Effect of whey fermented by Enterococcus faecium in consortium with Veilonella parvula on ruminal bacteria in vitro

Abstract

The objective of this research was to evaluate the effect of whey fermented by Enterococus faecium in consortium with Veilonella parvula in vitro on ruminal microorganisms in different substrates, with or without monensin. The first experiment was carried out in a completely randomized design, in a 6 × 3 factorial arrangement (six substrates × three whey levels) with two replicates. In experiment two, a 2 × 3 × 4 factorial arrangement (with and without monensin, three foods and four levels of fermented whey) was used, in a randomized design with four replicates, totaling 24 treatments. There was no interaction among the wheys and the substrates in the variable for pectin, starch, and carboxymethyl cellulose. There was a greater growth of amylolytic and pectinolytic microorganisms and a lower growth of proteolytic and cellulolytic microorganisms. A significant effect of optical density was found in the media without substrate and that containing trypticase and glucose due to the addition of fermented whey. There was interaction for the pH at 24 hours among whey, food and monensin. For ammonia at 24 hours there was effect for food, whey and monensin, and interaction among factors. For microbial protein at 24 hours, there was effect for food, whey, monensin and no interaction among sources of variation. The use of whey fermented by bacteria Enterococcus faecium and Veilonella parvula improves microbial protein synthesis by ruminal bacteria in media containing different energy sources. The combination of fermented whey and monensin shows variable results in relation to microbial growth.

ammonia; fermentation; microbial protein; monensin; rumen; ruminal pH

Introduction

Ruminants have the ability to use a large variety of foods as nutrient source due to the mutualistic relationship between the host (animal) and rumen microorganisms, which enables the use of complex compounds unusable for most other animals. Modifications in the rumen microbial ecosystem provide changes in nutrient availability for the ruminant.

Thus, there is much interest in alternatives to manipulate the ruminal microbiota. The rumen can be manipulated to improve the use of substrate and the efficiency of fermentation and use of food nutrients. Among the studied ruminal additives for ruminants, the organic acids and direct-fed microbials have stood out. These food additives act in different ways on ruminal fermentation, improving animal performance, without leaving residues in products of animal origin.

Organic acids in the rumen may stimulate consumption of lactate by Selenomonas ruminantium by preventing or correcting the drop of ruminal pH associated with ruminal acidosis; reduce methanogenesis by reducing energy loss associated with methane production in the rumen; and present a complementary effect like buffer on ruminal pH (Castillo et al., 2004).

The mechanism of action of direct-fed microbials (DFM) is not well understood yet, but it is believed that these microorganisms have attributes that enhance the rumen functionality (Weinberg et al., 2003). Research has shown beneficial effects of DFM in preventing ruminal acidosis (Krehbiel et al., 2003), improving dry matter digestibility and animal performance (Weinberg et al., 2003). However, some research studies did not show improvement of digestibility (Raeth-Knight et al., 2007).

A source of propionic acid and DFM can be produced from the fermentation of whey by two ruminal microorganisms: Enterococus faecium and Veilonella parvula. Lactose is a substrate from the genus Enterococcus sp that produces lactate. This is used as an energy source by bacteria of the genus Veilonella sp, which has propionic acid among its end products of the fermentation (Ribeiro et al., 2009).

In this context, the objective of this study was to evaluate the effect of whey fermented by Enterococus faecium in consortium with Veilonella parvula on ruminal microorganisms in vitro in different substrates, with or without the presence of monensin.

Material and Methods

The research was divided into two experiments. Both in vitro? experiments were performed in the Laboratory of Anaerobic Microbiology, Department of Microbiology, Universidade Federal de Viçosa, Viçosa, Minas Gerais State, Brazil.

In the two assays the same fermented whey was used. It was initially dehydrated and resuspended in water so that it contained 40 g/L lactose. Subsequently, the pH was adjusted to 7.0 with NaOH at 1.0 M. The whey was then autoclaved, saturated with carbon dioxide, and inoculated with Enterococcus faecium and Veilonella parvula (3% of the medium). The whey was kept for 48 hours at 39 °C with continuous CO₂ bubbling, and pH constantly corrected to 7.0 by adding NaOH; then, it was frozen for later use in incubations.

One liter of rumen fluid was collected from cattle fistulated in the rumen, and immediately transported to the laboratory in a thermos. It was then placed at rest for 30 minutes at 39 °C, and, after the formation of the liquid interfaces, the intermediary fluid was removed and centrifuged at 5000 xg for 10 minutes, discarding the supernatant to obtain the inoculum containing the active microbial population (pellet). The pellet formed, which contained the predominant microorganisms in the rumen fluid, was re-suspended in synthetic medium (40 mL of saline solution A - which contains, per liter: 7.3 g K₂HPO₄*3H₂O; 40 mL of saline solution B - which contains, per liter: 6.0 g of K₂HPO₄, 12.0 g of (NH₄)2SO₄, 12.0 g of NaCl, 2.5 g of MgSO₄*7H2O and 1.6 g of CaCl*2H₂O; 0.50 g of yeast extract; 1.0 g of trypticase - Trypticase, BBL Microbiology Systems, Cockesyille, MD; 0.60 g of cysteine hydrochloride; 1.0 mL of resazurin; 4.0 g of sodium carbonate; and 870 mL of water) autoclaved and saturated with carbon dioxide. Another centrifugation was performed at 5000 xg for 10 minutes, with the supernatant discarded again. The pellet formed in the last centrifugation was, then, re-suspended in synthetic medium autoclaved and saturated with carbon dioxide (Rumen Bacteria).

The fermented whey was centrifuged at 5,000 xg for 15 minutes and the supernatant from the centrifugation was used in the different combinations (whey). The centrifugation procedure was used so that the microorganisms inoculated in the whey did not constitute the fermented whey of the experiment, and thus, counted as ruminal microorganisms in the experimental units containing fermented whey, or were used as protein source.

The experimental design was completely randomized, in a 6 × 3 factorial arrangement (six substrates and three whey levels) with two replicates. The combinations were: no substrate (control), no substrate + 100 mL/L and 200 mL/L, respectively, of whey in the medium; trypticase, trypticase + 100 mL/L and 200 mL/L, respectively, of whey in the medium; starch, starch + 100 mL/L and 200 mL/L, respectively, of whey in the medium; carboxymethyl cellulose, carboxymethyl cellulose + 100 mL/L and 200 mL/L, respectively, of whey in the medium; pectin, pectin + 100 mL/L and 200 mL/L, respectively, of whey in the medium; and glucose, glucose + 100 mL/L and 200 mL/L, respectively, of whey in the medium.

All incubation tubes contained 0.2 mL of rumen bacteria, 40 mg of the substrate of each combination and synthetic medium autoclaved and saturated with carbon dioxide in quantities required to reach 10 mL of medium in total in all the combinations. The incubations were performed in anaerobic tubes, in which the medium was saturated with carbon dioxide. The tubes were sealed and kept at 39 °C.

After 24 hours of incubation, the optical density of each experimental unit was determined in the spectrophotometer Spectronic 20D + (Thermo Electron, Waltham, MA, USA) with wavelength of 600 nm (OD_600nm)_.

An interaction effect was found between the substrate and the whey level (P<0.05). Therefore, the data were evaluated by regression analysis according to the concentration of fermented whey in the culture medium in each substrate. The significance of the quantitative effects (α = 0.05) was taken as criterion for the choice of models.

In the second assay, the rumen fluid from a fistulated bovine was also collected and the same procedures were carried out as in the first assay to obtain the inoculum with active microorganisms. However, rather than re-suspending the pellet in saline solution, it was re-suspended in a synthetic medium.

The experimental design was completely randomized, in a 3 × 2 × 4 factorial arrangement (three substrates, two levels of monensin and four levels of whey) with four replicates. The combinations were: starch with and without monensin plus 0, 100, 250 and 500 mL/L, respectively, of whey in the medium; trypticase with and without monensin plus 0, 100, 250 and 500 mL/L, respectively, of whey in the medium; cellulose with and without monensin plus 0, 100, 250 and 500 mL/L, respectively, of whey in the medium.

All incubation tubes contained 4.5 mL of rumen bacteria, 150 mg substrate of each compound, 0.1 mL ethanol (pure or with monensin), 0 or 1.0 or 2.5 or 5.0 mL autoclaved whey and synthetic medium autoclaved and saturated with carbon dioxide in sufficient quantities to reach 10 mL medium in total in all the compounds. The substrates used were trypticase as a source of protein, starch as a source non-fibrous carbohydrate and ground Whatman paper number 1 as a source of cellulose. An amount of monensin was added to the ethanol solution so that the final concentration was 15 μM monensin in the culture medium.

The optical density of the medium at 600 nm was read by diluting 1.0 mL of the medium in approximately 10 mL of distilled water, to know the contents of cells in the treatments at 0 hour.

All incubation tubes were saturated with CO₂, sealed, and kept (lying) at 39 °C under stirring (80 rpm) for 24 hours.

At 0 and 24 hours, 2.0 mL samples from each experimental unit were collected, placed in Eppendorf tubes for pH reading and subsequently centrifuged at 5,200 xg for 10 minutes, and the supernatant was frozen for later analysis of ammonia concentration by the method of Chaney and Marbach (1962). The pellet was re-suspended in saline solution (0.9% NaCl), centrifuged again and separated from the supernatant, then re-suspended in saline solution (0.9% NaCl) and frozen for subsequent quantification of microbial protein by the method of Bradford (1976).

The results were submitted to analysis of variance and regression. The effect of whey levels was verified by the analysis of linear regression, adopting the significance of the regression parameters and the determination coefficient values as criteria for the choice of models. The different substrates were compared by Tukey's test at 5% significance in the first assay and by the average test at 5% probability in the second assay, using a statistical analysis program (SAEG, version 9.1).

Results

No interaction (P>0.05) was found among wheys and the substrates in the variable for pectin, starch and carboxymethyl cellulose. There was a higher growth of pectinolytic and amylolytic microorganisms and a lower growth of proteolytic and cellulolytic microorganisms (Table 1).

Table 1
Mean values of microbial growth in different substrates and in different concentrations of whey fermented by Enterococcus faecium and Veilonella parvula, expressed as optical density (OD600nm) after 24 hours of incubation

Substrate	Whey levels (mL/L), %
	0	100	200
	No substrate	0.110bC	0.175abC	0.211aB
Trypticase	0.105bC	0.231aC	0.288aB
Starch	0.510aA	0.560aA	0.488aA
Carboxymethyl cellulose	0.163aC	0.175aC	0.190aB
Pectin	0.489aA	0.572aA	0.489aA
Glucose	0.283bB	0.429aB	0.502aA
Coefficient of variation, %		10.20

There was effect (P<0.05) of the optical density in the media without substrate, which contained trypticase and glucose due to the addition of fermented whey in the medium.

For the pH at 0 hour, there was no effect (P>0.05) when adding monensin (Table 2); this was expected, since monensin does not have a rapid action.

Table 2
Mean pH values in the rumen in different substrates, with and without monensin and in different concentrations of whey fermented with Enterococcus faecium and Veilonella parvula after 0 hour of incubation

		Monensin
	Without		With
	6.87a		6.89a
Food		Whey levels (mL/L)
	0	100	250	500
Trypticase1	6.73B	6.80AB	6.97A	7.15A
Starch2	6.87A	6.92A	7.03A	7.22A
Carboxymethyl cellulose3	6.75AB	6.71B	6.90B	6.83B

• ^{1 Ŷ}
  = 6.7351 + 0.0084 X; r² = 0.98
• ^{2 Ŷ}
  = 6.8642 + 0.0071 X
• ^{3 Ŷ}
  = 6.7975
• ^{Coefficient of variation}
  = 1.63%

There was an interaction (P<0.05) between the foods and whey levels (Table 2), in which the fermented whey provided a linear increase in pH when the starch and trypticase were used as substrates, without adjusting the pattern for the increase in pH when using carboxymethyl cellulose as the substrate.

For pH at 24 hours, there was interaction (P<0.05) among whey, food and monensin (Table 3).

Table 3
Mean pH values in the rumen in different substrates, with and without monensin, and in different concentrations of whey fermented by Enterococcus faecium and Veilonella parvula after 24 hours of incubation

Without monensin
Food		Whey levels (mL/L)
	0	100	250	500
Trypticase1	6.97aA	7.02aA	7.12aA	7.17aA
Starch2	5.50bC	5.60bC	5.87bC	6.40aC
Carboxymethyl cellulose3	5.80bB	6.02bB	6.50bB	6.82aB
	With monensin
Food		Whey levels (mL/L)
	0	100	250	500
Trypticase4	6.95aA	7.00aA	7.07aA	7.12aA
Starch5	5.80aC	5.87aC	6.15aC	6.35aC
Carboxymethyl cellulose6	6.42aB	6.62aB	6.72aB	6.82aB

• ^{1 Ŷ}
  = 6.9888 + 0.0040 X; r² = 0.93
• ^{2 Ŷ}
  = 5.4519 + 0.0184 X; r² = 0.98
• ^{3 Ŷ}
  = 5.8447 + 0.0208 X; r² = 0.96
• ^{4 Ŷ}
  = 6.9635 + 0.0034 X; r² = 0.94
• ^{5 Ŷ}
  = 5.7998 + 0.0114 X; r² = 0.96
• ^{6 Ŷ}
  = 6.4964 + 0.0073 X; r² = 0.86
• ^{Coefficient of variation}
  = 2.05%

For ammonia at 0 hour of incubation (Table 4), there was no effect (P>0.05) for monensin, with the mean values of 10.30 and 10.22 mg/dL without addition and with addition of monensin, respectively, because this ionophore does not have a rapid action. An effect (P<0.05) was observed for food and whey, with no interaction between the sources of variation. The trypticase demonstrated greater effect among the other food used, with mean values of 13.07 mg/dL, while the starch showed 10.05 mg/dL and the carboxymethyl cellulose showed 7.64 mg/dL.

Table 4
Mean values of ammonia in the rumen in different concentrations of whey fermented by Enterococcus faecium and Veilonella parvula, expressed in mg/dL after 0 hour of incubation

Whey levels (mL/L)1
0	100	250	500
9.24	9.67	11.02	11.09

• ^{1 Ŷ}
  = 9.4363 + 0.0388 X; r² = 0.80
• ^{Coefficient of variation}
  = 14.03%

The mean values of ammonia in the rumen increased linearly (P<0.05) with the inclusion of whey levels. The results adjusted to the linear model: Ŷ = 9.4363 + 0.0388*X (r² = 0.80).

For ammonia at 24 hours, there was effect (P<0.05) for food, whey and monensin, and interaction among food, whey and monensin (Table 5).

Table 5
Mean values of ammonia in the rumen in different substrates, with and without monensin, and in different concentrations of whey fermented by Enterococcus faecium and Veilonella parvula, expressed in mg/dL after 24 hours of incubation

Without monensin
Food		Whey levels (mL/L)
	0	100	250	500
Trypticase1	90.89aA	102.07aA 103.82aA		87.34aA
Starch2	5.86aB	7.59aB	8.56aC	13.90aB
Carboxymethyl cellulose3	7.00bB	12.49aB	18.14aB	20.40aB
	With monensin
Food		Whey levels (mL/L)
	0	100	250	500
Trypticase4	54.92bA	58.53bA	55.69bA	52.58bA
Starch5	6.55aC	7.62aC	9.67aC	11.89aB
Carboxymethyl cellulose6	14.78aB	17.24aB	17.62aB	16.29aB

• ^{1 Ŷ}
  = 91.6123 + 1.1426 X . 0.0246 X²; r² = 0.98
• ^{2 Ŷ}
  = 5.6572 + 0.1563 X; r² = 0.96
• ^{3 Ŷ}
  = 9.0412 + 0.2574 X; r² = 0.86
• ^{4 Ŷ}
  = 55.7509 + 0.1507 X . 0.0043 X²; r² = 0.73
• ^{5 Ŷ}
  = 6.6426 + 0.1079 X; r² = 0.99
• ^{6 Ŷ}
  = 15.0188 + 0.2096 X . 0.0037 X²; r² = 0.91
• ^{Coefficient of variation}
  = 13.48%

For microbial protein at 0 hour, there was no effect (P>0.05) for monensin (Table 6), showing that monensin does not have a quick action. An interaction effect was observed between food and whey.

Table 6
Mean values of microbial growth in different substrates, with and without monensin, and in different concentrations of whey fermented by Enterococcus faecium and Veilonella parvula, expressed as microbial protein concentration (mg/L) after 0 hour of incubation

			Monensin
		Without		With
		1,028.31a		980.98a
Food			Whey levels (mL/L)
		0	100	250	500
Trypticase1		728.64A	904.74A	1,139.24AB	1,073.02B
Starch2		838.37A	872.70A	1,046.34B	1,589.91A
Carboxymethyl cellulose3		369.50B	700.84A	1,349.75A	1,442.96A

• ^{1 Ŷ}
  = 25.2765 + 715.4057 X . 0.3611X²; r² = 0.98
• ^{2 Ŷ}
  = 757.3141 + 15.5068 X; r² = 0.94
• ^{3 Ŷ}
  = 504.2903 + 21.7164 X; r² = 0.83
• ^{Coefficient of variation}
  = 20.70%

For microbial protein at 24 hours, there was effect (P<0.05) for food, whey and monensin, with no interaction among sources of variation (Table 7).

Table 7
Mean values of microbial growth in different substrates, with and without monensin, and in different concentrations of whey fermented by Enterococcus faecium and Veilonella parvula, expressed as microbial protein concentration (mg/L) after 24 hours of incubation

Monensin
Without			With
1,133.90a			914.12b
		Food
Trypticase	Starch	Carboxymethyl cellulose
950.37b	1,238.81a		882.84b
	Whey levels (mL/L)1
0	100	250	500
742.85	952.01	1,092.86	1,308.31

• ^{1 Ŷ}
  = 10.7253 + 796.0982 X; r² = 0.96
• ^{Coefficient of variation}
  = 23.13%

Discussion

The concentrations of ruminal microorganisms increased in the medium as fermented whey was added, which can be explained by the presence of organic acids in the whey that provided conditions for a more appropriate fermentation to proteolytic microorganisms and fermenters of nonstructural carbohydrates (Table 1).

The fermented whey stimulated the growth of bacteria in medium containing glucose or trypticase, due, perhaps, to the fact that part of the population of proteolytic microorganisms and fermenters of nonstructural carbohydrates are more resistant to higher levels of organic acids (propionic acid and lactate) in the medium, decreasing the substrate competition between these microorganisms and others sensitive to organic acid. In addition, the whey may have provided additional substrate (lactate) to be fermented by certain groups of bacteria, favoring microbial growth.

Several ruminal bacteria are able to grow in low pH media and use both glucose and lactate as energy source, such as Selenomonas ruminantium, which is present in large amounts in the rumen of animals, and Megasphaera elsdenii. Selenomonas ruminantium strains, which use lactate, grow in media rich in glucose, accumulating lactate that can be used to form acetate and propionate. Megasphaera elsdenii is another bacterium that ferments a variety of simple sugars, but has high affinity for lactic acid (Russell, 2002) and is also resistant to pH decrease.

Bacteria with high specific activity of fermenting amino acids use amino acids as the main energy substrate, degrading proteins more strongly than others (Russell, 2002). However, excessive deamination of amino acids resulting from the fermentation of these bacteria causes loss of nitrogen in ammonia form, decreasing the nitrogen utilization efficiency and microbial growth. According to Leopoldino et al. (2005), acidity reduces ammonia production by inhibiting the growth of proteolytic bacteria population.

There was no effect (P>0.05) when the substrate in the medium was starch or pectin, having no microbial growth with the inclusion of the fermented whey. There was a small increase in microbial growth with the substrate starch or pectin when there was 100 mL/L whey in the medium, and a decrease when 200 mL/L were added. The initial increase in microbial growth may also be due to the presence of organic acids of the whey that improved microbial fermentation. However, adding larger amounts of fermented whey in the medium may result in toxic levels of lactate and propionic acid to the amylolytic and pectinolytic microorganisms, inhibiting their growth, which explains the decrease with the addition of 20 mL/L whey. Amylolytic and pectinolytic microorganisms may be more sensitive to propionic acid and lactate than proteolytic microorganisms and other fermenters of nonstructural carbohydrate.

In the medium containing carboxymethyl cellulose as substrate, there was no effect (P>0.05) of fermented whey on microbial growth. This may be because cellulolytic microorganisms are not affected by constituents of fermented whey, more precisely by organic acids. Nevertheless, studies show that cellulolytic bacteria are one of the groups most susceptible to drop in pH (Russell and Strobel, 2005). As one of the main effects of propionic acid and lactate is decrease of pH, the results of this assay contradict the results obtained by Russell and Strobel (2005).

These increases with the addition of fermented whey occurred exactly because the whey already had a higher pH (Table 2).

The effect of monensin (P<0.05) was observed for starch and carboxymethyl cellulose, in which the media without monensin had their pH decreased. Oliveira et al. (2005) reported that animals fed diets with high percentages of grains have an increase in the growth of Streptococcus bovis, resulting in a higher lactate production, leading to a marked drop in pH and symptoms of acidosis. This shows that monensin is highly beneficial for inhibiting the development of these bacteria and increasing the ruminal pH (Krehbiel et al., 2003).

Concerning the foods, trypticase showed higher pH values both with and without monensin. In the same way, Lana et al. (2007), evaluating the in vitro degradability of some foods, found lower pH reduction for the foods with high protein content. Starch had the lowest values both with and without monensin (Table 3). The addition of fermented whey caused a linear increase (P<0.05) in pH values for all foods in both the presence and absence of monensin, which can be explained by the higher of pH the whey, since its effect was observed when it was added at 0 hour. Thus, as the amount of whey added to the medium is increased, the pH elevates.

The effect among the foods occurred because ammonia is the result of the fermentation process of protein; hence why trypticase showed the highest amount of ammonia. Trypticase is a protein source of easy degradation. Inversely, carboxymethyl cellulose and starch are sources of carbohydrates. The lowest value was obtained by carboxymethyl cellulose for ammonia production with an average of 7.64 mg/dL. It possibly occurred because the added whey already has a greater amount of ammonia due to its fermentation.

Monensin reduced ammonia production only when trypticase was used with substrate (Table 5), but did not reduce it in treatments containing starch and fiber, corroborating Russell and Strobel (1989), who claim that the ionophores have better results in diets containing a high degradable protein/fermentable carbohydrate ratio. The large amount of ammonia produced when the substrate was trypticase was due to the high degradability of its protein, which is consistent with the results found by Oliveira et al. (2004). This reduction in ammonia production was due to inhibition of microbial populations with high capacity of deamination of amino acids (Chen and Russell, 1989). Flythe (2009) observed that plants with high monensin contents inhibit bacteria that produce ammonia. This may be because ionophores are membrane-soluble molecules that shuttle ions down the transmembrane concentration gradients (Flythe, 2009). The dissipation of these gradients causes the loss of the ionmotive forces that drive membrane transport proteins, power motility and maintain cell turgor (Flythe, 2009).

The effect (P<0.05) among the different foods occurred because ammonia is the result of the fermentation process of protein (Table 6), which presented the highest mean values when incubated with trypticase and had no statistical difference when incubated with starch or fiber.

The effect (P<0.05) of fermented whey on ammonia production at 24 hours was observed differently among the different incubated foods. When trypticase was used as substrate, it presented a quadratic behavior with or without monensin, indicating that the addition of larger quantities of fermented whey in the medium may provide toxic levels of lactic acid and propionic acid, inhibiting the growth of these microorganisms.

When starch was used as substrate, it increased linearly as the levels of fermented whey were added. This is related to the increase in the concentration of ruminal microorganisms in the medium, in which addition of whey containing organic acids causes an increase in fermentation of proteolytic microorganisms, and consequently greater ammonia production.

For the substrate fiber, a linear effect was observed when monensin was not present, which is reported in the preceding paragraph, by the increase in the amount of organic acids with the addition of whey. On the other hand, when there was monensin in the medium, it had a quadratic behavior, probably because monensin inhibited microbial populations with high capacity of deamination of amino acids (Chen and Russell, 1989).

The increase observed as fermented whey was added was precisely due to the microorganisms contained therein (Table 6).

Monensin inhibited microbial growth (Table 7), as it was also reported for ammonia, in which monensin inhibits the growth of microbial populations, especially gram-positive bacteria (Martinele et al., 2008).

For the different foods, a higher microbial growth was observed in the medium in which the substrate was the starch. This increased microbial growth in part of amylolytic bacteria is because they have a faster fermentation than the cellulolytic and proteolytic bacteria.

The positive effect (P<0.05) found with the addition of whey on microbial protein concentration is probably because the organic acids contained in the whey stimulated microbial growth and whey constituents possibly served as a nutrient source for the microorganisms, as noted at 0 hour, when the same effect occurred. Brown et al. (2006), in the studies reviewed, verified that amylolytic bacteria became more numerous as more dietary concentrate was fed and lactate-utilizing bacteria increased more dramatically when the diet contained more than approximately 60% concentrate. Thus, whey probably enhanced lactate-utilizing bacteria because it contained lactate.

The combination of whey fermented by bacteria Enterococcus faecium and Veilonella parvula and the antibiotic monensin had variable results with respect to the parameters evaluated. Therefore, no benefit was found for the use of these two substances combined.

There was an effect of whey fermented by bacteria Enterococcus faecium and Veilonella parvula on the proteolytic microorganisms, fibrous carbohydrate fermenters and non-fibrous carbohydrate fermenters. However, the proteolytic bacteria were the most affected by fermented whey. This demonstrates that bacteria that ferment amino acids are sensitive to propionic and lactic acids contained in fermented whey.

The use of whey fermented by Enterococcus faecium and Veilonella parvula improves microbial protein synthesis by ruminal bacteria in media containing different energy sources (protein, fibrous carbohydrates and non-fibrous carbohydrates).

Conclusions

The use of whey fermented by bacteria Enterococcus faecium and Veilonella parvula improves microbial protein synthesis by ruminal bacteria in media containing different energy sources (protein, fibrous carbohydrates and non-fibrous carbohydrates).

The combination of whey fermented by bacteria Enterococcus faecium and Veilonella parvula and the antibiotic monensin has variable results in terms of microbial growth.

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Publication Dates

• Publication in this collection
  May 2014

History

• Received
  20 Aug 2013
• Accepted
  30 Jan 2014