A prebiotic, Celmanax™, decreases Escherichia coli O157:H7 colonization of bovine cells and feed-associated cytotoxicity in vitro
© Baines et al; licensee BioMed Central Ltd. 2011
Received: 20 May 2010
Accepted: 7 April 2011
Published: 7 April 2011
Escherichia coli O157:H7 is the most common serovar of enterohemorrhagic E. coli associated with serious human disease outbreaks. Cattle are the main reservoir with E. coli O157:H7 inducing hemorrhagic enteritis in persistent shedding beef cattle, however little is known about how this pathogen affects cattle health. Jejunal Hemorrhage Syndrome (JHS) has unclear etiology but the pathology is similar to that described for E. coli O157:H7 challenged beef cattle suggestive that E. coli O157:H7 could be involved. There are no effective treatments for JHS however new approaches to managing pathogen issues in livestock using prebiotics and probiotics are gaining support. The first objective of the current study was to characterize pathogen colonization in hemorrhaged jejunum of dairy cattle during natural JHS outbreaks. The second objective was to confirm the association of mycotoxigenic fungi in feeds with the development of JHS and also to identify the presence of potential mycotoxins. The third objective was to determine the impact of a prebiotic, Celmanax™, or probiotic, Dairyman's Choice™ paste, on the cytotoxicity associated with feed extracts in vitro. The fourth objective was to determine the impact of a prebiotic or a probiotic on E. coli O157:H7 colonization of mucosal explants and a bovine colonic cell line in vitro. The final objective was to determine if prebiotic and probiotic feed additives could modify the symptoms that preceded JHS losses and the development of new JHS cases.
Dairy cattle developed JHS after consuming feed containing several types of mycotoxigenic fungi including Fusarium culmorum, F. poae, F. verticillioides, F. sporotrichioides, Aspergillus flavus, Penicillium roqueforti, P. crustosum, P. paneum and P. citrinum. Mixtures of Shiga toxin - producing Escherichia coli (STEC) colonized the mucosa in the hemorrhaged tissues of the cattle and no other pathogen was identified. The STECs expressed Stx1 and Stx2, but more significantly, Stxs were also present in the blood clot blocking the jejunum. Mycotoxin analysis of the corn crop confirmed the presence of fumonisin, NIV, ZEAR, DON, 15-ADON, 3-ADON, NEO, DAS, HT-2 and T-2. Feed extracts were toxic to enterocytes and 0.1% Celmanax™ removed the cytotoxicity in vitro. There was no effect of Dairyman's Choice™ paste on feed-extract activity in vitro. Fumonisin, T-2, ZEAR and DON were toxic to bovine cells and 0.1% Celmanax™ removed the cytotoxicity in vitro. Celmanax™ also directly decreased E. coli O157:H7 colonization of mucosal explants and a colonic cell line in a dose-dependent manner. There was no effect of Dairyman's Choice™ paste on E. coli O157:H7 colonization in vitro. The inclusion of the prebiotic and probiotic in the feed was associated with a decline in disease.
The current study confirmed an association between mycotoxigenic fungi in the feed and the development of JHS in cattle. This association was further expanded to include mycotoxins in the feed and mixtures of STECs colonizing the severely hemorrhaged tissues. Future studies should examine the extent of involvement of the different STEC in the infection process. The prebiotic, Celmanax™, acted as an anti-adhesive for STEC colonization and a mycotoxin binder in vitro. Future studies should determine the extent of involvement of the prebiotic in altering disease.
Enterohemorrhagic Escherichia coli O157:H7 continues to cause serious human disease outbreaks despite extensive efforts at cattle processing facilities and feedlots to reduce the transmission of disease [1–3]. Cattle are the main reservoir for E. coli O157:H7 and like humans, the majority of cattle resolve experimental-challenge infections on their own, while a few highly colonized individuals develop hemorrhagic enteritis . It is currently unclear why earlier E. coli O157:H7 challenge studies did not report pathology, but we hypothesized that an unknown factor such as feed or water quality may be contributing to the development of disease. If E. coli O157:H7 does cause disease in cattle, the most likely candidates are diseases with unclear etiologies. Jejunal Hemorrhage Syndrome (JHS) is an emerging hemorrhagic disease in dairy cattle that has been associated with the presence of mycotoxigenic fungi in feed and the presence of Clostridium perfringens type A in hemorrhaged tissues, but there is some question as to whether this pathogen actually plays a role . Current treatments for JHS are ineffective suggesting that a novel approach to disease management must be undertaken. In monogastric livestock, probiotic and prebiotic feed additives mitigate pathogen issues in a number of ways including enhancing the presence of beneficial bacteria in the intestinal tract , improving mucosal barrier function [7, 8], increasing mucus production , inhibiting proinflammatory cytokines , enhancing the innate immune response , binding pathogen toxins  and interfering with colonization sites [8, 13]. Very little information is available concerning the benefits of probiotics or prebiotics for managing pathogens in ruminants. Probiotics do reduce E. coli O157:H7 shedding in experimental-challenged immature calves  and adult cattle . To be effective as pathogen mitigation agents, probiotics or prebiotics must escape fermentation in the rumen and digestion in the abomasum prior to reaching any pathogen colonization sites in the intestinal tract . There is evidence to suggest that prebiotics do survive the rumen environment  and as such, these agents may be useful for addressing pathogen issues and disease. The first objective of the current study was to characterize the pathogens associated with the hemorrhaged tissues during natural JHS outbreaks in dairy cattle. The second objective was to confirm the association of JHS development with the presence of mycotoxigenic fungi in feed and to determine if their mycotoxins or cytotoxins were also present. The third objective was to determine the impact of a prebiotic, Celmanax™, and a probiotic, Dairyman's Choice™ paste, on feed extract cytotoxicity in vitro. The fourth objective was to determine the impact of the prebiotic and probiotic on E. coli O157:H7 colonization of mucosal explants and a bovine colonic cell line in vitro. The final objective was to monitor the impact of the prebiotic and probiotic added to alleviate the reduction in milk production on the neurological symptoms and JHS development in dairy cattle during a natural JHS outbreak.
Dairy production site 1 (PS1) with no history of JHS
A natural outbreak of JHS occurred in a commercial dairy herd in December 2008 and January 2009 in Southern Alberta, Canada. From 1 to 3 animals per week developed disease symptoms and succumbed to the disease despite antibiotic interventions. Eleven mature cattle developed JHS and an average of 10 other animals per week had the neurological symptoms that preceded the development of JHS. The initial diagnosis was Acute Hemorrhagic Enteritis (AHE), however after further examination of tissues, this was changed to JHS. The principle difference in the diagnosis of these diseases is the location and extent of hemorrhaging in the intestinal tract. JHS presents with severe hemorrhaging in the jejunum with a large blood clot blocking the movement of digesta while AHE presents with hemorrhaging in several regions of the intestinal tract with smaller blood clots. The producer reported symptoms suggestive of a mycotoxicosis including lower milk production, staggering, hindlimb paralysis, wasting and higher than average mortality for the lactating cattle. To alleviate the reduction in milk production, the producer added a prebiotic (30 g) to the total mixed ration and a single application of a prebiotic + probiotic (400 ml:10 g) delivered to cattle within 24 hr after calving. The prebiotic, Celmanax™ (Vi-COR®, Mason City, IA, USA), consists of a non-living formulation of yeast cell walls or mannan oligosaccharide (MOS) and yeast metabolites. The probiotic, Dairyman's Choice™ paste (Animal Pro-Products, Arthur, ON, Canada), consists of two Bacillus isolates that provide enzymes for assisting digestion, vitamins and minerals. The Celmanax™ improves milk production in dairy cattle , while the Dairyman's Choice™ paste is applied during times of increased nutritional demands. We monitored the impact of the feed additives on the current neurological symptoms that preceded the development of JHS disease, the occurrence of new neurological symptoms and the development of new JHS cases.
Dairy production sites 2, 3 and 4 (PS2, PS3, PS4) with no previous history of JHS
From 2008 to 2010, other dairy production sites in Southern Alberta were experiencing sudden-onset cattle deaths, grey-green scours, reduced milk production, metritis, neurological symptoms (staggering), drooling, swollen joints and wasting associated with the consumption of mouldy feeds. Jejunal tissues from one animal per site were sampled. From 6 to 30 mature cattle developed JHS on each site with an average of 100 lactating cattle per site. As for PS1, an average of 1 animal per week had the neurological symptoms that preceded the JHS losses. The producers applied the prebiotic and probiotic to alleviate the reduction in milk production and we monitored the impact of the feed additives on the current neurological symptoms, the occurrence of new neurological symptoms and the development of new JHS cases.
Dairy production site 5 (PS5) with a history of JHS
A final production site was selected where the veterinarian had annual JHS cases in the herd. No feed additives were provided to the dairy cattle.
Escherichia coli O157:H7 isolation from PS1-PS5
One cow from PS1 died from complications associated with a c-section and the tissue served as a negative control. This animal had no neurological symptoms or other disease symptoms. One animal from PS2 and PS3 died from complications associated with leucosis and reproduction respectively. These animals served as negative controls and did not have any neurological symptoms. The tissue from 11 cattle confirmed the JHS status on PS1 based on the presence of acute hemorrhaging in the jejunum, blood clots in the small intestine and the lack of similar pathology in the control animals. To compare pathology associated with JHS diagnosis at multiple production sites, tissue samples were collected from PS1-PS4 and the pathology recorded. Finally, a sample was obtained from another veterinary practice (PS5) with a production site that had a history of JHS to determine whether there were any obvious differences in the gross pathology compared to PS1 to PS4. For all production sites, a 30 to 60 cm piece of tissue was removed from the acute hemorrhaged region of the jejunum within 4 hours after death and transported back to the laboratory at 4°C. The bloody digesta and clot were separated into sample tubes and serial dilutions were plated on Sorbitol MacConkey agar (SMAC; Dalynn Biologicals, Calgary, Alberta, Canada) to identify non-sorbitol fermenting bacterial colonies and on Potato Dextrose agar (PDA; Dalynn Biologicals, Calgary, Alberta, Canada) to isolate fungi. Adherent or tissue-colonizing bacteria were collected from the hemorrhaged regions. Each tissue was cut open, washed in cold PBS and 2.5 cm2 pieces cut out. Care was taken while cutting not to press down on the tissue and distort size. Each 2.5 cm2 intact tissue was incubated with 0.1% Triton X-100 overnight and plated on SMAC agar to determine the presence of non-sorbitol fermenting bacterial colonies. Any suspect colonies were tested as O157 and H7 using the RIM™ E. coli O157:H7 Latex test (Fisher Scientific, Ottawa, Ontario, Canada). To elucidate whether STEC virulence determinants were critical to the development of JHS, the blood clot that blocked the hemorrhaged jejunum and the E. coli O157:H7 isolates from the hemorrhaged regions were examined for Stx1 and Stx2 expression using the Meridian ImmunoCard STAT!® EHEC test (Somagen, Edmonton, Alberta, Canada). The Meridian ImmunoCard STAT!® EHEC test was optimized for use with cattle samples as follows: three-day old colonies on SMAC plates were used in the agar plate method, polymyxin B at 100 μg/ml, a longer Polymyxin B incubation period (45 min) and a 300 μl sample was applied to the test well. For the detection of Stx1 and Stx2 in the blood clot, a 1 ml volume of the blood was diluted in half with PBS and 300 ul was then applied to the test well.
PCR assay targeting O157 STEC and non-O157 STEC genes
Initial isolates were chosen from PS1-PS5 for additional PCR testing based upon their latex agglutination responses. The PS1, PS3 and PS4 isolates produced strong agglutination for both O157 and H7 in the RIM™ E. coli O157:H7 Latex test. One isolate representing this group was tested for identity. The isolates from the remaining sites produced weak agglutination with O157 and none to strong agglutination with H7 in the RIM™ E. coli O157:H7 Latex test. One isolate representing this group was tested for identity. The presumptive E. coli O157:H7 colonies were subjected to an E. coli O157:H7-specific PCR assay targeting the fliC, eaeA, and verotoxin (vt; VT1 and VT2) genes . In this assay, vt, eaeA and fliC PCR products are produced for E. coli O157:H7 strains while, vt PCR products are produced for non-O157 STEC strains.
DNA microarray assay targeting pathogenic E. coli genes
To further characterize the composition of the infections associated with JHS cases, isolates were re-examined in a DNA microarray assay targeting E. coli genes. To select isolates, the samples were transferred to SMAC, CT-SMAC and CHROMagar™ O157 and two to five STEC colonies were further characterized based upon differences in morphology and/or Stx production.
The microarray (MaxiVir1.0) used in this study was based on earlier published work  and carries 514 oligonucleotides of 70 bases in length targeting 348 virulence or virulence-related genes and 96 antimicrobial resistance or antimicrobial resistance-related genes found in gram-negative bacteria. The microarray, designed to detect a complete set of virulence genes representative of all E. coli pathotypes, includes virulence factors such as adhesins, locus of enterocyte effacement, colicins and microcins, toxins, iron acquisition and transport systems, capsular and somatic antigens, hemolysins and hemaglutinins, as well as newly recognized or putative E. coli virulence genes. Antimicrobial resistance genes included in the microarray represent different antimicrobial families such as β-lactams, aminoglycosides, tetracycline, phenicols, trimethoprim, sulfonamide and class I integron. The microarray also carries five positive oligonucleotide controls for E. coli derived from the sequences of genes encoding tryptophanase (tnaA), beta-glucuronidase (uidA), lactose permease (lacY), beta-galactosidase (lacZ), and glutamate decarboxylase (gad). Negative controls added to this microarray consist of oligonucleotides derived from the gene sequences for the green fluorescent protein of Aequorea victoria, the lactose permease of Citrobacter freundii, and the chlorophyll synthase from Arabidopsis thaliana.
Escherichia coli DNA labeling
Bacterial DNA was labeled using Bioprime DNA labeling system (Invitrogen Life Technologies, Burlington, ON, Canada). Fifteen μl of the supernatant containing DNA was added to a final volume of 32.5 μl containing 10 μl of a random primer solution, 0.5 μl of high-concentration DNA polymerase (Klenow fragment, 40 U/μl), 5 μl of a deoxyribonucleosidetriphosphate (dNTP) mixture (1.2 mM dATP, 1.2 mM dGTP, 1.2 mM dTTP, and 0.6 mM dCTP in 10 mM Tris [pH 8.0] and 1 mM EDTA), and 2 μl of 1 mMCy5-dCTP. Labeling reactions were performed in the dark at 37°C for 3.5 h and stopped by the addition of 5 μl Na2EDTA 0.5 M (pH 8.0). The labeled samples were then purified with a PureLink PCR purification kit (Invitrogen Life Technologies, Carlsbad, CA) according to the manufacturer's protocol. The amount of incorporated fluorescent Cy5 dye was then quantified by scanning the DNA sample with a NanoDrop ND-1000 spectrophotometer from 200 to 700 nm. Data were analyzed using a Web-based percent incorporation calculator http://www.pangloss.com/seidel/Protocols/percent_inc.html.
Hybridization of labeled DNA
Microarrays were prehybridized at 50°C for 1 hour under a Lifterslip (25 × 60 mm; Erie Scientific Company, Portsmouth, NH, USA) using a SlideBooster hybridization workstation (model SB800; Advalytix, Germany), with 50 μl of prewarmed (37°C) digoxigenin (DIG) Easy Hyb Buffer (Roche Diagnostics, Laval, Quebec, Canada) supplemented with 5% (vol/vol) bovine serum albumin (1 mg/ml; New England Biolabs Inc., Beverly, MA). After pre-hybridization, the lifterslip was removed by dipping the slides in 0.1 × SSC (saline-sodium citrate) and were air-dried. Before hybridization, the samples were dried and resuspended in 15 μl of hybridization buffer (DIG + 0.1 ug/ul ssDNA) and denatured for five minutes at 95°C. One microgram of labeled genomic DNA was hybridized on the MaxiVir1.0 microarray under a lifterslip (18 × 18 mm). The hybridization was carried out overnight at 50°C in a SlideBooster hybridization workstation. After hybridization, lifterslips were removed by dipping the slides in a 0.1 × SSC and 0.1% SDS (sodium dodecyl sulfate) solution. Post-hybridization washes were performed at 37°C: two washes with 0.1 × SSC and 0.1% SDS for ten and five minutes respectively and one last wash in 0.1 × SSC for five minutes. The microarrays were then air-dried.
Microarray slides were scanned at 5 μm resolution with a ScanArray Lite fluorescent microarray analysis system (Perkin-Elmer, Missasauga, Ontario, Canada). Acquisition of fluorescent spots was performed using the ScanArray Express software (Perkin-Elmer, Foster City, CA). Fluorescent spot intensities were quantified with ImaGene software version 8.0 (BioDiscovery, Inc., El Segundo, CA). All the microarrays were normalized using the same method. For each subarray, the mean value for each set of duplicate spotted oligonucleotides was divided by the correction factor taken from the negative controls spots. This value was then divided by the average of the empty spots to create a signal-to-noise ratio. Oligonucleotide spots with a signal-to-noise fluorescence ratio greater than the established threshold (3 in this case), were considered positive. These ratios were then converted into binary data where a value of 0 indicates a negative probe and a value of 1 a positive probe. A threshold of 3 was chosen because it best represented spot quantification. To verify that the results were accurate, we compared the .bmp image of a given sample and the quantified result.
Isolation of pathogens from hemorrhaged tissue in dairy cattle
Washed tissue samples (2.5 cm2) were placed in 0.1% TritonX-100 overnight and the released bacteria stored at -80°C or serial dilutions were direct plated. The digesta was also stored at -80°C or serial dilutions were direct plated. A 1 to 50 μl aliquot of a diluted sample was applied to CHROMagar™ Salmonella, CHROMagar™ E. coli, CHROMagar™ O157, CHROMagar™ Salmonella Plus, and CHROMagar™ Listeria plates (Dalynn Biologicals, Calgary, Alberta). To confirm identity, the presumptive isolates with the exception of the Listeria were subjected to a GN-ID A + B biochemical test (Alere™ Canada, Ottawa, Ontario). Presumptive Salmonella were also subjected to a Salmonella Latex Agglutination test (Alere™ Canada, Ottawa, Ontario, Canada). Presumptive Listeria was identified using a Listeria ID test (Alere™ Canada, Ottawa, Ontario). To detect Clostridium perfringens type A, samples were examined for characteristic features using a compound Nikon microscope set at 1000 × magnification. Digesta and tissue smears were examined for the presence of large, rectangular bacilli (rod) with or without spores (ovoid, sub-terminal). Sub-cultures on blood agar were examined for rapid spreading growth.
Isolation and identification of mycotoxigenic fungi
Feed components were collected from PS1-PS5. A 10 g sub-sample of corn silage, barley silage or hay was finely ground and a 5 ml volume added to a PDA plate. The plate was incubated for 1 to 7 days and individual fungal isolates transferred to new PDA plates. Fusarium isolates were identified by examination of micro-morphological characters according to Nelson et al.  and by PCR amplification and sequencing of a fragment of the EF1-a gene and comparing the sequence with the FUSARIUM-ID database . Penicillium isolates were identified by microscopic examination of morphology using the guide by Pitt . Aspergillus species were identified by microscopic examination of morphology using the guide provided by Klich .
Extraction of cytotoxins from mouldy feed
The methods used have been described previously . The corn silage was almost entirely moldy having a dark burgundy-red coloration for PS1 and visible pockets of white to blue mould were present in the barley silage. The barley silage had visible pockets of white and blue mold for PS2-PS5, while the hay had a pink coloration for PS3 and PS4. To extract the silages and hay, each sample was ground, a 25 ml aliquot of 50% ethanol or methanol was added to a 3 g sample of ground material and placed on a shaker at 200 rpm for 3 h. The supernatant was collected in another tube, and stored at 4°C until use.
The co-occurrence of mouldy feed and a high number of JHS cases suggested that a field survey of local corn crops was warranted for mycotoxin analysis. Cornfields from PS1 and the surrounding region in Lethbridge County were selected to compare mycotoxin profiles. A minimum of 20 intact cobs were collected from each field, the kernels removed, bagged and sent for commercial analysis (Animal Health Laboratory, University of Guelph, ON, Canada). The samples from PS1 were also submitted for analysis to Charm Sciences, Inc. who did the analysis without charge (Lawrence, MA USA).
Escherichia coli O157:H7 strain and culture conditions
Escherichia coli O157:H7 E318N is a human isolate (PT14) that was supplied by A. Borezyk, Enteric Reference Laboratory, Ministry of Health, Toronto, Ontario. The strain was maintained at -80°C in 25% glycerol: 75% Luria-Bertoli (LB) broth (Sigma-Aldrich, Oakville, Ontario, Canada) and was grown statically overnight at 37°C in LB broth (Fisher Scientific, Ottawa, Ontario, Canada) when required. The strain was serially diluted to the desired concentration with phosphate-buffered saline (PBS). Bacterial cell counts were determined by plating on SMAC agar and examined for non-sorbitol fermenting colonies that appeared as colorless colonies.
In vitro organ culture (IVOC) E. coli O157:H7 adherence assay
Healthy necropsy jejunal samples were obtained from steers using standard methods . Briefly, jejunal tissues (30 cm) were removed within 2 min of release of the intestinal tract from the carcass and each piece was maintained at 4°C for transport back to the laboratory. Upon arrival, the tissue was cut open, washed using PBS at 4°C and 2.5 cm2 pieces were excised. The IVOC adherence assay was conducted as previously described  using the E. coli O157:H7 E318N strain. This assay has been established as representing E. coli O157:H7 colonization in vivo and as a useful model system for E. coli O157:H7 colonization in cattle. To compare the ability of varying concentrations of the prebiotic, Celmanax™, to interfere with E. coli O157:H7 colonization of cattle intestinal tissue, 107 CFU/ml of E. coli O157:H7 was applied to the mucosal surface of tissue pieces to which 0%, 0.01%, 0.1%, 1% and 10% Celmanax™ diluted in DMEM was previously applied. Similarly, 0%, 0.01%, 0.1%, 1% and 10% Dairyman's Choice™ paste was added to cell monolayers and 107 CFU/ml of E. coli O157:H7 was applied to the mucosal surface. The treated mucosal explants were incubated for 4 h under standard culture conditions (37°C, 95% humidity and 5% CO2). After incubation, each tissue was washed six times with PBS to remove any unattached bacteria. The tissue was then turned mucosa-side down in 3 ml of PBS supplemented with 1% Triton X-100 (Sigma-Aldrich, Oakville, Ontario, Canada) and incubated at 4°C overnight. After 24 hr, serial dilutions of the released bacteria were plated on SMAC agar and the number of non-sorbitol fermenting colorless colonies recorded. The Triton X-100 effectively removed all the attached bacteria after 24 hr incubation at 4°C. The assay was replicated three times using the jejunum from three different animals.
In vitro cell culture (IVCC) E. coli O157:H7 E318N adherence assay
The methodology was described previously for comparing the colonization potential of E. coli O157:H7 strains belonging to different lineages . Briefly, the cell line was cultured in DMEM supplemented with 10% fetal bovine serum (Fisher Scientific, Oakville, Ontario, Canada) and gentamicin (Sigma-Aldrich, Oakville, Ontario Canada) under standard culture conditions. Cells were sub-cultured by trypsinization of the cell monolayer with 0.25% trypsin-EDTA solution (Sigma-Aldrich, Oakville, Ontario, Canada) for 5 min at 37°C, and the supernatant centrifuged at 2 087 × g for 10 min. The cell pellet was re-suspended in the culture medium and then, added to each well of a 6-well multi-well Falcon plate (Fisher Scientific, Oakville, Ontario, Canada) at a density of approximately 103 cells. The cells were grown until they formed a confluent monolayer consisting of 105 cells.
To determine the impact of the feed additives on E. coli O157:H7 E318N colonization of the colonic cell line, each well of confluent cells was washed once with PBS and then, 3 ml of DMEM with varying concentrations of the prebiotic, Celmanax™, or probiotic, Dairyman's choice™ paste, including 0%, 0.01%, 0.05% and 0.1%, was added. The concentrations of Celmanax™ used reflected the percentage achievable under standard feeding regiments for the prebiotics and probiotics given the dilution factor of the rumen and the passage rate for materials in the gastrointestinal tract. For the IVCC bioassay, we did not exceed 0.1% prebiotic or probiotic as it shifted the pH of the media and affected the health of the cells. Escherichia coli O157:H7 E318N was added to the cell monolayer to deliver a final exposure dose of 106 CFU/105 cells. The cell cultures were incubated for 3 h under standard culture conditions. At the end of the experiment, cell-monolayers were washed with PBS to remove any unattached bacteria and 2 ml of PBS supplemented with 0.1% Triton X-100 was added and incubated overnight at 4°C. Serial dilutions of the released bacteria were performed and quantified by plating onto SMAC plates. Plates were incubated at 37°C overnight and E. coli O157:H7 was quantified by counting the non-sorbitol fermenting colonies that appear colorless. The IVCC assay was replicated 6 times with a minimum of 3 different culture dates for the cell line.
Lawn assay for cytotoxicity associated with mouldy feed extracts and pure mycotoxins
The lawn assay has been described previously  and was used to examine the cytotoxicity of feed extracts and mycotoxins in the absence and presence of 0.1% Celmanax™ and Dairyman's Choice™ Paste. For the silage extracts, enterocytes isolated from the jejunum served as the cell lawn and the silage extracts were applied to assess for cytotoxicity. Briefly, a 1% SeaKem® Agarose (Mandel Scientific, Guelph, Ontario, Canada) support gel was poured into a petri dish. Next, the lawn agarose [3 ml of 3.7% SeaPlaque® agarose (Mandel Scientific, Guelph, ON, Canada)] was mixed with 3 ml of cell suspension and poured over the support agarose. For the pure mycotoxins, cell monolayers were prepared as described for the IVCC bioassay. A 400 μl aliquot of 0.4% SeaPlaque® agarose was poured over the cell monolayer and cooled for 15 min. The mycotoxins tested included DON (100 μg/ml), ZEAR (100 μg/ml), T-2 (100 μg/ml), and fumonisin B1 (50 μg/ml; Romer Labs, Union, MO, USA). A 5 μl aliquot of the stock mycotoxins was applied to the center of each cell monolayer. A 5 ul aliquot of the solvent used for the extraction process and the mycotoxin buffer served as negative controls. Each extract or mycotoxin (5 μl) was applied with or without 0.1% prebiotic or probiotic and the plate incubated for 4 h under standard culture conditions. The lawn was stained with 0.1% trypan blue (Sigma-Aldrich) and de-stained using PBS. Plates were scored the same day and the amount of extract cytotoxicity was scored as low (1), moderate (2) or high (3) which was visualized as a faint blue spot, a blue spot or a dark blue spot respectively. These activities were compared to two standards, ground corn containing 0.1 ppm aflatoxin that had a cytotoxicity score of 1 and 1 ppm aflatoxin that had a cytotoxicity score of 3. The assay was repeated a minimum of three times.
The IVOC adherence assay and IVCC adherence assay data were log transformed to normalize the data prior to analysis. All data were analyzed using ANOVA followed by a posthoc Tukey's test for comparison of the means. For the IVOC and IVCC data, the model consisted of two factors, passage number of the cell line or animal and dose. Results were considered significant if P < 0.05 and non-significant if P > 0.05.
Impact of a prebiotic and probiotic on the symptoms and development of JHS for PS1
The inclusion of Celmanax™ in the total mixed ration was associated with both a cessation of current neurological symptoms and no further development of neurological symptoms in the lactating cattle. The inclusion of Celmanax™ and Dairyman's Choice™ paste for freshening cattle changed the pattern for JHS development from 1 to 3 animals per week to 0 animals per week. This pattern was maintained throughout the winter while the cattle consumed the remaining mouldy corn and barley silage.
Impact of a prebiotic and probiotic on the symptoms and development of JHS for PS2-4
The inclusion of Celmanax™ and Dairyman's Choice™ in the total mixed ration was associated with both a cessation of the current neurological symptoms and no further development of neurological symptoms in the lactating cattle. The inclusion of Celmanax™ and Dairyman's Choice™paste for freshening cattle changed the pattern for JHS development from 1 animal per week to 0 animals per week. This pattern was maintained throughout the winter while the cattle consumed the remaining mouldy barley silage and/or hay.
Pathology associated with the jejunum PS1-PS5
Each tissue was examined and the pathology recorded. The control tissues had no pathology present. All hemorrhaged jejunum samples from JHS cases had the following common pathology: inflamed and raised Peyer's Patches in the jejunum, severe jejunal hemorrhages visible through the serosa, bloody digesta visible through the serosa, complete loss of mucosal structure in the hemorrhaged regions, dark-red erythema, large blood clots and edema. The main difference between PS5 and PS1-PS4 was the presence of a much larger blood clot that completely blocked the passage of digesta in the jejunum.
Shiga toxin - producing E. coli in the jejunum of cattle from PS1-PS4 with no history of JHS
Average number of STEC CFU per tissue type for dairy cattle with or without JHS.
Cattle with JHS (n = 12)
Mean Log CFU + SE
Cattle without JHS (n = 3)
Mean Log CFU + SE
Jejunum (per 2.5 cm 2 mucosa) 1
5.303 ± 0.184a
0.000 + 0.000b
Digesta (per ml)
4.487 ± 0.172a
0.000 + 0.000b
Escherichia coli O157:H7 and Stx in the jejunum of a cow from PS5 with a history of JHS cases
Adherent non-sorbitol fermenting colonies were identified at significant levels in the hemorrhaged regions of the jejunum. This animal had similar amounts of E. coli O157:H7 present as observed for the other production sites: 7 × 105 CFU/2.5 cm2 hemorrhaged jejunum, 1.6 × 104 CFU/ml bloody digesta, 6.0 × 104 CFU/2.5 cm2 intact severe focal hemorrhage, 1.7 × 105 CFU/2 cm2 jejunal Peyer's patch, 2.3 × 106 CFU/2.5 cm2 inflamed jejunum. To confirm a potential role for Stx in the development of JHS pathology, we evaluated the isolate for Stx expression and the blood clot blocking the hemorrhaged jejunum for the presence of Stx. The isolate did express Stx1 and Stx2, but more significantly, both toxins were detected in the blood clot.
Isolation of pathogens from dairy cattle with JHS
Bacterial pathogens in the digesta and hemorrhaged mucosa were isolated from the jejunum. CHROMagar™ is a selective media used for presumptive identification of specific pathogens including Salmonella, E. coli, E. coli O157 and Listeria[26–28]. Presumptive E. coli O157 were identified and appeared as regular mauve colonies (O157 STEC and non-O157 STEC), irregular mauve colonies or navy blue colonies with a small to large mauve halo (non-O157 STEC) on CHROMagar™ O157 plates. Presumptive E. coli O157 were confirmed as pathogenic E. coli in the GNID A + B test. Other presumptive pathogenic E. coli appeared as blue colonies on CHROMagar™ E. coli plates. All E. coli were confirmed as non-pathogenic E. coli in the GNID A + B test. White colonies were also found on this medium that were mauve on CHROMagar™ E. coli O157 and were identified as pathogenic E. coli in the GNID A + B Test. This provided a crosscheck for the results from the CHROMagar™ E. coli O157 and for the non-sorbitol or sorbitol fermenting colonies. Presumptive Salmonella were identified and appeared as mauve colonies on CHROMagar™ Salmonella plus plates, but were subsequently determined as false positives (pathogenic E. coli using the GNID A+ B kit and the Salmonella Latex Agglutination kit). Presumptive Listeria species were identified and appeared as pinpoint blue colonies with a halo on CHROMagar™ Listeria plates and these isolates were later determined to be Listeria grayi, a non-pathogenic strain. No Clostridium perfringens type A was detected. Thus, the only pathogen identified in the hemorrhaged tissues or bloody digesta for cattle with JHS regardless of the production site, were STECs.
PCR assay targeting O157 STEC and non-O157 STEC
The variation in the strength of the latex agglutination test and the possible identification of potential sorbitol-fermenting STEC suggested that closely related STECs were present in the tissues rather than E. coli O157:H7 alone. To confirm that not all isolates were E. coli O157:H7, PCR products produced from each isolate were characterized. The vt, eaeA and fliC PCR products were detected for isolates giving strong latex agglutination for O157 and H7 in the RIM™ E. coli O157:H7 Latex test defining the isolates from PS1, PS3 and PS5 as E. coli O157:H7. In contrast, only vt PCR products were detected for isolates giving weak latex agglutination for O157 and H7 in the RIM™ E. coli O157:H7 Latex test defining the isolates from PS2 and PS4 as non-O157 STECs.
DNA microarray assay targeting E. coli genes
The results from the bacterial isolations from the SMAC, CT-SMAC and CHROMagar™ O157 plates suggested that the tissues had multiple types of STEC present. There were several distinct morphologies on the CHROMagar™ O157 plates: mauve colonies with a circular form, raised elevation and entire or undulate margin; blue colonies with a mauve halo that had a circular form, raised elevation and an entire or undulate margin. These colonies were sorbitol or non-sorbitol-fermenting and tellurite-resistant. Two common STEC morphologies were observed in all tissues: regular mauve colonies having a circular form, raised elevation and entire margin; blue colonies with a mauve halo having a circular form, raised elevation and entire margin. The DNA microarray assay confirmed that mixtures of non-O157 STEC were colonizing the hemorrhaged tissues and these isolates have the locus of enterocyte effacement (LEE) pathogenicity island, stx1A, stx1B and hlyA. Finally, in addition to the genes mentioned above, variability in the presence of other virulence genes also supports the notion of a mixed STEC population. Interestingly, the absence of the stx2 gene in all the characterized isolates suggests that the detected Stx2 from the isolate and blood samples may represent a strain that was not ultimately isolated.
Mycotoxigenic fungi in silages for the production sites
Percent of samples positive for mycotoxigenic fungi for each corn silage, barley silage and hay sample from production sites (n = 5-10).
Quantitification of mycotoxins in corn from eight production sites in Lethbridge County.
IVOC E. coli O157:H7 adherence assay
IVCC E. coli O157:H7 adherence assay
Lawn assay for cytotoxicity associated with feed extracts and mycotoxins
The extracts from the corn silage from PS1 produced cytotoxicity equivalent to a 1 ppm aflatoxin (in corn) standard or cytotoxicity score of 3. Equivalent extracts from the barley silage produced a ten fold lower cytotoxicity equivalent to a 0.1 ppm aflatoxin (in corn) standard or a cytotoxicity score of 1. A 0.1% concentration of Celmanax™ eliminated the silage extract cytotoxicity regardless of the extraction buffer or the silage type. A 0.1% concentration of Dairyman's Choice™ paste had no effect on silage extract cytotoxicity (Figure 3, P > 0.05). The 50% methanol extracts of the barley silages from PS2-PS5 were equally cytotoxic to enterocytes producing cytotoxicity equivalent to 1 ppm aflatoxin (in corn) standard or a cytotoxicity score of 3. However, PS3 and PS4 also had the same activity associated with the 50% methanol hay extracts. Similarly, a 0.1% concentration of Celmanax™ significantly reduced the extract cytotoxicity regardless of the extraction buffer or the feed type (P = 0.001).
Impact of 0.1% Celmanax™ and Dairyman’s Choice™ paste on the cytotoxicity of T-2, DON, ZEAR and Fumonisin B1, n=3.
Cytotoxicity Index 1,2 (Mean ± S.E.)
Control (50% methanol)
0 ± 0 a
3 ± 0 b
2 ± 0.6 b
3 ± 0 b
3 ± 0 b
Celmanax™ + DON
0 ± 0 a
Celmanax™ + Zear
0 ± 0 a
Celmanax™ + T-2
0 ± 0 a
Celmanax™ + FUM B1
0 ± 0 a
Dairyman's Choice™ + DON
3 ± 0 b
Dairyman's Choice™ + ZEAR
2 ± 0.6 b
Dairyman's Choice™ + T-2
3 ± 0 b
Dairyman's Choice™ + FUM B1
3 ± 0 b
JHS is a hemorrhagic disease in dairy cattle with the main pathology presenting as hemorrhaging, severe inflammation, mucosal erosion and a major blood clot blocking the jejunum . Two factors are being investigated as causative agents namely mouldy feeds containing A. fumigatus and a pathogen C. perfringens type A. In the current study, we confirmed the presence of mycotoxigenic fungi but not A. fumigatus in the mouldy feeds consumed by cattle that developed JHS. In addition, we further expanded this association to include mycotoxins in feed components. Specific mycotoxins such as T-2 toxin do promote gastrointestinal lesions , but they do not induce hemorrhaging on their own. Since fumonisin B1 was present at significant levels in the corn crop and it can cause abdominal pain or diarrhea upon ingestion , the pain and abnormal feces observed in the current study suggest that there may be an interaction between pathogen colonization, mycotoxin concentrations and the development of JHS. In earlier JHS studies targeting the identification of potential pathogens, C. perfringens type A was detected, but there was some question as to whether this was relevant as it is a normal inhabitant of the intestine that quickly overgrows upon death. In the current study, no C. perfringens type A was detected but significant O157 STEC and non-O157 STEC were colonizing the hemorrhaged mucosa. STECs do cause diarrhea in other animal model systems  and their presence in the hemorrhaged region merits further investigation. With the exception of experimental challenge studies with E. coli O157:H7 , these pathogens are not known to cause disease in mature cattle. However, it is possible that this class of pathogens has been overlooked as most of the animals succumbing to JHS do so at production sites. If STECs are pathogens of cattle, they should express similar virulence traits described for serious forms of disease in other animals. One virulence determinant, Stx expression, is critical for the development of severe disease symptoms in susceptible animals [32–34]. Stxs have both lethal [35–37] and sublethal  effects on cells that benefit pathogen colonization by providing a foothold in the mucosa for replication and increasing the availability of non-intimate attachment sites. All of the STECs isolated from the cattle diagnosed with JHS expressed Stx and the Stxs were present in the blood clot that blocked the jejunum suggesting that the STECs did have the appropriate virulence traits to elicit serious disease. Future research should focus on examining the contribution of mycotoxins and STECs to the infection process associated with JHS.
Cattle supplemented with prebiotics or probiotics show improvements in performance measurements such as milk production and feed conversion efficiencies [15, 39–42]. Improvements in animal health are limited to observations of lower incidences of scours in calves , improved immune function in calves  or lower somatic cell counts in cattle [39, 45]. Given that both types of products can alter rumen microbial populations [16, 40] and prevent rumen acidosis [41, 42], these benefits have always been interpreted as an improvement in rumen function. Only a few animal studies have examined the potential use of probiotics or prebiotics to inhibit enteric pathogens such as E. coli O157:H7 in the gastrointestinal tract of cattle [14, 15] and as far as we are aware, no cattle tissue or cell studies have been attempted. In monogastric livestock, prebiotics directly act as anti-adhesives against E. coli O157:H7 by mimicking host cell receptor sites  and mucin binding sites . This reduces both the amount of E. coli O157:H7 colonization and the number of bacteria/microcolony. In the current study, the absence of an active immune system in the IVOC or IVCC bioassay together with the decrease in E. coli O157:H7 colonization in the presence of Celmanax™ supports an anti-adhesive behavior for the prebiotic. The second benefit of the prebiotic was that it blocked the cytotoxicity associated with the silages and the pure mycotoxins in vitro suggesting that it binds-up the toxic elements in a way that prevents cellular interactions. In contrast, the Dairyman's Choice™ paste had no such effect in the bioassays. The administration of the prebiotic or the prebiotic + probiotic to the cattle was associated with a cessation of neurological symptoms, no further development of neurological symptoms and no further development of new JHS cases. Future studies should examine the mechanisms responsible for the prebiotic or prebiotic:probiotic associated reduction in disease.
Prebiotics are non-digestible mannan oligosaccharides (MOS) that are used in feed rations of cattle to improve performance parameters . These products are obtained from disrupting cell walls of yeast with each product claiming to have a more effective, ruminant-specific starter strain or formulation. Other ingredients can also be present in prebiotic formulations including d-mannose which blocks pathogen type-1 pili binding to receptor sites [6, 45], glucomannan which absorbs feed-related toxins [12, 42, 46], and a yeast extract that provides a concentrated B vitamin supplement that can induce innate immune responses [10, 11]. The impact of prebiotics on livestock performance is variable [44, 47, 48] suggesting that the type of oligosaccharide or added ingredients may influence the measured changes in animal performance. In cattle, to be effective, prebiotics must navigate through the fermentation/digestion processes of the upper gastrointestinal tract prior to interacting with target sites in the intestinal tract. Therefore, the variation in responsiveness reported in studies could be related to the persistence of the prebiotic or additional ingredients in the gastrointestinal tract. The lower incidence of disease associated with prebiotic use in cattle [44, 45] together with the results of the current study suggest that a prebiotic, such as Celmanax™, warrant further investigation as disease management tools.
Escherichia coli pathogens initially adhere to the mucus layer in the intestinal tract prior to colonization of target intestinal cells . The IVOC or mucosal explant bioassay has a mucus layer and target cells while the IVCC bioassay has cells only. This suggests that the observed differences in bioassay sensitivity are related to the impact of the mucus layer on pathogen colonization. In addition, the larger reduction associated with the mucosal explant bioassay suggests a greater impact than predicted with the cell line bioassay in vivo. Previous studies with monogastric cell lines have shown that 1.6% prebiotic (GOS) reduced up to 70% E. coli pathogen colonization of Caco-2 and Hep-2 cells, while 0.1% prebiotic reduced E. coli pathogen colonization of Caco-2 cells by 10% . In contrast, 1% Celmanax™ reduced up to 98% O157 STEC colonization of mucosal explants and 0.1% Celmanax™ reduced up to 50% E. coli O157:H7 colonization of the bovine colonic cell line in vitro. Together, these results suggest that prebiotics could significantly alter STEC colonization at the mucosa and the amount of anti-adhesive behavior may be related to chemical composition. Future studies should characterize the mode of action of prebiotics to provide the basis for evaluating them as pathogen mitigation agents.
The current study confirmed that cattle developed JHS disease after consuming feed containing mycotoxigenic fungi, but also expands this association to include the mycotoxins deposited in the feed. Unlike earlier studies, we did not confirm the presence of C. perfringens type A. A mixture of novel pathogens was colonizing the hemorrhaged tissues, O157 STEC and non-O157 STEC. Shiga toxins were expressed by the STECs and were present in the blood clot blocking the hemorrhaged jejunum. A prebiotic, Celmanax™, acted as an anti-adhesive agent for STEC colonization and a mycotoxin binder in vitro. The addition of the prebiotic to alleviate milk production losses also was associated with a reduction in disease. Future studies should examine the extent of the involvement of the different STECs in the infection process that is associated with the development of JHS. In addition, further characterization of the mode of action of prebiotics is required to adequately assess them as disease management tools for cattle.
We gratefully acknowledge Keith A. Seifert and Dr. Tharcisse Barasubiye from the National Fungal Identification Service (Agriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, Ontario) for providing the identification of the initial fungal isolates from field samples. We also gratefully acknowledge Vic Gannon and Cassandra Jokinen from the Public Health Agency of Canada (Lethbridge, Alberta) for performing the initial PCR assays that separated the STEC groups. This research was supported by a grant from The Growing Forward Fund (Risk Mitigation Strategies Initiative RBPI # 1366) from Agriculture and Agri-Food Canada.
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