524
Views
0
CrossRef citations to date
0
Altmetric
Research Article

Effect of a peat-based feed additive and sow parity on the performance of suckling piglets: a case study

ORCID Icon, ORCID Icon, ORCID Icon & ORCID Icon
Pages 708-714 | Received 26 Jul 2021, Accepted 08 Nov 2022, Published online: 06 Dec 2022

ABSTRACT

This study was conducted to evaluate the benefit of a peat-based additive in reducing the neonatal diarrhoea of piglets, according to sow’s parity. From five consecutive batches, a total of 100 Large White x Landrace sows [50 primiparous (PR) and 50 multiparous (ML)] were randomly allocated to the control (CTR) or treated (TRT) group. The peat additive was provided to TRT piglets from the day of birth to day 7 of life (6 g/day/head). Overall, PR group resulted in lower piglets performance with higher enteric disease incidence compared with ML group. Compared with ML, PR sows had lower BCS at weaning (P < .001), fewer total piglets born, lower average piglet weaning weight (P < .01) and higher incidence of deaths due to enteric disease (P < .05). Regardless parity, TRT group showed a fewer number of litters affected by enteric disease (P < .05). No significant interaction between sow parity and treatment was observed.

Highlights

  • Peat-based feed additive led to reduce the number of litters affected by enteric disease during the pre-weaning phase in a commercial pig farm.

  • Primiparous sows had reduced piglets’ performance and higher incidence of enteric disease compared to multiparous sows.

Introduction

In swine production, the suckling period is a crucial phase affecting the future performance of the animals. At birth, piglets are immunodeficient and dependent upon maternal colostrum for passive immune transfer (Stokes et al. Citation2004). After 24 hours of age, there is a loss of absorptive ability of immunoglobulin (Ig), making the piglet particularly susceptible to infection during the first days of life (Rooke and Bland Citation2002; Stokes et al. Citation2004). The gut microbiota varies across piglets and is less stable than adult animal because parturition switches piglets from a sterile state in the uterus to a densely colonized external environment (Bian et al. Citation2016).

Neonatal diarrhoea is an ongoing problem in swine production that has a multifactorial aetiology and is correlated with animals' health and performance alterations (Nowland et al. Citation2019). The main causes include infectious factors, such as viruses (rotavirus, coronavirus), bacteria (Escherichia coli, Clostridium perfringens type A and C, Clostridium difficile) and coccidia (Isospora suis, Cryptosporidium spp.), and non-infectious factors, such as stress, herd management, nutrition strategies and environmental conditions (Calderaro et al. Citation2001; Wieler et al. Citation2001; Lippke et al. Citation2011; Vidal et al. Citation2019). Moreover, the development of genetic lines with hyperprolific sows has been associated with an increase in the number of piglets that are born underweight and thus are at greater risk for enteric problems in the first days of life (Peltoniemi et al. Citation2020).

Occurrence of enteric problems in very early life may affect the future performance of pigs and mortality rate during post-weaning and growing phases (Alvarez et al. Citation2015; Aghakeshmiri et al. Citation2017), and thus has economic implications. During the suckling period, a very crucial phase, piglets are fully fed on sows’ milk but, depending on the farm strategy, milk replacer and then creep feed may be used to supplement the sow low milk production, stimulate piglets gut mucosa development, enhance growth performance and/or stimulate the feeding behaviour to accustom them to the post-weaning diet (Okai et al. Citation1976; Fraser et al. Citation1994; Bruininx et al. Citation2002b).

Sow parity may also affect the piglet performance. The highest reproductive performance is reportedly observed from third parity sows (Hoving et al. Citation2011; Knecht et al. Citation2015), having a lower risk of piglet mortality (Guo et al. Citation2001). This could be influenced by colostrum and milk production, affecting also the passive immunity transfer (Friendship and O’Sullivan Citation2014). It is well known that piglets are born anaemic, with relative physiological deficiencies and an immunologically immature status (Lay et al. Citation2002); this likely contributes to pre-weaning mortality and enteric disease incidence. These findings could be emphasized by the influence of sow parity: primiparous progeny could be subjected to higher mortality and enteric disease challenges.

Due to the European banning of growth promoters in 2006, the use of feed additives has grown to enhance animal performance and health status, mainly by preventing gastrointestinal disorders (Pluske et al. Citation2007). This is in line also whit the communitarian aim of antimicrobial use reduction (More Citation2020).

The different types of feed additives currently available include prebiotics, probiotics, acids, minerals, nucleotides, phytoproducts and organic acids. However, the main criticism during pre-weaning phase is the effective feed intake related with the young age but also with the farm feeding strategy.

Among feed additives, peat is a completely natural material composed of water (from 50% to 70%), organic matter (including humus and plant debris) and minerals; since it is a natural material, the composition may vary by the origin and peat-forming plants (Xuehui and Jinming Citation2009). Peat can be considered as a source of biologically active substances, and is often used as a preventive and therapeutic agent against gastric and digestive problems both in human and animal medicine (Kühnert et al. Citation1989; Kuhnert et al. Citation1991; Banaszkiewicz and Drobnik Citation1994). According to its origin, it can be rich in humic substances (e.g. humic, fulvic, and ulmic acids, and humins) that could alter gut pH, nutrient uptake, feed efficiency, haematological profiles and animal performance (Trckova et al. Citation2005; Visscher et al. Citation2019).

The aim of this study was to assess the effect of feeding peat-based feed additive during the first seven days of life on performance and health status until weaning of piglets born from multiparous or primiparous.

Materials and methods

Animals and management

The study was performed in a commercial sow farm that is defined as site 1 of a multi-site production system located in the Mantova province (Lombardy, Italy). Pigs were raised in accordance with the protected designation of origin (PDO) Parma ham production regulation and with EC 120/2008 of the European Council (Council of the European Union, Citation2008) for pig welfare. This study was carried out on five consecutive batches from selected sows. Hundred sows (Large White x Landrace, ANAS line) and their litters (Duroc line as terminal sire) were monitored from farrowing to 28 days of life (weaning time). A total of 50 primiparous (PR) and 50 multiparous (ML) sows were included in the study. From each parity group, 25 were allocated to the peat treatment (TRT) and 25 were allocated to the control (CTR). From each batch, 20 sows were selected according to parity (10 primiparous, PR; and 10 multiparous, ML), body condition score (BCS), and reproductive performance (for multiparous sows), and randomly allocated to the control (CTR) or treated (TRT) group. Animals were housed in mechanically ventilated farrowing rooms in a single barn from seven days before farrowing. Twenty-four hours after farrowing, cross-fostering was performed between litters according to the sow parity and group, to standardize piglet numbers in order to have an average of 11 piglets for each sow. Overall, the animals were managed according to the general farm herd routine. The five batches of sows had 12.47 ± 0.50 newborn alive piglets per litter, 10.45 ± 0.20 weaned piglets per litter, and a loss during the suckling period equal to 11.30% ± 1.80%.

Diets

All sows were fed according their physiological phase according NRC recommendations (NRC, Citation2012). Liquid feed (solid:liquid ratio of 1:4) was provided once daily during gestation, and thrice daily after farrowing. and show the composition of the feeds provided to the sows during gestation and lactation and the related feed curves, respectively. As feed was bought from an authorized commercial feed mill, the percentage of each ingredient is unknown.

Table 1. Sow feed composition and feed curves during gestation.

Table 2. Sow feed composition and feed curves during lactation.

Starting from day 8 of age, suckling piglets were provided supplementary creep diets, first in a liquid form (from day 8 to13) and then in dry-meal form (from day 14 to28). The compositions of the three creep feeds are given in .

Table 3. Suckling piglet’s creep feed composition.

Additives

The peat additive was provided to piglets of the TRT groups from the day of birth to day 7 of life. During the first two days of treatment, peat was smeared on the sow mammary gland; thereafter, it was provided in a plastic creep feeder once daily at 6 g/day/head. shows the analytical and chemical parameters of the utilized peat.

Table 4. Analytical and chemical analysis of peat as fed.

Measurements

For each sow, visual body condition score (BCS; 1 = lowest, 5 = greatest; Coffey et al. Citation1999) was recorded the day before the scheduled farrowing date and the day of weaning, by qualified personnel. Data on the productive performance were collected, including the number of live-born, stillborn and mummified per litter. The weight of each litter was measured at farrowing after litter size standardization, and again on the weaning day. The feed consumption (from day 7 to the day of weaning) was measured for each litter. During the trial, all the enteric events and deaths were assessed and recorded by trained personnel.

Statistical analysis

The data were analysed for the normal distribution and homogeneity of the variance before statistical analysis. Data were then analysed according to a completely randomized experimental block design. The difference between averages was assessed using the linear mixed effect (LME) model function of NLME package (Pinheiro et al. Citation2017) of R v3.6.1 (Team R Development Core Citation2018). Treatment, parity and interaction between treatment and parity (TRT × Parity) were considered as fixed factors, while batch was taken as a random factor. The value of significance was established at P < .05, with P < .01 and P < .001 indicated where appropriate.

Results

Results for treatment differences are shown in . The trial sow subsamples (20 per batch) had 11.45 ± 0.20 born alive piglets, and 10.68 ± 0.08 weaned piglets and a pre-weaning piglet mortality rate of 7.00 ± 0.25%. The total number of piglets born differed by parity (P < .001), with higher performance observed in the ML group compared with the PR group. The weight of piglets at weaning was higher in the ML group (P < .001) than PR group. Compared with PR group, ML sows had a greater BCS at weaning (P < .001).

Table 5. Statistical analysis of animal performances according to sow parity, to group of treatment and interaction between parity and group of treatment.

The number of litters affected by enteric events was positively influenced by the treatment (P < .05), where TRT groups had a lower number of litters affected by enteric disorders compared to CTR group. Despite the lack of the interaction TRT × Parity effect, ML-TRT sows had lower average number of litters affected by enteric diseases than the PR-TRT group.

The enteric mortality was expressed as the percentage that died from enteric disease as a function of the overall percentage of piglets that died per litter. The enteric mortality was affected only by parity (P = .04). The ML sows registered the lower value.

Piglets’ feed consumption, from seven days of life to weaning, was comparable between PR and ML sows and between the TRT and CTR groups. However, piglets’ weight gain was significantly higher in the ML group (P < .001).

Discussion

The results obtained in this trial were not fully comparable with results found in the literature. Here, we tested the use of a peat-based additive for its ability to reduce the enteric mortality during the first days of life and, hence, improve the performance and survival of piglets. In fact, the studies available to date are mainly focused on fattening phase and only one study on pre-weaning stage, although providing peat from days 5 to 21 (Trckova et al. Citation2006). The same authors did not report any effect on body weight gain. Peat was also considered an economically ineffective additive in fattening pig stage due to the lack of effect on the growth performance, metabolic profile or health status (Trckova et al. Citation2005, Citation2006; Matlova et al. Citation2012).

In this study, the treatment did appear to reduce the number of litters affected by enteric disease. This might reflect the positive effects of humic and fulvic compounds, as these organic acids are naturally present in humus, which in turn have antioxidant and chelating activities that could indirectly improve the utilization of minerals by pigs (Ferronato and Prandini Citation2020). Visscher et al. (Citation2019) supplemented piglets with humic acid-rich peat and found no alteration of performance parameters but did observe changes in the fermentation level of cecal and colon contents with a reduction of short-fatty acids in the cecal content and differences for bacterial relative abundance. Instead the direct supplementation of humic substances (i.e. humic acids, fulvic acids, humate) showed greater benefits on the reduction of enteric problems (Golbs et al. Citation1986; Fuchs et al. Citation1990; Trckova et al. Citation2017; Tunc and Yoruk Citation2017).

We did not find a significant effect of the interaction between peat treatment and sow parity but there was a significant effect of the latter on reproductive performance, which is in line with previous works. A previous study showed that the parity of sows impacts the performance of their offspring (Moore Citation2001). Here, we observed that PR sows had decreased performance in terms of BCS loss, the number of piglets weaned, total number of stillborn piglets and the weight of piglets at weaning. The lower PR performance could be due to several factors including the rearing of gilts, age at first mating and farrowing, environmental factors and feeding management, which are associated with the greater needs of energy and growth in primiparous sows.

The lower piglet weaning weight found herein for the PR group could be explained by poorer milk and colostrum production and quality, which would correlate with a reduced passive immune (IgG) transfer to piglets. In contrast to the reports of Craig et al. (Citation2017, Citation2019), the live-born weight did not differ between the PR and ML groups. This would result in the average weight gain of piglets being higher for ML sows than PR sows. Indeed, Moore (Citation2001), Milligan et al. (Citation2002) and Miller et al. (Citation2012) found reduced performance in piglets of PR sows, and suggested the need to addressed this by providing supplemental milk during the suckling period. The pre-weaning mortality was similar between the PR and ML groups and slightly lower than Koketsu (Citation2000), while the average enteric rate and the number of litters affected by enteric disease in the PR group were double of the ML group. Craig et al. (Citation2019) reported that reduced performance of primiparous progeny could be due to reduced production of colostrum and milk instead of reduced concentrations of IgG, protein or fat. Conversely, Pinheiro et al. (Citation2017) suggested that IgG content could be reduced in primiparous sow-derived piglets due to their incomplete acquisition of specific immunity. The remaining mortalities could be explained by piglets being crushed as the sow changes position (Lay et al. Citation2002). Among non-infectious factors listed as causes of pre-weaning mortality, there are piglets’ factors (i.e. birth weight, vitality, gender), environmental factors (i.e. season and temperature, housing, management) as well as sow factors. Among the latter, there are the colostrum composition, maternal stress during farrowing time, parity and sow nutrition. The negative correlation between pre-weaning mortality and primiparous sows may be explained by the lower piglets weight, the lower colostrum yield and farrowing experience (Muns et al. Citation2016). Ferrari et al. (Citation2014) reported that piglets suckled by multiparous sows have better growth performance than primiparous piglets even if sow parity of the biological dam did not affect piglets’ survival and growth.

The average creep-feed intake (0.360 kg/piglet) was in the range previously proposed by several authors (Bruininx et al. Citation2002a, Citation2004; Sulabo et al. Citation2010). Even if creep-feed consumption was not different between the groups, the increased weight gain and weight at weaning time seen in the ML group could be explained by improvements in the mucosal adsorptive capacity and nutrient uptake. We could speculate that the improved feed efficiency among piglets could have interacted with the sow BCS, reducing the loss of BCS by decreasing milk demand and ameliorating the negative energy balance (Buckley et al. Citation2003; Yan et al. Citation2011; Pustal et al. Citation2015).

Instead of (or in addition to) providing benefits as a feed additive, the peat could have acted as a stimulus to explore the environment, promote solid feed ingestion and reduce aggression during the post-weaning phase (Kuller et al. Citation2010; Vanheukelom et al. Citation2011; Middelkoop et al. Citation2019). This is relevant because we did not monitor the piglets’ behaviour in the present study, and thus cannot be assured that the peat was fully ingested.

Conclusions

This study showed that peat could also be administered in the suckling phase to support gut health and reduce enteric disease in suckling piglets, starting from birth.

However, considering the lower performance of litters primiparous sows, there was no significant interaction between treatment and sow parity. Further studies should be developed considering a longer period of peat-based feed administration and evaluating the effects in the later post-weaning period.

Ethical approval

This study complied with Italian laws on animal experimentation (DL n. 26, 04/03/2014).

Disclosure statement

No potential conflict of interest was reported by the author(s).

References

  • Aghakeshmiri F, Azizzadeh M, Farzaneh N, Gorjidooz M. 2017. Effects of neonatal diarrhea and other conditions on subsequent productive and reproductive performance of heifer calves. Vet Res Commun. 41:107–112.
  • Alvarez J, Sarradell J, Morrison R, Perez A. 2015. Impact of porcine epidemic diarrhea on performance of growing pigs. PLoS One. 10:e0120532.
  • Banaszkiewicz W, Drobnik M. 1994. Wpływ borowiny naturalnej i roztworu izolowanych kwasów huminowych na niektóre wskaźniki przemiany materii i równowagi kwasowo-zasadowej u zwierzat doświadczalnych [The influence of natural peat and isolated humic acid solution on certain indices of metabolism and of acid-base equilibrium in experimental animals]. Rocz Panstw Zakl Hig. 45(4):353–60. Polish. PMID: 7792525.
  • Bian G, Ma S, Zhu Z, Su Y, Zoetendal EG, Mackie R, Liu J, Mu C, Huang R, Smidt H, Zhu W. 2016. Age, introduction of solid feed and weaning are more important determinants of gut bacterial succession in piglets than breed and nursing mother as revealed by a reciprocal cross-fostering model. Environ Microbiol. 18:1566–1577.
  • Bruininx EMAM, Binnendijk GP, Van Der Peet-Schwering CMC, Schrama JW, Den Hartog LA, Everts H, Beynen AC. 2002. Effect of creep feed consumption on individual feed intake characteristics and performance of group-housed weanling pigs1. J Anim Sci. 80:1413–1418.
  • Bruininx EMAM, Heetkamp MJW, Van Den Bogaart D, Van Der Peet-Schwering CMC, Beynen AC, Everts H, Den Hartog LA, Schrama JW. 2002. A prolonged photoperiod improves feed intake and energy metabolism of weanling pigs. J Anim Sci. 80,:1736–1745.
  • Bruininx EMAM, Schellingerhout AB, Binnendijk GP, Van Der Peet-Schwering CMC, Schrama JW, Den Hartog LA, Everts H, Beynen AC. 2004. Individually assessed creep food consumption by suckled piglets: influence on post-weaning food intake characteristics and indicators of gut structure and hind-gut fermentation. Anim Sci. 78:67–75.
  • Buckley F, O’Sullivan K, Mee JF, Evans RD, Dillon P. 2003. Relationships among milk yield, body condition, cow weight, and reproduction in spring-calved Holstein-Friesians. J Dairy Sci. 86:2308–2319.
  • Calderaro FF, Baccaro MR, Moreno AM, Ferreira AJP, Jerez AJ, Pena HJF. 2001. Frequencia De agentes causadores De enterites Em leitões lactentes provenientes De sistemas De produção De suínos Do Estado de São Paulo. Arq Inst Biol (Sao Paulo). 68:29–34.
  • Coffey RD, Parker GR, Laurent KM. 1999. Assessing sow body condition. Lexington, KY: Publ. ASC, Univ. Kentucky Coop. Ext. Serv.
  • Council of the European Union. 2008. Council Directive 2008/120/EC laying down minimum standards for the protection of pigs. Off J Eur. Union L47/5-13.
  • Craig JR, Collins CL, Bunter KL, Cottrell JJ, Dunshea FR, Pluske JR. 2017. Poorer lifetime growth performance of gilt progeny compared with sow progeny is largely due to weight differences at birth and reduced growth in the preweaning period, and is not improved by progeny segregation after weaning1. J Anim Sci. 95:4904–4916.
  • Craig JR, Dunshea FR, Cottrell JJ, Wijesiriwardana UA, Pluske JR. 2019. Primiparous and multiparous sows have largely similar colostrum and milk composition profiles throughout lactation. Animals (Basel). 9:35.
  • Ferrari CV, Sbardella PE, Bernardi ML, Coutinho ML, Vaz IS, Wentz I, Bortolozzo FP. 2014. Effect of birth weight and colostrum intake on mortality and performance of piglets after cross-fostering in sows of different parities. Prev Vet Med. 114:259–266.
  • Ferronato G, Prandini A. 2020. Dietary supplementation of inorganic, organic, and fatty acids in pig: A review. Animals (Basel). 10:1740–1727.
  • Fraser D, Pajor EA, Feddes JJR. 1994. The relationship between creep feeding behavior of piglets and adaptation to weaning: Effect of diet quality. Can J Anim Sci. 74:1–6.
  • Friendship R, O’Sullivan T. 2014. Sow health.
  • Fuchs V, Kühnert M, Golbs S, Dedek W. 1990. The enteral absorption of iron (II) from humic acid-iron complexes in suckling piglets using radiolabeled iron (59Fe). Dtsch Tierarztl Wochenschr. 97:208–209.
  • Golbs S, Kuehnert M, Fuchs V. 1986. The effects of veterinary drugs based on humic acids in the treatment of enteritis in young animals.
  • Guo SF, Gianola D, Rekaya R, Short T. 2001. Bayesian analysis of lifetime performance and prolificacy in Landrace sows using a linear mixed model with censoring. Livest Prod Sci. 72:243–252.
  • Hoving LL, Soede NM, Graat EAM, Feitsma H, Kemp B. 2011. Reproductive performance of second parity sows: Relations with subsequent reproduction. Livest Sci. 140:124–130.
  • Knecht D, Środoń S, Duziński K. 2015. The impact of season, parity and breed on selected reproductive performance parameters of sows. Arch Anim Breed. 58:49–56.
  • Koketsu Y. 2000. Productivity characteristics of high-performing commercial swine breeding farms. J Am Vet Med Assoc. 216:376–379.
  • Kuhnert M, Bartles KP, Kroll S, Lange N. 1991. Veterinary pharmaceuticals containing humic-acid for therapy and prophylaxis for gastrointestinal-diseases of dog and cat. Monatsh Veterinarmed. 46(1):4–8.
  • Kühnert M, Fuchs V, Golbs S. 1989. Pharmakologisch-toxikologische Eigenschaften von Huminsäuren und ihre Wirkungsprofile für eine veterinärmedizinische Therapie [Pharmacologic and toxicologic properties of humic acids and their activity profile for veterinary medicine therapy]. Dtsch Tierarztl Wochenschr. 96(1):3–10. German. PMID: 2522037.
  • Kuller WI, Tobias TJ, van Nes A. 2010. Creep feed intake in unweaned piglets is increased by exploration stimulating feeder. Livest Sci. 129:228–231.
  • Lay D, Matteri R, Carroll J, Fangman T, Safranski T. 2002. Economics of visceral energy metabolism in ruminants: Toll keeping or internal revenue service? J Anim Sci. 80:E74–E84.
  • Lippke RT, Borowski SM, Marques SMT, Paesi SO, Almeida LL, Moreno AM, Corbellini LG, de Barcellos DESN. 2011. Matched case-control study evaluating the frequency of the main agents associated with neonatal diarrhea in piglets. Pesquisa Veterinária Brasileira. 31:505–510.
  • Matlova L, Kaevska M, Moravkova M, Beran V, Shitaye JE, Pavlik I. 2012. Mycobacteria in peat used as a supplement for pigs: failure of different decontamination methods to eliminate the risk. Veterinární Medicína. 57:212–217.
  • Middelkoop A, Costermans N, Kemp B, Bolhuis JE. 2019. Feed intake of the sow and playful creep feeding of piglets influence piglet behaviour and performance before and after weaning. Sci Rep. 9.
  • Miller YJ, Collins AM, Smits RJ, Thomson PC, Holyoake PK. 2012. Providing supplemental milk to piglets preweaning improves the growth but not survival of gilt progeny compared with sow progeny1. J Anim Sci. 90:5078–5085.
  • Milligan BN, Dewey CE, De Grau AF. 2002. Neonatal-piglet weight variation and its relation to pre-weaning mortality and weight gain on commercial farms. Prev Vet Med. 56:119–127.
  • Moore C. 2001. Segregated production: How far could we go? Allen D. Leman Swine Conf. 203–206.
  • More SJ. 2020. Using examination performance data and focus groups to inform teaching – a case study from final year students of veterinary medicine. Ir Vet J. 73:1–12.
  • Muns R, Nuntapaitoon M, Tummaruk P. 2016. Non-infectious causes of pre-weaning mortality in piglets. Livest Sci. 84:46–57.
  • Nowland TL, Plush KJ, Barton M, Kirkwood RN. 2019. Development and function of the intestinal microbiome and potential implications for pig production. Animals (Basel). 9:76.
  • NRC. 2012. Nutrient requirements of swine. National Academies Press.
  • Okai DB, Aherne FX, Hardin RT. 1976. Effects of creep and starter composition on feed intake and performance of young pigs. Can J Anim Sci. 56:573–586.
  • Peltoniemi O, Oliviero C, Yun J, Grahofer A, Björkman S. 2020. Management practices to optimize the parturition process in the hyperprolific sow. J Anim Sci. 98:S96–S106.
  • Pinheiro J, Bates D, DebRoy S, Sarkar D, EISPACK, Heisterkamp S, Van Willigen B. 2017. Linear and nonlinear mixed effects models description. R Package. version 3:1–336.
  • Pluske J, Hansen C, Payne H, Mullan B. 2007. Gut health in the pig. Pages 147–158 in Manipulating Pig Production XI. Proceedings of the 11th Australasian Pig Science Association Biennal Conference, 25–28 October, Brisbane, Australia.
  • Pustal J, Traulsen I, Preißler R, Müller K, Beilage Tg, Börries U, Kemper N. 2015. Providing supplementary, artificial milk for large litters during lactation: effects on performance and health of sows and piglets: a case study. Porcine Health Management. 1.
  • Rooke JA, Bland IM. 2002. The acquisition of passive immunity in the new-born piglet. Pages 13–23 in Livestock Production Science.
  • Stokes CR, Bailey M, Haverson K, Harris C, Jones P, Inman C, Pié S, Oswald IP, Williams BA, Akkermans ADL, et al. 2004. Postnatal development of intestinal immune system in piglets: Implications for the process of weaning. Pages 325–334 in Animal Research.
  • Sulabo RC, Jacela JY, Tokach MD, Dritz SS, Goodband RD, Derouchey JM, Nelssen JL. 2010. Effects of lactation feed intake and creep feeding on sow and piglet performance1. J Anim Sci. 88:3145–3153.
  • Team R Development Core. 2018. A language and environment for statistical computing. R Found. Stat. Comput. 2. https://www.R-project.org
  • Trckova M, Matlova L, Hudcova H, Faldyna M, Zraly Z, Dvorska L, Beran V, Pavlik I. 2005. Peat as a feed supplement for animals: A review. Vet. Med. (Praha). 50:361–377. doi:10.17221/5635-VETMED.
  • Trckova M, Zraly Z, Bejcek P, Matlova L, Beran V, Horvathova A, Faldyna M, Moravkova M, Shitaye JE, Svobodová J, Pavlik I. 2006. Effect of feeding treated peat as a supplement to newborn piglets on the growth, health status and occurrence of conditionally pathogenic mycobacteria. Vet. Med. (Praha). 51:544–554. doi:10.17221/5589-VETMED.
  • Trckova M, Lorencova A, Babak V, Neca J, Ciganek M. 2017. Effects of sodium humate and zinc oxide used in prophylaxis of post-weaning diarrhoea on the health, oxidative stress status and fatty acid profile in weaned piglets. Veterinární Medicína. 62:16–28.
  • Tunc MA, Yoruk MA. 2017. Effects of humate and probiotic on the number of Escherichia coli, blood and antioxidant parameters in suckling period of calves. Asian J Anim Vet Adv. 12:169–176.
  • Vanheukelom V, Driessen B, Maenhout D, Geers R. 2011. Peat as environmental enrichment for piglets: the effect on behaviour, skin lesions and production results. Appl Anim Behav Sci. 134:42–47.
  • Vidal A, Martín-Valls GE, Tello M, Mateu E, Martín M, Darwich L. 2019. Prevalence of enteric pathogens in diarrheic and non-diarrheic samples from pig farms with neonatal diarrhea in the North East of Spain. Vet Microbiol. 237.
  • Visscher C, Hankel J, Nies A, Keller B, Galvez E, Strowig T, Keller C, Breves G. 2019. Performance, fermentation characteristics and composition of the microbiome in the digest of piglets kept on a feed with humic acid-rich peat. Front Vet Sci. 6:29.
  • Wieler LH, Ilieff A, Herbst W, Bauer C, Vieler E, Bauerfeind R, Failing K, Klös H, Wengert D, Baljer G, Zahner H. 2001. Prevalence of enteropathogens in suckling and weaned piglets with diarrhoea in Southern Germany. J Vet Med Ser B. 48:151–159.
  • Xuehui M, Jinming H. 2009. Classification of Peat and peatland: v, 2. II. E.P.C. Ltd, ed.
  • Yan L, Jang HD, Kim IH. 2011. Effects of varying creep feed duration on pre-weaning and post-weaning performance and behavior of piglet and sow. Asian-Australas J Anim Sci. 24:1601–1606.