Title of Invention

A COMPOSITION CONTAINING LACTIC ACID BACTERIA STRAINS CAPABLE OF PREVENTING DIARRHOEA

Abstract

ABSTRACT "A COMPOSITION CONTAINING LACTIC ACID BACTERIA STRAINS CAPABLE OF PREVENTING DIARRHOEA" The present invention pertains to novel microorganisms of the family Lactobacillaceae, especially to microorganisms of the genus Lactobacillus, that are useful in preventing or treating diarrhea. In particular, the present invention relates to the use of said micro¬organisms for the preparation of an ingestible support and to a composition containing the same

Full Text

The present invention pertains to novel microorganisms of the family Lactobacillaceae, especially to microorganisms of the genus Lactobacillus, that are useful in preventing or treating diarrhoea. In particular, the present invention relates to the use of said microorganisms for the preparation of an ingestable support and to a composition containing the same. Organisms that produce lactic acid as a major metabolic component have been known for a long time. These bacteria may be found in milk or in milk processing factories, respectively, living or decaying plants but also in the intestine of man and animals. These microorganisms, summarized under the term "lactic acid bacteria", represent a rather inhomogeneous group and comprise e.g. the genera Lactococcus, Lactobacillus, Streptococcus, Bifidobacterium, Pediococcus etc.. Lactic acid bacteria have been utilized as fermenting agents for the preservations of food taking benefit of a low pH and the action of fermentation products generated during the fermentative activity thereof to inhibit the growth of spoilage bacteria. To this end, lactic acid bacteria have been used for preparing a variety of different foodsmff such as cheese, yogurt and other fermented dairy products from milk. Quite recently lactic acid bacteria have attracted a great deal of attention in that some strains have been found to exhibit valuable properties to man and animals upon ingestion. In particular, specific strains of Lactobacillus or Bifidobacterium have been found to be able to colonize the intestinal mucosa and to assist in the maintenance of the well-being of man and animal. In this respect, EP 0 768 375 discloses specific strains of the genus Bifidobacterium, that are capable to become implanted in the intestinal flora and may adhere to intestinal cells. These Bifidobacteria are reported to assist in immunomodulation, being capable to competitively exclude adhesion of pathogenic bacteria to intestinal cells, thus assisting in the maintenance of the individual's health. During the last few years research has also focused on the potential use of lactic acid bacteria as probiotic agents. Probiotics are considered to be viable microbial pre¬parations which promote the individual's health by preserving the namral microflora in the intestine. A microbial preparation may be commonly accepted as a probiotic in case the effectual microbes thereof and their mode of action are known. Probiotics are deemed to attach to the intestine's mucosa, colonize the intestinal tract and likewise prevent attachment of harmful microorganisms thereon. A crucial prerequisite for their action resides in that they have to reach the gut's mucosa in a proper and viable form and do not get destroyed in the upper part of the gastrointestinal tract, especially by the influence of the low pH prevailing in the stomach. In this respect, WO 97/00078 discloses a specific strain, termed Lactobacillus GG (ATCC 53103), as such a probiotic. The microorganism is particularly employed in a method of preventing or treating food induced hypersensitivity reactions in that it is administered to a recipient together with a food material that has been subjected to a hydrolysis treatment with pepsin and/or trypsin. The Lactobacillus strain selected is described as exhibiting adhesive and colonizing properties and showing a protease enzyme system, so that the protein material contained in the foodstuff to be administered is further hydrolysed by means of proteases secreted by the specific Lactobacillus strain. The method discussed in this document shall eventually result in the uptake of protein material by the gut that does not show a substantial amount of allergenic material anymore. Further, in EP 0 577 903 reference is made to the use of such lactic acid bacteria having the ability of replacing Heliobacter pylori, the acknowledged cause for the development of ulcer, in the preparation of a support intended for the therapeutic or prophylactic treatment of an ulcer associated with the action of Heliobacter pylori. In knowledge of the valuable properties particular strains of lactic acid bacteria may provide there is a desire in the art for additional lactic acid bacterial strains that are beneficial to the well being of man and/or animal. Consequently, a problem of the present invention is to provide additional bacterial strains that exhibit new properties beneficial for man and/or animals. The above problem has been solved by providing novel microorganisms, namely lactic acid bacteria, belonging to the genus Lactobacillus having the traits of being capable to adhere to and essentially colonize the intestinal mucosa and to prevent infection of intestinal epithelial cells by rotaviruses. According to a preferred embodiment the Lactobacillus strains are capable to grow in the presence of up to 0.4 % bile salts, so that they may easily pass the gastrointestinal tract and stay essentially active. According to another preferred embodiment the lactic acid bacterium is selected from the group consisting of Lactobacillus rhamnosus or Lactobacillus paracasei, preferably Lactobacillus paracasei, and is more preferably Lactobacillus paracasei CNCM1-2116. The microorganisms of the present invention have been shown to exhibit the following properties, they are gram positive, catalase negative, NH3 form arginine negative and COj production negative. They produce L(+) lactic acid, are capable to grow in the presence of bile salts in a concentration of up to about 0.4 % and may essentially prevent infection of epithelial cells by rotaviruses. The novel microorganisms may be used for the preparation of a variety of ingestable support materials, such as e.g. milk, yogurt, curd, fermented milks, milk based fermented products, fermented cereal based products, milk based powders, infant formulae and may be included in the support in an amount of from about 10^ cfu / g to about 10" cfii / g. For the purpose of the present invention the abbreviation cfu shall designate a "colony forming unit" that is defined as number of bacterial cells as revealed by microbiological counts on agar plates. The present invention also provides a food or a pharmaceutical composition containing at least one of the Lactobacillus strains having the above traits. For preparing a food composition according to the present invention at least one of the Lactobacillus strains according to the present invention is incorporated in a suitable support, in an amount of from about 10' cfii / g to about 10" cfti / g, preferably from about 10* cfu / g to about 10'° cfu / g, more preferably from about 10' cfu / g to about 10' cfu / g. In case of a pharmaceutical preparation the product may be prepared in forms of tablets, liquid bacterial suspensions, dried oral supplements, wet oral supplements, dry mbe feeding or a wet mbe feeding etc., with the amount of Lactobacillus strains to be incorporated therein being in the range of up to 10'^ cfu / g, preferably from about 10' cfu / g to about 10" cfu / g, more preferably from about 10' cfti / g to about 10'° cfu / g . The activity of the novel microorganisms in the individual's intestine is naturally dose dependent. That is, the more the novel microorganisms are incorporated by means of ingesting the above food material or the pharmaceutical composition the higher the protective and/or curing activity of the microorganisms. Since the novel micro¬organisms are not detrimental to mankind and animals and have eventually been isolated from baby feces a high amount thereof may be incorporated so that essentially a high proportion of the individual's intestine will be colonized by the novel microorganisms. In the figures, Fig. 1 shows a scheme illustrating the cell culture screening for assessing rotaviral protective properties of bacteria! strains. Fig. 2 shows the acidification of the L. casei strain CNCM 1-2116 (termed STU) in different growth media. Fig. 3 shows the survival rate of the L. casei strain STll at 10 °C measured during 30 days. Fig. 4 shows the mRNA pattern of IL-12 and IL-10 in mouse adherent cells derived from bone marrow after incubation of the cells with serial dilutions of STll. Fig. 5 shows the outcome of Th2 differentiation as resulting in decreased IL-4 production. During the extensive stodies leading to the present invention the inventors have investigated baby feces and isolated a variety of different bacterial strains tiierefrom. These strains were subsequently examined for their capability to prevent infection of epithelial cells with rotaviruses that are known to cause diarrhoea. Several bacterial genera comprising Lactobacillus, Lactococcus, Streptococcus were screened for their rotavirus inhibitory properties. The tests for the inhibitory property were essentially performed with three rotavirus serotypes representing the major etiological agents of human viral diarrhoea (serotypes Gl, G3 and 04). The various lactic acid bacteria were grown in a suitable medium, such as MRS, Hugo-Jago or M17 medium at temperamres of from about 30 to 40'C corresponding to their optimal growth temperature. After reaching stationary growth the bacteria were collected by centrifugation and resuspended in physiological NaCl solution. Between the different tests the bacterial cells were stored frozen (-20°C). The various rotavirus stocks were prepared by infection of confluent cell monolayers. The rotaviruses were incubated before infection. The cells were infected with 20 tissue culture infectious doses. For assessing anti-rotaviral properties two different protocols were applied. According to one protocol the various bacterial strains were examined for their direct interaction with the rotavirus while in the second protocol the bacteria were screened for those strains that interact with cellular rotavirus receptors. The first protocol involved contacting the respective bacterial suspension each with a different rotavirus strain and incubating in suitable media. Subsequently, the virus-bacterium mixture was applied to a monolayer of cells of the human undifferentiated colon adenoma cells HT-29 and incubation was continued. Virus replication was then assayed. The second protocol involved incubating the respective bacterial suspension first together with a monolayer of cells of the human undifferentiated colon adenoma cells HT-29 and adding the virus subsequently. After continued mcubation virus replication was assayed. Rotavirus replication may easily be assessed by histo-immunological staining of rotavirus proteins in infected cells. A rotavirus inhibitory effect was attributed to a given bacterium when the number of infected cells was reduced by 90% in the cell culture inoculated with rotavirus plus the indicated bacteria in comparison with cells inoculated only with rotavirus. Out of a total of 260 different bacterial strains primarily isolated merely 9 could be shown to essentially inhibit rotaviral replication. The different bacteria were ascertained to belong to the genus Lactobacillus subspecies rhamnosiis or paracasei. One strain, termed Lactobacillus casei STll, that has been deposited in accordance with the Budapest Treaty and has received the deposit numbers NCC 2461 (1-2116), has been shown to be extremely effective in preventing infection of human cells by rotavirus. Moreover, this particular strain shows excellent growing properties as may be shown by acidification in different media. The strain also shows good performance as regards the survival rate during storage at low temperatures of about 10 °C, which makes it an excellent candidate for being included in food stuff or pharmaceutical compositions to be stored at refrigerator conditions. In addition to the above finding it could also be shown that the strains surprisingly also exhibit anti-allergenic properties in that said strains have an impact on the synthesis of different immunological mediators. It is generally acknowledged that humoral immune responses and allergic reactions are mediated by CD4"*' T cells bearing the type 2 phenotype (Th2). Th2-cells are characterized by the production of high levels of interleukin 4 (IL-4), a cytokine required for the secretion of IgE, which is the major antibody class involved in allergic reactions. The differentiation of Th2 cells is impaired by IFN-y, a particular cytokine that arises from the mutually exclusive Thl subset of CD4* T cells. Said Thl cells are in turn strongly induced by interleukin 12 (IL-12). In contrast thereto IL-10, another cytokine, has been shown to have a strong suppressing impact on the proliferation of Thl cells and is therefore deemed to play a role in immunosupressive mechanisms. In summary, both IL-12 and IL-10 have strong modulatory effects on CD4"^ T cell development by influencing the development of the Thl subset. IL-12 is a key regulatory cytokine for the induction of Thl differentiation and thus inhibits the generation of Th2 responses. A major pathway for inhibition of Th2 cells is therefore seen in the stimulation of IL-12 synthesis by accessory cells. It is well known that some components of gram negative bacteria, such as LPS, induce high levels of IL-12 in adherent cells, such as macrophages and dendritic cells. Consistently, it has been found that gram negative bacteria can strongly bias CD4* T cell differentiation towards the Thl phenotype. The microorganism STll as an example of the Lactobacillus strains of the present invention has been tested for a potential role in the induction of cytokines involved in the regulation of CD4"^ T cell differentiation. In particular, the effect of STll on the phenotype of CD4'*' T cells undergoing Th2 differentiation has been studied. In this respect the capacity of STll to induce the synthesis of mRNA encoding these two regulatory cytokines in mouse adherent cells derived from bone marrow was compared with 4 other strains of Lactobacilli and with a control of gram negative bacteria (E.coli K12). The mRNA was measured by semi-quantitative RT-PCR after 6 hours of incubation of the cells with serial dilutions of bacteria ranging from 10' to lO'cfu/ml. Although all strains of Lactobacillus could induce transcription of IL-12 mRNA to a certain degree, STll could be shown to be the strongest inducer, since as a strong PCR signal could be detected even at the-lowest bacterial dose. In fact, the capacity of STll to induce IL-12 mRNA transcription was as strong as that of E. coli. Induction of IL-10 mRNA was in general weaker than for IL-12 mRNA, as only at higher bacterial doses a signal could be detected. Nevertheless, STll was the strongest inducer of IL-10 mRNA, as compared to the other lactobactilli and the E.coli control. Thus, STll is deemed to be efficient in inducing immunoregulatory cytokines involved in CD4"*' T cell differentiation. Its strong capacity to induce IL-12 makes it a candidate to inhibit Th2 responses and its measurable IL-10 induction may prevent inflammatory responses. In addition to the above finding it was also determined whether STll had an inhibitory effect on CD4'^ T cells undergoing Th2 differentiation and a positive effect on Thl functions. A well established cell differentiation culture system was utilized, where precursor CD4* T cells were polyclonally activated and modulated to undergo either Thl or Th2 differentiation, depending on the type of co-stimuli provided in the culture medium. Thl/Th2 differentiation was induced during a 7-days primary culture, after which the cells were then restimulated for 2 days in a secondary culmre containing medium alone and acquisition of a specific phenotype (Thl or Th2) was assessed by measuring the types of cytokines produced in the supernatant (IFN-y vs. IL-4). It is known that precursor CD4* T cells from mice of the BALB/c background preferentially differentiate to predominant Th2 phenotype (high IL-4, low IFN-y in the 2ry culmre supernatants) after activation under neutral conditions (medium alone in the Iry culture). This phenotype could be completely reverted to a Thl pattern (high IFN-y, low IL-4) upon addition of a blocking monoclonal antibody to IL-4 in the Iry culture. To investigate a potential role for ST 11 on Th2 inhibition, purified precursor CD4"^ T cells from BALB/c mice were activated in the presence of bone marrow adherent cells as accessory cells during the Iry culture. These cells were co-cultured either in medium alone, or in the presence of 1 mg/ml LPS, or 10* cfu/ml ST 11, or 10* cfu/ml of another Lactobacillus. After this time, the cells were washed and CD4' T cells were purified once again and restimulated in the 2ry culture in medium alone. Cytokines produced by the differentiated CD4^ T cells wer? measured after 2 days. As expected, cells differentiated in the presence of medium alone displayed a dominant Th2 phenotype. Addition of STll to the Iry cultures strongly modulated the outcome of Th2 differentiation, as it resulted in an 8-foid decrease in IL-4 production. This inhibition was of similar magnitude as that observed in culmres derived from cells differentiated in the presence of LPS. In contrast, the other Lactobacillus strain had no measurable impact on IL-4 levels. Interestingly, IFN-y levels were not increased upon addition of STll in the Iry cultures. In summary, STll specifically impaired IL-4 production by CD4+ T cells undergoing Th2 differentiation, but did not significantly increase IFN-y secretion. The fact that STll does not increase IFN-y production may be due to its capacity to induce IL-10 with the consequence that it may keep a low inflammatory impact despite its anti-Th2 activity. In consequence, it could be shown that STU is a Lactobacillus strain that has a good anti-Th2 profile which makes it an excellent candidate for its use as a bacterium with anti-allergic, probiotic activity. The present invention will now be described by way of example. Media and solutions: MRS (Difco), Hugo-Jago (Tryptone Difco 30 g/1, Yeast Extract Difco 10 g/1, Lactose Difco 5 g/1, KH2PO4 5 g/1, Beef Extract Difco 2 g/1, agar Difco 2 g/1) M17 (Difco) Ml99 (Seromed) Ringer solution (Oxoid) PBS (NaCl 8g/l, KCl 0.2 g/1, Na^HPO^ 1.15 g/1, KH2PO4 0.2 g/1)) Tryptose phosphate broth (Flow) Trypsin-EDTA solution (Seromed) Human rotavirus Wa (Gl serotype) and simian rotavirus SA-U (G3 serotype) were obtained from P.A. Offit, Children's Hospital of Philadelphia, U.S.A. The DS-IxRRV reassortant virus was obtained from A. Kapikian, NIH Bethesda, U.S.A. The serotype 4 human rotavirus Hochi was obtained from P. Bachmann, University of Munich, Germany. Example 1 Isolation of lactic acid bacteria from baby feces Fresh feces were harvested from diapers of 16 healthy babies 15 to 27 days old. 1 g of fresh feces was placed under anaerobic conditions for transportation to the laboratory and microbiological analyses were run within 2 hours from sampling by serial dilutions in Ringer solution and plating on selective media. MRS agar plus antibiotics (phosphomycine 80 )ig/ml, sulfamethoxazole 93 ^g/ml, trimethoprime 5\ig/m\) incubated at 37°C for 48 hours was used to isolate lactic acid bacteria. Colonies were randomly picked up and purified. Physiological and genetic characterisation was performed on the isolates. Example 2 Testing of strains in cell culture for anti-rotaviral activity Several bacterial genera comprising Lactobacillus, Lactococcus, Streptococcus were selected and tested for members which showed anti-rotavirus activity in the cell culture inhibition test. The genus Lactococcus was represented by a single species (Lc. lactis) consisting of two subspecies (Lc. lactis supsp. lactis and cremoris). A total of 30 strains were tested. The Streptococcus genus was represented by a single species (S. thermophilus) with 45 strains. The Leuconostoc and Propionibacterium genus were only represented by a single species (6 strains), while the Enterococcus and Staphylococcus genus was represented by two species each and a total of 17 strains. In total, 260 bacterial strains were tested for rotavirus inhibitory activity. 1" protocol: 30 fil of bacterial suspension (containing at average 3x10* bacteria) were mixed with 70 pi Ml99 medium supplemented with 10% tryptose phosphate broth (Flow) and 5% trypsin-EDTA solution (Seromed) (1:4 diluted in the case of HT-29 cells) and 100 pi of virus in supplemented M199 medium. The virus-bacterium mixmre was incubated for 1 hour at 4°C and for 1 hour at 37°C. Cells of the human undifferentiated colon adenoma cells HT-29 growing as a confluent monolayer in 96-well microtiter plates were washed three times with phosphate-buffered saline (PBS ; pH 7.2). The virus-bacterium mixmre was applied to the cells and the microtiter plates were incubated for 18 h in a COj incubator (Heraeus). Virus replication was assayed as described below. 2"^ protocol: 30 pi of the bacterial suspension (supra) were mixed with 70 pi M199 medium supplemented with 10% tryptose phosphate broth (Flow) and 5% trypsin-EDTA solution (Seromed ) (1 : 4 diluted in the case of HT-29 cells) and applied directly on the cells in the microtiter plates. After one hour incubation at 37°C 100 \i\ of virus in supplemented Ml99 medium was added to the cells in the microtiter plates. The incubation was continued for 18 h in a CO2 incubator (Heraeus). Virus replication was assayed as described below. The rotavirus replication was assessed by histo-immunological staining of rotavirus proteins in infected cells as described hereafter. One day after infection, the cell culture medium was discarded from the microtiter plates and the cells were fixed with absolute ethanol for 10 min. Ethanol was discarded, and the plates were washed three times in PBS buffer. Then 50 \x\ of an anti-rotavirus serum (mainly directed against VP6 protein), produced in rabbits (obtained from the ISREC University of Lausanne) and diluted 1 :2000 in PBS was added to each well and incubated for 1 h at 37°C with a cover slip to prevent desiccation of the wells. The antiserum was discarded afterwards and the plates were washed three times with PBS. Then 50 \i\ of anti-rabbit immunoglobulin G (IgG) antiserum produced in goats and coupled to peroxidase (GAR-IgG-PO; Nordic) were added at a dilution of 1 : 500 in PBS to each well and the plates were incubated for 1 hour at 37 "C. The serum was discarded and the plates were once again washed three times with PBS. Then 100 |j.l of the following substrate mixture was added to each well : 10 ml of 0.05 M Tris-hydrochloride (pH 7.8), 1 ml of HjOj (30% suprapur, diluted 1 -.600 in HjO ; Merck) and 200 |il of 3-amino-9-ethylcarbazole (0.1 g/10 ml of ethanol stored in 200 |J.1 aliquots at -80 *C ; A-5754 ; Sigma). The plates were incubated for at least 30 min at room temperature. The substrate was discarded and the wells were filled with 200 \i\ of HjO to stop the reaction. Infected cell foci were counted with an inverted microscope (Diavert; Leitz). Only very few bacterial strains interacted with rotaviruses. Merely 9 out of the 260 bacterial cells primarily selected inhibited rotavirus replication in at least one protocol. Lactobacillus paracasei NCC 2461 (ST 11) showed an extremely high activity against Serotype 1 Rotavirus, Serotype 3 rotavirus SA-U and Serotype 4 rotavirus Hochi. Example 3 Properties of STll ST 11 has been subjected to incubation in simulated gastric juice. The simulated gastric juice was prepared by suspending pepsin (3 g/1) in sterile saline (0.5% w/v) and adjusting the pH to 2.0 and pH 3, respectively, with concentrated HCl. ST 11 has been grown in varying amounts in the above media and the resistance of the microorganisms has been determined. The results are summarized in table I below . Table I pH cfu/ml at T 0 cfu at T Imin Cfu at T 15 cfu at T 30 cfu at T 60 2.0 2.0 X 10' 1.8x10' 1.2 x 10' 3.7 X 10' 7.0 X 10' 3.0 2.0 X 10' 1.9x10' 1.7x10' 1.7x10' 8.4 X 10* STll has the following properties as defined according to methods disclosed in the genera of lactic acid bacteria, Ed. B.J.B. Wood and W.H. Holzapfel, Blackie A&P. - gram positive, - catalase negative, - NH3 form arginine negative - CO2 production negative - production of L(+) lactic acid - growth in the presence of bile salts in a concentration of up to about 0.4 %. Example 4 Growth of ST 11 under different conditions STll was incubated at 37 °C in tomato based medium (4% tomato powder rehydrated in distilled water) supplemented with sucrose (0, 0.5, 1 or 2%) or soya peptone (0.5%) or glucose (0.5%) for different periods of time. The results are shown in fig. 2. STll was further added in an amount of 2.5 % to a medium composed of rice flour (3%), wheat flour (2%) and sucrose (3%) and incubated at 37°C until a pH of 4.4 was reached. After cooling the product was packed with or without addition of vit.C and stored at 10°C. Example 5 Induction of IL-12 and ILIO- mRNA synthesis in mouse adherent cells by STll Bone marrow cells were isolated from the femur and tibia of 8 week-old specific pathogen-free C57BL/6 mice and were incubated at a concentration of 2x10* cells/ml in RPMI medium (Gibco) containing 10% fetal bovine serum, 1 mM L-Glutamine, 12 mM Hepes, 0.05 mM 2-mercaptoethanol, 100 U/ml penicillin and 100 ^g/ml streptomycin (all reagents from Gibco) for 12 hours at 37°C in a 5% CO2 atmosphere. Non-adherent cells were discarded by 3 consecutive washes with warm culture medium and the remaining adherent cells were harvested and incubated at a concentration of 10^ cells/ml for 6 hours in the presence or absence of bacteria. It was previously determined that 6 hours represents an optimal time-point for cytokine mRNA synthesis by mouse adherent cells in response to LPS. Bacteria were added at different concentrations ranging from 10' to 10' cfu/ml. Bacteria were grown and stored as indicated above (page 6). At the end of the 6-hour culture period, cells were isolated by centrifugation and lysed using the TRIzol reagent kit (GibcoBRL, Cat. No. 15596-018) following the manufacturer's instructions. Total RNA was isolated by isopropanol precipitation and reverse-transcribed into cDNA for 90 min at 42°C using 200 U reverse transcriptase (Superscript II, BRL) in a 40-^1 reaction volume containing 200 mM Tris pH 8.3, 25 mM KCl, 1 /ig/ml oligo d(T),5 (Boehringer Mannheim), 1 mM DTT (Boehringer Mannheim), 4 mM of each dNTP (Boehringer Mannheim) and 40 U/ml Rnasin (Promega). PCR primers and conditions were used as already described in Kopf et al. (Journal of Experimental Medecine 1996 Sep l;184(3):1127-36). Amounts of cDNA were normalized within the samples using primers specific for a house-keeping gene (P-2-microglobulin). PCR products were separated on a 2% agarose gel and bands were analyzed under UV. As shown in Figure 4, STll showed the strongest induction of IL-12 and IL-10 mRNA, which was comparable to levels observed with the positive control (E. coli). Differences are best seen at the lowest bacteria concentrations (10^ cfu/ml). Example 6 Suppression of IL-4 synthesis by STll CD4* T cells were purified from the spleen of specific pathogen-free BALB/c mice using the MiniMACS kit from Miltenyi Biotec (Cat. No. 492-01). The CD4^ T cells were cultured at a concentration of 2x10' cells/ml in RPMI medium containing 10% fetal bovine serum, 1 mM L-Glutamine, 12 mM Hepes, 0.05 mM 2-mercaptoethanol, 100 U/ml penicillin and 100 ^g/ml streptomycin and activated during one week by cross-linking with plate-bound monoclonal antibodies to CD3 (clone 2C11) and CD28 (clone 37.51, both antibodies from Pharmingen). During this Iry culnire, the CD4^ T cells were co-cultured with bone marrow adherent cells (isolated as described above) as accessory cells and with 10* cfu/ml STll, or 10* cfu/ml Lal, or 1 mg/ml LPS, or medium alone. After this time, the cells were washed and CD4"' T cells were purified once again using MiniMACS kit technology and restimulated in a 2ry culture containing medium alone. Cytokines produced by the differentiated CD4* T cells were measured in the supernatants after 2 days using sandwich ELISA (kits from Endogen and Pharmingen). Results are shown in Fig. 5. Cells differentiated in the presence of medium alone displayed a dominant Th2 phenotype characterized by high levels of IL-4. Addition of STll to the Iry cultures strongly modulated the outcome of Th2 differentiation, as it resulted in an 8-fold decrease in IL-4 production. This inhibition was of similar magnitude as that observed in cultures derived from cells differentiated in the presence of LPS. In contrast thereto, the other Lactobacillus strain had no measurable impact on IL-4 levels. Interestingly, IFN-y levels were not increased upon addition of STll in the Iry cultures. As may be seen from the above the strains of the present invention may be well prepared for the production of a food and/or a pharmaceutical carrier taking advantage of the valuable properties of the microorganisms. Example 7 The STl 1 strain was tested in a clinical trial in a community on the outskirts of Guatemala City on its ability to influence the transmission and experience of acute rainy-season diarrhoeal disease experienced by most of the children in this area. A total of 203 children, aged 35 to 70 months were enrolled in the study and received a target dose of 10'° viable organisms (STll) or none (placebo) over a feeding period of 29 days. The children selected for both sample and placebo, respectively, had the typical deficits in weight-for-age and height-for-age characteristic due to undernutrition. Before initiating the feeding trial in preschool children, a safety evaluation was conducted based on in vitro and in vivo studies. In vitro studies showed antibiotic resistance pattern similar to those of other lactobacilli used in food applications, and no potential for forming biogenic amines, for degrading mucin and for deconjugating bile salts. In a placebo-controlled clinical study involving 42 adult volunteers, ST 11 was well tolerated and did not induce any adverse effects, among the potential manifestations monitored, such as flamlence, number of stools per day and stool consistency; the levels of acute-phase proteins in serum did not raise any concern with respect to a potential inflammatory reaction. The samples and placebo's have been packed in sachets at the Nestle Product Technology Center manufacturing facility in Konolfingen, Switzerland, and shipped refrigerated to Guatemala. Each 10 g sachet consisted of a chocolate flavored vehicle and either 0.2 g of STll (10'" cfu) or, in case of the placebo, 0.2 g milk powder. The chocolate flavored vehicle consisted of cocoa powder, sugar, soy lecithin, vanillin,'and cinnamon. The sachets were stored at 4° to 6°C until two hours before use. Before use the sachet had to be dissolved in 100 ml water provided by Nestle, which was free of any bacterial contamination. According to the protocol applied diarrhoea was defined as the occurrence of three or more liquid or unformed fecal evacuation during a period of 24 hrs. A diarrhoeal episode was defined as an event that presented the evidence of diarrhoea (3 diarrhoeal evacuations over 24 hrs). Its total duration in hrs was calculated from the moment of the first of the three index stools to the appearance of the first formed stool or a period 24 h without any defecation. For a child to have a "new" episode, 48 hours had to have elapsed the termination of the prior episode. If not, it was considered a continuation of the same episode and the total duration was then used for evaluation. A case was a child who experienced one or more documented episodes of diarrhoea through the 29-day obser\'ation period. Intensity of a diarrhoeal episode was based on the total number of loose stools produced. The elements of severity of the episode embraced the presence of blood, mucus or pus in stools, along with symptoms of fever and vomiting. An intensity of 7 stools per 24 h or the need for intervention by a health professional at a clinic, health center or hospital also classified an episode as severe. When a diarrhoeal episode was diagnosed through the surveillance system, a specimen of a diarrhoeal stool was collected for microscopic examination and culture to identify potential etiological pathogens for that episode. The specimen was diagnosed for rotavirus antigen, Giardia, and E. histolytica, in case the sample was dysenteric, and for bacterial pathogens including Shigella, Salmonella, Aeromonas, Plesiomonas shigelloides, E. Coli and possibly V. cholerae. During the period of investigation product samples were collected to examine the viability of the microorganisms included during the period of administration. It could be shown that the microorganism stayed viable in the sachets during the entire study so that also at the end of the study the sachets were capable to convey 10'° viable microorganism upon reconstitution with water. The study revealed that the sample containing the probiotic microorganism could decrease the occurrence of diarrhoea in contrast to the control group (placebo) by about 30 %. Yet, also the control group already exhibited a decreased number of diarrhoeal occurrence over the normal population receiving none of the samples or placebo, respectively. This latter finding may in part be explained on the basis of the children receiving additional valuable nutrition and contamination free water. However, since the study was performed in the field it may clearly be derived that STl 1 can surely reduce the occurrence of diarrhoea in vivo. The present invention pertains to novel microorganisms of the family Lactobacillaceae, especially to microorganisms of the genus Lactobacillus, that are useful in preventing or treating diarrhoea. In particular, the present invention relates to the use of said microorganisms for the preparation of an ingestable support and to a composition containing the same. Organisms that produce lactic acid as a major metabolic component have been known for a long time. These bacteria may be found in milk or in milk processing factories, respectively, living or decaying plants but also in the intestine of man and animals. These microorganisms, summarized under the term "lactic acid bacteria", represent a rather inhomogeneous group and comprise e.g. the genera Lactococcus, Lactobacillus, Streptococcus, Bifidobacterium, Pediococcus etc.. Lactic acid bacteria have been utilized as fermenting agents for the preservations of food taking benefit of a low pH and the action of fermentation products generated during the fermentative activity thereof to inhibit the growth of spoilage bacteria. To this end, lactic acid bacteria have been used for preparing a variety of different foodstuff such as cheese, yogurt and other fermented dairy products from milk. Quite recently lactic acid bacteria have attracted a great deal of attention in that some strains have been found to exhibit valuable properties to man and animals upon ingestion. In particular, specific strains of Lactobacillus or Bifidobacterium have been found to be able to colonize the intestinal mucosa and to assist in the maintenance of the well-being of man and animal. In this respect, EP 0 768 375 discloses specific strains of the genus Bifidobacterium, that are capable to become implanted in the intestinal flora and may adhere to •■•.- intestinal cells. These Bifidobacteria are reported to assist in immunomodulation, being capable to competitively exclude adhesion of pathogenic bacteria to intestinal cells, thus assisting in the maintenance of the individual's health. During the last few years research has also focused on the potential use of lactic acid bacteria as probiotic agents. Probiotics are considered to be viable microbial pre¬parations which promote the individual's health by preserving the natural microflora in the intestine. A microbial preparation may be commonly accepted as a probiotic in case the effectual microbes thereof and their mode of action are known. Probiotics are deemed to attach to the intestine's mucosa, colonize the intestinal tract and likewise prevent attachment of harmful microorganisms thereon. A crucial prerequisite for their action resides in that they have to reach the gut's mucosa in a proper and viable form and do not get destroyed in the upper part of the gastrointestinal tract, especially by the influence of the low pH prevailing in the stomach. In this respect, WO 97/00078 discloses a specific strain, termed Lactobacillus GG (ATCC 53103), as such a probiotic. The microorganism is particularly employed in a method of preventing or treating food induced hypersensitivity reactions in that it is administered to a recipient together with a food material that has been subjected to a hydrolysis treatment with pepsin and/or trypsin. The Lactobacillus strain selected is described as exhibiting adhesive and colonizing properties and showing a protease enzyme system, so that the protein material contained in the foodstuff to be administered is further hydrolysed by means of proteases secreted by the specific Lactobacillus strain. The method discussed in this document shall eventually result in the uptake of protein material by the gut that does not show a substantial amount of allergenic material anymore. Further, in EP 0 577 903 reference is made to the use of such lactic acid bacteria having the ability of replacing Heliobacter pylori, the acknowledged cause for the s development of ulcer, in the preparation of a support intended for the therapeutic or prophylactic treatment of an ulcer associated with the action of Heliobacter pylori. In knowledge of the valuable properties particular strains of lactic acid bacteria may provide there is a desire in the art for additional lactic acid bacterial strains that are beneficial to the well being of man and/or animal. Consequently, a problem of the present invention is to provide additional bacterial strains that exhibit new properties beneficial for man and/or animals. The above problem has been solved by providing novel microorganisms, namely lactic acid bacteria, belonging to the genus Lactobacillus having the traits of being capable to adhere to and essentially colonize the intestinal mucosa and to prevent infection of intestinal epithelial cells by rotaviruses. According to a preferred embodiment the Lactobacillus strains are capable to grow in the presence of up to 0.4 % bile salts, so that they may easily pass the gastrointestinal tract and stay essentially active. According to another preferred embodiment the lactic acid bacterium is selected from the group consisting of Lactobacillus rhamnosus or Lactobacillus paracasei, preferably Lactobacillus paracasei, and is more preferably Lactobacillus paracasei CNCM1-2116. The microorganisms of the present invention have been shown to exhibit the following properties, they are gram positive, catalase negative, NH3 form arginine negative and C02 production negative. They produce L(+) lactic acid, are capable to grow in the presence of bile salts in a concentration of up to about 0.4 % and may essentially prevent infection of epithelial cells by rotaviruses. The novel microorganisms may be used for the preparation of a variety of ingestable support materials, such as e.g. milk, yogurt, curd, fermented milks, milk based fermented products, fermented cereal based products, milk based powders, infant formulae and may be included in the support in an amount of from about 10s cfu / g to about 10" cfu / g. For the purpose of the present invention the abbreviation cfu shall designate a "colony forming unit" that is defined as number of bacterial cells as revealed by microbiological counts on agar plates. The present invention also provides a food or a pharmaceutical composition containing at least one of the Lactobacillus strains having the above traits. For preparing a food composition according to the present invention at least one of the Lactobacillus strains according to the present invention is incorporated in a suitable support, in an amount of from about 105 cfu / g to about 10" cfu / g, preferably from about 106 cfu / g to about 1010 cfu / g, more preferably from about 107 cfu / g to about 109 cfu / g. In case of a pharmaceutical preparation the product may be prepared in forms of tablets, liquid bacterial suspensions, dried oral supplements, wet oral supplements, dry tube feeding or a wet tube feeding etc., with the amount of Lactobacillus strains to be incorporated therein being in the range of up to 1012 cfu / g, preferably from about 107 cfu / g to about 10" cfu / g, more preferably from about 107 cfu / g to about 1010 cfu / g . The activity of the novel microorganisms in the individual's intestine is naturally dose dependent. That is, the more the novel microorganisms are incorporated by means of ingesting the above food material or the pharmaceutical composition the higher the protective and/or curing activity of the microorganisms. Since the novel micro¬organisms are not detrimental to mankind and animals and have eventually been isolated from baby feces a high amount thereof may be incorporated so that essentially a high proportion of the individual's intestine will be colonized by the novel microorganisms. In the figures, Fig. 1 shows a scheme illustrating the cell culture screening for assessing rotaviral protective properties of bacteria! strains. Fig. 2 shows the acidification of the L. casei strain CNCM 1-2116 (termed ST11) in different growth media. Fig. 3 shows the survival rate of the L. casei strain ST11 at 10 °C measured during 30 days. Fig. 4 shows the mRNA pattern of IL-12 and IL-10 in mouse adherent cells derived from bone marrow after incubation of the cells with serial dilutions of ST11. Fig. 5 shows the outcome of Th2 differentiation as resulting in decreased IL-4 production. During the extensive studies leading to the present invention the inventors have investigated baby feces and isolated a variety of different bacterial strains therefrom. These strains were subsequently examined for their capability to prevent infection of epithelial cells with rotaviruses that are known to cause diarrhoea. Several bacterial genera comprising Lactobacillus, Lactococcus, Streptococcus were screened for their rotavirus inhibitory properties. The tests for the inhibitory property were essentially performed with three rotavirus serotypes representing the major etiological agents of human viral diarrhoea (serotypes Gl, G3 and G4). The various lactic acid bacteria were grown in a suitable medium, such as MRS, Hugo-Jago or M17 medium at temperatures of from about 30 to 40 °C corresponding to their optimal growth temperature. After reaching stationary growth the bacteria were collected by centrifugation and resuspended in physiological NaCl solution. Between the different tests the bacterial cells were stored frozen (-20°C). The various rotavirus stocks were prepared by infection of confluent cell monolayers. The rotaviruses were incubated before infection. The cells were infected with 20 tissue culture infectious doses. For assessing anti-rotaviral properties two different protocols were applied. According to one protocol the various bacterial strains were examined for their direct interaction with the rotavirus while in the second protocol the bacteria were screened for those strains that interact with cellular rotavirus receptors. The first protocol involved contacting the respective bacterial suspension each with a different rotavirus strain and incubating in suitable media. Subsequently, the virus-bacterium mixture was applied to a monolayer of cells of the human undifferentiated colon adenoma cells HT-29 and incubation was continued. Virus replication was then assayed. The second protocol involved incubating the respective bacterial suspension first together with a monolayer of cells of the human undifferentiated colon adenoma cells HT-29 and adding the virus subsequently. After continued incubation virus replication was assayed. Rotavirus replication may easily be assessed by histo-immunological staining of rotavirus proteins in infected cells. A rotavirus inhibitory effect was attributed to a given bacterium when the number of infected cells was reduced by 90% in the cell culture inoculated with rotavirus plus the indicated bacteria in comparison with cells inoculated only with rotavirus. Out of a total of 260 different bacterial strains primarily isolated merely 9 could be shown to essentially inhibit rotaviral replication. The different bacteria were ascertained to belong to the genus Lactobacillus subspecies rhamnosus or paracasei. One strain, termed Lactobacillus casei ST11, that has been deposited in accordance with the Budapest Treaty and has received the deposit numbers NCC 2461 (1-2116), has been shown to be extremely effective in preventing infection of human cells by rotavirus. Moreover, this particular strain shows excellent growing properties as may be shown by acidification in different media. The strain also shows good performance as regards the survival rate during storage at low temperatures of about 10 °C, which makes it an excellent candidate for being included in food stuff or pharmaceutical compositions to be stored at refrigerator conditions. In addition to the above finding it could also be shown that the strains surprisingly also exhibit anti-allergenic properties in that said strains have an impact on the synthesis of different immunological mediators. It is generally acknowledged that humoral immune responses and allergic reactions are mediated by CD4+ T cells bearing the type 2 phenotype (Th2). Th2-cells are characterized by the production of high levels of interleukin 4 (IL-4), a cytokine required for the secretion of IgE, which is the major antibody class involved in allergic reactions. The differentiation of Th2 cells is impaired by IFN-y, a particular cytokine that arises from the mutually exclusive Thl subset of CD4+ T cells. Said Thl cells are in turn strongly induced by interleukin 12 (IL-12). In contrast thereto IL-10, another cytokine, has been shown to have a strong suppressing impact on the proliferation of Thl cells and is therefore deemed to play a role in immunosupressive mechanisms. In summary, both IL-12 and IL-10 have strong modulatory effects on CD4+ T cell development by influencing the development of the Thl subset. IL-12 is a key regulatory cytokine for the induction of Thl differentiation and thus inhibits the generation of Th2 responses. A major pathway for inhibition of Th2 cells is therefore seen in the stimulation of IL-12 synthesis by accessory cells. It is well known that some components of gram negative bacteria, such as LPS, induce high levels of IL-12 in adherent cells, such as macrophages and dendritic cells. Consistently, it has been found that gram negative bacteria can strongly bias CD4+ T cell differentiation towards the Thl phenotype. The microorganism ST11 as an example of the Lactobacillus strains of the present invention has been tested for a potential role in the induction of cytokines involved in the regulation of CD4+ T cell differentiation. In particular, the effect of ST11 on the phenotype of CD4+ T cells undergoing Th2 differentiation has been studied. In this respect the capacity of ST 11 to induce the synthesis of mRNA encoding these two regulatory cytokines in mouse adherent cells derived from bone marrow was compared with 4 other strains of Lactobacilli and with a control of gram negative bacteria (E.coli K12). The mRNA was measured by semi-quantitative RT-PCR after 6 hours of incubation of the cells with serial dilutions of bacteria ranging from 109 to 107cfu/ml. Although all strains of Lactobacillus could induce transcription of IL-12 mRNA to a certain degree, ST11 could be shown to be the strongest inducer, since as a strong PCR signal could be detected even at the-lowest bacterial dose. In fact, the capacity of ST11 to induce IL-12 mRNA transcription was as strong as that of E. coli. Induction of IL-10 mRNA was in general weaker than for IL-12 mRNA, as only at higher bacterial doses a signal could be detected. Nevertheless, ST11 was the strongest inducer of IL-10 mRNA, as compared to the other lactobactilli and the E.coli control. Thus, ST11 is deemed to be efficient in inducing immunoregulatory cytokines involved in CD4+ T cell differentiation. Its strong capacity to induce IL-12 makes it a candidate to inhibit Th2 responses and its measurable IL-10 induction may prevent inflammatory responses. In addition to the above finding it was also determined whether ST 11 had an inhibitory effect on CD4+ T cells undergoing Th2 differentiation and a positive effect on Thl functions. A well established cell differentiation culture system was utilized, where precursor CD4+ T cells were polyclonally activated and modulated to undergo either Thl or Th2 differentiation, depending on the type of co-stimuli provided in the culture medium. Thl/Th2 differentiation was induced during a 7-days primary culture, after which the cells were then restimulated for 2 days in a secondary culture containing medium alone and acquisition of a specific phenotype (Thl or Th2) was assessed by measuring the types of cytokines produced in the supernatant (IFN-y vs. IL-4). It is known that precursor CD4+ T cells from mice of the BALB/c background preferentially differentiate to predominant Th2 phenotype (high IL-4, low IFN-y in the 2ry culture supernatants) after activation under neutral conditions (medium alone in the lry culture). This phenotype could be completely reverted to a Thl pattern (high IFN-y, low IL-4) upon addition of a blocking monoclonal antibody to IL-4 in the lry culture. To investigate a potential role for ST 11 on Th2 inhibition, purified precursor CD4+ T cells from BALB/c mice were activated in the presence of bone marrow adherent cells as accessory cells during the lry culture. These cells were co-cultured either in medium alone, or in the presence of 1 mg/ml LPS, or 108 cfu/ml ST11, or 108 cfu/ml of another Lactobacillus. After this time, the cells were washed and CD4+ T cells were purified once again and restimulated in the 2ry culture in medium alone. Cytokines produced by the differentiated CD4+ T cells were measured after 2 days. As expected, cells differentiated in the presence of medium alone displayed a dominant Th2 phenotype. Addition of ST11 to the lry cultures strongly modulated the outcome of Th2 differentiation, as it resulted in an 8-fold decrease in IL-4 production. This inhibition was of similar magnitude as that observed in cultures derived from cells differentiated in the presence of LPS. In contrast, the other Lactobacillus strain had no measurable impact on IL-4 levels. Interestingly, IFN-y levels were not increased upon addition of ST 11 in the lry cultures. In summary, ST 11 specifically impaired IL-4 production by CD4+ T cells undergoing Th2 differentiation, but did not significantly increase IFN-y secretion. The fact that ST11 does not increase IFN-y production may be due to its capacity to induce IL-10 with the consequence that it may keep a low inflammatory impact despite its anti-Th2 activity. In consequence, it could be shown that ST 11 is a Lactobacillus strain that has a good anti-Th2 profile which makes it an excellent candidate for its use as a bacterium with anti-allergic, probiotic activity. The present invention will now be described by way of example. Media and solutions: MRS (Difco), Hugo-Jago (Tryptone Difco 30 g/1, Yeast Extract Difco 10 g/1, Lactose Difco 5 g/1, KH2P04 5 g/1, Beef Extract Difco 2 g/1, agar Difco 2 g/1) M17 (Difco) Ml99 (Seromed) Ringer solution (Oxoid) PBS (NaCl 8g/l, KC1 0.2 g/1, Na2HP04 1.15 g/1, KH2P04 0.2 g/1)) Tryptose phosphate broth (Flow) Trypsin-EDTA solution (Seromed) Human rotavirus Wa (Gl serotype) and simian rotavirus SA-11 (G3 serotype) were obtained from P.A. Offit, Children's Hospital of Philadelphia, U.S.A. The DS-lxRRV reassortant virus was obtained from A. Kapikian, NIH Bethesda, U.S.A. The serotype 4 human rotavirus Hochi was obtained from P. Bachmann, University of Munich, Germany. Example 1 Isolation of lactic acid bacteria from baby feces Fresh feces were harvested from diapers of 16 healthy babies 15 to 27 days old. 1 g of fresh feces was placed under anaerobic conditions for transportation to the laboratory and microbiological analyses were run within 2 hours from sampling by serial dilutions in Ringer solution and plating on selective media. MRS agar plus antibiotics (phosphomycine 80 jig/ml, sulfamethoxazole 93 ug/ml, trimethoprime 5u.g/ml) incubated at 37°C for 48 hours was used to isolate lactic acid bacteria. Colonies were randomly picked up and purified. Physiological and genetic characterisation was performed on the isolates. Example 2 Testing of strains in cell culture for anti-rotaviral activity Several bacterial genera comprising Lactobacillus, Lactococcus, Streptococcus were selected and tested for members which showed anti-rotavirus activity in the cell culture inhibition test. The genus Lactococcus was represented by a single species (Lc. lactis) consisting of two subspecies (Lc. lactis supsp. lactis and cremoris). A total of 30 strains were tested. The Streptococcus genus was represented by a single species (S. thermophilus) with 45 strains. The Leuconostoc and Propionibacterium genus were only represented by a single species (6 strains), while the Enterococcus and Staphylococcus genus was represented by two species each and a total of 17 strains. In total, 260 bacterial strains were tested for rotavirus inhibitory activity. 1st protocol: 30 ul of bacterial suspension (containing at average 3x106 bacteria) were mixed with 70 u.1 Ml99 medium supplemented with 10% tryptose phosphate broth (Flow) and 5% trypsin-EDTA solution (Seromed) (1:4 diluted in the case of HT-29 cells) and 100 u.1 of virus in supplemented M199 medium. The virus-bacterium mixture was incubated for 1 hour at 4°C and for 1 hour at 37°C. Cells of the human undifferentiated colon adenoma cells HT-29 growing as a confluent monolayer in 96-well microtiter plates were washed three times with phosphate-buffered saline (PBS ; pH 7.2). The virus-bacterium mixture was applied to the cells and the microtiter plates were incubated for 18 h in a C02 incubator (Heraeus). Virus replication was assayed as described below. 2nd protocol: 30 u.1 of the bacterial suspension (supra) were mixed with 70 ul M.199 medium supplemented with 10% tryptose phosphate broth (Flow) and 5% trypsin-EDTA solution (Seromed ) (1 : 4 diluted in the case of HT-29 cells) and applied directly on the cells in the microtiter plates. After one hour incubation at 37°C 100 u.1 of virus in supplemented Ml99 medium was added to the cells in the microtiter plates. The incubation was continued for 18 h in a C02 incubator (Heraeus). Virus replication was assayed as described below. The rotavirus replication was assessed by histo-immunological staining of rotavirus proteins in infected cells as described hereafter. One day after infection, the cell culture medium was discarded from the microtiter plates and the cells were fixed with absolute ethanol for 10 min. Ethanol was discarded, and the plates were washed three times in PBS buffer. Then 50 ul of an anti-rotavirus serum (mainly directed against VP6 protein), produced in rabbits (obtained from the ISREC University of Lausanne) and diluted 1 :2000 in PBS was added to each well and incubated for 1 h at 37°C with a cover slip to prevent desiccation of the wells. The antiserum was discarded afterwards and the plates were washed three times with PBS. Then 50 ul of anti-rabbit immunoglobulin G (IgG) antiserum produced in goats and coupled to peroxidase (GAR-IgG-PO; Nordic) were added at a dilution of 1 : 500 in PBS to each well and the plates were incubated for 1 hour at 37 °C. The serum was discarded and the plates were once again washed three times with PBS. Then 100 u,l of the following substrate mixture was added to each well : 10 ml of 0.05 M Tris-hydrochloride (pH 7.8), 1 ml of H202 (30% suprapur, diluted 1 :600 in H20 ; Merck) and 200 ul of 3-amino-9-ethylcarbazole (0.1 g/10 ml of ethanol stored in 200 u.1 aliquots at -80 °C ; A-5754 ; Sigma). The plates were incubated for at least 30 min at room temperature. The substrate was discarded and the wells were filled with 200 ul of H20 to stop the reaction. Infected cell foci were counted with an inverted microscope (Diavert; Leitz). Only very few bacterial strains interacted with rotaviruses. Merely 9 out of the 260 bacterial cells primarily selected inhibited rotavirus replication in at least one protocol. Lactobacillus paracasei NCC 2461 (ST11) showed an extremely high activity against Serotype 1 Rotavirus, Serotype 3 rotavirus SA-11 and Serotype 4 rotavirus Hochi. Example 3 Properties of ST11 ST 11 has been subjected to incubation in simulated gastric juice. The simulated gastric juice was prepared by suspending pepsin (3 g/1) in sterile saline (0.5% w/v) and adjusting the pH to 2.0 and pH 3, respectively, with concentrated HC1. ST 11 has been grown in varying amounts in the above media and the resistance of the microorganisms has been determined. ST11 has the following properties as defined according to methods disclosed in the genera of lactic acid bacteria, Ed. B.J.B. Wood and W.H. Holzapfel, Blackie A&P. - gram positive, - catalase negative, - NH3 form arginine negative - C02 production negative - production of L(+) lactic acid - growth in the presence of bile salts in a concentration of up to about 0.4 %. Example 4 Growth of ST 11 under different conditions ST 11 was incubated at 37 °C in tomato based medium (4% tomato powder rehydrated in distilled water) supplemented with sucrose (0, 0.5, 1 or 2%) or soya peptone (0.5%) or glucose (0.5%) for different periods of time. The results are shown in fig. 2. ST11 was further added in an amount of 2.5 % to a medium composed of rice flour (3%), wheat flour (2%) and sucrose (3%) and incubated at 37°C until a pH of 4.4 was reached. After cooling the product was packed with or without addition of vit.C and stored at 10°C. Example 5 Induction of IL-12 and IL10- mRNA synthesis in mouse adherent cells by ST11 Bone marrow cells were isolated from the femur and tibia of 8 week-old specific pathogen-free C57BL/6 mice and were incubated at a concentration of 2xl06 cells/ml in RPMI medium (Gibco) containing 10% fetal bovine serum, 1 mM L-Glutamine, 12 mM Hepes, 0.05 mM 2-mercaptoethanol, 100 U/ml penicillin and 100 ^g/ml streptomycin (all reagents from Gibco) for 12 hours at 37°C in a 5% C02 atmosphere. Non-adherent cells were discarded by 3 consecutive washes with warm culture medium and the remaining adherent cells were harvested and incubated at a concentration of 106 cells/ml for 6 hours in the presence or absence of bacteria. It was previously determined that 6 hours represents an optimal time-point for cytokine mRNA synthesis by mouse adherent cells in response to LPS. Bacteria were added at different concentrations ranging from 109 to 107 cfu/ml. Bacteria were grown and stored as indicated above (page 6). At the end of the 6-hour culture period, cells were isolated by centrifugation and lysed using the TRIzol reagent kit (GibcoBRL, Cat. No. 15596-018) following the manufacturer's instructions. Total RNA was isolated by isopropanol precipitation and reverse-transcribed into cDNA for 90 min at 42°C using 200 U reverse transcriptase (Superscript II, BRL) in a 40-^1 reaction volume containing 200 mM Tris pH 8.3, 25 mM KC1, 1 /ig/ml oligo d(T)15 (Boehringer Mannheim), 1 mM DTT (Boehringer Mannheim), 4 mM of each dNTP (Boehringer Mannheim) and 40 U/ml Rnasin (Promega). PCR primers and conditions were used as already described in Kopf et al. (Journal of Experimental Medecine 1996 Sep 1;184(3): 1127-36). Amounts of cDNA were normalized within the samples using primers specific for a house-keeping gene ((3-2-microglobulin). PCR products were separated on a 2% agarose gel and bands were analyzed under UV. As shown in Figure 4, ST11 showed the strongest induction of IL-12 and IL-10 mRNA, which was comparable to levels observed with the positive control (E. coli). Differences are best seen at the lowest bacteria concentrations (107 cfu/ml). Example 6 Suppression of IL-4 synthesis by ST11 CD4+ T cells were purified from the spleen of specific pathogen-free BALB/c mice using the MiniMACS kit from Miltenyi Biotec (Cat. No. 492-01). The CD4+ T cells were cultured at a concentration of 2xl05 cells/ml in RPMI medium containing 10% fetal bovine serum, 1 mM L-Glutamine, 12 mM Hepes, 0.05 mM 2-mercaptoethanol, 100 U/ml penicillin and 100 jig/ml streptomycin and activated during one week by cross-linking with plate-bound monoclonal antibodies to CD3 (clone 2C11) and CD28 (clone 37.51, both antibodies from Pharmingen). During this lry culture, the CD4+ T cells were co-cultured with bone marrow adherent cells (isolated as described above) as accessory cells and with 108 cfu/ml ST11, or 10s cfu/ml Lai, or 1 mg/ml LPS, or medium alone. After this time, the cells were washed and CD4+ T cells were purified once again using MiniMACS kit technology and restimulated in a 2ry culture containing medium alone. Cytokines produced by the differentiated CD4+ T cells were measured in the supernatants after 2 days using sandwich ELISA (kits from Endogen and Pharmingen). Results are shown in Fig. 5. Cells differentiated in the presence of medium alone displayed a dominant Th2 phenotype characterized by high levels of IL-4. Addition of ST11 to the lry cultures strongly modulated the outcome of Th2 differentiation, as it resulted in an 8-fold decrease in IL-4 production. This inhibition was of similar magnitude as that observed in cultures derived from cells differentiated in the presence of LPS. In contrast thereto, the other Lactobacillus strain had no measurable impact on IL-4 levels. Interestingly, IFN-y levels were not increased upon addition of ST 11 in the lry cultures. As may be seen from the above the strains of the present invention may be well prepared for the production of a food and/or a pharmaceutical carrier taking advantage of the valuable properties of the microorganisms. Example 7 The ST11 strain was tested in a clinical trial in a community on the outskirts of Guatemala City on its ability to influence the transmission and experience of acute rainy-season diarrhoeal disease experienced by most of the children in this area. A total of 203 children, aged 35 to 70 months were enrolled in the study and received a target dose of 1010 viable organisms (ST11) or none (placebo) over a feeding period of 29 days. The children selected for both sample and placebo, respectively, had the typical deficits in weight-for-age and height-for-age characteristic due to undernutrition. Before initiating the feeding trial in preschool children, a safety evaluation was conducted based on in vitro and in vivo studies. In vitro studies showed antibiotic resistance pattern similar to those of other lactobacilli used in food applications, and no potential for forming biogenic amines, for degrading mucin and for deconjugating bile salts. In a placebo-controlled clinical study involving 42 adult volunteers, ST11 was well tolerated and did not induce any adverse effects, among the potential manifestations monitored, such as flatulence, number of stools per day and stool consistency; the levels of acute-phase proteins in serum did not raise any concern with respect to a potential inflammatory reaction. The samples and placebo's have been packed in sachets at the Nestle Product Technology Center manufacturing facility in Konolfingen, Switzerland, and shipped refrigerated to Guatemala. Each 10 g sachet consisted of a chocolate flavored vehicle and either 0.2 g of ST11 (10'° cfu) or, in case of the placebo, 0.2 g milk powder. The chocolate flavored vehicle consisted of cocoa powder, sugar, soy lecithin, vanillin.'and cinnamon. The sachets were stored at 4° to 6°C until two hours before use. Before use the sachet had to be dissolved in 100 ml water provided by Nestle, which was free of any bacterial contamination. According to the protocol applied diarrhoea was defined as the occurrence of three or more liquid or unformed fecal evacuation during a period of 24 hrs. A diarrhoeal episode was defined as an event that presented the evidence of diarrhoea (3 diarrhoeal evacuations over 24 hrs). Its total duration in hrs was calculated from the moment of the first of the three index stools to the appearance of the first formed stool or a period 24 h without any defecation. For a child to have a "new" episode, 48 hours had to have elapsed the termination of the prior episode. If not, it was considered a continuation of the same episode and the total duration was then used for evaluation. A case was a child who experienced one or more documented episodes of diarrhoea through the 29-day observation period. Intensity of a diarrhoeal episode was based on the total number of loose stools produced. The elements of severity of the episode embraced the presence of blood, mucus or pus in stools, along with symptoms of fever and vomiting. An intensity of 7 stools per 24 h or the need for intervention by a health professional at a clinic, health center or hospital also classified an episode as severe. When a diarrhoeal episode was diagnosed through the surveillance system, a specimen of a diarrhoeal stool was collected for microscopic examination and culture to identify potential etiological pathogens for that episode. The specimen was diagnosed for rotavirus antigen, Giardia, and E. histolytica, in case the sample was dysenteric, and for bacterial pathogens including Shigella, Salmonella, Aeromonas, Plesiomonas shigelloides, E. Coli and possibly V. cholerae. During the period of investigation product samples were collected to examine the viability of the microorganisms included during the period of administration. It could be shown that the microorganism stayed viable in the sachets during the entire study so that also at the end of the study the sachets were capable to convey 1010 viable microorganism upon reconstitution with water. The study revealed that the sample containing the probiotic microorganism could decrease the occurrence of diarrhoea in contrast to the control group (placebo) by about 30 %. Yet, also the control group already exhibited a decreased number of diarrhoeal occurrence over the normal population receiving none of the samples or placebo, respectively. This latter finding may in part be explained on the basis of the children receiving additional valuable nutrition and contamination free water. However, since the study was performed in the field it may clearly be derived that ST11 can surely reduce the occurrence of diarrhoea in vivo. We claim: 1. A food or pharmaceutical composition comprising of genus Lactobacillus capable of adhering to and essentially colonizing the intestinal mucosal and capable of preventing infection of intestinal epithelial cells by rotavirus and being capable to grow in the presence of 0.4% bile salts. 2. The composition as claimed in claim 1, which is selected from the group consisting of Lactobacillus rhamnosus or Lactobacillus paracasei. 3. The composition as claimed in claim 2 wherein the lactobacillus is Lactobacillus paracasei. 4. The composition as claimed in claim 3 wherein said strain is Lactobacillus paracasei CNCM1-2116. 5. The composition as claimed in claims 1 to 4 containing Lactobacillus strain in an amount of 105 cfu/g to 1012 cfu/g. 6. The composition as claimed in claims 1 to 5, wherein said food composition is selected from milk, yogurt, curd, cheese, fermented milks, milk based fermented products, ice-creams, fermented cereal based products, milk based powders, infant formulae. 7. The composition as claimed in claim 1 to 5 wherein said pharma composition is in form of tablets, liquid bacterial suspensions, dried oral supplement, wet oral supplement, dry tube feeding or wet tube feeding. 8. The composition as claimed in claim 6 to 7 intended for the prevention of diarrhoea caused by rotavirus. We claim: 1. A food or pharmaceutical composition comprising of genus Lactobacillus capable of adhering to and essentially colonizing the intestinal mucosal and capable of preventing infection of intestinal epithelial cells by rotavirus and being capable to grow in the presence of 0.4% bile salts. 2. The composition as claimed in claim 1, which is selected from the group consisting of Lactobacillus rhamnosus or Lactobacillus paracasei. 3. The composition as claimed in claim 2 wherein the lactobacillus is Lactobacillus paracasei. 4. The composition as claimed in claim 3 wherein said strain is Lactobacillus paracasei CNCM1-2116. 5. The composition as claimed in claims 1 to 4 containing Lactobacillus strain in an amount of 10^ cfu/g to lO'^ cfu/g. 6. The composition as claimed in claims 1 to 5, wherein said food composition is selected from milk, yogurt, curd, cheese, fermented milks, milk based fermented products, ice-creams, fermented cereal based products, milk based powders, infant formulae. 7. The composition as claimed in claim 1 to 5 wherein said pharma composition is in form of tablets, liquid bacterial suspensions, dried oral supplement, wet oral supplement, dry tube feeding or wet tube feeding. 8. The composition as claimed in claim 6 to 7 intended for the prevention of diarrhoea caused by rotavirus.

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in-pct-2001-1195-che others.pdf

in-pct-2001-1195-che pct.pdf

in-pct-2001-1195-che petition.pdf