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Effects of feeding polyclonal antibody preparations on ruminal bacterial populations and ruminal pH of steers fed high-grain diets

N. DiLorenzo^*, F. Diez-Gonzalez and A. DiCostanzo^*,1

^* Departments of Animal Science and and Food Science and Nutrition, University of Minnesota, St. Paul 55108

	Abstract

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Three experiments with factorial arrangements of treatments were designed to test the efficacy of avian-derived polyclonal antibody preparations (PAP) against Streptococcus bovis (PAP-Sb) or Fusobacterium necrophorum (PAP-Fn) in reducing ruminal counts of target bacteria in beef steers supplemented or not with feed additives (300 mg of monensin/d and 90 mg of tylosin/d; MT). Feeding increasing doses of PAP-Sb in Exp. 1 or a single dose in Exp. 2 reduced S. bovis counts in a cubic fashion (P = 0.014). In Exp. 1 and 2, inclusion of MT in the diet had no effect (P > 0.05) on ruminal S. bovis counts. In Exp. 2, ruminal pH was increased (P < 0.05) by feeding PAP-Sb, MT, and PAP-Sb plus MT. Ruminal F. necrophorum counts were reduced by feeding PAP-Fn (P = 0.002) and MT (P < 0.001). Reduction in ruminal F. necrophorum counts was greater (P = 0.008) when feeding MT alone than when feeding PAP-Fn and MT together. In Exp. 3, ruminal S. bovis counts were not affected (P = 0.64) by PAP-Fn. Ruminal pH was not affected (P = 0.61) by feeding PAP-Fn, and the total anaerobic bacterial count was not affected (P > 0.05) by either PAP-Sb or PAP-Fn in Exp. 1 or Exp. 3. In conclusion, PAP of avian origin and against S. bovis or F. necrophorum were effective in reducing target ruminal bacterial populations. These PAP could be effective in preventing the deleterious effects associated with these bacteria, and possibly in enhancing animal performance.

Key Words: Streptococcus bovis • Fusobacterium necrophorum • polyclonal antibodies

	INTRODUCTION

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Ionophores and antibiotics are extensively used to increase animal performance by modifying ruminal bacterial populations to obtain more efficient fermentation. However, the use of antibiotics in animal agriculture is perceived by some to be a major public health concern because antibiotics are thought to contribute to the emergence of antibiotic-resistant microorganisms (Salyers, 2002). As an alternative to antibiotics, direct-fed microbial agents have been tested to enhance animal performance, but their effectiveness is inconsistent (Ghorbani et al., 2002; Brashears et al., 2003; Elam et al., 2003). The use of naturally occurring microbial or plant extracts has also been postulated to improve animal productivity, but further development is needed to obtain efficacious natural feed additives (Newbold et al., 2001).

An alternative to feeding ionophores or direct-fed microbial agents that has not received as much attention until recently is immunization. Vaccination against ruminal Streptococcus bovis and Lactobacillus spp. led to reductions in ruminal lactate concentration and target bacteria (Shu et al., 1999). Similarly, passive immunization achieved by feeding colostrum or eggs successfully prevented bovine coronavirus diarrhea (Ikemori et al., 1997) in bottle-fed calves. Feeding avian antibodies is a possible alternative because immunoglobulin Y, the main source of immunoglobulins in avian antibodies, is resistant to heat, acid digestion, and proteolysis (Shimizu et al., 1988). Polyclonal antibody preparations (PAP) against various microorganisms are produced by Camas Inc. (LeCenter, MN), but they have not been tested for their ability to affect target bacteria. An objective of the present series of studies was to evaluate effects of feeding avian-derived PAP against S. bovis or Fusobacterium necrophorum on ruminal populations of target bacteria and ruminal pH of steers fed a high-grain diet supplemented or not with feed additives (MT, monensin and tylosin). A second objective (Exp. 2) was to evaluate effects of PAP and time postfeeding on ruminal populations of target bacteria and ruminal pH of steers fed a high-grain diet supplemented or not with MT.

	MATERIALS AND METHODS

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Procedures for PAP preparation, diets, animal management, ruminal fluid collection, bacterial enumeration, and statistical analysis were the same for all 3 experiments. All animal care personnel were trained, and animals were cared for, according to the guidelines established by the University of Minnesota Institutional Animal Care and Use Committee.

Polyclonal Antibody Preparations
Polyclonal antibodies are produced under patented and proprietary procedures (Camas Inc., Le Center, MN); thus, only portions of the procedure are described herein. Immunogens were extracted from model bacteria grown under proprietary conditions to express the surface antigens that the organism uses to attach to cells. Antigens were then purified from the culture, and isolated "adherin" immunogens were made for injection into egg-laying hens with no adjuvant. The model organisms for this study were Streptococcus bovis (ATCC 9809) and Fusobacterium necrophorum (ATCC 27852). These organisms were used for the initial testing, to which wild-type organisms isolated from the rumen of normal cattle were later added. More than 600 hens were immunized per each immunogen. Eggs collected were analyzed weekly by specific ELISA test plates to monitor antibody binding.

For the study preparations, approximately 200 immunized hens were randomly selected from the total group of hens used for egg collection. Eggs were collected for 3 d, and the product was made from eggs pooled from this collection. The PAP product was made using a mixture of egg protein, molasses, soy oil, and PBS at pH 7.4. At the single dose, the PAP product was fed at 2.5 mL/d. Approximately 2 mL of the egg protein was present in each 2.5-mL aliquot of the PAP product. Titers by ELISA averaged between 1:50,000 and 1:1,000,000. The preparations contained immunoglobulin Y, immunoglobulin M, and immunoglobulin A. Counts of 10¹⁸ antibody molecules per mL of egg protein were observed. This included approximately 10 to 20% of the preparation that was not active. Because antibodies against many bacteria are found in most eggs, commercially available egg products or eggs were tested for antibodies to specific microbes using the same protocols used to produce egg protein. Although there were small amounts of antibodies in these products and eggs to specific bacteria such as Streptococcus spp. or Escherichia coli, they did not bind specific organisms to beads coated with these antibodies. In addition, the ELISA titers did not indicate binding to the specific attachment factors.

Animals and Management
In all experiments, ruminally cannulated, crossbred steers were housed in each of 2 concrete-surfaced pens (7.3 x 9.8 m) in a total confinement barn. Pens were bedded as needed with hardwood sawdust to minimize bedding consumption. Each pen was fitted with a Calan-Broadbent System (American Calan, Northwood, NH) that accommodated 12 individual bunks (0.61 m each). Steers had free-choice access to a common water trough (0.91 m).

Diets
The diet consisted of 83% dry-rolled corn grain, 13% corn silage (average particle size of 8 mm), and 4% supplement on a DM basis (Table 1). Diets were fed once daily at 0900, and the soyhull pellets with PAP or control solution were top-dressed. Each PAP or control solution was sprayed onto 120 g of soyhull pellets/d using a 10-mL syringe and hand-mixed before feeding. Steers were permitted to consume feed ad libitum. A supplement was formulated with protein, vitamins, and minerals (Table 1), with or without MT. Steers were individually fed (through a Calan-Broadbent system); feed offerings and refusals were measured daily. Samples of feed ingredients, including pellets, were collected weekly, and those of feed refusals were collected daily. Ingredient and refusal samples were composited for each study period (from 14 to 29 d). Samples were then stored frozen (– 20 ° C) until they were analyzed for DM, CP (methods 930.15, and 990.02, respectively; AOAC, 1997), NDF, and ADF. Concentrations of NDF (with heat-stable -amylase and sodium sulfite) and ADF were determined using a fiber analyzer (Model 200, Ankom Technology, Fairport, NY).

Experiment 2.
Seventeen ruminally cannulated crossbred steers (643 ± 110 kg of BW) were used in a completely randomized design with a 2 x 2 factorial arrangement of treatments. Factors were inclusion or not of 2.5 mL of PAP-Sb/d, with or without MT.

Experiment 3.
Seventeen ruminally cannulated crossbred steers (675 ± 113 kg of BW) were used in a completely randomized design with a 2 x 2 factorial arrangements of treatments. Two steers were removed from the experiment (1 each from MT and PAP-Fn treatments, respectively) due to conditions unrelated to the experiment. Factors were inclusion or not of 2.5 mL/d of a PAP against F. necrophorum (PAP-Fn), and with or without MT.

Sample Collection
Experiment 1.
Steers were gradually adapted to the diets over a 21-d period before initiation of treatments. After the adaptation period, steers were sampled (d 0) for ruminal bacterial populations (S. bovis, F. necrophorum, and total anaerobes) in the morning, before delivery of feed and PAP treatments. A second collection took place 14 d later before feed delivery.

Experiment 2.
Steers were adapted to the diet and dietary treatments for 29 d before ruminal fluid collection. On d 29, samples for measurement of ruminal bacterial populations were taken at 0 (before delivery of feed and PAP treatments) and 5.5 h postfeeding.

Experiment 3.
Steers were adapted to the diet for at least 29 d before initiation of treatments. Ruminal fluid for pH and bacterial enumeration (S. bovis and F. necrophorum) was collected on d 0 (first day for dosing PAP-Fn) and d 12 in the morning, before delivery of feed and PAP treatments.

Ruminal Bacterial Enumerations
Quantification of S. bovis.
Ruminal fluid (150 mL) was collected by hand from 3 areas in the rumen and strained through 4 layers of cheesecloth. A subsample (approximately 48 mL) was transferred to a 50-mL vial, kept at 39 ° C, and immediately transported to the microbiology laboratory. Vials were introduced into an anaerobic glove box (Coy Laboratories Inc., Grass Lake, MI) containing an O₂-free atmosphere of CO₂ (98%) and H₂. Vials were vortexed inside the glove box, and a 20-µL aliquot was transferred to each of 3 wells in a 96-well microtitration plate containing minimal medium (Russell et al., 1981).

Serial 10-fold dilutions were performed in triplicate to determine the most probable number (MPN) of S. bovis per milliliter of ruminal fluid (Anderson et al., 1987; Dehority et al., 1989). Minimal medium permitted selective enrichment of S. bovis because this bacterium can utilize ammonium salts as the only source of nitrogen (Wolin et al., 1959). Previous research in our laboratory indicated that growth of S. bovis in minimal medium did not differ from that in a nonselective medium, indicating that the use of a minimal medium did not inhibit the growth of S. bovis, and thus was suitable for use as an enrichment step.

The composition of the minimal medium was (per L): 40 mL of mineral solution 1 (0.6% K₂HPO₄), 40 mL of mineral solution 2 [0.6% KH₂PO₄, 0.6% (NH₄)₂SO₄, 1.2% NaCl, 0.25% MgSO₄ · 7H₂O, 0.16% CaCl₂ · 2H₂O], 10 mL of vitamin B solution, 5 mL of metal solution, 4.0 g of Na₂CO₃, 2 g of glucose, 0.5 g of cysteine hydrochloride, 1 mg of resazurin, and 1 mg of hemin. The vitamin B stock solution contained (per 100 mL): 20 mg each of thiamin hydrochloride, calcium D-pantothenate, nicotinamide, riboflavin, and pyridoxine hydrochloride; 10 mg of biotin; 1 mg of p-aminobenzoic acid; 0.5 mg of folic acid; and 0.2 mg of cyanocobalamin. The metal solution contained (per 100 mL): 50 mg of Na₄EDTA, 20 mg of FeSO₄ · 7H₂O, 20 mg of MnCl · 4H₂O, 2 mg of H₃BO₃, 2 mg of CoCl₂ · 6H₂O, 1 mg of ZnSO₄ · 7H₂O, 0.3 mg of NaMoO₄ · 2H₂O, 0.2 mg of NiCl₂, and 0.1 mg of CuCl₂ · 2H₂O. The pH of the medium was adjusted to 6.5 by adding NaOH, bottled anaerobically under oxygen-free CO₂, sealed, autoclaved, and stored at 4 ° C until used.

The 96-well plates were incubated inside the glove box at 39 ° C for 48 h. The contents of wells that demonstrated bacterial growth (visually assessed by the extent of turbidity in the well) were spread-plated (0.1 mL) onto an Enterococcosel agar medium (Becton, Dickinson, and Co., Sparks, MD) for confirmation of the presence of S. bovis and incubated anaerobically for 24 h at 39 ° C. Enterococcosel agar is a selective and differential medium for group D streptococci (such as S. bovis). The selectiveness is given by the presence of sodium azide and bile salts, and differentiation is achieved by the esculin hydrolysis, which produces darkening of the medium (Facklam and Moody, 1970; Anderson et al., 1987). A final (conclusive) test for confirmation of S. bovis was performed using API 20 Strep strips (bioMerieux, Inc., Hazelwood, MO).

Quantification of F. necrophorum.
Ruminal fluid collection procedures for enumeration of F. necrophorum were the same as described for S. bovis. After ruminal fluid samples were placed inside the anaerobic glove box, a 20-µL aliquot was added to each of 3 wells of a 96-well microtitration plate containing 180 µL of modified lactate medium (Tan et al., 1994). Selectiveness of modified lactate medium is based on the presence of lactate as the only carbon source and the presence of 3 antibiotics (bacitracin, gentamycin sulfate, and streptomycin sulfate). Wells that demonstrated bacterial growth were tested for the presumptive presence of F. necrophorum by adding a drop of Kovac’s reagent. If indole production was observed, well contents were streaked on brain heart infusion agar plates and incubated anaerobically at 39 ° C for 24 h. Counts of F. necrophorum per milliliter of ruminal fluid were determined by the MPN technique based on triplicate 10-fold dilutions. Isolates were confirmed as F. necrophorum using API 20A strips (bioMerieux, Inc.).

Quantification of Total Anaerobic Bacteria.
Procedures for collection of ruminal fluid for quantification of total anaerobic bacteria were the same as described above. A nonselective medium that included a variety of carbon sources was used (Bryant and Robinson, 1961). The composition of the medium was (per L): 2.5 g of glucose, 2.5 g of cellobiose, 0.5 g of soluble starch, 0.5 g of yeast extract, 10 mL of vitamin B solution, 1 mg of resazurin, 37.5 mL of mineral solution 1, 37.5 mL of mineral solution 2, 2 g of Na₂CO₃, 0.5 g of cysteine HCl, and 200 mL of centrifuged ruminal fluid (25,000 x g, 15 min). Compositions of mineral and vitamin B solutions were the same as described for S. bovis quantification. The pH of the medium was adjusted to 6.5 before autoclaving by adding NaOH. The medium was bottled anaerobically under oxygen-free CO₂, sealed, autoclaved, and stored at 4 ° C until used. Bacterial growth in each well was assessed visually by the extent of turbidity. Serial 10-fold dilutions were performed in triplicate to determine the MPN per milliliter of ruminal fluid.

Laboratory Methods
Ruminal pH was measured immediately using a model 345 Corning pH meter equipped with an immersible probe (Corning, Inc., Corning, NY) after ruminal contents were strained (approximately 100 mL) through 4 layers of cheesecloth. Ruminal pH measurements were conducted at 20 ° C.

Statistical Analyses
For the analysis of ruminal bacterial populations, data were converted before analysis using log₁₀ transformation, and arithmetic means are presented. Data on populations of ruminal bacteria or pH were analyzed as a repeated measures, completely randomized design (Steel and Torrie, 1980) using the Mixed procedure of SAS (SAS Inst., Inc., Cary, NC) with a factorial arrangement of treatments (PAP or MT). Means were separated using least squares procedures when terms for main effects or interactions were significant (P < 0.05). Means in Exp. 1 were also separated using orthogonal polynomial contrasts to determine linear, quadratic, or cubic responses.

	RESULTS

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Experiment 1.
Polynomial orthogonal contrasts were used to evaluate dose response (Table 2). Feeding increasing concentrations of PAP-Sb with or without MT reduced the ruminal counts of S. bovis in a cubic (P = 0.014) manner. This was due to the fact that feeding 2 x had no effect (P = 0.64) on S. bovis counts relative to those in steers fed no PAP. However, feeding 1 x or 3 x doses for 14 d resulted in 80 and 75% lower (P < 0.05) ruminal counts of S. bovis, respectively, relative to those in steers fed no PAP. There was no (P = 0.69) MT x PAP-Sb interaction, but a day x dose interaction (P = 0.04) was observed as result of variable reductions in S. bovis counts 14 d after feeding PAP-Sb doses. Ruminal S. bovis counts before delivery of PAP-Sb (d 0) were similar (P > 0.05) for all doses. After 14 d of PAP-Sb feeding, ruminal counts of S. bovis were similar (P = 0.79) for 1 x and 3 x doses, and lower (P < 0.05) than those in the rumen of steers fed no PAP-Sb. When comparing ruminal S. bovis counts at d 0 and 14 within a given dose, a reduction (P = 0.02) in ruminal S. bovis counts was achieved only with the 3 x dose. No effects (P > 0.05) of feeding MT with or without PAP-Sb were observed on ruminal S. bovis counts (Table 3).

Experiment 2.
There were no interactions (P > 0.05) between MT or PAP-Sb and sampling time on populations of S. bovis or pH. Results demonstrated no MT x PAP-Sb interaction (P = 0.149) for ruminal S. bovis counts or pH (P = 0.087; Table 4). Feeding MT had no effect (P > 0.05) on ruminal S. bovis counts or pH. Feeding PAP-Sb reduced (P = 0.045) ruminal S. bovis counts and increased (P = 0.014) ruminal pH (Table 4).

	DISCUSSION

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The extent of S. bovis count reduction was 80 or 75% for the 1 x or 3 x dose, respectively, and was comparable to a 79% reduction in ruminal S. bovis counts obtained by feeding 250 mg of virginiamycin/d to steers consuming a high-grain diet (Coe et al., 1999). Reductions in ruminal S. bovis counts of 99% were reported for steers vaccinated (i.m.) against S. bovis 16 h after an abrupt change from a forage diet to a high-grain diet (Shu et al., 1999). Differences observed in the magnitude of response by ruminal S. bovis counts between the study conducted by Shu et al. (1999) and our study are probably due to substantial differences in methodology approaches. Feeding PAP-Sb is considered a passive immunization method, because antibodies against S. bovis are produced by immunized hens and then fed to steers. The immunization method followed by Shu et al. (1999) led to active immunization, because steers were exposed to the antigen and adjuvant to develop their own immune response (Ghaffar, 2004).

When 2.5 mL of PAP-Sb/d (1 x dose) was fed (Exp. 2) for 29 d, a 67% reduction in ruminal S. bovis counts was observed when compared with steers fed no PAP-Sb. This reduction was lower than that achieved in Exp. 1 (80%) with the same dose. Lower ruminal S. bovis counts in Exp. 2 as well as lack of differences in ruminal S. bovis between 0 and 5.5 h postfeeding in Exp. 2 could be because counts of S. bovis in the rumens of animals adapted to high-grain diets do not tend to deviate much from 10⁷/mL of ruminal fluid (Dehority, 2003). Because Exp. 1 was conducted for 14 d after adaptation to eating high-grain diets and Exp. 2 was conducted for 29 d after adaptation, a longer period of exposure of steers in Exp. 2 to the high-grain diet may have led to differences in ruminal S. bovis counts and their magnitude of response to feeding PAP-Sb between the 2 experiments. Other studies revealed no differences in counts of starch-utilizing bacteria in the rumen of steers fed high-grain diets between 0 and 12 h postfeeding after a 12-d adaptation period (Leedle et al., 1982).

When considerable quantities of starch enter the rumen after feeding, the numbers of starch-utilizing bacteria increase as starch is rapidly hydrolyzed, peaking at 16 h postfeeding (Leedle et al., 1982). We chose to sample ruminal fluid 5.5 h postfeeding to correspond with lowest pH observed during 24-h pH measurements for steers fed high-grain diets (Cooper et al., 2002). When immunizing against S. bovis using an intramuscular vaccine, Shu et al. (1999) observed reduced counts of ruminal S. bovis 16 h after challenging grazing steers with a high-grain diet; however, 24 h after the challenge, no differences were found in ruminal S. bovis counts between immunized and nonimmunized steers. In Exp. 2, ruminal S. bovis counts were not affected by time postfeeding, agreeing with the observations of Leedle et al. (1982). Further research needs to be conducted to elucidate diurnal fluctuations of S. bovis in response to feeding PAP-Sb or MT, or under dietary changes.

In contrast to previous observations by several authors (Dennis et al., 1981; Nagaraja et al., 1981; Coe et al., 1999), feeding a supplement formulated to deliver 300 mg of monensin/d and 90 mg of tylosin/d did not affect the population of ruminal S. bovis in Exp. 1. A reduction of 60% in ruminal S. bovis concentrations was reported when 250 mg of monensin/d plus 90 mg of tylosin/d were fed to steers on a high-grain diet (Coe et al., 1999). We also observed a 67% reduction in S. bovis counts due to PAP-Sb feeding compared with steers fed no PAP-Sb; however, no effects on S. bovis were observed due to MT feeding during Exp. 2. Although some of these differences may be attributable to the size and breed of experimental animals (Coe et al., 1999 used 288- to 318-kg Holstein steers), differences may be due to response to monensin by S. bovis strains. Dennis et al. (1981) conducted an extensive study to determine the minimum inhibitory concentrations of monensin needed to impair the growth of most lactate-producing bacteria of the rumen. Interestingly, 2 of the 3 strains of S. bovis tested were sensitive to monensin, indicating some of the lowest minimum inhibitory concentrations of all species and strains tested. However, the third strain tested (S. bovis 124) was resistant to monensin at the concentrations tested (48 µg/mL of medium). This resistant strain of S. bovis is considered one of the exemptions to the general belief that monensin inhibits gram-positive bacteria (Westley, 1977; Nagaraja et al., 1981). Dawson and Boling (1983) indicated that monensin-resistant bacteria might be found in greater numbers in rumens of animals fed monensin-supplemented diets than those not fed monensin. However, this phenomenon was not necessarily associated with altered fermentation patterns. It is possible that differences in S. bovis response to MT feeding in our experiments was caused by differential response of S. bovis strains to continuous monensin feeding.

No effect on ruminal S. bovis counts was observed when PAP-Fn was fed indicating a specificity of this PAP to S. bovis. The specificity of avian antibodies was discussed by other authors (Shimizu et al., 1988; Ikemori et al., 1992) and their conclusions support our observations indicating that avian antibodies are highly specific.

Effects on Ruminal F. necrophorum.
Ruminal counts of F. necrophorum were not affected by feeding PAP-Sb, confirming the specificity of avian antibodies to F. necrophorum. However, an antagonistic effect was apparent between MT and PAP-Fn. When MT was fed without PAP-Fn, counts of ruminal F. necrophorum were lowest. Counts of ruminal F. necrophorum did not differ between steers fed PAP-Fn alone or in combination with MT, but were lower than those in steers fed no PAP-Fn. The antagonistic effect of PAP-Fn when fed in combination with monensin and tylosin could be due to an alteration of ruminal microbial population equilibrium as yet undefined. Further studies regarding changes in ruminal bacterial population under the diets and treatments tested should be conducted to better understand this interaction.

Feeding MT in Exp. 1 reduced ruminal F. necrophorum counts by 83%. In Exp. 3, a reduction of 96% in ruminal F. necrophorum counts relative to control was observed for MT, compared with the 82% reduction relative to control with PAP-Fn. Similar reductions (98%) in ruminal F. necrophorum counts were found when 250 mg of monensin/d plus 90 mg of tylosin/d were fed to steers on a high-grain diet (Coe et al., 1999). Feeding 90 mg of tylosin/d caused a reduction of 89% in ruminal F. necrophorum counts in steers fed a high-grain diet for 17 d (Nagaraja et al., 1999). Differences in the magnitudes of reduction in our studies between MT and PAP-Fn could be attributed to differences in the mode of action. Tylosin is a macrolide antibiotic and acts by directly interfering with bacterial protein synthesis, whereas antibodies are thought to bind with the bacterium, impairing reproduction.

Fusobacterium necrophorum is inhibited at a pH below 5 (Coe et al., 1999). The fact that the lowest pH found in our experiments was 5.43 (control steers, Exp. 2) indicates that inhibition of F. necrophorum due to low ruminal pH was not likely to have occurred in any of the experiments.

Effects on Ruminal pH.
In spite of a reduction in ruminal counts of F. necrophorum in response to feeding PAP-Fn, no effects on ruminal pH were observed indicating no major impact of this bacterium on ruminal pH despite its role in ruminal lactate use. Similar findings were reported by Nagaraja et al. (1999).

Feeding monensin and tylosin did not affect ruminal pH in Exp. 3. These results agree with previous studies reporting no effects on ruminal pH when monensin or tylosin or both were fed in high-grain diets (Zinn, 1988; Coe et al., 1999; Nagaraja et al., 1999). The lack of effect of tylosin on ruminal lactate or total VFA concentration in steers fed high-grain diets might have resulted in the lack of effect on ruminal pH (Nagaraja et al., 1999). Feeding PAP-Sb increased ruminal pH in Exp. 2; likely due to a reduction in ruminal S. bovis counts (Owens et al., 1998).

Effects on Total Anaerobic Bacteria.
Total anaerobic bacteria were not affected by PAP-Sb or MT in Exp. 1. Dawson and Boling (1983) evaluated the response by calves fed diets containing monensin and observed similar total anaerobic bacterial counts to calves not fed monensin. The complexity of the ruminal microbial ecosystem is such that, in general, when groups or species of microorganisms are decreased in numbers, other groups or species develop because of substrate availability; a relatively constant number of total bacteria for a given diet is thus maintained. Variations in ruminal bacterial counts are expected, however, with different diets, levels of intake, and postprandial sampling times (Leedle et al., 1982; Dehority and Orpin, 1988). Products that affect total anaerobic bacterial counts are not commonly used in production agriculture. Day-to-day stability in total anaerobic bacteria numbers was documented previously (Leedle et al., 1982). Maintaining total anaerobic bacteria at similar numbers as those found in control steers is a reflection of the innocuous effect of feeding MT or PAP-Sb on total anaerobic bacterial counts.

	IMPLICATIONS

Top Abstract INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION IMPLICATIONS LITERATURE CITED

 
Feeding a polyclonal antibody preparation against Streptococcus bovis or Fusobacterium necrophorum reduced ruminal counts of the target bacteria in steers fed high-grain diets. The polyclonal antibody preparation did not seem to cross-react within the 2 bacterial species tested, indicating some specificity of avian antibodies. Because S. bovis and F. necrophorum play a key role in the development of ruminal acidosis and abscessed livers, respectively, reducing the ruminal counts of these bacteria could be effective in preventing these deleterious conditions and enhancing animal performance.

¹ Corresponding author: dicos001{at}umn.edu

Received for publication September 1, 2005. Accepted for publication March 15, 2006.

	LITERATURE CITED

Top Abstract INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION IMPLICATIONS LITERATURE CITED

 


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