Printer Friendly

Effect of lactobacillus acidophilus & epidermal growth factor on experimentally induced clostridium difficile infection.

Clostridium difficile-associated disease (CDAD) remains an important nosocomial disease resulting in significant morbidity and mortality. In recent years, there has been an upward trend in the incidence of this condition with continuing high rates of recurrent disease (1). Antimicrobial therapeutic measures viz., vancomycin and metronidazole are being used for the treatment of CDAD but with inconsistent results. It has been reported that 80 per cent of the patients with CDAD respond well to the initial treatment of vancomycin or metronidazole. However, the remaining 20 per cent may develop subsequent episodes of CDAD, which may persist over several years, despite repeated antimicrobial treatment (2). Moreover, neither of the above two antibiotics nor any other antimicrobial regimen is reliably effective in eradicating the C. difficile carrier state, probably because the spores of the organism are resistant to their action, unlike the vegetative forms. Severe complications in patients, an increasing frequency of nosocomial outbreaks and cases of recurrent CDAD have necessitated the search for alternative treatments that may be more effective in the management of the disease (3).

There is an increasing interest in therapeutic approaches employing probiotics to the management of gastrointestinal diseases. Treatment strategies that involve the disruption of intestinal microflora by antibiotics may be particularly effective with probiotics (4). Probiotics may offer potential effective therapy for CDAD by re-establishing the disrupted microflora, enhancing immune responses and clearing pathogens and their toxins from the host. Several research trials have been done using probiotics for the treatment of CDAD (5,6). However, the lack of definitive evidence regarding efficacy and safety has limited the use of this type of treatment strategy (4). Similarly epidermal growth factor (EGF), a potent mitogenic peptide that heals gastric ulcers and reduces bacterial colonisation (7) could be investigated as an alternative approach. The literature on the role of EGF in the management of CDAD is scarce. In our recently published study we found that probiotics and EGF reduced the severity of cyclosporine induced CDAD in animals (8). In the present study BALB/c mice experimentally inoculated with C. difficile were investigated to assess the beneficial effects of L. acidophilus and EGF for the management of ampicillin and lansoprazole induced CDAD.

Material & Methods

Experimental design: The study was conducted in the Microbiology and Histopathology Divisions of the Department of Superspeciality of Gastroenterology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, India. The study was approved by the PGIMER Research Ethics Committee and Institutional Animal Ethics Committee. The investigations were conducted from August 2004 to April 2006. Healthy, adult male BALB/c mice, 4-6 wk old and weighing approximately 25 g each were used in the study. The animals (n = 60) included in the experimental study were divided into 10 groups with group 1 serving as controls and receiving no inoculum. All the animals in groups 2-10 received C. difficile. Apart from this, animals belonging to groups 3, 6 and 9 received L. acidophilus (LA-5) and those belonging to groups 4, 7 and 10 received EGF for one week after C. difficile infection. Animals in groups 5-7 were pretreated with ampicillin daily for one week and those in groups 8-10 with lansoprazole daily for two weeks prior to C. difficile infection. The dosage, period of various inocula given as well as the day of sacrifice of the animals have been given in Table I.

Preparation of various inocula: A toxigenic strain of C. difficile serogroup A (W1194, ATCC 43594) positive for both toxins A and B (kindly provided by Dr M. Delmee, Belgium) was used to prepare the C. difficile inoculum ([10.sup.8] cfu/ml) for administration as described earlier (9). C. difficile inoculum was administered orogastrically at a dose of 1 ml/animal. L. acidophilus inoculum ([10.sup.6] cfu /ml) was prepared using LactoBacil capsule (Organon India Limited, India). EGF (Sigma, USA) inoculum was prepared in sterile distilled water at a final dose of 100 [micro]g/kg body weight. Ampicillin inoculum was prepared using 500 mg ampicillin capsules (Ranbaxy Laboratories Limited, New Delhi) at a final dose of 66 mg/kg administered daily in two divided doses. Lansoprazole inoculum was prepared using 30 mg lansoprazole capsules (Brown & Burk Pharmaceutical Limited, Tamil Nadu) in sterile distilled water at a final dose of 0.5 mg/kg.

The body weight of the animals was recorded at the start of the experiment (baseline), weekly during the experiment and lastly at the time of sacrifice (final weight). The change in body weight was recorded as the difference of the baseline and the final weight.

All the animals in groups 2-10 were sacrificed one week post C. difficile infection using anaesthetic ether via inhalation. The animals in control group were sacrificed along with the animals in group 2 (Table I).

The intestinal tract of each animal was dissected out aseptically using a surgical blade. The colon, caecum and the ileal segments were separated out for further processing. The content from the caecum was immediately washed out with 1 ml sterile saline and this constituted 'initial dilution' (ID) for C. difficile counts and toxin assays. The colon was washed with sterile physiological saline to clear out the adherent faecal material. Two centimetres of the proximal end was kept in 10 mM proteolysis inhibitor containing ectoin and hydroxyectoin (HiMedia, Mumbai, India) for myeloperoxidase (MPO) activity. The caecum, the ileum and the distal part of the colon were immediately transferred to separate vials containing 10 per cent buffered formalin for histopathological studies.

C. difficile colonisation : C. difficile counts were assessed in the washed out caecal content by inoculating different dilutions on cefoxitin cycloserine fructose agar and incubating anaerobically at 37[degrees]C for 48 h. The colony forming units per ml (cfu/ml) of the original samples were obtained by multiplying the counts obtained with the dilution factor as described earlier9.

C. difficile toxin assay: C. difficile toxins were detected in the caecal content supernatant by latex agglutination assay as described earlier10 using antisera for toxins A and B (kindly gifted by Dr M. Warny, USA). All positive samples were subjected to further titration by doubling dilutions. The titre of the toxins (A and B) was recorded as the highest dilution of the supernatant which gave a positive agglutination reaction using C. difficile anti-toxin coated latex beads.

Myeloperoxidase activity: Myeloperoxidase activity in the colonic tissue was estimated by enzyme linked immunosorbent assay (ELISA) as described by Bradely et al (11) with some modifications. Briefly, colonic tissue (2 cm) was homogenized in 2 ml of 0.5 per cent hexadecyltrimethylammonium bromide (Sigma, USA) buffer (pH 6.0) in an ice bath and freezed-thawed for three cycles. It was sonicated on ice for 10 sec and centrifuged at 4472 g for 20 min at 4[degrees]C. The supernatant was transferred to fresh vial and the protein content estimated (12). Next, 14 (l of the supernatant was taken in an ELISA plate to which 200 [micro]l of reactive buffer (O-dianisidine and hydrogen peroxide) was added. Incubation was carried out for 15 min at room temperature in dark. Human MPO (Sigma, USA) at a concentration of 0.5 Units/ml was used as a positive control and phosphate buffer (50 mM) as a negative control. The absorbance was read at 450 nm by an ELISA reader (Multiskan, Finland). Each sample was tested in duplicate. The mean MPO value of each sample was expressed as Units/g of protein.

Histopathological studies: Formalin fixed specimens of ileum, caecum and colonic segments were processed and stained with haematoxylin and eosin for histopathological evaluation. Particular attention was paid to record the inflammatory changes in the mucosa for surface epithelial injury, change in shape of cells with mucodepletion, presence or absence of erosion/ ulcer of surface epithelium, intraepithelial leucocytes (lymphocytes/neutrophils), crypt abscess/cryptitis, lamina propria infiltrate (lymphocytes, neutrophils and eosinophils). The severity of inflammation was graded by a score of 0-3 and represented in the form of mean [+ or -] standard error of mean (SEM). Absence of inflammation or no change was recorded as 0; mild, moderate and severe inflammatory changes were recorded as 1, 2 and 3 respectively.

Statistical analysis: C. difficile colony counts were converted to [log.sub.10] values. Mean, median, standard deviation and ranges were calculated. Kruskal-Wallis test was applied to see the significance for parameters like colonisation by C. difficile, toxin A and B titres, MPO activity and histopathological changes among the 10 groups. Mann-Whitney U test was applied to compare between two different groups. Analysis of variance test was applied for analyzing significant differences for weight changes. P<0.05 was considered significant.

Results

The animals in control group remained healthy during the experimental period. All the animals in each group survived till the end of the experiment.

There was a significant decrease (P<0.05) in body weight of animals receiving C. difficile (group 2) compared to group 1. The increase in body weight in the groups receiving probiotic (group 3) and EGF (group 4) was significant (P<0.05) compared to group 2, which did not receive either L. acidophilus or EGF after C. difficile administration. A significant decrease (P<0.05) in body weight of animals belonging to group 6 (antibiotic, C. difficile and probiotic) was observed compared to controls. Though a decrease in body weight was also observed in group 5 (antibiotic and C. difficile) the reduction was insignificant. In contrast to the above two groups, there was an increase in body weight of animals receiving EGF after antibiotic and C. difficile administration (group 7). Similarly there was an increase in the body weight similar to the uninoculated controls in all the animals receiving lansoprazole prior to C. difficile inoculum (groups 8-10). This increase was more significant (P<0.05) in animals receiving probiotic (group 9) compared to those that did not receive either L. acidophilus or EGF (group 8) (Fig. ).

[FIGURE OMITTED]

C. difficile count differed significantly (P<0.001) in all the groups (Table II). During inter-group comparison, C. difficile count was significantly reduced in animals receiving either probiotic (P=0.003) or EGF (P=0.015) in addition to C. difficile (groups 3 and 4 respectively) compared to those receiving only C. difficile (group 2). C. difficile count was significantly lower in animals receiving EGF (P=0.004) but did not show significant difference (P=0.808) in animals receiving probiotic (group 6) when compared with those not receiving either probiotic or EGF after pretreatment with antibiotic (group 5). C. difficile count was significantly lower in groups 9 (P=0.030) and 10 (P=0.013) receiving either L. acidophilus or EGF in addition to lansoprazole, compared to those not receiving either probiotic or EGF after pre-treatment with PPI (group 8).

C. difficile toxins A and B were not detected in animals belonging to groups 1-4 (Table III). However, in animals receiving ampicillin and C. difficile (group 5) toxin A was detected in 100 per cent (positive to 103) and toxin B in 83.3 per cent (undetected to 103) of the animals. With probiotic administration, toxin A was detected in 33.3 per cent (undetected to 103) and toxin B in 50 per cent (undetected to 101) of the animals. In animals receiving EGF (group 7), toxin A was present in 33.3 per cent (undetected to 102) and toxin B in 66.6 per cent (undetected to 101) of the animals. In animals receiving lansoprazole (group 8) toxin A was detected in 83.3 per cent (undetected to 102) and B in 100 per cent (ID to 101) in the caecal content supernatant. In animals receiving probiotic after lansoprazole administration (group 9) toxin A was present in 83.3 per cent and B in 33.3 per cent of them with the titre of both the toxins ranging from undetected to ID. With the administration of EGF (group 10), toxin A was not detected in any of the animals whereas toxin B was present in only 50 per cent of the animals (undetected to positive).

Kruskal-Wallis test showed significant difference for toxin A (P<0.01) and toxin B (P<0.05) among the various groups. Toxin A titres showed significant reduction in animals receiving EGF after antibiotic pretreatment when compared to group 5. Toxin B titres showed insignificant reduction for toxin B (P=0.11), whereas titres for both the toxins reduced significantly (toxin A, P<0.01 and toxin B, P<0.05) in animals receiving EGF after lansoprazole pre-treatment when compared to those not receiving EGF (group 8).

MPO activity (Table IV) did not show any significant difference in groups 2 to 4 compared to controls. MPO activity was significantly reduced in animals receiving either L. acidophilus (P<0.01) or EGF (P<0.01) when compared to those that did not receive either L. acidophilus or EGF (group 5). The MPO activity was also significantly lower in L. acidophilus (P<0.05) or EGF (P<0.05) receiving groups (group 9-10) compared to those not receiving either L. acidophilus or EGF (group 8).

No pathological changes were found in the ileal, caecal and colonic segments of animals belonging to groups 1-4. The ileal segments in all the remaining groups showed no pathological alterations. When Kruskal-Wallis test was applied to the inflammatory parameters [mucodepletion (caecum, P<0.05; colon, P<0.001); neutrophilic infiltrate (caecum, P<0.05; colon, P<0.001), eosinophilic infiltrate (caecum, P<0.05); and cryptitis (caecum, P<0.01), a significant difference was found for all the parameters among groups 5-10 except lymphocytic infiltrate. The severity of acute inflammation was significantly lowered (P<0.05) in caecal and colonic segments for mucodepletion, neutrophilic infiltrate after administration of L. acidophilus compared to those in group 5. Cryptitis was significantly lowered (P<0.001) in the caecum of animals receiving probiotic after pre-treatment with antibiotic. The severity of acute inflammation was also significantly lowered (P<0.05) in caecal and colonic segments for neutrophilic infiltrate after administration of EGF compared to those in group 5. Although the severity of acute inflammation was lowered in the caecal and colonic segment of animals receiving either L. acidophilus or EGF after pre-treatment with lansoprazole, the reduction was not significant compared to those in group 8.

Discussion

Among the alternative therapies for CDAD, probiotics have been used by many. As it is difficult to do controlled studies in human beings, we have used the murine model for investigating therapeutic approaches like probiotic L. acidophilus or EGF in the management of CDAD. The mouse model of C. difficile infection has been used successfully for the investigation of histological changes in intestinal mucosa and shifts in intestinal microflora in animal fed with different diets (13). Wilson et al (14) reported induction of C. difficile diarrhoea in cefoxitin-treated conventional BALB/c mice with the morphological findings in the colon similar to changes in the human intestine.

In the present study, the administration of L. acidophilus led to a significant increase in body weight in animals in the lansoprazole group. Probiotic administration also resulted in significant reduction of C. difficile toxins in animals receiving either ampicillin or lansoprazole. Similar observations were reported by Plummer et al (6) in patients receiving probiotic compared to placebo. Administration of L. acidophilus results in its colonisation of the distal end of small intestine and the colon, protecting against C. difficile through a 'barrier effect' and/or production of antimicrobial components such as bacteriocins. It is also known that lactobacilli are more antagonistic to C. difficile, as the former produce hydrogen peroxide and high levels of lactic acid more frequently (15).

After an inflammatory stimulus, goblet cells, present in the intestine, release mucous. The enhanced presence of goblet cells would insure an improved synthesis of mucous, which improve the intestinal barrier and functioning, and thereby increase host protection against infections (16). In the present study also mucodepletion was significantly lowered in L. acidophilus receiving animals.

Black et al (17) observed the inhibition of C. difficile growth in vitro by L. acidophilus and clinical elimination of relapsing pseudomembranous colitis. Probiotic L. acidophilus and Bifidobacterium bifidum reduced the incidence of faecal samples positive for C. difficile toxins from 7.25 per cent in placebo-control group to 2.9 per cent in probiotic group (6). However, from their study it was not clear as to which of the two probiotics proved beneficial and whether both benefited in synergy or individually. In the present study, a single probiotic L. acidophilus administered showed protective effect against C. difficile infection. Gotz et al (18) reported no case of antibiotic associated diarrhoea when a commercial mixture of L. acidophilus and L. bulgaricus was given to 79 hospitalised patients receiving ampicillin compared to 6 of 43 patients on placebo. However, another study failed to find any protective effect of the probiotic preparation (19).

We tested the efficacy of EGF in prevention of C. difficile colonisation and disease production. Inhibition of bacterial growth by EGF may occur through several ways and need not be due to direct antibacterial effect (20). Riegler et al (21) described the possible mechanism of the preventive effect of EGF in toxin-induced damage involving binding of EGF to its cell surface receptors and stimulating the tyrosine kinase activity of the receptor. This initiates a signal transduction cascade resulting in biochemical changes within the cell, ultimately leading to DNA synthesis and cell proliferation (22). High levels of EGF can suppress inflammatory mediators and may stimulate mucosal healing by enhancing the production of other growth factors, including transforming growth factor a and heparin-binding EGF23. Besides repair of mucosal surface, EGF plays a protective role in the gastrointestinal tract by accelerated ulcer healing and preventing bacterial invasion as effectively as antibiotic treatment (20), a property that makes it extremely useful as a therapeutic agent.

Increase in body weight was observed in animals receiving EGF in the present study. Additionally, EGF reduced C. difficile count and toxin production significantly regardless of whether an antibiotic or an anti-ulcer drug was given. Buret et al (20) administered EGF to rabbits before oral inoculation with enteropathogenic E. coli and demonstrated inhibition of bacterial colonisation, a reduction in microvillus injury and disaccharidase deficiencies.

Mild to moderate inflammation was found in the caecum and colon of animals pre-treated with ampicillin or lansoprazole before C. difficile infection in a previous study (9). Administration of EGF normalised the concentration of inflammatory marker i.e. MPO in the colonic segments after C. difficile challenge in the present study. This observation is corroborated by significant reduction in the severity of inflammation in the colons of the animals. Less to lesser degree of mucodepletion and neutrophilic infiltration was observed in animals receiving EGF in the drug induced C. difficile infections in animals. EGF stimulates epithelial restitution of human colonic mucosa in vitro (21) and promotes enterocyte migration and resurfacing of epithelial discontinuities thereby accelerating the healing of gastric ulcers and colitis (24).

To conclude, our study confirms the usefulness of probiotic L. acidophilus in preventing C. difficile colonisation as well as toxin production. Our findings also show the potential benefits of EGF as an alternative strategy in prevention of C. difficile infection. However, further clinical trials would be required to use EGF as the therapeutic agent for the management of CDAD.

Acknowledgment

The study was carried out by the internal grants of the Institute. Ms Sukhminderjit Kaur received the Senior Research Fellowship from the Indian Council of Medical Research, New Delhi, India. Authors thank Dr M. Delmee, Belgium, for giving the standard C. difficile strain, Dr M. Warny, USA, for donating antisera for C. difficile toxin A and toxin B, Dr C. Pothoulakis, USA, for providing protocol for myeloperoxidase activity, and Ms Kusum Lata for statistical evaluation of the data.

Received July 3, 2009

References

(1.) Senok AC, Rotimi VO. The management of Clostridium difficile infection: antibiotics, probiotics and other strategies. J Chemother 2008; 20 : 5-13.

(2.) McFarland LV, Surawicz CM, Rubin M, Fekety R, Elmer GW, Greenberg RN. Recurrent Clostridium difficile disease: epidemiology and clinical characteristics. Infect Control Hosp Epidemiol 1999; 20 : 43-50.

(3.) Valiquette L, Low DE, Pepin J, McGeer A. Clostridium difficile infection in hospitals: a brewing storm. CMAJ 2004; 171 : 27-9.

(4.) McFarland LV. Meta-analysis of probiotics for the prevention of antibiotic associated diarrhea and the treatment of Clostridium difficile disease. Am J Gastroenterol 2006; 101 : 812-22.

(5.) Wullet M, Hagslatt ML, Odenholt I. Lactobacillus plantarum 299v for the treatment of recurrent Clostridium difficile-associated diarrhea: a double-blind placebo-controlled trial. Scand J Infect Dis 2003; 35 : 365-7.

(6.) Plummer S, Weaver MA, Harris JC, Dee P, Hunter J. Clostridium difficile pilot study: effects of probiotic supplementation on the incidence of C. difficile diarrhea. Int Microbiol 2004; 7 : 59-62.

(7.) Elliott SN, Wallace JL, McKnight W, Gall DJ, Hardin JA, Oslon M, et al. Bacterial colonization and healing of gastric ulcers: the effects of epidermal growth factor. Am J Physiol Gastrointest Liver Physiol 2000; 278 : G105-12.

(8.) Kaur S, Vaishnavi C, Ray P, Kochhar R, Prasad KK. Effect of biotherapeutics on cyclosporin-induced Clostridium difficile infection in mice. J Gastroenterol Hepatol 2010; 25 : 832-8.

(9.) Kaur S, Vaishnavi C, Prasad KK, Ray P, Kochhar R. Comparative role of antibiotic and proton pump inhibitor in experimental Clostridium difficile infection in mice. Microbiol Immunol 2007; 51 : 1209-14.

(10.) Vaishnavi C, Kochhar R, Bhasin DK, Thapa BR, Singh K. Detection of Clostridium difficile toxin by an indigenously developed latex agglutination assay. Trop Gastroenterol 1999; 20 : 33-5.

(11.) Bradely PP, Priebet DA, Christensen RD, Rothstein G. Measurement of cutaneous inflammation: estimation of neutrophil content with enzyme marker. J Invest Dermatol 1982; 78 : 206-9.

(12.) Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem 1951; 193 : 265-75.

(13.) May T, Mackie RI, Garleb KA. Effect of dietary oligosaccharides on intestinal growth of and tissue damage by Clostridium difficile. Microecol Ther 1995; 23 : 158-70.

(14.) Wilson KH, Sheagren JN, Freter R, Weatherbee L, Lyerly D. Gnotobiotic models for study of the microbial ecology of Clostridium difficile and Escherichia coli. J Infect Dis 1986; 153 : 547-51.

(15.) Naaber P, Mikelsaar RH, Salminen S, Mikelsaar, M. Bacterial translocation, intestinal microflora and morphological changes of intestinal mucosa in experimental models of Clostridium difficile infection. J Med Microbiol 1998; 47 : 591-8.

(16.) Vinderola G, Matar C, Perdigon G. Milk fermentation products of L. helveticus R389 activate calcineurin as a signal to promote gut mucosal immunity. BMC Immunol 2007; 8 : 19.

(17.) Black F, Einarsson K, Lidbeck A, Orrhage K, Nord CE. Effect of lactic acid producing bacteria on the human intestinal microflora during ampicillin treatment. Scand J Infect Dis 1991; 23 : 247-54.

(18.) Gotz V, Romankiewicz JA, Moss J, Murray HW. Prophylaxis against ampicillin associated diarrhoea with Lactobacillus preparation. Am J Hosp Pharm 1979; 36 : 754-7.

(19.) Tankanow RM, Ross MB, Ertel IJ, Dickinson DG, McCormick LS, Garfinkel JF. Double blind, placebo-controlled study of the efficacy of Lactinex in the prophylaxis of amoxicillin induced diarrhoea. Drug Interaction Clinical Pharmacy. Ann Pharm 1990; 24 : 382-4.

(20.) Buret A, Oslon ME, Gall DJ, Hardin JA. Effects of orally administered epidermal growth factor on enteropathogenic Escherichia coli infection in rabbits. Infect Immun 1998; 66 : 4917-23.

(21.) Riegler M, Sedivy R, Sogukoglu T, Castagliuolo I, Pothoulakis C, Cosentini E, et al. Epidermal growth factor attenuates Clostridium difficile toxin A- and B-induced damage of human colonic mucosa. Am J Physiol 1997; 273 : G1014-22.

(22.) Fallon JH, Serology KB, Loughlin SE, Morrison RS, Bradshaw RA, Knaver DJ, et al. Epidermal growth factor immunoreactive material in the central nervous system: location and development. Science 1994; 224 : 1107-9.

(23.) Beck PL, Podolsky DK. Growth factors in inflammatory bowel disease. Inflamm Bowel Dis 1999; 5 : 44-60.

(24.) Procaccino F, Reinshagen M, Hoffmann P, Zeeh JM, Lakshmanan J, McRoberts JA, et al. Protective effect of epidermal growth factor in an experimental model of colitis in rats. Gastroenterology 1994; 107 : 12-7.

Sukhminderjit Kaur, Chetana Vaishnavi, Kaushal Kishor Prasad, Pallab Ray, * & Rakesh Kochhar

Departments of Gastroenterology & * Medical Microbiology, Postgraduate Institute of Medical Education & Research, Chandigarh, India

Reprint requests: Dr C. Vaishnavi, Additional Professor (GE Microbiology), Department of Gastroenterology, Postgraduate Institute of Medical Education & Research, Chandigarh 160 012, India

e-mail: cvaishnavi@rediffmail.com, cvaishnavi@sify.com
Table I. Study design giving the dosage, period
of inocula and day of sacrifice of the animals

                     Group 1  Group 2  Group 3  Group 4  Group 5
                     Control    CD      CD+PB   CD+EGF    AB+CD

Ampicillin             --       --       --       --     Day 1-7
(66 mg/kg)

Lansoprazole           --       --       --       --       --
(0.5 mg/kg)

C. difficile                   Day 1    Day 1    Day 1    Day 8
([10.sup.8] cfu/ml)

L. acidophilus         --       --     Day 2-7    --       --
([10.sup.6] cfu/ml)

EGF                    --       --       --     Day 2-7    --
(100 [micro]g/kg)

Sacrifice             Day 8    Day 8    Day 8    Day 8   Day 15

                     Group 6   Group 7   Group 8   Group 9    Group 10
                     AB+CD+PB  AB+CD+EGF PPI + CD  PPI+CD+PB PPI+CD+EGF

Ampicillin           Day 1-7   Day 1-7      --        --         --
(66 mg/kg)

Lansoprazole            --        --     Day 1-14  Day 1-14   Day 1-14
(0.5 mg/kg)

C. difficile          Day 8     Day 8     Day 15    Day 15     Day 15
([10.sup.8] cfu/ml)

L. acidophilus       Day 9-14     --        --     Day 16-21     --
([10.sup.6] cfu/ml)

EGF                     --     Day 9-14     --        --     Day 16-21
(100 [micro]g/kg)

Sacrifice             Day 15    Day 15    Day 22    Day 22     Day 22

AB, antibiotic; PPI, proton pump inhibitor; CD,
C. difficile; PB, probiotic; EGF, epidermal growth factor

Table II. Mean cfu/ml, [Log.sub.10] values of C. difficile
isolated from caecal contents

Group
No.     Inocula          Mean      SD        Range     Median

1.      Control         0.0000   0.00000   0.00-0.0    0.0000
2.      CD **           4.1833   0.51153   3.40-4.90   4.1500
3.      CD+PB *         0.5000   0.54772   0.00-1.0    0.5000
4.      CD+EGF **       3.0500   0.77910    2.00-4     2.9500
5.      AB+CD **        5.6633   0.56092   5.00-6.30   5.8200
6.      AB+CD+PB **     5.6400   0.46217   5.00-6.40   5.5500
7.      AB+CD+EGF **    4.1367   0.53850   3.30-4.84   4.0400
8.      PPI+CD **       5.2033   0.84687   4.00-6.34   5.3000
9.      PPI+CD+PB **    3.7350   1.15765   2.30-5.11   3.5000
10.     PPI+CD+EGF **   3.5767   0.95326   2.00-4.90   3.6300

CD, C. difficile; PB, probiotic; EGF, epidermal growth
factor; AB, antibiotic; PPI, proton pump inhibitor

P * <0.05, ** <0.01 compared to control

Table III. C. difficile toxin A and B
titres in different groups of animals

        Groups 1-4  Group 5       Group 6       Group 7
                    AB+CD         AB+CD+PB      AB+CD+EGF

Animal  Tox A & B   Tox A  Tox B  Tox A  Tox B  Tox A  Tox B
No.
1           ND      8112    218    ID     ND     256    ID
2           ND       ID     ND     ND     ND     ND     ID
3           ND        8     ID     ND     ID     ND     ID
4           ND       ID     ID    8112    16     ND     ND
5           ND      8112   1024    ND     ND     ND      8
6           ND       ID     512    ND     ID     ID     ND

        Group 8       Group 9       Group 10
        PPI + CD      PPI+CD+PB     PPI+CD+EGF

Animal  Tox A  Tox B  Tox A  Tox B  Tox A  Tox B
No.
1        256    ID     ID     ND     ND     ID
2        128     8     ID     ID     ND     ND
3        ND      8     ID     ND     ND     ID
4        ID     ID     ID     ID     ND     ID
5        128    32     ID     ND     ND     ND
6        256    ID     ND     ND     ND     ND

Groups 1-4, Group 1 (Control), Group 2 (CD), Group 3 (CB+PB),
& Group 4 (CD+EGF); Tox, toxin; AB, antibiotic; PPI, proton pump
inhibitor; CD, C. difficile; PB, probiotic; EGF, epidermal growth
factor; ND, not detected; ID, initially diluted

Table IV. Mean MPO (units/g protein)
activity in various groups of animals

Group
No.    Inocula        Mean       SD       Range      Median

1.     Control        672.50   335.328   350-1123    600.00
2.     CD          1306.33 *   292.361   840-1747   1322.00
3.     CD+PB          840.33   349.358   538-1494    794.50
4.     CD+EGF         926.00   540.573   333-1703    839.00
5.     AB+CD       2270.33 *   846.725  1316-3456   1913.00
6.     AB+CD+PB      1034.33   314.049   419-1283   1141.00
7.     AB+CD+EGF      983.67   440.964   479-1710    943.50
8.     PPI+CD      1896.83 *   861.982  1061-3325   1627.00
9.     PPI+CD+PB      974.00   355.947   663-1543    812.00
10.    PPI+CD+EGF    1045.17   416.722   327-1520   1033.00

CD, C. difficile; PB, probiotic; EGF, epidermal growth
factor; AB, antibiotic; PPI, proton pump inhibitor

* P <0.05 compared to control
COPYRIGHT 2011 Indian Council of Medical Research
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2011 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Author:Kaur, Sukhminderjit; Vaishnavi, Chetana; Prasad, Kaushal Kishor; Ray, Pallab; Kochhar, Rakesh
Publication:Indian Journal of Medical Research
Article Type:Clinical report
Geographic Code:9INDI
Date:Apr 1, 2011
Words:4741
Previous Article:Occurrence & antibiogram of Salmonella Typhi & S. Paratyphi A isolated from Rourkela, Orissa.
Next Article:Utility of molecular studies in incontinentia pigmenti patients.
Topics:

Terms of use | Privacy policy | Copyright © 2019 Farlex, Inc. | Feedback | For webmasters