Reducing microbial ureolytic activity in the rumen by immunization against urease therein
© Zhao et al.; licensee BioMed Central. 2015
Received: 22 October 2014
Accepted: 7 April 2015
Published: 14 April 2015
Ureolytic activity of rumen bacteria leads to rapid urea conversion to ammonia in the rumen of dairy cows, resulting possible toxicity, excessive ammonia excretion to the environment, and poor nitrogen utilization. The present study investigated immunization of dairy cows against urease in the rumen as an approach to mitigate bacterial ureolytic activity therein.
Most alpha subunit of rumen urease (UreC) proteins shared very similar amino acid sequences, which were also highly similar to that of H. pylori. Anti-urease titers in the serum and the saliva of the immunized cows were evaluated following repeated immunization with the UreC of H. pylori as the vaccine. After the fourth booster, the vaccinated cows had a significantly reduced urease activity (by 17%) in the rumen than the control cows that were mock immunized cows. The anti-urease antibody significantly reduced ureolysis and corresponding ammonia formation in rumen fluid in vitro. Western blotting revealed that the H. pylori UreC had high immunological homology with the UreC from rumen bacteria.
Vaccine developed based on UreC of H. pylori can be a useful approach to decrease bacterial ureolysis in the rumen.
Ruminal microbial urease plays an important role in the nitrogen metabolism in ruminants such as cattle and sheep. The urea from diet or recycled from blood to rumen is hydrolyzed by urease to ammonia, the major source of nitrogen for many ruminal bacteria including several known cellulolytic bacteria . The traditional recommendation for urea feeding is less than 1% of the concentrate portion of the diet, approximately 135 g/cow daily . Between 40 and 80% of the urea-N synthesized by the liver also return to the rumen and gut, where 35 to 55% of this N is used in microbial anabolism in both cattle and sheep . However, the rate of urea hydrolysis (ureolysis) is about four fold greater than that of ammonia assimilation, resulting in ammonia accumulation, which can lead to toxicity, excessive ammonia excretion to the environment, and poor N utilization when diets contain a high urea content [2,4]. To alleviate this problem, different urease inhibitors have been evaluated to reduced ureolytic activity, including acetohydroxamic acid, phenyl phosphorodiamidate, N-(n-butyl) thiophosphoric triamide, boric acid, and bismuth compounds, to slow down production of ammonia in the rumen . However, their efficacy decreases over time due to microbial adaptation , and some of these compounds pose potential risk animal and human health, precluding their use in production.
Recent studies have shown that immunization is a potential approach to mitigate methane emissions [7-9], lactic acidosis , and to decrease protozoal population  in the rumen. We hypothesize that immunization against rumen urease can be an effective approach to slow down ureolysis in the rumen. Bacterial urease consists of two (alpha and beta) or three (alpha, beta and gamma) structural subunits. The alpha subunit (UreC) contains a urea binding site and a catalytic site. The ureC gene has been used as a gene marker to examine UreC diversity in bacterial communities because it is quite conserved among different bacterial species . In one study, the UreC of jack bean urease has been tried as an antigen to immunize sheep to inhibit rumen ureolysis in sheep rumen ; however, no obvious anti-urease activity was achieved probably because of low immunological homology between jack bean urease and rumen bacterial urease. The objectives of the present study were to examine the diversity of UreC in the rumen, identify an antigen that has high immunological homology with rumen UreC, develop an anti-urease vaccine from bacterial UreC, and evaluate anti-urease immunization as an approach to decrease ruminal ureolysis.
Diversity of rumen bacterial urease gene
Immunological homology between purified rumen urease and H. pylori urease
Vaccine and specific antibody titers
The above ureC diversity data showed that the majority (86%) of the UreC in the rumen share high homology (84-100% aa sequence identity) with the UreC of H. pylori. The urease of H. pylori also share high immunological homology with the urease of rumen bacteria. Therefore, H. pylori UreC was selected as the antigen to elicit immunization against urease in the rumen of dairy cows. Another reason to choose the UreC of H. pylori was the availability of full-length sequence of its ureC gene so that this UreC protein can be overexpressed in E. coli. The UreC of H. pylori was successfully expressed in E.coli BL21(DE3) following induction with IPTG. The molecular weight of the expressed UreC was about 66 kDa, consistent with the molecular mass predicted from the UreC sequence (see Additional file 1). About 20 mg purified UreC was obtained. The expressed UreC protein, together with Freund’s adjuvant, was used as the vaccine to immunize the dairy cows.
Urease activity and rumen fermentation after immunization
Inhibition of urea hydrolysis by anti-urease serum in vitro
Most of the ureases in the rumen are produced by bacteria, but little is known about the diversity of the urease-producing bacteria because only 6.5% of the rumen bacteria have been cultured or characterized [14,15]. The urease genes carried by rumen ureolytic bacteria have not been systematically examined. In a study conducted in 1970′s, Cook et al.  found that urease from rumen bacteria, such as Staphylococcus spp., was either intracellular or bound to the surface of the cell wall. The diversity of ureolytic bacteria and their urease gene have to be identified before highly effective urease vaccine can be developed. The present study is the first study that examined the diversity of ureC genes in the rumen of dairy cows using a cultivation-independent approach. About 86% of the recovered UreC sequences shared high sequence identity (84-100%) to that of H. pylori; however, interestingly, none of the recovered UreC sequences matched that previously recovered from any cultured rumen microbes. The UreC from H. pylori has been verified to have high immunogenicity in mice and human . In the present study, overexpressed UreC of H. pylori was shown to be highly immunologically homologous to rumen UreC of dairy cows. The observed inhibition to urease activity and corresponding decrease in ammonia accumulation suggest that specific antibodies against rumen bacterial urease were produced by the dairy cows vaccinated with the overexpressed UreC of H. pylori.
As demonstrated in the present study, urease vaccination did elicit a humoral immune response as indicated by the elevated serum and saliva specific antibody titers observed in the vaccinated cows but not in the control cows. Specific IgG and IgA titers in the serum and the saliva were further increased following booster immunization and peaked after the third and second booster immunization, respectively. The IgG and IgA titers in the serum had high positive correlation with those in the saliva. The specific IgG and IgA could flow into rumen fluid with saliva, because the liquid in the rumen is primarily (>70%) derived from saliva . Although rumen contains proteolytic bacteria, no significant degradation of IgG molecules within the first 4 h of incubation in fresh rumen fluid [19,20]. As such, anti-urease antibodies produced by vaccination can persist long enough in the rumen to bind to urease and reduce ureolytic activity.
Immunization with jack bean urease failed to reduce urease activity or urea kinetics in sheep rumen  or produce antibody against the urease of Helicobacter in vaccinated mice . This inability is probably attributed to a lack of immunological homology between bacterial urease and jack bean urease. The reduced urease activity by the bovine anti-urease antibody elicited by the UreC of H. pylori, both in vitro and in vivo, clearly indicates that the UreC of H. pylori has high immunological homology with rumen bacterial ureases, at least many of them, and can be used as an effective vaccine in cows. The Western blotting further confirmed the immunological homology between the rumen bacterial urease and the H. pylori urease. However, given the diverse UreC present in the rumen (Figure 1), a vaccine prepared from a combination of representatives of different rumen UreC clusters may be more effective than UreC of H. pylori or single rumen bacterial UreC. Future studies are also needed to identify ureolytic bacteria and their ureases so that anti-urease antibodies with greater efficacy might be developed.
The alpha subunit of H. pylori urease may serve as a vaccine to immunize cows to slow down ureolysis in the rumen. Combined representatives of rumen bacterial UreC may be an even more effective vaccine to improve urea utilization efficiency without the adverse effects associated with chemical urease inhibitors.
Diversity of rumen bacterial urease gene
Rumen digesta samples were collected from four rumen-fistulated Chinese Holstein dairy cows before morning feeding. Total microbial DNA was extracted using the RBB + C method . A degenerate primer set specific for the ureC gene (ureC forward:5′-TGGGCCTTAARMTHCAYGARGAYTGGG-3′, and ureC reverse:5′-GTGRTGRCAMACCATNANCATRTC-3′)  was used in PCR amplification of the UreC in the rumen samples. A 25 μL PCR reaction contained 2.5 μL PCR buffer (Invitrogen, Carlsbad, CA), 0.75 μL MgCl2 (50 mM), 0.5 μL dNTP (10 mM), 1.5 μL each forward and reverse primer (10 μm), 0.3 μL Platinum Taq DNA polymerase (Invitrogen, Carlsbad, CA), 1 μL rumen microbial DNA (~100 ng μL−1), and 16.95 μL sterile ddH2O. The PCR cycling included 94°C for 5 min; 30 cycles of 94°C for 30 s, 50°C for 30 s, and 72°C for 30 s; 72°C for 15 min; and 10°C for 30 min. The expected PCR amplicons of about 324 bp were visualized on agarose (2%) gel and then purified using a Gel Purification Kit (Qiagen, Valencia, CA), cloned into the pMD19-T vector (TaKaRa, Dalian, LN, China), and then transformed into competent E.coli JM109 cells (TaKaRa, Dalian, LN). Random clones were sequenced with the T7 primer using a BigDye Terminator v3.1 cycle sequencing kit (Applied Biosystems, Inc., Foster, CA). All sequences were trimmed to remove the vector regions and low-quality ends using the PREGAP4 program of the STADEN software package . The sequences were then compared to GenBank sequences using Blastx, and the most similar UreC sequences derived from known bacterial species were downloaded and combined with the UreC protein sequences recovered in this study. A phylogenetic tree was constructed from the combined UreC sequences using the MEGA software .
Expression and purification of urease alpha subunit (UreC)
The gene encoding the UreC of H. pylori was amplified from the genomic DNA of H. pylori UMAB41 using a forward primer (5′-AAAACATATGAAAAAGATTAGCAGGAAAG-3′) with a NdeI cutting site (italic) and a reverse primer (5′-CCGCTCGAGCTACCGCGCCATCTTCCACCAG-3′) with a XhoI cutting site (italic). Following double digestion with NdeI and XhoI, the purified full-length gene was ligated into correspondingly double-digested pET-30a(+) (Novagen, Madison, WI). The recombinant plasmids were then transformed into competent E.coli BL21 (DE3) (Promega, Madison, WI). The transformants were grown until an OD600 of 0.6, and over expression of the cloned UreC was induced at 30°C by IPTG (1.0 mM). The E. coli cells were harvested by centrifugation, and total cell protein was isolated using the BugBuster® Protein Extraction Reagent (Novagen, Madison, WI). Purification of the overexpressed UreC was achieved using a Ni-NTA kit (Novagen, Madison, WI) per manufacturer’s instructions. The UreC protein was analyzed by SDS-PAGE and visualized after staining with Coomassie Blue R-250. The UreC protein concentration was determined using the Bradford assay (Bio-Rad, Hercules, CA).
Purification of rumen urease and western blotting using UreC of H. pylori
Rumen fluid was collected fistulated dairy cows fed a total mixed ration (TMR) (see Additional file 3). The bacterial cells were isolated by gradient centrifugation and then disrupted by ultrasonication (300 W, 15 min). The cellular proteins were concentrated using ultrafiltration (50 kDa) and then a Hi Trap Capto Q ion exchange column (GE Healthcare, Little Chalfont, UK) that was pre-equilibrated with a Tris–HCl buffer (20 mm, pH 8.0). Gradient elution was used to separate urease protein using the same Tris–HCl buffer with a NaCl concentration ranging from 0 to 1 M at a flow rate of 1 mL min−1. The fractions with positive urease activities were pooled and concentrated by lyophilization .
The urease protein was separated on SDS-PAGE and transferred to a nitrocellulose membrane (Sigma, St Louis, MO, USA) for immune blotting analysis. The membrane was blocked with 5% low-fat dry milk dissolved in TBS-T buffer for 1 h at room temperature and then stained overnight with the bovine anti-urease serum (1:1000). Following three washes for 10 min each in TBS-T buffer, the membrane was incubated in diluted (1:1000 diluted) horseradish peroxidase-conjugated sheep anti-bovine antibody (Bethyl Laboratories, Montgomery, TX) for 1 h at room temperature before incubation in 6 mL of chemiluminescence reagent (Sigma, St Louis, MO, USA) for 1 min. Positive immunostaining was determined based on the presence of a visible band corresponding to the expected UreC protein.
Immunization of dairy cows
Eight rumen-fistulated lactating Chinese Holstein dairy cows, with a body weight of 556 ± 19 kg, were randomly allocated to two treatment groups (n = 4), with one group (control) mock vaccinated with physiological saline containing the Freund’s adjuvant only, while the other group (vaccinated) was vaccinated with the overexpressed UreC of H. pylori. Briefly, an UreC protein solution (0.4 mg mL−1 UreC protein) was combined with an equal volume of Freund’s complete adjuvant. The mixture was emulsified, resulting in an UreC vaccine containing 0.2 mg mL−1 UreC protein. Each cow in the vaccinated group was injected subcutaneously on the neck and intramuscularly on the buttock  with 0.5 mL UreC vaccine at day 0. The injections were repeated at days 14, 28 and 42 as boosters, but with the Freund’s complete adjuvant being replaced by Freund’s incomplete adjuvant. The control group received the same injection procedures in parallel but with physiological saline containing Freund’s adjuvant only. All cows were housed under identical conditions and fed the same TMR (see Additional file 3) thrice daily. The animals were strictly cared for following the standard protocols approved specifically for this study by the Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China (Permit Number: RNL10/08).
Animal sample collection and analysis
At days 0, 7, 21, 35, and 49, samples of blood, saliva, and rumen fluid were collected about 2 h after morning feeding. Blood samples were collected from the caudal vein of each cow into evacuated tubes and centrifuged at 3000 × g for 10 min to separate the serum. Saliva samples were collected from the oral cavity of the cows using a suction tube and then centrifuged at 10000 × g for 15 min to collect the supernatant. Rumen fluid samples were collected through rumen fistula and filtered through four layers of cheesecloth. Subsamples of rumen fluid were also collected for analysis of urease activity. At day 56, 60 g urea was infused directly into the rumen of the cows of both groups through the rumen fistula after morning feeding. Rumen fluid was then collected at 0, 1, 2, 4, 6 and 8 h post infusion and analyzed for pH, ammonia concentration, and VFA profile.
The titers of specific anti-urease IgG and IgA in the serum and the saliva samples were determined using a modified ELISA protocol . Briefly, the plates were coated with 100 μL well−1 UreC solution (40 μg mL−1) and incubated overnight at 4°C. After washing, the plates were blocked with 150 μL well−1 of 1% (vol./vol.) chicken serum for 90 min at 37°C. An aliquot of 100 μL well−1 serially diluted serum (1:400 to 1:25600 for IgG, 1:500 to 1:32000 for IgA) and saliva (1:640 to 1:10240 for IgG, 1:20 to 1:640 for IgA) from either the vaccinated cows or the cows in the control group was added. Fetal calf serum was used as a negative control. The plates were incubated at 37°C for 2 h. Then, 100 μL donkey anti-bovine IgG or IgA alkaline phosphatase conjugate (Promega, Madison, WI) (1:10000 diluted) was added to each well and incubated at 37°C for 2 h. Following dilution to a final concentration of 1.5 mg mL−1 in a buffer containing 1 M diethanolamine and 0.5 mM MgCl2, the substrate chromogen tetramethylbenzidine (100 μL) was added to each well. After incubation for 30 min at 37°C, the reaction was terminated by adding 50 μL of 2 N NaOH to each well. The absorbance was recorded at 405 nm using an ELISA plate-reader (Infinite F200; Tecan, Mannedorf Switzerland). The reaction was defined as positive when the absorbance exceeded twice that of the negative control. Antibody titers were expressed as the highest dilution that gave a positive reaction.
Urease activity was determined by measuring the amount of ammonia released from urea . One unit of urease activity was defined as one μmol ammonia released per min per mL rumen fluid or mg microbial protein. Ammonia concentration was determined by the phenol-hypochlorite reaction as described by Weatherburn et al. . Concentrations of VFA were analyzed by gas chromatography (model 6890, Series II; Hewlett Packard Co., Avondale, PA) as described by Mohammed et al. .
Evaluation of the anti-urease antibody on urea hydrolysis in rumen fluid in vitro
The TMR diet, which was the same as that fed to the cows, was weighed into serum bottles (0.25 g bottle−1) containing 20 mL McDougall’s buffer, 10 mL of strained fresh rumen fluid, and urea (final concentration of 1 g L−1). To each bottle, bovine serum from either the control group or the vaccinated group was added. Two bovine serum concentrations from the vaccinated group was used in two treatments: Trt1 (IgG titer, 1:40000) and Trt2 (IgG titer, 1:80000). Three replicates were used both the control and the anti-urease serum treatments. The bottles were gassed with CO2, sealed with rubber stoppers, and incubated in a 39°C shaking water bath. Subsamples were collected at 0, 1, 2, 4, 8 and 12 h post incubation, and the pH was measured immediately. Ammonia concentrations were determined colorimetrically as described above. Urea concentration was determined with the diacetyl monoxime method of Marsh et al. . Rates of urea disappearance and concomitant ammonia N formation were computed as the slope of regression of the natural logarithm of urea and ammonia N concentration, respectively, over the course of the incubation.
All data were subjected to analysis of variance using the MIXED procedure of SAS (version 9.0, SAS Institute Inc., Cary, NC). The REPEATED statement was used for variables measured over days (titers of IgA and IgG, and urease activity) or times (pH, VFA, NH3-N). Tukey multiple comparison test was used to separate the means when significant differences were indicated by the MIXED procedure. Differences were considered significant at P < 0.05.
Nucleotide sequence accession numbers
The ureC sequences obtained in this study were deposited in the GenBank database under accession numbers JQ611755 to JQ612071.
This work was supported by Natural Science Foundation of China (31430081), Basic Research Program (973) of China (2011CB100804), and Agricultural Science and Technology Innovation Program (ASTIP-IAS12).
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