for identifying a bacterium capable of interacting with the growth of pathogens (or harmful microorganisms) comprising the following successive steps:
    BE2018 / 5504 we take (select) a bacterium to test (identify) or a collection of bacteria to test (identify);
    one or more pathogens (and / or harmful microorganisms) are removed (selected);
    the culture conditions allowing the growth of both this pathogen (s) (and / or harmful microorganism) and this bacteria are determined and / or a culture supernatant of this bacteria to be identified is taken; determining the growth of the pathogen (s) (and / or harmful microorganism) (i) in the absence of this bacterium and (ii) in the presence of this bacterium and / or determining the growth of the pathogen in the presence culture supernatant of this bacteria;
    a bacteria is identified which causes a specific reduction in the growth of at least one of the pathogens. In the context of the present invention, the terminology “reduction (specific) of growth” means that the quantity of the pathogen in condition (ii), therefore in the presence of the bacteria to be tested or of the culture supernatant of the bacteria to be tested, is less than in condition (i), therefore in the absence of the bacteria to be tested. Advantageously, the quantity of the pathogen after culture in condition (ii) can also be less than the quantity seeded.
    In the context of the present invention, the terminology "specific reduction (of growth)" means that the bacteria does not have a general biocidal effect. The bacteria of the invention may, for example, act by competition with the pathogen (or the harmful microorganism), or produce a factor which specifically disturbs the metabolism of the pathogen (or the harmful microorganism).
    BE2018 / 5504
    Measurement (ii) above can be done in several ways which can be cumulated. In particular, it is possible to take a supernatant from a culture of the bacteria to be tested and to measure the effect of this supernatant on the growth of pathogens or of the harmful microorganism (in monoculture).
    An alternative is to carry out a coculture test in which a predetermined quantity of the bacteria and of the pathogen (or of the harmful microorganism) are seeded. Advantageously, different quantity ratios between the bacteria and the pathogen are tested.
    The pathogen is advantageously cultured on a surface (but preferably not as a biofilm). This makes it possible to highlight a possible phenomenon of competition for the substrate, or even the presence of an inhibiting factor which would be produced by the bacteria to be tested (eg presence of an inhibition halo). However, a co-culture test in liquid medium is possible. Advantageously, the two tests, on surface and in liquid medium, are practiced.
    In the case of coculture in a liquid medium, it is advantageous to measure the optimal amount of bacteria to be seeded, or the optimal ratio (amount of bacteria to be seeded: amount of pathogen) or, at a minimum, to test 3, 4, 5 or even 10 different ratios, presenting a range of variation by a factor of at least 10 (for example 1: 1 and 20: 1).
    A preferred culture medium for co-culture comprises yeast extracts, protein hydrolyzates (peptone) and metabolizable sugars, for example glucose. Preferably, the pH of the medium is controlled and maintained during the culture. The skilled person knows
    BE2018 / 5504 how to determine the optimum pH, whether for single culture, and for co-culture.
    In the context of the present invention, the bacterium to be tested can be any bacterium which would not penalize the properties of the detergent composition. Thus, these bacteria have no known toxicity to humans or animals and have no general biocidal effect. These bacteria are preferably natural, that is to say that they are not modified by genetic engineering.
    A preferred strain of these bacteria is found in the Bacillus subtilis complex. Preferably Bacillus amyloliquefaciens or Bacillus velezensis. More preferably, the bacteria to be tested have an element of their genome having at least 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, (approximately) 95% , 96%, 97%, 98%, 99% or even have 100% identity with at least 100 contiguous nucleotides of the ribosomal RNA 16S or 23S of Bacillus amyloliquefaciens (e.g. strains ATCC 39374 and 39320; see SEQ. ID.Nos: 1, 2) or Bacillus velezensis (e.g. strain NRRL B-41580; SEQ.ID.NO: 3), or having at least 70%, 75%, 80%, 85%, 90% , 91%, 92%, 93%, 94%, (approximately) 95%, 96%, 97%, 98%, 99% or even have 100% identity with at least 100 contiguous nucleotides of the DNA of the alpha unit of Gyrase (see SEQ.ID.NO: 4, Bacillus amyloliquefaciens strain CP 1604 and / or SEQ.ID.NO: 5, Bacillus velezensis, strain B-41580). Such a sequence comparison can advantageously be done using BLASTn, well known to those skilled in the art.
    A related aspect of the present invention is that of the use of the bacteria described above for
    BE2018 / 5504 reduce, for example on a surface, the quantity of bacteria, yeasts and / or nosocomial fungi and / or which can cause diseases and / or undesirable.
    These are advantageously chosen from the group consisting of Actinomyces, Bacillus anthracis, Brucella, Campylobacter, Clostridium sp. (C. botuminium, C. perfringens, C. tetani), Borrelia sp. , Corynebacterium sp., Enterobacter sp., Escherichia coli, Flavobacterium meningosepticum, Haemophilus sp. , Helicobacter pylori, Klebsiella sp. , Legionella sp. , Listeria ivanovii, Listeria monocytogenes, Mycobacterium sp., Neisseria meningitidis, Pasteurella sp., Proteus mirabilis, Pseudomonas aeruginosa, Salmonella sp (eg S. typhimurium), Shigella dysenteriae, Staphylococcus aureus, Streptococcus sp. (e.g. S. pneumoniae) Vibrio sp (e.g. V. cholerae), Yersinia sp (e.g. Y. pest is and Y. enterolitica), Aspergillus fumigatus, Candida albicans, Trichphyton sp, Bacillus cereus, Cladosporidium sp., Penicillium sp ., Aspergillus sp. , Alternaria alternats and Ulocladium botrytis.
    Among the bacteria, yeasts and / or fungi which are nosocomial and / or which can cause diseases, there are in particular certain strains of Escherichia coli, of Staphyloccocus aureus, in particular the strains resistant to methicillin (MRSA), of Pseudomonas aeruginosa and Candida albicans.
    Another related aspect of the present invention is the use (or incorporation) of the bacteria identified above in detergent compositions. The preferred detergent compositions are those for the treatment of surfaces, in particular the surfaces of communities such as hospitals, nurseries
    BE2018 / 5504 for young children, nursing homes for the elderly or in rehabilitation, department stores (including the handles of shopping carts), canteens. This advantageously makes it possible to clean these surfaces, while directly reducing the abundance of pathogens which would be present there.
    In the context of the present invention, the detergent compositions are not particularly limited.
    However, the detergent compositions are liquids. They preferably have the pH (in general the detergent compositions contain water, which does not exclude the presence, even the majority, of organic solvents) and the various compounds in concentration which are compatible with the life of the bacteria (described above) for a sufficiently long period (for example several weeks or more; in general, the compositions are stable for several months, for example 10 months or more).
    If this is not possible, the bacterium of the invention can be formulated in an intermediate composition, preferably liquid, which must be mixed just before use with the detergent composition, preferably in simple proportions (eg between 1: 100 and 100: 1, preferably between 1: 10 and 10: 1).
    In the context of the present invention, the detergent composition is a liquid solution (aqueous and / or comprising one or more organic solvents) and this solution comprises (in addition to the bacteria described above) at least one molecule having surface properties and / or surfactant and / or amphiphilic such as surfactants and soaps (preferably less than 30% by weight) and one (at least one) preservative (and / or
    BE2018 / 5504 stabilizer) (up to 10% by weight for the total of the preservatives present). When the detergent composition is aqueous, including a composition comprising one or more organic solvents, its pH is fixed, preferably between 2.5 and 11.5, advantageously between 4 and 10, or even between Ί and 10.
    The composition also advantageously comprises waxes and / or polymers (preferably less than 30% by weight), bleaching agents (preferably less than 15% by weight), acids, bases (preferred) or salts (preferably a total of less than 30% by weight), as well as one or more compounds chosen from the group consisting of chelating agents, enzymes, thickeners and corrosion inhibitors.
    The detergent composition can optionally comprise one or more perfume (s) and / or one or more coloring agent (s).
    Another related aspect of the present invention is the bacteria identified above in a liquid medium at a concentration of at least 200,000 cfu / ml, for example at least 500,000 cfu / ml, at least 1 million cfu / ml, at least 5 million cfu / ml, at least 10 million cfu / ml, for example about 40 to about 70 million cfu / ml. Cfu is the acronym in English for “colony forming unit”, which is the usual way of quantifying the presence of a bacterium by its capacity to generate colonies, once this bacterium is seeded on an appropriate culture support.
    Preferably, this liquid medium also comprises at least one molecule having surface and / or surfactant and / or amphiphilic properties such as surfactants and soaps (preferably less than 30% by weight) and a
    BE2018 / 5504 preservative (stabilizer) (up to 10% by weight, preferably up to 1% by weight).
    The liquid medium advantageously further comprises one or more compounds for promoting the growth of the bacteria of the invention (once placed on a surface to be cleaned), preferably chosen from nucleotides (eg; adenine, guanine; 0.1 to 1% w: w m u liquid iii e) r a phytohormone, for example 1'indole 3-acetic acid (from 0.01% to 0.1% by weight Gd üquide mi i) mineral nitrogen (eg NH4SO4. : 0.1 to 1 · δ in liquid weight) a source of carbon (eg glucose). This compound for promoting the growth of the bacteria of the invention is particularly useful for formulations where the concentration of the bacteria of the invention is lower (eg 200,000 cfu / ml, 500,000 cfu / ml, 1,000,000 cfu / ml)
    The liquid medium can be aqueous, which means that it includes water and can also include non-aqueous solvents.
    A preferred liquid medium comprises at least 50% by weight (weight organic solvent: weight of all of the solvents) of a solvent (that is to say a nonaqueous substance liquid at room temperature) chosen from the group consisting of alcohols (eg benzyl, ethanol, isopropanol), glycol ethers (eg butyldiglycol, monopropylene glycol, dipropylene glycol), petroleum distillates (eg "white spirit", petroleum ether, paraffin oil), amino compounds (e.g. monoethanolamine), ketone and aldehyde derivatives (e.g. methylal, dimethoxy methane).
    The preservative (s) (stabilizer (s)) are present at concentrations of 10% by weight maximum, preferably between 0.001% and 10%, more preferably, between _ ____________________________ BE2018 / 5504
    0.01% and 1%, even more preferably, between 0.05% and 0.2% (weight of the preservative (s) present (s): weight of the composition).
    The preservative (s) (stabilizers) are preferably chosen from the group consisting of isothiazolinone (eg 1,2-Benzisothiazol “3-one; 2-Methyl-2H-isothiazol-3one; 5-Chloro- 2-methyl-isothiazolin-3 (2H) -one (CMI); 2methylisothiazolin-3 (2H) -one (MI)), formaldehyde and its liberators (ex glutaraldehyde; 2-bromo-2nitropropane-1,3-diol ; 5-bromo-5-nitro-1,3-dioxane), preservatives (stabilizers) with an amine function (ex Diazolinidylurea; Chloroacetamide), preservatives (stabilizers) with an alcohol function (ex: Phenoxypropanol; Benzyl alcohol; o -Phenylphenol; Phenoxy-ethanol), benzoate and its derivatives, parabens and derivatives, methyldibromoglutaronitrile, sodium hydroxy methyl glycinate, triclosan and sorbate (and / or sorbic acid), as well as mixtures of several of these preservatives (stabilizers). For example, a CMI + MI mixture in mass proportions of 3: 1.
    Examples
    Example 1. Pathogenic strains (SP).
    Candida albicans (CA) ATCC 64124 Staphylococcus aureus (MRSA) ATCC 33591 Escherichia coli (EC) ATCC BAA-2452 Klebsiella pneumoniae (KP) ATCC BAA-2146 Pseudomonas aeruginosa (PA) ATCC BAA-2108
    Example 2. Development of a liquid medium common to the bacteria of the invention and to SP.
    BE2018 / 5504
    The inventor has noticed that all of the above SP strains (even CA, the culture of which is recommended rather at pH 5.6), but also the bacteria of the invention, are capable of growing in medium A comprising a yeast extract , peptone and glucose at pH 7 and at room temperature.
    Example 3. Analysis of the interaction between the Bacterium of the invention and SP in liquid culture.
    The starting inoculum of the strain of the bacteria of the invention was fixed at a high concentration. To do this, a colony of the bacterium of the invention is taken from an agar dish and inoculated in 10 ml of medium A in a flask. The number of CFU / ml is determined after an incubation of 24 h on the particle counter.
    The concentration of the starting inoculum of the SP strains is 5.10 2 CFU / ml. Given the difficulty of measuring such low concentrations on the particle counter, several colonies are taken from an agar dish and suspended in a precise volume of medium A. This culture is then counted on the particle counter and then diluted to the desired concentration.
    As shown in Figures 1-3, in liquid culture, the bacteria of the invention reduced the growth of EC, greatly reduced the growth of CA and had an even more marked effect on MRSA.
    On the other hand, the bacterium of the present invention had no significant effect in liquid culture on the growth of KP or PA, which shows that the bacterium
    BE2018 / 5504 of the invention has no general biocidal properties, and suggests a specific effect.
    Example 3. Analysis of the interaction between the Bacterium of the invention and SP in solid medium.
    The interaction between the bacteria of the invention and each strain of SP was studied in agar medium: on the one hand, the effect of the culture supernatant was tested on a agar culture of each SP; on the other hand, the effect of the bacterium of the invention on the growth of the SP strains was tested by streaking or by adding colonies of the bacterium of the invention to an SP carpet.
    CA and EC were grown, and show carpet growth. The addition of the culture supernatant of the bacteria of the invention inhibited the growth of CA and EC. An inhibitory effect was less evident in the case of the other SPs.
    The measurement of streak interactions showed a significant growth of the bacteria of the invention, and a low number of CA colonies. The effect is even more dramatic in the case of MRSA, and also observable in the case of EC.
    The inventor also put the SP in culture on agar, then after drying, 3 colonies of the bacteria of the invention. In the case of CA, the bacteria of the invention had a significant growth, which covers CA. The inventor observed that the bacteria of the invention, where it was seeded, caused halos of inhibiting the growth of MRSA. The effect is less marked for the other SPs.
    权利要求:
    Claims (12)
    [1]
    1. Liquid detergent composition comprising one or more molecule (s) having surface and / or surfactant and / or amphiphilic properties in an amount by weight of between 1% and 30%; one or more preservative (s) in a quantity by weight of between 0.001% and 10% and a bacteria antagonist of one or more pathogenic or undesirable microorganism (s).
    [2]
    2. Liquid detergent composition according to claim 1 in which the bacterium antagonist of one or more pathogenic or undesirable microorganism (s) acts by competition with the pathogenic microorganism (s) ) or undesirable (s), or produces a factor which specifically disrupts the metabolism of the pathogenic or undesirable microorganism (s).
    [3]
    3. Liquid detergent composition comprising one or more molecule (s) having surface and / or surfactant and / or amphiphilic properties in an amount by weight of between 1% and 30%; one or more preservative (s) in a quantity by weight of between 0.001% and 10% and a bacterium capable of being obtained by a method comprising the following successive steps:
    - a bacteria to be tested is taken;
    - one or more pathogenic or undesirable microorganism (s) is taken;
    - the culture conditions allowing the growth of both said pathogenic or undesirable microorganism (s) and said bacteria are determined and / or a culture supernatant of said bacteria is taken;
    - the growth of said pathogenic or undesirable microorganism (s) is determined
    BE2018 / 5504 (i) in the absence of said bacteria and (ii) in the presence of said bacteria or of said culture supernatant of said bacteria;
    - A bacterium is identified which causes a specific reduction in the growth of at least one of said pathogenic or undesirable microorganism (s).
    [4]
    4. Detergent composition according to any one of the preceding claims, in which at least 100 contiguous nucleotides of the genome of the bacterium a
    at least 75% identity with at less 100 nucleotides contiguous from SEQ.ID. NO : 1 or of SEQ.ID.NO: 3 and / or SEQ.ID.NO : 4 and or of SEQ.ID.NO: 5 " 5. Composition detergent according to one any of the
    previous claims wherein the bacterium is from the group Bacillus amyloliquefaciens.
    [5]
    6. Detergent composition according to any one of the preceding claims, in which the preservative is chosen from the group consisting of isothiazolinone, formaldehyde and its liberators, preservatives with an amine function, preservatives with an alcohol function, benzoate and its derivatives, parabens and derivatives, quaternary ammoniums, methyldibromoglutaronitrile, Sodium hydroxy methyl glycinate, triclosan and Sorbate (and / or sorbic acid).
    [6]
    7. A detergent composition according to any one of the preceding claims, in which the bacteria is present at a concentration of at least 200,000 cfu / ml, preferably at least 1,000,000 cfu / ml, even more preferably at a concentration of at least 10,000,000 cfu / ml.
    [7]
    8. Detergent composition according to any one of the preceding claims, further comprising one or more compound (s) chosen from
    BE2018 / 5504 nucleotides, a phytohormone, mineral nitrogen and a source of carbon.
    [8]
    9. A detergent composition according to any preceding claim, in which the pathogenic or undesirable microorganism (s) include Escherichia coli, Staphylococcus aureus (MRSA), and another pathogen chosen from Pseudomonas aeruginosa , a yeast and a fungus, preferably where one, 2, or each of said pathogen (s) is (are) resistant to antibiotic treatment.
    [9]
    10. A detergent composition according to any one of the preceding claims, wherein the pathogens are known to cause diseases, for example nosocomial diseases.
    [10]
    11. Liquid composition comprising at least 200,000 cfu / ml, preferably at least 1,000,000 cfu / ml, even more preferably at least 10,000,000 cfu / ml of a bacterium with at least 100 contiguous nucleotides of its genome at least 75% identity with at least 100 contiguous nucleotides of
    SEQ.ID. NO: 1 or SEQ.ID.NO: 3 and / or
    SEQ.ID.NO: 4 and / or SEQ.ID.NO: 5.
    [11]
    12. A liquid composition according to claim 11 further comprising a preservative.
    [12]
    13. Liquid composition according to claim 11 or 12 further comprising one or more compound (s) chosen from nucleotides, a phytohormone, mineral nitrogen and a carbon source.
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    EP2922946A1|2012-11-26|2015-09-30|Realco S.A.|Method for eliminating biofilms for cleaning medical instruments, in particular for combating nosocomial infections|
    法律状态:
    2019-05-02| FG| Patent granted|Effective date: 20190315 |
    优先权:
    申请号 | 申请日 | 专利标题
    BE2017/5916A|BE1025305B1|2017-12-08|2017-12-08|Detergent composition|
    BEBE2017/5916|2017-12-08|CA3121541A| CA3121541A1|2017-12-08|2018-12-07|Detergent composition|
    EP18811851.7A| EP3526342A1|2017-12-08|2018-12-07|Detergent composition|
    PCT/EP2018/084001| WO2019110811A1|2017-12-08|2018-12-07|Detergent composition|
    US16/768,732| US20210171877A1|2017-12-08|2018-12-07|Detergent Composition|
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