SciELO - Scientific Electronic Library Online

 
vol.13 número2Estrés por calor en ganado lechero con énfasis en la producción de leche y los hábitos de consumo de alimento y agua. RevisiónApis mellifera en México: producción de miel, flora melífera y aspectos de polinización. Revisión índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

Links relacionados

  • No hay artículos similaresSimilares en SciELO

Compartir


Revista mexicana de ciencias pecuarias

versión On-line ISSN 2448-6698versión impresa ISSN 2007-1124

Rev. mex. de cienc. pecuarias vol.13 no.2 Mérida abr./jun. 2022  Epub 20-Jun-2022

https://doi.org/10.22319/rmcp.v13i2.5980 

Review

Potato protein concentrate: a possible alternative to the use of antibiotics in diets for weaned piglets. Review

Erick Alejandro Parra Alarcóna 

Teresita de Jesús Hijuitl Valerianob 

Gerardo Mariscal Landína  b  c 

Tércia Cesária Reis de Souzaa  b  * 

a Universidad Nacional Autónoma de México. Facultad de Medicina Veterinaria y Zootecnia Maestría en Ciencias de la Producción y de la Salud Animal. Ciudad de México, México.

b Universidad Autónoma de Querétaro. Facultad de Ciencias Naturales. Maestría en Salud y Producción Animal Sustentable. Av. De las Ciencias s/n. Querétaro, Querétaro, México.

c Instituto Nacional de Investigaciones Forestales, Agrícolas y Pecuarias (INIFAP). Centro Nacional de Investigación Disciplinaria en Fisiología y Mejoramiento Animal. Ajuchitlán, Querétaro, México.


Abstract

The weaning period is critical in the life of piglets and can cause gastrointestinal disorders and low growth, which are lessened with the use of antibiotics in starter feeds. However, due to the need to eliminate antibiotics from animal nutrition, some possible alternatives to their use are mentioned. In this literature review, antimicrobial peptides and plant-derived protease inhibitor compounds are described, especially those from potatoes, which have traditionally been recognized for their potential biomedical application and activity against pathogenic bacteria and fungi. The characteristics and applications of potato protein concentrate (PPC) from the starch industry, which is distinguished by its amino acid profile and high digestibility, were reviewed. Molecules that are present in the protein fraction and that can contribute to the intestinal health of piglets stand out in PPC, so it is emerging as an ingredient with potential to be used in antibiotic-free diets. However, it is necessary to have more bibliographic information on PPC to verify whether the health response is consistent or not, and to recommend its inclusion in starter diets for newly weaned piglets as an alternative to antibiotics.

Key words Piglets; Weaning; Antimicrobial peptides; Protease inhibitors; Potato

Resumen

El periodo del destete es crítico en la vida de los lechones y puede generar trastornos gastrointestinales y un bajo crecimiento, que son aminorados con el uso de antibióticos en los alimentos iniciadores. Sin embargo, debido a la necesidad de eliminar los antibióticos de la nutrición animal, se mencionan algunas posibles alternativas a su uso. En la presente revisión bibliográfica, se describen los péptidos antimicrobianos y compuestos inhibidores de proteasas de origen vegetal, sobre todo los provenientes de la papa, que han sido tradicionalmente reconocidos por su potencial aplicación biomédica y actividad contra bacterias patógenas y hongos. Se revisaron las características y aplicaciones del concentrado de proteína de papa (CPP) proveniente de la industria del almidón, que se distingue por su perfil de aminoácidos y alta digestibilidad. Se destacan en el CPP moléculas que están presentes en la fracción proteica y que pueden contribuir a la salud intestinal de los lechones, por lo que se perfila como un ingrediente con potencial para ser utilizado en dietas libres de antibióticos. Sin embargo, es necesario tener más información bibliográfica sobre el CPP para verificar si la respuesta sanitaria es consistente o no, y recomendar su inclusión en las dietas iniciadoras para lechones recién destetados como una alternativa a los antibióticos.

Palabras clave Lechones; Destete; Péptidos antimicrobianos; Inhibidores de proteasas; Papa

Introduction

The newborn piglet has a low intestinal capacity to digest and absorb solid feeds, especially those of vegetable origin, so its digestive system must mature quickly to ensure its survival1,2. Enteral nutrition (colostrum and milk) plays a fundamental role in the maturity of the piglet1; however, milk soon ceases to cover the nutritional demand of the piglet and it begins a gradual consumption of other feeds, allowing the gradual maturity of the nervous, immune and digestive systems. This maturation process of the digestive tract is stimulated by the colonization of different bacterial genera(3.4), which use some nutrients and produce enzymes2,5 and, through competitive exclusion, prevent the adhesion of pathogens4.

Under natural conditions, piglet weaning occurs between weeks 10 to 22 of life6,7. However, under commercial conditions, weaning is carried out between 21 and 28 d of age in order to allow the maximum productive efficiency of the female; higher number of births and piglets per sow per year, reduce the cost of facilities, etc.6. Commercial weaning, unlike natural weaning, is not gradual but an abrupt and sudden event, which is extremely stressful for the still immature piglet. This fact is characterized by the separation of the mother, the environmental change and from a dairy diet to a solid one (mainly composed of cereals). All this, added to the presence of new pathogens, causes neuroendocrine, immunological and digestive complications2,7, with piglets showing in the first 24 to 48 h after weaning a low, and even zero, feed consumption, weight loss, atrophy of the intestinal structure and with it of the digestive and absorption capacity, as well as an increase in the incidence of post-weaning diarrheas6,8.

The presence of post-weaning diarrheas is widely related to the sudden change in diet, as well as gastrointestinal infections. Both factors promote rapid dysbiosis, that is, an imbalance in the composition of bacterial populations, with an increase in E. coli, which contributes to the loss of intestinal structure9, as well as an abrupt reduction of Lactobacillus spp. The incidence of these post-weaning digestive disorders generates great economic losses10. To combat these gastrointestinal complications, antibiotics have been used as growth promoters (GPAs) in diets in recent years, since their use in animal feed favors the growth rate and reduces the incidence of diseases and mortality11,12. These molecules decrease the number of pathogens and with it the atrophy of the intestinal villi and hypertrophy of the crypts are prevented. This leads to a greater and early consumption of feed, adequate digestive capacity and better feed efficiency, thus increasing the retention of nitrogen and energy from the diet13,14. However, in recent years, the inclusion of GPAs in animal diets has been questioned, and even banned in some countries, since they represent a serious problem for public health, due to the development of bacterial resistance to antibiotics, which can potentially reduce the treatment of diseases in animals and possibly in humans. Therefore, the search for substitutes or alternatives to antibiotics is of great relevance for pig farming15,16.

With the growing human population, the demand for safe food resources by the pig industry has increased dramatically in recent years17. Due to its nutritional and possibly therapeutic characteristics, potato protein concentrate (PPC), obtained after starch extraction, seems to be a good choice as a protein source. Therefore, the present work aims to review some characteristics of this protein ingredient, which place it as a nutritional alternative with potential to improve the intestinal health of newly weaned piglets.

Alternatives to growth-promoting antibiotics (GPAs)

The crisis of bacterial resistance to antibiotics shows no signs of a solution in the short term and the lack of new antimicrobial drugs, as well as the few companies that invest in this area, threatens the ability to treat and prevent infections. One reason for the shortage of new antibiotics is that typical points of action, such as cell wall and protein synthesis, as well as that of DNA/RNA, have perhaps been overexploited. Currently, thanks to access to complete bacterial genomes, strategies based on new molecular targets are sought; however, this approach has not been fully developed18.

However, the antibiotic crisis demands measures that contemplate a new approach and different therapeutic strategies18. There are many literature reviews on the different alternatives to GPAs. Among the most studied alternatives the following stand out: plant extracts, chicken egg antibodies, organic acids and enzymes12, as well as essential oils10, probiotics19, prebiotics20, minerals such as copper and zinc11, as well as animal plasma21 and plant proteins such as potato protein concentrate22.

Among the most successful alternatives for the control of post-weaning digestive disorders, animal proteins stand out, such as animal plasma and fishmeal, which, due to their high digestibility and amino acid profile, favor feed consumption and growth rate23,24. However, ingredients of animal origin are expensive and inadequate handling during storage could favor the transmission of some pathogens. Fishmeal is the essential protein in piglet feeds, but marine overfishing has caused a vertiginous increase in prices, reducing its availability.

The results of including these ingredients in piglet diets can sometimes be inconsistent and hardly able to match the effect of antibiotics in productive terms, however, benefits to intestinal health are reported, which should be considered when using antibiotic-free diets. Plant-based antimicrobial peptides (AMPs) are an alternative to GPAs that have shown potential use12.

Plant-based antimicrobial peptides

AMPs are developed by different plants and tubers as a defense mechanism and in response to microbial aggressions and infections25-27. These peptides are expressed and stored in different plant tissues25. AMPs are encoded by genes that have a wide range of activity against Gram-negative, Gram-positive bacteria, fungi and bacilli of the genus Mycobacterium. They have been isolated and characterized from tissues and organisms that represent practically all kingdoms and phyla28. These peptides play an important role in the mechanisms responsible for eliminating or preventing the growth of pathogens, both inside and outside plant organisms29. AMPs exist in different molecular forms, the most common are linear, although there are also cyclic forms. Most AMPs have 2 to 6 cysteine residues26, which give them high thermal, enzymatic and chemical stability30. They are polypeptides with less than 200 amino acids (AAs), commonly less than 50 AAs, of low molecular weight (approximately 10 kDa), basic character and are generally cations at physiological pH due to their residues loaded with arginine and lysine25.

Cystine-rich AMPs are classified into families according to their sequence similarity, cysteine motifs, that is, the cysteine combinations that accumulate in the tertiary structure of the peptide and disulfide bond patterns. Families of cystine-rich plant AMPs include thionines, defensins, hevein-type peptides, knottin-type peptides (linear and cyclic), lipid transfer proteins, α-hairpinines and snakins25,26. It should be clarified that there are AMPs rich in other amino acids (glycine, histidine). The ability of plant AMPs to organize into families with conserved structural characteristics allows the variation of the sequence of residues that are not cysteine in the same structure within a particular family to perform multiple functions26.

Plant AMPs have activity against bacteria, fungi, viruses and parasites. The mechanism of action of AMP is generally believed to be related to membrane lysis or peptide penetration followed by attack on intracellular targets. The cationic nature and amphipathic capacity of AMPs allows interaction with the (anionic) wall and phospholipid membrane of microorganisms25,26. Mechanisms of action such as pore formation and membrane depolarization, disruption of bacterial energy metabolism and interference with biosynthetic pathways for the antimicrobial activity of several AMPs that contain disulfide bridges31 have been suggested. The aforementioned characteristics profile them as an important alternative for the development of antibiotic and anti-inflammatory molecules25. These characteristics, in addition to cysteine residues, are classic of the families of thionines and defensins. Other families of AMPs such as hevein-type peptides bind to chitins, and lipid transfer proteins bind to cell membrane lipids to disrupt microbial penetration into cells26.

Some authors28,32,33 suggest that PPC may be an alternative to feeds medicated with antibiotics, because it showed antimicrobial activity by effectively reducing the population of coliform bacteria. It is suggested33 that potato protein may have an additional potential advantage over antibiotics by selectively inhibiting the in vitro growth of pathogenic bacteria (Staphylococcus aureus, Salmonella gallinarum and E. coli). The explanation of the antimicrobial effects of PPC could be related to the action of certain antimicrobial peptides that can be found in the protein of the tuber Solanum tuberosum34, since peptides with antimicrobial activity are produced by the potato in its defense against pathogens.

Antimicrobial potato peptides

Potato proteins are divided into three groups: patatin, protease inhibitors (PIs) and other proteins that are also involved in the defense of the potato, as they all have antifungal or antimicrobial actions35. PIs represent a high proportion of the total potato protein36, and are a structurally heterogeneous group (Table 1) with a wide range of antifungal and antimicrobial activities35.

Table 1 Potato protease inhibitors35  

Protease inhibitor Molecular
mass
(kDa)
Isoelectric point SU Inhibited
enzyme
Protease inhibitor l 7.68 - 7.87 5.1-6.3-7.2-7.8 5 T, Q
Protease inhibitors ll 20.02 - 20.68 5.5-5.8-5.9-6.0-6.1-6.5-6.9 2 T, Q
Aspartate protease inhibitor 19.87 - 22.03 6.2-7.5-8.2-8.4-8.6-8.7 1 T, Q, CD
Cysteine protease inhibitor 20.1 - 22.7 5.8-6.6-6.7-7.1-8.0-8.3->9 1 T, Q, Pap.
Kunitz-type protease inhibitor 20.19 - 20.24 8.0-9.0 1 T, Q
Other serine protease inhibitors 21.03 - 21.80 7.5-8.8 1-2 T, Q
Carboxypolypeptidase inhibitor 4.20 not determined 1 CA

SU= subunits. T = trypsin; Q= chymotrypsin; CD= cathepsin D; Pap= papain; CA= carboxypolypeptidase A.

In the past, PIs were only considered antinutritional factors; however, they have recently aroused interest because they have multiple biological activities. Potato PIs have been studied for their antimicrobial effect, anticancer activity and regulation of feed consumption related to the modulation of cholecystokinin through trypsin inhibition35.

The high stability of antifungal activity of potato PIs I and II at high temperatures opens a new market for starch producers, due to the potential use of these peptides in the food, pharmaceutical or agricultural industry27.

In some experiments35,37, potato PIs I and II reduced the growth of several fungi; while members of the Kunitz family (proteins Potide-G, AFP-J, Potamin-1 and PG-2) inhibited pathogenic bacteria (Staphylococcus aureus, Listeria monocytogenes, Escherichia coli or Candida albicans). In an in vitro study37, Potamin-1 inhibited the growth of different plant pathogens, and also had inhibitory activity against the enzymes trypsin, chymotrypsin and papain. The peptide Potamin-1 is currently the most mentioned in the literature to explain the mechanism of action of PPC in animals38.

Other potato proteins

Within the group called “other potato proteins”, cysteine-rich peptides such as thionines, defensins, lectins and snakins are included39. Thionines base their antimicrobial activity on the interaction with the phospholipid membrane of pathogenic microorganisms. Defensins seem to act on specific membrane receptors, however, information on these peptides is limited35.

Snakin peptides are part of an independent group. They are within the classification of other potato proteins due to their practically zero similarity to any other type of potato peptide35,40. Snakins are involved in biological processes such as cell division, elongation, and growth and signaling in potato defense. Two types of snakin peptides are found [snakin-1 (SN1) and snakin-2 (SN-2)] and although they only share 38 % of their structure, they have similar functions. Both are peptides rich in cysteine residues with reported activity against Gram-negative and Gram-positive bacteria (C. michiganensis, R. solanacearum, E. chrysanthemi and R. meliloti), as well as against some fungi35,39. Their spectrum of antimicrobial activity against bacterial and fungal pathogens is quite similar to each other and different from that of defensin peptides from the same tissues. However, the expression of the SN2 gene is induced in the potato by a local wound and shows differential responses to infection by pathogens. The expression patterns and antimicrobial activities of SN2 are consistent with its participation in the constitutive and inducible defense barriers of the potato41.

Potato protein concentrate in the feed of weaned piglets

There are about 5,000 varieties of potato, originating mainly from the Andes, with variants in size, shape, color, texture, as well as nutritional profile. About 10 varieties are cultivated, and the most cultivated variety worldwide is the species Solanum tuberosum. China is responsible for 80 % of the world’s production of this variety. The chemical composition of the potato is modulated by different factors such as geographical area and cultivation practices; its protein content in the fresh state varies between 0.49 and 2.7 %42,43.

In addition to consumption in fresh form, the potato is also used to obtain starch, fiber and juice. In the European Union alone, 8 million tonnes of potatoes are processed annually. PPC is a coproduct of the starch industry, by recovering the liquid fraction that remains after its extraction44. The process is based on thermal coagulation followed by protein separation and drying27,45. Potato proteins are typically classified according to their molecular mass and electrophoretic separation into three large groups: patatins, protease inhibitors and other proteins35. Patatins represent about half of potato proteins and are glycoproteins with molecular weights of 39 to 43 kDa, with enzymatic activities (hydrolases, phospholipases and glucanases)35.

The potato has some antinutritional factors such as glycoalkaloids of solanines (927 - 2,632 mg/kg) and trypsin inhibitors (0.97 - 3.70 mg/kg), where the concentration can be variable according to the conditions of processing44. Thermal processing (100°/15 min) before drying is capable of inactivating up to 48 % of protease inhibitors and up to 89 % of glycoalkaloids46.

PPC is an ingredient that contains adequate amounts of essential amino acids, which can replace animal protein in piglet diets47, as it has been characterized by a highly balanced amino acid profile and is especially rich in lysine, methionine, threonine, tryptophan and valine. In piglets that received a diet with PPC with the same level of inclusion as fishmeal, an improvement in the growth rate of piglets was observed48, which can be attributed to the quality of its amino acid profile. Thus, the nutritional value of PPC is related to the concentration and availability of amino acids since it has a profile similar to that of soybean49 and some animal proteins50. The proportion of eight essential amino acids (threonine, valine, methionine, isoleucine, leucine, phenylalanine, lysine and tryptophan) corresponds to 40.7 % of the PPC protein42. The amino acid profile of potato protein completes or exceeds the ideal protein profile, except for tryptophan and lysine with 64.5 and 89.75 % of the requirement, respectively.

In 2008 and 2009, three articles were published 28,32,33 in which a refined potato protein (RPP or PP) purified at laboratory level from a special variety of potato (Solanum tuberosum L. cv. Golden valley) was used. This protein fraction showed an inhibitory effect on the in vitro growth of pathogenic bacteria, so they studied the incorporation of RPP or PP at different levels in the diet of newly weaned piglets and compared it with a control diet with antibiotics. Results varied between studies, and an advantage of using the diet with antibiotics was observed in the three studies.

When the authors33 used diets with 0, 200, 400 and 600 ppm of RPP, it was reported that the increase in levels of inclusion in the diets linearly improved the productive performance and reduced the populations of total bacteria, coliforms and Staphylococcus spp. in the contents of the colon and rectum and in feces. The apparent fecal digestibility of dry matter and crude protein, as well as apparent ileal digestibility of amino acids, did not differ between pigs fed the control diet (0 ppm) with antibiotics and diets with RPP33.

With higher levels of inclusion (0.0, 2.5, 5.00 and 7.50 g PP/kg of diet), researchers28 also observed a linear improvement in feed efficiency during the 28 experimental days and an increase in the apparent fecal digestibility of dry matter in phase II (0 to 14 days post-weaning) with the increase in the level of inclusion of PP. A linear decrease in fecal bacteria was also observed on days 21 and 28 with the increase in the level of inclusion of PP. Piglets that consumed the diets with PP had a linear reduction of total bacteria, coliforms and Staphylococcus spp. in the cecum and rectum. The apparent ileal digestibility of amino acids and the morphology of intestinal villi and crypts were not affected by the consumption of experimental diets28.

In another study32 with piglets fed diets with 0.0, 0.25, 0.50 or 0.75 % potato protein (PP) during phase I (0 to 14 d post-weaning) and phase II (14 to 28 days post-weaning), the authors observed that increasing levels of PP linearly improved daily weight gain, daily feed consumption and feed efficiency in both phases (I and II); in addition to increasing the digestibility of the dry matter in phase II. Consumption of diets with increasing levels of PP linearly reduced bacterial populations in feces and contents of the cecum, colon and rectum. The height of the villi and the depth of the intestinal crypts did not vary with the increase in the level of PP in the diet. These three studies28,32,33 opened an area of opportunity for the use of potato protein concentrate generated in the starch industry in animal feed.

The use of PPC of commercial origin22 in growing pigs (25 kg live weight) showed a high ileal digestibility of nitrogen, both standardized (93.0 %) and apparent (85.8 %). The apparent ileal digestibility and the digestibility of most AAs were similar to the digestibility of soybean protein concentrate and isolate, with the highest standardized and apparent ileal digestibility of leucine (96.3 and 94.7 %, respectively) and threonine (94.7 % and 86.9 %, respectively) standing out in PPC22.

In another study47 with growing pigs (21 kg live weight), the inclusion in the diet of 17.5 % PPC with a low concentration of glycoalkaloids and low trypsin inhibitory activity did not affect daily weight gain, daily feed consumption or the relative weight of stomach, duodenum and jejunum, as well as other aspects of intestinal morphology. Protein digestibility was lower in pigs fed the diet with PPC than with the diet with casein, however, the apparent ileal digestibility of fat was better in piglets with PPC. The authors conclude that the diet with a high level of PPC was well used by growing pigs47.

The good results to the consumption of PPC observed in growing pigs are probably related to its nutritional characteristics; however, due to the reported antimicrobial properties, the use of PPC is more recommended for its inclusion in diets for newly weaned piglets.

In 2005, it had already been observed48 that piglets fed diets with 6 % PPC had a greater daily weight gain in the first 1-21 and 21-50 d post-weaning than piglets fed diets in which they included fishmeal, sunflower meal and gluten meal in similar amounts. Mortality in the period was low (about 4 %) and the severity of diarrheas was slight (1.6 points) in all piglets48.

Some authors51, using PPC with a low level of glycoalkaloids (PPCLG) in diets of newly weaned pigs, found no differences in the productive behavior with respect to diets with animal plasma. The authors observed a quadratic response in weight gain and feed consumption in weaned piglets when using increasing levels of inclusion of PPCLG, replacing 25, 50, 75 and 100 % of animal plasma in the diet. Feed efficiency improved linearly with the inclusion of PPCLG. It was concluded that PPCLG may be an effective substitute for a part of the pig plasma in diets for weaned piglets51.

During the first week after weaning52, it was observed that daily weight gain and feed efficiency were also not different between piglets that consumed dehydrated porcine plasma or PPC in their diets. During the second week post-weaning and in the total experimental period, the daily feed consumption was similar among all animals. The apparent ileal digestibility of crude protein was higher in piglets fed antibiotic and PPC. The apparent total digestibility of dry matter and energy was higher for piglets fed PPC than the other diets. The severity index of diarrheas in piglets fed the PPC diet was similar among piglets fed the control diet with antibiotic52. These results demonstrate a potential use of PPC for newly weaned piglets.

Conclusions

In recent years, the search for alternatives to the use of antibiotics in feeds as promoters of growth and intestinal health in newly weaned piglets has increased. The potato is some food rich in antimicrobial peptides (AMPs) and other proteins that are involved in its defense system, which have already been purified at the laboratory level. The industry of starch extraction from the potato generates a large amount of a protein concentrate, which probably preserves these AMPs. In this context, potato protein concentrate could exert a positive effect on the productive development of pigs due to its nutritional value, in addition to the possible benefits of its AMPs on intestinal health. However, for it to be considered as an alternative to the use of antibiotics in starter diets, it is necessary to have more bibliographic evidence on the presence of these peptides in commercial products based on potato protein concentrate available on the market, and if their beneficial effects persist at the gastrointestinal level, decreasing post-weaning diarrheas.

Literatura citada

1. Buddington RK, Sangild PT, Hance B, Huang EY, Black DD. Prenatal gastrointestinal development in the pig and responses after preterm birth. J Anim Sci 2012;90(suppl 4):290-298. [ Links ]

2. Pohl CS, Medland JE, Moeser AJ. Early-life stress origins of gastrointestinal disease: animal models, intestinal pathophysiology, and translational implications. Am J Physiol Gastrointest Liver Physiol 2015;309(12):927- 941. [ Links ]

3. Maradiaga N, Zeineldin M, Aldridge B, Lowe J. Influence of maternal microbial communities on the mucosal microbiome of neonatal pigs. AASV 2014;2014(1):1-39. [ Links ]

4. Mach N, Berri M, Estellé J, Levenez F, Lemonnier CD, Leplant CC, et al. Early life establishment of the swine gut microbiome and impact on host phenotypes. Environ Microbiol Rep 2015;7(3):554-569. [ Links ]

5. McCormack UM, Curião T, Buzoianu SG, Prieto ML, Ryan T, Varley P, et al. Exploring a possible link between the intestinal microbiota and feed efficiency in pigs. Appl Environ Microbiol 2017;83(15):1-16. [ Links ]

6. Insuasti ASG, Collazos DV, Argote F. Efecto de la dieta y edad del destete sobre la fisiología digestiva del lechón. Rev Fac Cienc Agrar 2008;6(1):32-41. [ Links ]

7. Moeser AJ, Pohl SC, Rajput M. Weaning stress and gastrointestinal barrier development: implications for lifelong gut health in pigs. Anim Nutr 2017;3(4):313-321. [ Links ]

8. Campbell JM, Crenshaw DJ, Polo J. The biological stress of early weaned piglets. J Anim Sci Biotechnol 2013;4(1):1-4. [ Links ]

9. Rhouma M, Fairbrother JM, Beaudry F, Letellier A. Post weaning diarrhea in pigs: risk factors and non-colistin-based control strategies. Acta Vet Scand 2017;59(1):2-19. [ Links ]

10. Gresse R, Chaucheyras-Durand F, Fleury MA, Van de Wiele T, Forano E, Blanquet-Diot S. Gut Microbiota Dysbiosis in Postweaning Piglets: Understanding the Keys to Health. Trends Microbiol 2017;25(10):851-873. [ Links ]

11. Puskle J. Feed- and feed additives-related aspects of gut health and development in weanling pigs. J Anim Sci Biotechnol 2013;4(1):2-7. [ Links ]

12. Thacker PA. Alternatives to antibiotics as growth promoters for use in swine production: a review. J Anim Sci Biotechnol 2013;4(35):1-12. [ Links ]

13. Wu S, Zhang F, Huang Z, Liu H, Xie C, Zhang J, et al. Effects of the antimicrobial peptide cecropin AD on performance and intestinal health in weaned piglets challenged with Escherichia coli. Peptides 2012;35(2):225-230. [ Links ]

14. Kiarie E, Voth C, Wey D, Zhu C, Vingerhoeds P, Borucki S, et al. Comparative efficacy of antibiotic growth promoter and benzoic acid on growth performance, nutrient utilization and indices of gut health in nursery pigs fed corn-wheat-soybean meal diet. Can J Anim Sci 2018;98 (4):868-874. [ Links ]

15. Levy SB, Marshall B. Antibacterial resistance worldwide: causes, challenges and responses. Nat Med 2004;10(12):122-129. [ Links ]

16. Zhao J, Harper AF, Estienne MJ, Webb JKE, McElroy AP, Denbow DM. Growth performance and intestinal morphology responses in early weaned pigs to supplementation of antibiotic-free diets with an organic copper complex and spray-dried plasma protein in sanitary and nonsanitary environments. J Anim Sci 2007;85(5):1032-1310. [ Links ]

17. Yu M, Li Z, Chen W, Wang G, Rong T, Liu Z, et al. Hermetia illucens larvae as a fishmeal replacement alters intestinal specific bacterial populations and immune homeostasis in weanling piglets. J Anim Sci 2020;98(3):1-13. [ Links ]

18. Culp E, Wright G. Bacterial proteases, untapped antimicrobial drug targets. J Antibiot 2017;17(4):366-377. [ Links ]

19. Vondruskova H, Slamova R, Trckova M, Zraly Z, Pavlik I. Alternatives to antibiotic growth promoters in prevention of diarrhoea in weaned piglets: a review. Vet Med 2010;55(5):199-224. [ Links ]

20. Oliveira ER, Silva CA, Da Castro-Gómez RJH, Lozano AP, Gavioli DF, Frietzen J, et al. Chito-oligosaccharide as growth promoter replacement for weaned piglets: performance, morphometry, and immune system. Semin Cienc Agrar 2017;38(5):3253-3269. [ Links ]

21. Crenshaw JD, Campbell JM, Polo J, Stein HH. Effects of specialty proteins as alternatives to bovine or porcine spray-dried plasma in non-medicated diets fed to weaned pigs housed in an unsanitary environment. Transl Anim Sci 2017;1(3):333-342. [ Links ]

22. Cotten B, Ragland D, Thomson JE, Adeola O. Amino acid digestibility of plant protein feed ingredients for growing pigs. J Anim Sci 2016;94(3):1073-1082. [ Links ]

23. Torrallardona D. Spray dried animal plasma as an alternative to antibiotics in weanling pigs. A review. Asian-Aust J Anim Sci 2010;23(1):131-148. [ Links ]

24. Pérez-Bosque A, Polo J, Torrallardona D. Spray dried plasma as an alternative to antibiotics in piglet feeds, mode of action and biosafety. Porc Health Manag 2016;2(1):1-10. [ Links ]

25. Benko-Iseppon M, Galdino SL, Calsa T Jr, Kido A, Tossi A, Belarmino C, Crovella S. Overview on plant antimicrobial peptides. Curr Protein Pept Sci 2010;11(3):181-188. [ Links ]

26. Tam, P, Wang S, Wong H, Tan L. Antimicrobial Peptides from Plants. Pharmaceuticals 2015;8(4):711-757. [ Links ]

27. Bártová V, Bárta J, Vlačihová A, Šedo O, Zdráhal Z, Konečná H, et al. Proteomic characterization and antifungal activity of potato tuber proteins isolated from starch production waste under different temperature regimes. Appl Microbiol Biotechnol 2018;102(24):10551-10560. [ Links ]

28. Jin Z, Yang YX, Choi JY, Shinde PL, Yoon SY, Hahn TW, Lim HT et al. Effects of potato (Solanum tuberosum L. cv. Golden valley) protein having antimicrobial activity on the growth performance, and intestinal microflora and morphology in weanling pigs. Anim Feed Sci Technol 2008;140(1):139-154. [ Links ]

29. Islas-Flores I, Minero-García Y, James AC. Proteínas contra las infecciones de las plantas. Ciencia 2005;3(1):64-74. [ Links ]

30. Contreras P, Diaz C, Taron D. Ciclótidos, proteínas circulares producidas por plantas con potencial farmacológico. Rev Cubana Farm 2015;49(2):84-93. [ Links ]

31. Marshall SH, Arenas G. Antimicrobial peptides: A natural alternative to chemical antibiotics and a potential for applied biotechnology. Elect J Biotechn 2003;6(3):271-284. [ Links ]

32. Jin Z, Yang YX, Choi JY, Shinde PL, Yoon SY, Hahn TW, Lim HT, et al. Potato (Solanum tuberosum L. cv. Gogu valley) protein as a novel antimicrobial agent in weanling pigs. J Anim Sci 2008;86(7):1562-1572. [ Links ]

33. Jin Z, Shinde PL, Yang YX, Choi JY, Yoon SY, Hahn TW, et al. Use of refined potato (Solanum tuberosum L. cv. Gogu valley) protein as an alternative to antibiotics in weanling pigs. Livest Sci 2009;124(1-3):26-32. [ Links ]

34. Waglay A, Karboune S, Alli I. Potato protein isolates: Recovery and characterization of their properties. Food Chem 2014;142(1):373-382. [ Links ]

35. Bártová V, Bárta J, Jarošová M. Antifungal and antimicrobial proteins and peptides of potato (Solanum tuberosum L.) tubers and their applications. Appl Microbiol Biotechnol 2019;103(14):5533-5547. [ Links ]

36. Waglay A, Karboune S. Potato Proteins Functional Food Ingredients. In: Jaspreet Singh, Lovedeep Kaur editors. Advances in Potato Chemistry and Technology. 2 ed. Academic Press, London, UK: Elsevier Books; 2016:75-104. [ Links ]

37. Kim JY, Park SC, Kim MH, Lim HT, Park Y, Hahm KS. Antimicrobial activity studies on a trypsin-chymotrypsin protease inhibitor obtained from potato. Biochem Biophys Res Commun 2005;330(3): 921- 927. [ Links ]

38. Cisneros JS, Cotabarren J, Parisi MG, Vasconcelos MW, Obregón WD. Purification and characterization of a novel trypsin inhibitor from Solanum tuberosum subsp. andigenum var. overa: Study of the expression levels and preliminary evaluation of its antimicrobial activity. Int J Biol Macromol 2020;158(1):1279-1287. [ Links ]

39. Kovalskaya N, Hammond RW. Expression and functional characterization of the plant antimicrobial snakin-1 and defensin recombinant proteins. Protein Expr Purif 2009;63(1):12-17. [ Links ]

40. Segura A, Moreno M, Madueño F, Molina A, García-Olmedo F. Snakin-1, a peptide from potato that is active against plant pathogens. Mol Plant Microbe Interact 1999;12(1):16-23. [ Links ]

41. Berrocal-Lobo M, Segura A, Moreno M, López G, Garcıa-Olmedo F, Molina A. Snakin-2, an antimicrobial peptide from potato whose gene is locally induced by wounding and responds to pathogen infection. Plant Physiol 2002;128(3):951-961. [ Links ]

42. Mu TH, Tan SS, Xue YL. The amino acid composition, solubility and emulsifying properties of sweet potato protein. Food Chem 2009;112(4):1002-1005. [ Links ]

43. Wijesinha-Bettoni R, Mouillé B. The contribution of potatoes to global food security, nutrition and healthy diets. Am J Potato Res 2019;96(2):139-149. [ Links ]

44. Taciak M, Tuśnio A, Pastuszewska B. The effects of feeding diets containing potato protein concentrate on reproductive performance of rats and quality of the offspring. J Anim Physiol Anim Nutr 2011;95(5):556-563. [ Links ]

45. Pastuszewska B, Tuśnio A, Taciak M, Mazurczyk W. Variability in the composition of potato protein concentrate produced in different starch factories-A preliminary survey. Anim Feed Sci Tech 2009;154(3-4):260-264. [ Links ]

46. Wojnowska I, Poznanski S y Bednarski W. Processing of potato protein concentrates and their properties. J Food Sci 1982;47(1):167-172. [ Links ]

47. Tuśnio A, Pastuszewska B, Święch, Taciak M. Response of young pigs to feeding potato protein and potato fibre - nutritional, physiological and biochemical parameters. J Anim Feed Sci 2011;20(3):361-378. [ Links ]

48. Sardi L, Paganelli R, Parisini P, Simioli M, Martelli G. The replacement of fishmeal by plant proteins in piglet production. Ital J Anim Sci 2005;4(suppl. 2):449-451. [ Links ]

49. Froidmont E, Wathelet B, Oger R, Romnée JM, Colinet A, Cloet D, et al. Nutritional properties of potato protein concentrate compared with soybean meal as the main protein source in feed for the double-muscled Belgian Blue bull. Animal 2008;3(2):200-208. [ Links ]

50. Refstie S, Tiekstra HA. Potato protein concentrate with low content of solanidine glycoalkaloids in diets for Atlantic salmon (Salmo salar). Aquaculture 2003;216(1-4):283-298. [ Links ]

51. Kerr CA, Goodband RD, Smith JW, Musser RE, Bergström JR, Nessmith Jr WB, et al. Evaluation of potato proteins on the growth performance of early-weaned pigs. J Anim Sci 1998;76(12):3024-3033. [ Links ]

52. Reis de Souza TC, Aguilera AB, Rubio SR, Machado WG, Escobar KG, Gómez JGG, et al. Growth performance, diarrhoea incidence, and nutrient digestibility in weaned piglets fed an antibiotic-free diet with dehydrated porcine plasma or potato protein concentrate. Ann Anim Sci 2019;19(1):59-172. [ Links ]

Received: April 07, 2021; Accepted: August 26, 2021

Creative Commons License Este es un artículo publicado en acceso abierto bajo una licencia Creative Commons