Weaning is one of the most stressful periods in the life of a pig, resulting in lower feed intake, poorer growth, and higher morbidity and mortality, particularly during the first weeks after weaning or until the immune system has become more fully developed. Weaning is a stress, independent of weaning age, caused by the abrupt separation from the sow and by other stressors related to changes in the physical and social environment, mingling with pigs from different litters, dietary transitions, and exposure to different pathogens or antigens.1 Weaning stress causes intestinal inflammation and damage to mucosal barrier structure and function.2-5 Therefore, it is crucial that the pig overcomes weaning stress rapidly to survive and be productive through the commercial production cycle.
Along with good husbandry and health management, dietary interventions may be a viable and practical way to help pigs adapt and transition through the complexities associated with weaning stress. Many studies have demonstrated consistently better performance with the use of spray-dried plasma (SDP) than with other protein sources, independent of its origin (porcine, bovine, or a blend), in diets for weaned pigs.1,6,7 Several studies have also reported that SDP reduces the incidence of diarrhea during the post-weaning phase,8,9 and improved performance has been described in pigs kept under less hygienic research conditions or commercial circumstances10 or in younger pigs with less mature immune systems.11 In addition, some studies also show that the intestinal mucosal immune response is better in animals fed diets containing SDP.12-14 Taken together, these studies suggest that diets containing plasma proteins improve the immunological response to stress without compromising the response to pathogens, allowing the animal to use more nutrients for growth and other productive functions instead of for maintaining the immune response.
Spray-dried whole egg (SDE) without shells is an excellent nutrient source due to its high digestibility, favorable amino acid balance, fat content, and high metabolizable energy (ME).15,16 In addition, SDE derived from hens not hyperimmunized against specific pig pathogens contains active components such as immunoglobulins (IgY),17 lysozyme, and antimicrobial proteins.18 Inclusion of SDE in nursery pig diets did not consistently promote better performance than did other high-quality protein ingredients, eg, SDP, milk proteins, and fish meal.19
Egg-yolk antibodies (EYA) from eggs produced by hens hyperimmunized against specific bacterial antigens have been suggested as a more efficient source of SDE and as an effective way to control diarrhea in post-weaned pigs.20-23 Positive responses to EYA have been consistent when the microorganism used to challenge the pigs is the same as that used to hyperimmunize the hens.20-23 However, limited published information is available about the use of EYA under commercial conditions when sanitation is suboptimal.
The purpose of this study was to investigate the effects on performance of weaned pigs reared under unsanitary conditions (pens not cleaned and sanitized after previously housing pigs) and fed diets containing either EYA or one of two dietary inclusion levels of SDP of porcine origin (SDPP).
Materials and methods
The experimental procedures with animals described in this study were conducted after approval from the Institut de Recerca i Tecnologia Agroalimentàries (IRTA) Ethical Committee on Animal Experimentation. The IRTA is a research institute belonging to the Catalonia government.
Animals and housing
The study was conducted in the post-weaning facility of the experimental farm of IRTA Animal Nutrition (Centre Mas de Bover, Constantí, Spain). The pigs were housed in two nursery rooms with 24 and 12 pens, respectively, each 1.7 m2 (0.96 m × 1.77 m), with four pigs per pen. All pens were identically equipped with one single-sided hopper feeder with four eating spaces, and a cup-type drinker system. The rooms had automatic heating, forced ventilation, and completely slatted floors. The experimental facilities were not cleaned prior to the entry of the study animals in order to impose an environmental challenge.
One hundred and forty-four newly weaned intact male pigs (Duroc × Landrace), obtained from a commercial farm at 21 days of age, were used in the study. Average initial body weight (BW) was 6.3 kg (standard deviation [SD], 0.80 kg). At the start of the study, the pigs were sorted by BW and divided into 36 groups of four animals, so that the first four groups (ie, 16 animals) belonged to block 1, the next four to block 2 and so on, up to block 9. The four animals in a given group were randomly distributed, using the random number generator function in Excel (Microsoft Corporation, Redmond, Washington), among the four replicates (pens) in the corresponding block, and the same was done for the other groups in the same block. This was repeated for all blocks, so that nine blocks with four replicates (pens of four piglets) were generated. The four pens belonging to a block were adjacent to each other and in the same room, so that location was also considered within the block effect. Once the pigs had been assigned to the 36 replicates, the four experimental treatments were randomly assigned, using the random generator function in Excel, to the four replicates in each block.
Experimental design and treatments
The experimental diets (13.8 MJ metabolizable energy [ME]; 13.5 g per kg lysine) were offered for a period of 14 days (pre-starter phase). Between days 15 and 28, a common starter diet (without SDPP or EYA) was offered (13.6 MJ ME; 12.5 g per kg lysine). Diets were formulated to meet the nutrient requirements of the National Research Council (NRC; 1998).24 Feed was presented in mash form and offered ad libitum. Ingredient and nutritive compositions of the diets are shown in Table 1 and Table 2, respectively.
The four feed treatments consisted of a control group (Control); two treatments containing SDPP (AP820P from APC Europe, SA, Granollers, Spain) at 3% and 6%, replacing soy protein concentrate in the Control diet (SDPP3 and SDPP6 groups); and a fourth treatment containing a commercial EYA product (Globigen; EW Nutrition GmbH, Visbek, Germany) at the manufacturer-recommended dietary inclusion rate (0.2%), also replacing soy protein concentrate (EYA group). According to the manufacturer’s literature, the Globigen EYA product contains specific antibodies (immunoglobulins) against a number of pathogens described as “Escherichia coli K88, E coli K99, E coli 987P, E coli Oedema, Salmonella typhimurium, transmissible gastroenteritis virus, Cryptosporidium, Rotavirus, Clostridium perfringens, circovirus.” The experimental feeds were offered from day 1 through day 14 post weaning, and a common starter diet was fed to all animals from day 15 through day 28.
Feed and piglets were weighed at the start of the study, at day 14, and at the end of the study (day 28). Initial and final BW, average daily gain (ADG), average daily feed intake (ADFI), and gain-to-feed ratio (G:F) were calculated.
Statistical analysis
The experimental unit was the pen, and average pen values were used for the performance parameters. For statistical analysis (GLM procedure; SAS Inc, Raleigh, North Carolina), a randomized block design was used, with initial weight and pen location as block criteria. Least squares means, probabilities of differences, and standard errors of the mean were obtained to evaluate differences among treatment means.
In addition, orthogonal contrasts were used to compare production parameters in pigs in the Control or the EYA treatments versus the two SDPP treatments, and to determine the linear response to the increasing dose of SDPP supplementation. Results were considered statistically significant at P < .05 and a trend was defined at P < .10.
Results
During the pre-starter period (days 0 to14), four piglets died with signs of diarrhea (two in the Control group and two in the SDPP3 group). During the common starter phase (days 15 to 28), another four piglets died (one in the Control group, two in the SDPP6 group, and one in the EYA group). Four animals from the SDPP3 treatment group were culled due to extremely poor body condition. The data from these animals were considered missing values and were not used in the calculations. Their feed intake was calculated with a model that estimates the individual feed intake of pigs in group feeding,25 and was subtracted from the total intake of the corresponding pen.
Between days 0 and 14 (Table 3), ADG was greater in the SDPP6 group (P < .05) than in the Control and EYA groups. For BW, ADG, and ADFI, performance in the SDPP3 group was intermediate between the Control and SDPP6 groups. Gain-to-feed ratio for EYA treatment was the lowest in this period. Linear improvements (P < .05) in BW and ADG and tendencies (P < .10) for higher ADFI and G:F were observed with increasing SDPP during this period. In addition, groups fed SDPP had greater ADG, ADFI, and G:F than the group fed EYA (P < .05), and tended to have greater ADG than the Control group (P < .10). Performance data did not differ between pigs fed the diet including EYA and those fed the Control diet.
During days 15 to 28 (Table 4), when a common starter diet was fed to all animals, no significant differences in ADG and ADFI were observed among treatments. However, pigs that had been previously fed SDPP had lower G:F than did the Control and EYA groups (P < .01).
For days 0 through 28, no differences for any parameters were observed among treatment groups. However, relative to the Control group, in pigs previously fed SDPP6, final BW was 0.46 kg higher, while in pigs previously fed the SDPP3 and EYA diets, final BW was 0.59 and 0.43 kg lower, respectively.
Discussion
In this study, pigs were subjected to challenging conditions by being weaned and housed in pens uncleaned since previous use. These conditions were effective in inducing post-weaning growth depression, as can be observed from the generally low growth rates of these animals, compared to normal production values in the industry or experience before and after the current trial in the same facilities. In the study facility, ADG of similar pigs on similar diets, but weaned into a clean environment, ranged from 175 to 250 grams per day at 0 to 14 days post weaning. The pathogens associated with these stressful conditions were not determined, but signs of watery diarrhea and poor feed conversion were observed.
Although the nutrient compositions of the experimental diets met the nutrient recommendations of the NRC (1998),24 it could be argued that the diets were limiting for sodium and some essential amino acids, according to the values proposed more recently (NRC; 2012).26 Even if some nutrients were limiting, the magnitude of their limitation cannot explain the poor performances observed. Instead, it is more likely that poor performance was driven mainly by the markedly lower feed intake of the study pigs. Under the conditions of the current trial, health status of the animals might have been compromised, resulting in the observed poor appetite.
The better performance observed with the inclusion of SDPP in the feed during the initial 14 days was consistent with previous publications indicating that formulating diets with SDPP improves post-weaning performance of pigs, especially when sanitary conditions are not optimal.1,10 Several publications have demonstrated that when SDPP is included in the diet of animals challenged with a diversity of pathogens (Escherichia coli, Salmonella, rotavirus, porcine reproductive and respiratory syndrome, and porcine epidemic diarrhea virus [PEDV]), the animals had better health and more rapid recovery from these pathogens.27-33 Enhanced performance provided by SDPP in diets for weaned pigs may be related to beneficial effects on intestinal barrier function, inflammation, and diarrhea.13
During the common starter phase (days 15 through 28), the two groups of pigs previously fed SDPP diets had lower G:F than did the Control or EYA groups. Over the entire study period (days 0 to 28), pigs previously fed the SDPP6 diet had numerically better final BW, ADG, and ADFI than did the Control group, but this was not the case for the SDPP3 and EYA groups. The reasons for these observations in the current study are unknown. However, it has been reported13 that pigs fed a diet with 5% SDPP for 14 days post weaning had less secretory activity, lower diarrhea scores, and less pro-inflammatory cytokine (mRNA TNF-α) in colon tissue, resulting in less damage to gut barrier function than in pigs fed diets with either 0% or 2.5% SDPP.13 In addition, a recent study30 demonstrated that the dietary inclusion rate of SDPP and feeding duration post weaning is important for maintaining longer-term gastrointestinal tract function after SDPP is removed from the diet. In that study,30 pigs were fed diets with either 0%, 2.5%, or 5.0% SDPP (5.0% SDPP in a diet fed for 14 days versus 2.5% SDPP in a diet fed for 7 days), and at day 34 in the nursery (50 days of age) pigs were transported to a different facility and challenged with Salmonella Typhimurium. At day 2 post challenge, distal ileum samples were collected and subjected to various chemical and physical measures. Results indicated pigs previously fed the 5.0% SDP diet for 14 days post weaning had lower histological scores, myeloperoxidase and IL-8 concentrations, and 4 kDa fluorescein isothiocyanate dextran (FD4) flux rates, along with higher concentrations of plasma and ileal TNF-α than in other groups, suggesting that inclusion rate and duration of feeding SDPP in diets can influence subsequent immunological and intestinal injury induced by Salmonella challenge. The data from the current study indicate that the inclusion rate of SDPP in the diet may need to be higher than 3% to maintain the performance benefits obtained during the initial 14 days post weaning.
Likewise, some studies suggest a growth-promoting effect of EYA in early-weaned pigs challenged with specific pathogens.20-23 In most studies demonstrating improvements in animal performance when EYA has been fed, the animals had been challenged with the same pathogen for which the hens had been inoculated to produce the specific EYA. For example, a study22 reported the effect on performance of pigs challenged with enterotoxigenic Escherichia coli (ETEC) K88 when a pea-protein-based diet was supplemented with EYA from hens immunized with ETEC K88 antigen. The results indicated that the pigs fed a diet with EYA had higher ADG than those fed a Control diet without EYA. In the same study,22 pigs fed a diet with SDPP also had a higher ADG than the Control group, but no differences were observed between the groups supplemented with SDPP or EYA. In addition, the authors reported less severe diarrhea and lower mortality when either EYA or SDPP was included in the diets. Both the EYA and SDPP diets contained specific antibodies against ETEC K88 and F18, and therefore the authors suggested that the antibodies in these two products may have prevented ETEC K88 from binding to the mucosal receptors.22 A different study19 in weaned pigs fed diets containing SDE without antibodies against specific pathogens reported that pigs fed the SDE diet had higher ADFI during the first 7 days post weaning than did the pigs fed the control diet, but other performance parameters did not differ. However, pigs fed a diet containing SDP had significantly higher ADG, ADFI, and G:F than the control group. Similarly, in an earlier study,34 weaned pigs were fed a diet containing egg-yolk powder with antibodies against Salmonella Typhimurium or a diet containing SDP, or were treated with antibiotics starting at day 3 of the trial. At day 7, all pigs were challenged with the strain of Salmonella Typhimurium used in the egg-yolk powder. The authors found that the percentage of pigs shedding Salmonella was lower in the antibiotic treatment group than in the other groups. However, E coli antibiotic resistance was greater in pigs fed antibiotics than in pigs in the other treatment groups. Health and performance indicators (weight gains, white blood cell counts, and plasma concentrations of Salmonella antibodies) did not differ among treatment groups, indicating that feeding those antibodies may not have been effective in reducing Salmonella shedding. Further, in another study,35 weaned pigs challenged with K88+ E coli and fed diets with 0.00%, 0.32%, or 3.20% EYA (IgY) developed watery diarrhea and became dehydrated, compared to an unchallenged Control group. No quantifiable concentrations of IgY were detected either in treated or Control pigs by testing small intestinal content using an enzyme-linked immunosorbent assay. According to the authors, the E coli challenge was successful in creating a clinical syndrome similar to field cases. The presence of chicken egg-yolk antibodies in the feed did not appear to be effective in preventing the disease.
During the process of manufacturing commercial spray-dried plasma, one single production lot of SDPP is derived from the pooled blood of 6000 to 10,000 pigs.36 Each lot of SDPP contains antibodies against multiple pathogens circulating in the pig population at any time. Therefore, it is not surprising that SDPP may contain antibodies with neutralizing capacity against the unknown pathogens affecting the pigs used in our study, as it has been demonstrated that commercial SDPP contains neutralizing antibodies against common swine pathogens.37 However, there is substantial literature demonstrating that the effects of dietary SDPP are due to the presence not only of immunoglobulins, but also other functional proteins, growth factors, cytokines, and biologically active compounds like functional peptides and amino acids that contribute to its beneficial effects on animal performance and health.12,38 However, the exact roles of each of the functional components present in plasma that contribute to the physiological improvements of gastrointestinal barrier function have yet to be completely elucidated. These proteins can interact with immune cells in the mucosa, thus changing the cytokine environment. In addition to this luminal effect, spray-dried plasma also has systemic effects. For example, it can reduce the expression of pro-inflammatory cytokines in peripheral tissues of pigs challenged with lipopolysaccharides (LPS) from E coli39 and prevent the increase in activated lymphocyte populations in an LPS-induced lung inflammation model.40 In addition, it has been demonstrated that dietary SDP decreased the uterine concentrations of TNF-α and IFN-γ, and serum TNF-α, C-reactive protein, and cortisol, but increased uterine anti-inflammatory cytokine (TGF-β1) concentration in a pregnancy animal model study. 41 Since the organized gut-associated lymphoid tissue is an inductive site that connects with both local and peripheral effector sites (respiratory tract, glandular tissues, and the uterine mucosa), it can be further hypothesized that spray-dried plasma may favorably modulate the broader common mucosal immune system.
A recent study33 evaluated a potential positive effect of SDPP or EYA on pigs challenged with PEDV. That EYA product consisted of a liquid egg formulation that, according to company specifications, was tested to contain anti-coronavirus antibodies. The pigs in all the infected groups (Control, SDPP, and EYA) began shedding PEDV in feces by day 3 post infection, and under the study conditions, SDPP or EYA addition did not significantly alter PEDV shedding or overall disease course after experimental challenge, except that the pigs in the SDPP group appeared more active during the acute PEDV disease stage, with less pronounced diarrhea. In addition, fecal PEDV shedding in treated pigs (SDPP or EYA) was lower than in the Control pigs in the early stage of infection, which could contribute to lower environmental PEDV loads and lower transmission rates to uninfected contact pigs. Furthermore, in the same study,33 at day 3 post infection, adherent E coli in the intestine were detected in two of three pigs fed the Control diet and two of three pigs in the EYA group, but none (zero of three) in the SDPP-fed group, indicating that in the PEDV-challenged pigs fed the diet with SDPP, concurrent opportunistic pathogens like E coli were prevented.
In summary, the results of the current study indicate that, under the unsanitary conditions described, performance of pigs fed diets with SDPP during the initial 14 days after weaning was better than that of the EYA and Control groups, but longer-term performance (days 0 to 28) did not differ among groups. In this study, challenge pathogens were not identified and antibodies against those specific pathogens were not identified in the EYA fed. Under these conditions, better pig performance was not observed when diets were supplemented with EYA.
Implications
- Under the conditions of this study, spray-dried porcine plasma linearly increases performance in weaned pigs reared in an unknown challenge environment during the period that the ingredient is fed.
- Under the conditions of this study, the performance benefit of feeding spray-dried porcine plasma from day 0 to 14 post weaning is maintained to day 28 when the inclusion rate is 6%, but not when the inclusion rate is 3%.
- Under the conditions of this study, egg-yolk antibodies from eggs of hens hyperimmunized with specific bacterial antigens do not benefit performance in a non-specific pathogenic environment.
Conflict of interest
Javier Polo is employed by APC Europe, SA, Granollers, Spain, a company that manufactures and sells spray-dried plasma. However, APC Europe did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. David Torrallardona has no conflict of interest.
Acknowledgements
The authors gratefully acknowledge the technical advice and help writing and revising the manuscript of Dr Joe D. Crenshaw.
Disclaimer
Scientific manuscripts published in the Journal of Swine Health and Production are peer reviewed. However, information on medications, feed, and management techniques may be specific to the research or commercial situation presented in the manuscript. It is the responsibility of the reader to use information responsibly and in accordance with the rules and regulations governing research or the practice of veterinary medicine in their country or region.
This article was originally published in Journal of Swine Health & Production 2016; 24(1):21–28.
References
1. Torrallardona D. Spray dried animal plasma as an alternative to antibiotics in weanling pigs – A review. Asian-Aust J Anim Sci. 2010;23:131–148.
2. Spreeuwenberg MAM, Verdonk JMAJ, Gaskins HR, Verstegen MWA. Small intestine epithelial barrier function is compromised in pigs with low feed intake at weaning. J Nutr. 2001;131:1520–1527.
3. Boudry G, Peron V, Le Huerou-Luron I, Lalles JP, Seve B. Weaning induces both transient and long-lasting modifications of absorptive, secretory and barrier properties of piglet intestine. J Nutr. 2004;134:2256–2262.
4. Pie S, Lalles JP, Blazy F, Laffitte J, Seve B, Oswald IP. Weaning is associated with an upregulation of expression of inflammatory cytokines in the intestine of piglets. J Nutr. 2004;134:641–647.
5. Smith F, Clark JE, Overman BL, Tozel CC, Huang JH, Rivier JEF, Blisklager AT, Moeser AJ. Early weaning stress impairs development of mucosal barrier function in the porcine intestine. Amer J Physiol Gastrointest Liver Physiol. 2010;298:G352– G363.
6. Coffey RD, Cromwell GL. Use of spray-dried animal plasma in diets for weanling pigs. Pig News Inf. 2001;22:39–48.
7. Van Dijk AJ, Everts H, Nabuurs MJA, Margry R, Beynen AC. Growth performance of weanling pigs fed spray-dried animal plasma: a review. Livest Prod Sci. 2001;68:263–274.
*8. Gatnau R, Zimmerman DR. Spray dried porcine plasma (SDPP) as a source of protein for weanling pigs in two environments [abstract]. J Anim Sci. 1991;69(Suppl1):103.
*9. Cain CM, Zimmerman DR. Effect of spray dried plasma (SDP) on fecal shedding of hemolytic Escherichia coli (HEC) and rotavirus by pigs in a segregated early-weaned (SEW) environment [abstract]. J Anim Sci. 1997;75(Suppl1):61.
10. Coffey RD, Cromwell GL. The impact of environment and antimicrobial agents on the growth response of early-weaned pigs to spray-dried porcine plasma. J Anim Sci. 1995;73:2532–2539.
11. Torrallardona D, Conde R, Esteve-Garcia E, Brufau J. Use of spray dried animal plasma as an alternative to antimicrobial medication in weanling pigs. Anim Feed Sci Technol. 2002;99:119–129.
12. Moretó M, Pérez-Bosque A. Dietary plasma proteins, the intestinal immune system, and the barrier functions of the intestinal mucosa. J Anim Sci. 2009;87:E92–E100.
13. Peace RM, Campbell J, Polo J, Crenshaw J, Russell L, Moeser A. Spray-dried porcine plasma influences intestinal barrier function, inflammation and diarrhea in weaned pigs. J Nutr. 2011;141:1312–1317.
14. Gao YY, Jiang ZY, Lin YC, Zheng CT, Zhou GL, Chen F. Effects of spray-dried animal plasma on serous and intestinal redox status and cytokines of neonatal piglets. J Anim Sci. 2011;89:150–157.
15. Norberg SE, Dilger RN, Dong H, Harmon BG, Adeola O, Latour MA. Utilization of energy and amino acids of spray-dried egg, plasma protein, and soybean meal by ducks. Poult Sci. 2004;83:939–945.
16. Harmon BG, Richert BT. Spray dried egg as a rich source of immune globulins in diets for weaned pigs: metabolizable energy determination. Proc 13th Int Conf Prod Dis Farm Anim. Leipzig, Germany. 2007;550.
17. Harmon BG, Latour MA, Norberg SE. Sprayed dried eggs as a source of immune globulins for SEW pigs. Purdue Swine Day. Purdue University, West Lafayette. 2002;31–35.
18. Schmidt LD, Blank G, Boros D, Slominski BA. The nutritive value of egg by-products and their potential bactericidal activity: in vitro and in vivo studies. J Sci Food Agric. 2007;87:378–387.
19. Song M, Che TM, Liu Y, Soares JA, Harmon BG, Pettigrew JE. Effects of dietary spray-dried egg on growth performance and health of weaned pigs. J Anim Sci. 2012;90:3080–3087.
20. Yokoyama H, Peralta RC, Diaz R, Sendo S, Ikemori Y, Kodama Y. Passive protective effect of chicken egg-yolk immunoglobulins against experimental enterotoxigenic Escherichia coli. Infect Immun. 1992;60:998–1007.
21. Owusu-Asiedu A, Baidoo SK, Nyachoti CM, Marquardt RR. Response of early-weaned pigs to spray-dried porcine or animal plasma-based diets supplemented with egg-yolk antibodies against enterotoxigenic Escherichia coli. J Anim Sci. 2002;80:2895–2903.
22. Owusu-Asiedu A, Nyachoti CM, Baidoo SK, Marquardt RR, Yang X. Response of early-weaned pigs to an enterotoxigenic Escherichia coli (K88) challenge when fed diets containing spray-dried porcine plasma or pea protein isolate plus egg yolk antibody. J Anim Sci. 2003;81:1781–1789.
23. Owusu-Asiedu A, Nyachoti CM, Marquardt RR. Response of early-weaned pigs to an enterotoxigenic Escherichia coli (K88) challenge when fed diets containing spray-dried porcine plasma or pea protein isolate plus egg yolk antibody, zinc oxide, fumaric acid, or antibiotic. J Anim Sci. 2003;81:1790–1798.
24. National Research Council. Nutrient Requirements of Swine. 10th ed. Washington DC: National Academy Press; 1998:110–123.
25. Lindemann MD, Kim BG. Technical note: A model to estimate individual feed intake of swine in group feeding. J Anim Sci. 2006;85:972–975.
26. National Research Council. Nutrient Requirements of Swine. 11th ed. Washington DC: National Academy Press; 2012:208–238.
27. Bosi P, Han IK, Jung HJ, Heo KN, Perini S, Castellazzi AM, Casini L, Creston D, Cremokilini C. Effect of different spray dried plasmas on growth, ileal digestibility, nutrient deposition, immunity and health of early-weaned pigs challenged with E. coli K88. Asian-Aust J Anim Sci. 2001;14:1138–1143.
28. Bosi P, Casini L, Finamore C, Cremokilini C, Merialdi P, Trevisi P, Nobili F, Mengheri E. Spray-dried plasma improves growth performance and reduces inflammatory status of weanling pigs challenged with enterotoxigenic Escherichia coli K88. J Anim Sci. 2004;82:1764–1772.
29. Torrallardona D, Conde MR, Badiola I, Polo J, Brufau J. Effect of fishmeal replacement with spray-dried animal plasma and colistin on intestinal structure, intestinal microbiology, and performance of weanling pigs challenged with Escherichia coli K99. J Anim Sci. 2003;81:1220–1226.
30. Boyer PE, D’Costa S, Edwards LL, Milloway M, Susick E, Borst LB, Thakur S, Campbell JM, Crenshaw JD, Polo J, Moeser AJ. Early-life dietary spray-dried plasma influences immunological and intestinal injury responses to later-life Salmonella typhimurium challenge. Brit J Nutr. 2015. doi:10.1017/S000711451400422X.
31. Corl, BA, Harrell RJ, Moon HK, Phillips O, Weaver EM, Campbell JM, Arthington JD, Odle J. Effect of animal plasma proteins on intestinal damage and recovery of neonatal pigs infected with rotavirus. J Nutr Biochem. 2007;18:778–784.
*32. Díaz I, Lorca C, Gallindo I, Campbell J, Barranco I, Kuzemtseva L, Rodríguez-Gómez IM, Crenshaw J, Russell L, Polo J, Pujols J. Potential positive effect of commercial spray-dried porcine plasma on pigs challenged with PRRS virus. Proc IPVS Cong. Vancouver, Canada. 2010;560.
33. Opriessnig T, Xiao CT, Gerber PF, Zhang J, Halbur PG. Porcine epidemic diarrhea virus RNA present in commercial spray-dried porcine plasma is not infectious to naive pigs. PLoS one. 2014;9(8):1–10. doi;10.1371/journal.pone.0104766.
34. Mathew AG, Rattanatabtimtong S, Nyachoti CM, Fang L. Effects of in-feed yolk antibodies on Salmonella shedding, bacterial antibiotic resistance, and health of pigs. J Food Prot. 2009;72:267–273.
35. Chernysheva LV, Friendship RM, Dewey CE, Gyles CL. The effect of dietary chicken egg-yolk antibodies on the clinical response in weaned pigs challenged with a K88+ Escherichia coli isolate. J Swine Health Prod. 2004;12:119–122.
*36. Borg BS, Campbell JM, Polo J, Russell LE, Rodríguez C, Rodenas J. Evaluation of the chemical and biological characteristics of spray-dried plasma protein collected from various locations around the world. Proc AASV. Kansas City, Missouri. 2002;97–100.
37. Polo J, Opriessnig T, O’Neill KC, Rodríguez C, Russell LE, Campbell JM, Crenshaw J, Segalés J, Pujols J. Neutralizing antibodies against porcine circovirus type 2 in liquid pooled plasma contributed to the biosafety of commercially manufactured spray-dried porcine plasma. J Anim Sci. 2013;91:2192– 2198.
38. Lallès JP, Bosi P, Janczyk P, Koopmans SJ, Torrallardona D. Impact of bioactive substances on the gastrointestinal tract and performance of weaned piglets: A review. Animal. 2009;3:1625–1643.
39. Touchette KJ, Carroll JA, Allee GL, Matteri RL, Dyer CJ, Beausang LA, Zannelli ME. Effect of spray-dried plasma and lipopolysaccharide exposure on weaned pigs: I. Effects on the immune axis of weaned pigs. J Anim Sci. 2002;80:494–501.
40. Maijó M, Miró L, Polo J, Campbell J, Russell L, Crenshaw J, Weaver E, Moretó M, Pérez-Bosque A. Dietary plasma proteins modulate the adaptive immune response in mice with acute lung inflammation. J Nutr. 2012;142:264–270.
41. Song M, Liu Y, Lee JJ, Che TM, Soares- Almeida JA, Chun JL, Campbell JM, Polo J, Crenshaw JD, Seo SW, Pettigrew JE. Spray-dried plasma attenuates inflammation and improves pregnancy rate of mated female mice. J Anim Sci. 2015;93:298–305. doi:10.2527/jas2014-7259.