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Page 1: Nursery Pig Growth And Health Are Improved When ... · Animal fat – 2.01 Monocalcium phosphate 1.21 1.30 Limestone 0.87 0.80 L-lysine HC1 0.232 0.305 DL-methionine 0.127 0.145

9

6

3

0

Buty

rate

(mM

)

Wheat/Barley Corn/Soy/DDGSCorn/Soy

Substrate

3.43a

4.92b

7.37c

2.57a3.14b

4.24c

2.40a2.92b

6.66c 0.30*

Control XPC Prototype

Table 1. Composition of Control Diets1,2.

Ingredient, % Phase 1 (d 1 to 9) Phase 2 (d 10 to 21) Corn (maize) 37.14 49.10Soybean meal (48% CP) 22.61 27.64Whey powder 25.13 12.56Blood plasma 5.03 1.26Blood cells – 0.34Fish meal 2.16 2.51Soybean oil 4.02 –Animal fat – 2.01Monocalcium phosphate 1.21 1.30Limestone 0.87 0.80L-lysine HC1 0.232 0.305DL-methionine 0.127 0.145L-threonine – 0.022Salt 0.187 0.519Choline chloride (60%) 0.076 0.051Zinc oxide (72% Zn) 0.402 0.251Copper sulfate (25.2% Cu) 0.101 0.105Tiamulin3 0.176 –Chlortetracycline3 0.201 –Tilmicosin3 – 0.754Vitamin & mineral premix 0.328 0.328Total 100 100 1 All diets were formulated to meet or exceed the nutrient requirements of swine (NRC, 1998).2 The feed additives Diamond V Original XPC and Lactobacillus acidophilus- based fermentation prototype (LAFP) replaced corn (maize) at their respective treatment levels. 3 Dietary antibiotics.

ResultsPhase 1 Performance (d 1-9)

Phase 2 Performance (d 10-21)

120

100

80

60

40

20

0

g/d

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

31.3a

83.0b

112.0b

0.30*

Average Daily Gain

103.4b

200

150

100

50

0

g/d

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

93.9a

126.1b

161.5b0.30*

Average Daily Feed Intake

162.4b

1.00

0.75

0.50

0.25

0.00

ADG

/ ADF

I

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

0.33

0.66 0.690.30*

Feed E�ciency

0.64

7.8

7.6

7.4

7.2

7.0

6.8

6.6

kg

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

7.03a

7.37ab

7.67b

0.30*

Body Weight (d 9)

7.58b

360

340

320

300

280

260

g/d

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

296a

312ab

345b

0.30*

Average Daily Gain

347b

500

400

300

200

g/d

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

368a 388ab

451c

0.30*

Average Daily Feed Intake

440bc

1.00

0.80

0.60

0.40

G : F

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

P = 0.16

0.804 0.8030.765

0.30*

Feed E�ciency

0.789

12.0

11.5

11.0

10.5

10.0

9.5

kg

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

10.46a

11.13ab

11.61b

0.30*

Final Body Weight (d 21)

11.75b

30

25

20

15

10

5

0

# of

inje

ctio

ns

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

P = 0.2724

15

0

0.30*

Phase 1 (d 1-9)

0

15

10

5

0

# of

inje

ctio

ns

Control XPC 1 g/kg LAFP 1 g/kg LAFP 2 g/kg

P = 0.5014

5

1

0.30*

Phase 2 (d 10-21)

2

9

6

3

0

Buty

rate

(mM

)

Wheat/Barley Corn/Soy/DDGSCorn/Soy

Substrate

3.43a

4.92b

7.37c

2.57a3.14b

4.24c

2.40a2.92b

6.66c 0.30*

Control XPC Prototype

Nursery Pig Growth And Health Are Improved When Supplemented With A Microbial

Fementation Prototype Feed Additive

Introduction• Research in pigs evaluating the impact of feeding XPC has shown a number of beneficial affects including: • Improved growth rate and feed conversion (Shen et al., 2009; van der Peet-Schwering, et. al., 2007). • Improved gut health and immune response to challenges (Chaytor et al., 2011; Kiarie et. al. 2011; Kiarie et. al. 2012; Price et al., 2011). • Recently, Severson et al. (2010) demonstrated increased bacterial production of butyrate when XPC or a Lactobacillus acidophilus-based fermentation prototype was evaluated in an in vitro assay using fresh fecal inoculum from pigs (Figure 1). figure 1. In Vito Butyrate Production During a 12 hr Incubation.

• Further research is needed to evaluate the effects of the Lactobacillus acidophilus-based fermentation prototype on pig performance and health.

Objective• To evaluate the impact of feeding Saccharomyces cerevisiae fermentation product (Diamond V Original XPCTM) and the newly developed Lactobacillus acidophilus-based microbial fermentation prototype (LAFP) on nursery pig growth and health.

Materials and Methods• A total of 120 pigs weaned at 19 d of age and weighing 6.7 kg were use in this study. • Pigs were allotted to 1 of 4 treatments and housed 2 pigs/pen with 15 replications per treatment. • Dietary Treatments: 1. Control 2. As 1 + XPC 1 g/kg 3. As 1 + LAFP 1 g/kg 4. As 1 + LAFP 2 g/kg• The Control diet contained antibiotics and pharmacolog- ical levels of copper and zinc supplementation (Table 1). • The XPC and LAFP treatments were supplemented to the Control diet in place of corn (maize).• The treatments were fed in two dietary phases (Phase 1: d 1 to 9 and Phase 2: d 10 to 21). • Pig body weight and feed intake were recorded at the beginning of the trial and at the end of each Phase.• The number of injectable medications administered to the pigs to treat health problems during Phase 1 and 2 were also recorded by treatment. Daily animal caretakers were blinded to the experimental treatments.

Jason W. Frank & Mark Scott | Diamond V | Cedar Rapids, Iowa, USA

Pig medicaTions

Conclusions• The results of this research demonstrate that feeding LAFP, a Lactobacillus acidophilus-based microbial fermentation prototype, can significantly improve growth performance of pigs.• Pig body weight, growth rate, and feed intake were greatest in pigs fed 2 g/kg of LAFP.• Feeding either 1 g/kg or 2 g/kg of LAFP reduced the number of injectable medications.• These improvements in animal health and production may be related to improved endogenous butyrate production in the gastrointestinal tract; however, additional research is required to better understand the mode of action.

ReferencesChaytor, A.C., M. T. See, J. A. Hansen, D. C. Kendall, T. F. Middleton, P. R. O’Quinn, and S. W. Kim. 2011. Efficacy of yeast based feed additives to reduce the effects of chronic exposure to deoxynivalenol and zearalenone on internal organ health of pigs. J. Anim. Sci. 89 (E-suppl. 2): 128.Kiarie, E., S. Bhandari, M. Scott, D. O. Krause and C. M. Nyachoti. 2011. Growth performance and gastrointestinal microbial ecology responses of piglets receiving Saccharomyces cerevisiae fermentation products after an oral challenge with Escherichia coli (K88). J. Anim. Sci. 89: 1062–1078.Kiarie, E., M. Scott, D. O. Krause, H. Khazanehei, E. Khafipour, and C. M. Nyachoti. 2012. Interactions of S. cerevisiae fermentation product and in-feed antibiotic on gastrointestinal and immunological responses in piglets challenged with E.coli K88+. XII International Symposium on Digestive Physiology of Pigs. Keystone, CO, USA. Abstract #1012, page 42-43.NRC. 1998. Nutrient Requirements of Swine. 10th rev. ed. Natl. Acad. Press, Washington, DC.Price, K.L., H.R. Totty, H.B. Lee, M.D. Utt, G.E. Fitzner, I. Yoon, M.A. Ponder, and J. Escobar. 2010. Use of Saccharomyces cerevisiae fermentation product on growth performance and microbiota of weaned pigs during Salmonella infection. J. Anim. Sci. 88:3896-3908.Severson, D., I. Yoon, J. Butler, and M. Scott. 2010. Saccharomyces cerevisiae fermentation product and fermentation prototype stimulate bacterial production of butyrate in vitro with swine fecal inoculum. J. Anim. Sci. 88 (E-suppl. 3): 257.Shen, Y. B., X. S. Piao, S. W. Kim, L. Wang, P. Liu, I. Yoon and Y. G. Zhen. 2009. Effects of yeast culture supplementation on growth performance, intestinal health, and immune response of nursery pigs. J. Anim. Sci. 87: 2614–2624.van der Peet-Schwering, C.M.C., A.J.M. Jansman, H. Smidt, and I. Yoon. 2007. Effects of yeast culture on performance, gut integrity, and blood cell composition of weanling pigs. J. Anim. Sci. 85: 3099-3109.

AbstractPrevious research demonstrated increased bacterial production of butyrate when a Saccharomyces cerevisiae fermentation product (Diamond V Original XPC) or a fermentation prototype was evaluated in an in vitro assay using fresh fecal inoculum from pigs. These results led to an in vivo trial in pigs to test these feed additives. The objective of the study was to evaluate the impact of feeding XPC and the newly developed Lactobacillus acidophilus-based microbial fermentation prototype (LAFP) on nursery pig growth and health. A total of 120 pigs weaned at 19 d of age and weighing 6.7 kg were use in this study. Pigs were allotted to 1 of 4 treatments and housed 2 pigs/pen with 15 replications/treatment. The treatments were Control, XPC (1 g/kg), and LAFP at 1 g/kg and 2 g/kg. The Control diet contained antibiotics and pharmacological levels of copper and zinc supplementation. The XPC and LAFP treatments were supplemented to the Control diet and treatments were fed in two dietary phases (Phase 1: d 1 to 9 and Phase 2: d 10 to 21). Pig body weight and feed intake were recorded, as well as the number of injectable medications administered to the pigs to treat health problems during Phase 1 and 2. Pigs supplemented with XPC or LAFP had significantly greater growth rate and feed intake than pigs fed the Control diet during Phase 1 (P < 0.05). Pig weights at the end of Phase 1 for Control, XPC, and LAFP at 1 g/kg and 2 g/kg were 7.03, 7.37, 7.67, and 7.58 kg, respectively, with the weights of LAFP fed pigs being significantly greater than Control (P < 0.05). Pigs supplemented with LAFP did not require any injectable antibiotics during Phase 1, while pigs fed Control and XPC required 24 and 15 injections, respectively (P = 0.27). During Phase 2, growth rate in pigs supplemented with LAFP at 2 g/kg was significantly greater than Control (P < 0.05). In addition, pigs supplemented with LAFP at both inclusion rates had significantly greater feed intake than Control during Phase 2 (P < 0.01). At the end of Phase 2, pigs receiving LAFP at 1 g/kg and 2 g/kg were 1.16 and 1.29 kg heavier (P < 0.05) than Control. The number of injectable medications administered (P < 0.50) to the pigs during Phase 2 for Control, XPC, LAFP at 1 g/kg, and LAFP at 2 g/kg were 14, 5, 1, and 2; respectively. The results of this research demonstrate that feeding LAFP, a Lactobacillus acidophilus-based microbial fermentation prototype, can improve growth performance and health of pigs. These improvements in animal health and production may be related to improved endogenous butyrate production in the gastrointestinal tract. However, additional research is required to better understand the mode of action.

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