List of breeds of sheep in the United States.
Abstract
Sheep play a significant role in agriculture, serving as a primary source of meat, milk, and wool fiber. They constitute a unique class of animals distinguished by their specialized digestive organs. As our population increases, there is a high demand for sheep meat and products from developed and developing countries. In livestock production, disease poses a significant challenge, and the use of antimicrobial and antiparasitic drugs facilitates the control of infections, thereby improving animal welfare, health, and productivity. The use of antimicrobials in sheep farming has become prevalent and has led to antimicrobial resistance. This chapter will focus on the alternatives to antimicrobials used in sheep and how they benefit sheep health and production.
Keywords
- antimicrobials
- gastrointestinal parasites
- immunity
- probiotics
- sheep
1. Introduction
One of the biggest issues facing development in the upcoming years will be the ability of the world’s food markets to meet the demands of a fast-rising population. The increasing demand for safe, quality foods is driven by exponential population growth. It has been estimated that the human population is expected to exceed 9 billion by 2050 [1] and peak at 9.73 billion in 2064 [2]. Livestock plays a pivotal role in the economy and sustenance of numerous communities, with sheep emerging as the most prevalent livestock species [3, 4]. The growing demand to increase animal protein foods such as meat, milk, and eggs is premised on the increasing world population, whose need for safe, nutritious, and high-quality foods must be met. The current production systems and appliances utilized in livestock farming and veterinary medicine show numerous hindrances and drawbacks to producing sufficient animal foods without compromising environmental health.
Sheep are essential livestock and companion animal species. Sheep (
Breed name | Purpose | Year introduced in the US |
---|---|---|
American Blackbelly | Hunting and Hair | — |
Awassi | Milk and Wool | 2012 |
Babydoll Southdown | Pets, Wool, and Meat | — |
Barbados Blackbelly | Hair | 1904 |
Black Welsh Mountain | Black fleece (wool) | 1973 |
Bluefaced Leicester | Long Wool | 1980 |
Booroola Merino | Fine Wool and Prolific | — |
Border Cheviot | Medium Wool and Meat | 1838 |
Border Leicester | Long Wool and Meat | 1920 |
California Red | Wool and Meat | 1970 |
California Variegated Mutant | Wool | 1900 |
Charollais | Terminal Sires and Meat | — |
Clun Forest | Wool and Meat | 1970 |
Columbia | Medium Wool and Meat | 1900 |
Coopworth | Long Wool | 1970 |
Cormo | Fine Wool | 1976 |
Corriedale | Meat and Wool | 1914 |
Cotswold | Long Wool | 1831 |
Debouillet | Fine Wool | — |
Delaine Merino | Fine Wool | 1800 |
Dorper | Hair | 1990 |
Dorset | Medium Wool | 1885 |
East Friesian | Milk | 1993 |
Finnsheep | Medium Wool and Prolific | 1968 |
Gotland | Wool | 2003 |
Gulf Coast Native | Medium Wool | — |
Hampshire | Medium Wool and Meat | 1860 |
Herdwick | Wool | 2008 |
Hog Island | Medium Wool | 1700 |
Icelandic | Meat Wool and Milk | 1993 |
Ile de France | Terminal Sires and Meat | — |
Jacob | Wool | 1900 |
Karakul | Wool | 1900 |
Katahdin | Wool | — |
Kerry Hill | Medium Wool | 2006 |
Lacaune | Dairy | 1996 |
Leicester Longwool | Long Wool | 1700 |
Lincoln | Long Wool | 1800 |
Montadale | Medium Wool | 1930 |
Navajo Churro | Colored | 1600 |
North Country Cheviot | Medium Wool | 1944 |
Oxford | Medium Wool (Terminal Sire) | 1846 |
Painted Desert | Hair (Exotic) | — |
Panama | Medium Wool | 1912 |
Perendale | Long Wool | 1950 |
Polypay | Medium Wool (Prolific) | 1970 |
Racka | Long Wool | 2005 |
Rambouillet | Fine Wool (Dual Purpose) | 1800 |
Rideau Arcott | Medium Wool | 1990 |
Romanov | Terminal Sire | 1980 |
Romney | Long Wool | 1904 |
Royal White | Hair | 1990 |
Santa Cruz | Medium | — |
Scottish Blackface | Wool | — |
Shetland | Wool | — |
Shropshire | Medium Wool (Terminal Sire) | 1855 |
Soay | Colored | — |
SAMM | Fine Wool | 1999 |
Southdown | Medium Wool | 1820 |
St. Augustine | Hair | 1990 |
St. Croix | Hair | — |
Suffolk | Medium Wool | 1888 |
Targhee | Medium Fine | 1926 |
Teeswater | Long Wool | 1996 |
Texel | Medium Wool (Terminal Sire) | 1990 |
Tunis | Medium Wool | 1799 |
Valais Blacknose | Long Wool | 2018 |
Wensleydale | Long Wool | 1990 |
Wiltipoll | Hair | — |
Wiltshire Horn | Hair | 1600 |
1.1 Use of antibiotics in sheep production
Since the middle of the twentieth century, antibiotics have been widely employed to increase livestock productivity and, as a result, lower the price of animal protein to support food security. Despite this increase, sheep production has faced several losses due to infections by parasites and other health-related problems faced by ruminants. Most producers have relied on the use of antibiotics to treat these infections. Antibiotics have reduced the cost of animal-derived protein worldwide, thereby significantly improving the quality of life for billions of people. Several antibiotics used in sheep production include cydectin, fenbendazole, oxytetracycline, penicillin, lasalocid, sulfadimethoxine, decoquinate, aminoglycoside, lincomycin, macrolides, fluoroquinolones, etc. Nevertheless, despite their enormous benefits, the unintentionally growing issue of antibiotic resistance impedes the use of antibiotics in animal production. Antimicrobial resistance (AMR) is an emerging global threat to public health. The World Health Organization (WHO) considers AMR a major threat to global public health. Antibiotics are essential to livestock production to prevent a major drop in the health and productivity of sheep that would affect the security of the human food supply. To remedy this and stop the loss of livestock, it is imperative to create novel approaches and instruments that enhance animal well-being and productivity, like the way antibiotics were once employed. The need for effective alternatives to antibiotics in food-producing animals due to the development of resistant bacteria and the accumulation of antibiotic residue is discussed in this chapter.
2. Methodology used for sheep studies
Several phenotypic data are collected and analyzed following treatments with several alternatives to antibiotics. Body weight is collected using a weighing scale. The body condition score is measured on a scale of 1–5 by physically examining the sheep’s body [7]. Packed cell volume, used as an indicator of anemia, is determined from blood samples in sheep. The FAMACHA (Faffa Malan Chart) scoring system was used to clinically evaluate anemia in sheep. It is a useful tool that farmers can use to determine which animals require treatment. Fecal samples are collected from sheep to determine the number of fecal eggs. For molecular studies, protein analysis is conducted by enzyme-linked immunosorbent assay (ELISA), a molecular technique used to quantify and detect specific antigens or antibodies. The presence and level of secretion of proteins were determined using ELISA [7]. The detection and expression of genes were determined using real-time polymerase chain reaction (PCR).
3. Alternatives to antibiotics used in sheep production
Small ruminant production has been a growing industry in the United States due to demographic changes and the high demand for grass-fed livestock. Globally, healthy sheep are crucial for the long-term success of the sheep industry. In the United States, sheep are raised on pasture, making them more susceptible to the impacts of climatic factors. There have been growing concerns and safety issues surrounding the use of antibiotics for sheep production, leading many countries to seek different alternatives. Alternatives to antibiotics have been the subject of extensive research over the last 20 years. The widely used approach for treatment is drug therapy or the use of anthelmintics. The measures used to reduce parasite infection include reducing stock density and maximizing pasture to reduce parasite numbers [7]. Several alternatives have been proposed to combat parasitic infection and maintain the health status of sheep. The most widely researched alternatives include prebiotics, probiotics, phytobiotics/plant extracts, and essential oils. Understanding these alternatives will aid in designing immunomodulatory strategies to induce an immune response in sheep.
3.1 Prebiotics
According to the Food and Agriculture Organization (FAO), prebiotics are defined as nondigestible substances that benefit the host by selectively stimulating the favorable growth of several beneficial bacteria. Prebiotics are bypass carbohydrate materials that positively directly or indirectly influence the host’s intestinal microbes’ ecology through the proliferation of the gut’s beneficial bacteria, such as anaerobes,
![](http://cdnintech.com/media/chapter/89454/1716213421-1256707053/media/F1.png)
Figure 1.
Classification of prebiotics. Source: Author own development. Data source: Ref. [
3.2 Probiotics
The gastrointestinal tract (GIT) is known to have a highly diverse microbiota that includes bacteria, viruses, archaea, and protozoa [14]. Probiotics are defined as live microorganisms that, when administered in adequate amounts, confer a health benefit on the host. Research has shown that bacteria constitute the dominant group in the gastrointestinal tract (GIT), with at least 500 known bacterial species [15]. Probiotics are microbial substances capable of stimulating the expansion of another microorganism. They are living microbial feed additives that improve the host animals’ intestinal microbial balance and offer health values by establishing a better-suited microbial population by transforming the equilibrium of beneficial and harmful microorganisms. Probiotics work by inhibiting pathogen adherence, producing antimicrobial components, competitively excluding pathogenic microbes, enhancing barrier function, lowering luminal pH, and modulating the immune system, among other mechanisms [16].
Gastrointestinal nematode (GIN) parasite is a critical parasite that affects sheep. Gastrointestinal nematode infections are considered the most important limiting factor in ruminant production systems worldwide, resulting in substantial economic losses to producers [7, 17]. The resistance of this parasite to most anthelmintic drugs poses a significant economic challenge for sheep farming and remains a major obstacle that must be addressed [18]. The damage inflicted by the parasite leads to the loss of substantial blood volume in affected animals, resulting in severe anemia, weakness, nutritional deficiencies, body weight loss, and, in numerous cases, death. Among the parasites that affect sheep,
The role of probiotics in ruminants is to influence the intricate microbial population of the rumen, which degrades ingested feed materials and can indirectly enhance the immune system to fight parasitic infection, as reviewed in the chapter “Probiotics and ruminant health” [22, 23]. Studies by Sanders et al. [21] showed that treatment with paraprobiotics reduced the parasitic load of sheep infected with
The effects of probiotics have generally led to improved digestibility by increasing enzyme activity in the GIT. Mass et al. [25] reported that applying
Probiotic | Effect on Sheep/Lamb | Reference |
---|---|---|
Increased body weight gain, improved intestinal microbiota, strengthened the immune system, and maintained normal physiological processes | [27] | |
Significantly increased the total weight gain, microbial abundance, and diversity | [28] | |
Combination of | Improved the activities of superoxide dismutase and glutathione peroxidase. Increased growth hormones and immunoglobulin G levels, volatile fatty acids, and acetate | [29] |
Increased dry matter, organic matter, crude protein, and neutral detergent fiber intakes. Increased blood urea nitrogen, weaning weight, average daily weight gain, and improved health status in lambs. | [30] | |
Combination of | Regulated intestinal metabolites (SCFAs) and improved the tenderness of meat. | [31] |
Improved immune function and the fatty acid profile of the meat | [32] | |
Combination of | Improved growth performance indices (average daily gain, growth rate, and total weight gain). Increased plasma total protein, glucose, urea nitrogen, and aspartate aminotransferase | [33] |
Improved nutrient digestibility, daily gain, feed conversion, and economic efficiency | [34] | |
Combination | Increased digestibility of crude dry matter, organic matter, and neutral detergent fiber, improved meat quality | [35] |
A mixture of | Increased body weight and height at withers, circumference of chest, body proportion, and anamorphosis indices. Increased hemoglobin and red blood cells | [36] |
Decreased the area, length, and number of eggs from the recovered | [37] | |
Improved lamb growth and maximized economic efficiency of production. | [38] | |
Improved milk yield with minimal effect on blood plasma metabolite contents and enzyme activities | [39] | |
Decreased concentrate consumption and increased energy utilization efficiency. Decreased the meat cholesterol content of local sheep. | [40] | |
Improved dry matter intake, growth performance, feed conversion ratio, and nutrient digestibility during pre- and postweaning periods. | [41] | |
Increased intramuscular fat and improved the composition of fatty acids by modulating adenosine 5′-monophosphate-activated protein kinase (AMPK) signaling pathway | [42] | |
Influenced animal behavior (feed consumption) and altered the native rumen community structure or function | [43] | |
Improved blood lipid parameters, expression of lipid metabolismrelated genes, tail fat metabolites, and volatile flavor compounds | [44] | |
Improved meat quality without the occurrence of pathological kidney and liver lesions. | [45] | |
Improved metabolic and killing activity of phagocytes. Significantly increased | [46] | |
Increased intestinal slgA, reduced mRNA expression of toollike/MyD88/NF-kB/MAPK | [47] | |
Significantly increased IL-10 levels | [48] | |
Increased IgG, lgG1, and IgG2 Increased mRNA transcript of | [49] |
Table 2.
Immunomodulatory effects of probiotics strains in sheep.
Probiotics are vital in solving food production problems by replacing antibiotic use. However, there is a need to identify the optimum condition for a probiotic to survive, colonize, expand, and render its effects to the hosts. Also important are detailed dosage-dependent studies to confirm the organism’s identity using molecular testing at a reference laboratory.
3.3 Phytobiotic/plant extracts
Incorporating plant extracts as an alternative to antibiotics in sheep production is a tangible application of the One Health concept, promoting the well-being of animals, humans, and the environment in an integrated and interconnected manner. Phytobiotics encompasses a spectrum of natural bioactive compounds from plants, including herbs, spices, essential oils, and oleoresins [53]. Plant components and extracts are often relatively cheap, widely available, natural, and nontoxic. Phytobiotics have various effects, including antibacterial, antioxidant, and anti-inflammatory properties, gut microbiota alteration, intestinal barrier and nutrient absorption, and immunological modulation, which are advantageous to improving animal growth performance, health, and meat quality [54, 55, 56, 57, 58, 59]. Peptides that have antibacterial activity against
For instance, a study by Hashemzadeh et al. [62] showed that supplementation of a photogenic-rich herbal mixture (rosemary, cinnamon, turmeric roots, and clove buds) promoted feed intake, enhanced serum and liver antioxidant status, and improved growth performance of heat-stressed feedlot lambs. Phytobiotics have been employed in the rumen microbiota in grazing sheep, as seen in a study by Zhang et al. [63], where
As a growth promoter, Yaxing et al. [68] evaluated the effects of
The continuous use of antiparasitic drugs against gastrointestinal nematodes (GINs), which are the principal parasites that impact sheep production and health, incurring economic losses in grazing systems worldwide, could ultimately lead to resistance. Therefore, using phytobiotics (herbs) as anthelmintics could be a better alternative against these parasites [69]. Medicinal plant extract, rich in secondary compounds, has been shown to reduce GIN infection [70]. Mejia-Delgadillo et al. [71] reported that treating Peptasan reduced ewes’ nematode counts (mostly
Moharam & Kamal [72] investigated the blood antioxidative status of ewes in late pregnancy and early after parturition and examined the anthelmintic effects of black seeds (
Saparova and Zubova [76] researched the development and evaluation of the effects of novel environmentally safe herbal remedies derived from a combination of extracts from
One of the significant attributes of phytobiotics/plant extracts is their capacity to contribute essential nutrients to livestock while concurrently stimulating the endocrine system, thereby facilitating nutrient metabolism. Furthermore, certain phytobiotics/plant extracts are pivotal in reducing microbial toxins by stabilizing the microbiome [77], consequently diminishing inflammation. This redirection of resources toward growth promotion, rather than immune modulation, results in a more efficient allocation of protein production [78, 79].
3.4 Essential oils
Essential oils contain concentrated and complex mixtures of volatile nonpolar compounds extracted from plant sources. Essential oils are produced worldwide for flavor and pharmaceutical applications [80]. They are widely used for their natural antibacterial, anti-inflammatory, antioxidant, antifungal, and antispasmodic effects [81]. Essential oils represent one of the most promising alternatives to antibiotics in reducing some of the problems associated with the sheep industry.
In grazing ruminants worldwide, gastrointestinal nematodes (GINs) continue to be the most common parasites that cause illness, especially in sheep and goats [7, 82]. Gastrointestinal parasites are responsible for most economic and productive losses around the world. Previous studies conducted by Strabac et al. [83] reported that essential oils could be used as an anthelmintic agent in sheep farms, which affected gastrointestinal parasites. Also, previous studies conducted by Camurca et al. [84] reported using essential oil to control gastrointestinal nematodes in sheep. Mesquita-Sousa reported the use of essential oil in the treatment of sheep infected with gastrointestinal nematodes. Their report shows that essential oils reduced the shedding of nematode eggs by 78%. Despite all the positive reports on using essential oils in sheep production, a better understanding of the mechanism of action is needed, especially when combined with other drugs. da Silva et al. [85] evaluated the effect of orange essential oil on parasitic infection in lambs. They reported that essential oils reduced the severity of the parasitic infection and constantly diminished pasture contamination of gastrointestinal parasites when used with other methods.
Terpenes and terpenoids are the most prevalent components in plant essential oils. Ferreira et al. [18] showed the
Numerous studies show that essential oils have bioactivities, such as selective antibacterial activity, ruminal methane emission inhibition, ruminal propionate proportion enhancement, and bypass protein, to the intestine [86]. It has been shown that the addition of essential oil to the diet of sheep improves fiber digestibility. Based on some of these reports, it can be suggested that essential oils could be used as a diet supplement to improve the health status of sheep.
4. Conclusion
The demand for sheep products continuously increases as our population increases. It is essential to look into these alternatives to antibiotics that will provide the animal with beneficial effects for health and production in the host animal by modulating the host immune system. These studies provide a deep insight into the different alternatives to antibiotics used in sheep production. Treatment with prebiotics, probiotics, phytobiotics/plant extracts, and essential oil is promising and could be used in designing immunomodulatory strategies to induce immune responses in sheep.
References
- 1.
Adam D. How far will global population rise? Researchers can’t agree. Nature. 2021; 597 (7877):462-465 - 2.
Vollset SE, Goren E, Yuan C, Cao J, Smith AE, Hsiao T, et al. Fertility, mortality, migration, and population scenarios for 195 countries and territories from 2017 to 2100: A forecasting analysis for the global burden of disease study. The Lancet. 2020; 396 (10258):1285-1306 - 3.
Grandin T. Grazing cattle, sheep, and goats are important parts of a sustainable agricultural future. Animals. 2022; 12 :2092. DOI: 10.3390/ani12162092 - 4.
Markemann A, Stemmer A, Siegmund-Schultze M, Piepho H, Valle ZA. Stated preferences of llama keeping functions in Bolivia. Livestock Science. 2009; 124 (1):119-125 - 5.
Crane AR. Breeds of sheep and goats. In: Dikeman M, editor. Encyclopedia of Meat Sciences. 3rd ed. Oxford: Elsevier; 2024. pp. 741-748 - 6.
National Research Council. Changes in the Sheep Industry in the United States: Making the Transition from Tradition. Washington DC, United States: National Academies Press; 2008 - 7.
Ekwemalor K, Adjei-Fremah S, Asiamah E, Worku M. Molecular genetics and genome biology of goats. Goat. Science. 2018; 1 . 978-1-78923-203-5. DOI: 10.5772/intechopen.72414 - 8.
Megur A, Daliri EBM, Baltriukienė D, Burokas A. Prebiotics as a tool for the prevention and treatment of obesity and diabetes: Classification and ability to modulate the gut microbiota. International Journal of Molecular Sciences. 2022; 23 (11):6097 - 9.
Shoukry MM, El-Nomeary YAAE, Salman FM, Shakweer WME. Improving the productive performance of growing lambs using prebiotic and probiotic as growth promoters. Tropical Animal Health and Production. 2023; 55 (6):375 - 10.
Soliman SM, El-Shinnawy AM, El-Morsy AM. Effect of probiotic or prebiotic supplementation on the productive performance of Barki lambs. Journal of Animal and Poultry Production. 2016; 7 (10):369-346 - 11.
Zapata O, Cervantes A, Barreras A, Monge-Navarro F, González-Vizcarra VM, Estrada-Angulo A, et al. Effects of single or combined supplementation of probiotics and prebiotics on ruminal fermentation, ruminal bacteria and total tract digestion in lambs. Small Ruminant Research. 2021; 204 :106538 - 12.
Murthy AK, Chakravarthi MK. Effect of supplementation of probiotic, prebiotic and Synbiotic on growth performance in Nellore Brown lambs. Indian Journal of Animal Production and Management. 2023; 37 (3):225-227 - 13.
Lettat A, Nozière P, Silberberg M, Morgavi DP, Berger C, Martin C. Rumen microbial and fermentation characteristics are affected differently by bacterial probiotic supplementation during induced lactic and subacute acidosis in sheep. BMC Microbiology. 2012; 12 :1-12 - 14.
Melara EG, Avellaneda MC, Valdivié M, García-Hernández Y, Aroche R, Martínez Y. Probiotics: Symbiotic relationship with the animal host. Animals. 2022; 12 (6):719 - 15.
Canny GO, McCormick BA. Bacteria in the intestine, helpful residents or enemies from within? Infection and Immunity. 2008; 76 (8):3360-3373 - 16.
Anee IJ, Alam S, Begum RA, Shahjahan RM, Khandaker AM. The role of probiotics on animal health and nutrition. The Journal of Basic and Applied Zoology. 2021; 82 :1-16 - 17.
Ekwemalor K, Asiamah E, Adjei-Fremah S, Eluka-Okoludoh E, Mulakala B, Osei B, et al. Diverse pathogen-associated molecular patterns affect transcription of genes in the toll-like receptor signaling pathway in goat blood. Animal Biotechnology. 2023; 34 (8):3729-3738 - 18.
Ferreira LE, Benincasa BI, Fachin AL, França SC, Contini SSHT, Chagas ACS, et al. Thymus vulgaris L. essential oil and its main component thymol: Anthelmintic effects against Haemonchus contortus from sheep. Veterinary Parasitology. 2016; 228 :70-76 - 19.
Selemon M. Review on control of Haemonchus contortus in sheep and goat. Journal of Veterinary Medicine and Research. 2018; 5 (5):1139 - 20.
Getachew T, Dorchies P, Jacquiet P. Trends and challenges in the effective and sustainable control of Haemonchus contortus infection in sheep. Review. Parasite. 2007; 14 (1):3-14 - 21.
Sanders J, Xie Y, Gazzola D, Li H, Abraham A, Flanagan K, et al. A new paraprobiotic-based treatment for control of Haemonchus contortus in sheep. International Journal for Parasitology: Drugs and Drug Resistance. 2020; 14 :230-236 - 22.
Adjei-Fremah S, Ekwemalor K, Worku M, Ibrahim S. Probiotics and ruminant health. Probiotics-Current Knowledge and Future Prospects. 2018; 1 :133-150 - 23.
Adjei-Fremah S, Worku M, Ibrahim S. Immune-modulation and gut microbiome. The Gut Microbiota in Health and Disease. 2023; 1 :179-191 - 24.
Alimi D, Rekik M, Akkari H. Comparative in vitro efficacy of kefir produced from camel, goat, ewe and cow milk on Haemonchus contortus. Journal of Helminthology. 2019; 93 (4):440-446 - 25.
Maas RM, Verdegem MC, Debnath S, Marchal L, Schrama JW. Effect of enzymes (phytase and xylanase), probiotics (B. Amyloliquefaciens) and their combination on growth performance and nutrient utilisation in Nile tilapia. Aquaculture. 2021; 533 :736226 - 26.
Ekwemalor K, Asiamah E, Adjei-Fremah S, Worku M. Effect of a mushroom (Coriolus versicolor) based probiotic on goat health. American Journal of Animal and Veterinary Sciences. 2016; 11 (3):108-118 - 27.
Devyatkin V, Mishurov A, Kolodina E. Probiotic effect of Bacillus subtilis B-2998D, B-3057D, and bacillus licheniformis B-2999D complex on sheep and lambs. Journal of Advanced Veterinary and Animal Research. 2021; 8 (1):146 - 28.
Gao Y, Wei W, Tian F, Li J, Wang Y, Qi J, et al. Corn straw total mix dietary supplementation of bacillus subtilis-enhanced growth performance of lambs by Favorably modulating rumen bacterial microbiome. Fermentation. 2022; 9 (1):32 - 29.
Mao H, Ji W, Yun Y, Zhang Y, Li Z, Wang C. Influence of probiotic supplementation on the growth performance, plasma variables and ruminal bacterial community of growth-retarded Lamb. Frontiers in Microbiology. 2023; 14 :1216534 - 30.
Khattab IM, Abdel-Wahed AM, Khattab AS, Anele UY, El-Keredy A, Zaher M. Effect of dietary probiotics supplementation on intake and production performance of ewes fed Atriplex hay-based diet. Livestock Science. 2020; 237 :104065 - 31.
Liu T, Bai Y, Wang C, Zhang T, Su R, Wang B, et al. Effects of probiotics supplementation on the intestinal metabolites, muscle fiber properties, and meat quality of Sunit lamb. Animals. 2023; 13 (4):762 - 32.
Santillo A, Annicchiarico G, Caroprese M, Marino R, Sevi A, Albenzio M. Probiotics in milk replacer influence lamb immune function and meat quality. Animal. 2012; 6 (2):339-345 - 33.
Hussein AF. Effect of probiotics on growth, some plasma biochemical parameters and immunoglobulins of growing Najdi lambs. World's Veterinary Journal. 2018; 8 (4):80-89 - 34.
Lila ZA, Mohammed N, Kanda S, Kamada T, Itabashi H. Effect of sarsaponin on ruminal fermentation with particular reference to methane production in vitro. Journal of Dairy Science. 2003; 86 (10):3330-3336 - 35.
Hamdon HA, Kassab AY, Vargas-Bello-Pérez E, Abdel Hafez GA, Sayed TA, Farghaly MM, et al. Using probiotics to improve the utilization of chopped dried date palm leaves as a feed in diets of growing Farafra lambs. Frontiers in Veterinary Science. 2022; 9 :1048409 - 36.
El-Sayed AA, Mousa SA. Effects of administration of probiotic on body growth and hematobiochemical profile in growing Barki lambs. Comparative Clinical Pathology. 2020; 29 (1):297-303 - 37.
Santana DAD, Machado MO, de Azevedo BZ, Weber SH, Sotomaior CS, Ollhoff RD. Influence of probiotic supplementation on parasitological parameters in lambs. Veterinary Parasitology. 2023; 318 :109934 - 38.
El-Katcha MI, Soltan MA, Essi MS. Effect of Pediococcus spp. supplementation on growth performance, nutrient digestibility and some blood serum biochemical changes of fattening lambs. Alexandria Journal for Veterinary Sciences. 2016; 49 (1):44-54 - 39.
Kafilzadeh F, Payandeh S, Gómez-Cortés P, Ghadimi D, Schiavone A, Martínez Marín AL. Effects of probiotic supplementation on milk production, blood metabolite profile and enzyme activities of ewes during lactation. Italian Journal of Animal Science. 2019; 18 (1):134-139 - 40.
Herdian H, Sofyan A, Sakti AA, Juendra H, Karimy MF, Suryani AE, et al. Performance and meat quality of local sheep administered with feed additive containing probiotic and organic mineral complex. Media Peternakan. 2013; 36 (3):203 - 41.
Saleem AM, Zanouny AI, Singer AM. Growth performance, nutrients digestibility, and blood metabolites of lambs fed diets supplemented with probiotics during pre-and post-weaning period. Asian-Australasian Journal of Animal Sciences. 2017; 30 (4):523 - 42.
Zhang Y, Yao D, Huang H, Zhang M, Sun L, Su L, et al. Probiotics increase intramuscular fat and improve the composition of fatty acids in Sunit sheep through the adenosine 5′-monophosphate-activated protein kinase (AMPK) signaling pathway. Food Science of Animal Resources. 2023; 43 (5):805 - 43.
Schofield BJ, Lachner N, Le OT, McNeill DM, Dart P, Ouwerkerk D, et al. Beneficial changes in rumen bacterial community profile in sheep and dairy calves as a result of feeding the probiotic bacillus amyloliquefaciens H57. Journal of Applied Microbiology. 2018; 124 (3):855-866 - 44.
Liu T, Zhang T, Zhang Y, Yang L, Duan Y, Su L, et al. Impact of feeding probiotics on blood parameters, tail fat metabolites, and volatile flavor components of Sunit sheep. Food. 2022; 11 (17):2644 - 45.
Ding H, Liu W, Erdene K, Du H, Ao C. Effects of dietary supplementation with Allium mongolicum regel extracts on growth performance, serum metabolites, immune responses, antioxidant status, and meat quality of lambs. Animal Nutrition. 2021; 7 (2):530-538 - 46.
Wojcik R. Effect of brewer's yeast (Saccharomyces cerevisiae) extract on selected parameters of humoral and cellular immunity in lambs. Bulletin of the Veterinary Institute in Pulawy. 2010; 54 :181-187 - 47.
He X, Ye G, Xu S, Chen X, He X, Gong Z. Effects of three different probiotics of Tibetan sheep origin and their complex probiotics on intestinal damage, immunity, and immune signaling pathways of mice infected with Clostridium perfringens type C. Frontiers in Microbiology. 2023; 14 :1177232 - 48.
Pinheiro NB, Gaspar EB, Minho AP, Domingues R, de Moura MQ , Junior ASV, et al. Sheep immune-stimulated with saccharomyces boulardii show reduced prolificacy of Haemonchus contortus. Parasite Immunology. 2022; 44 (12):e12954 - 49.
Santos FDS, Maubrigades LR, Gonçalves VS, Ferreira MRA, Brasil CL, Cunha RC, et al. Immunomodulatory effect of short-term supplementation with bacillus toyonensis BCT-7112T and saccharomyces boulardii CNCM I-745 in sheep vaccinated with clostridium chauvoei. Veterinary Immunology and Immunopathology. 2021; 237 :110272 - 50.
Dagnaw, Fenta M, Gebremariam AA, Mebratu AS. Effectiveness of probiotic and combinations of probiotic with prebiotics and probiotic with rumenotorics in experimentally induced ruminal acidosis sheep. In: Veterinary Medicine: Research and Reports. United Kingdom: Taylor & Francis; 2023. pp. 63-78 - 51.
Han G, Gao X, Duan J, Zhang H, Zheng Y, He J, et al. Effects of yeasts on rumen bacterial flora, abnormal metabolites, and blood gas in sheep with induced subacute ruminal acidosis. Animal Feed Science and Technology. 2021; 280 :115042 - 52.
Singh D, Gupta SK, Sharma N, Kumar A. Bovine ruminal acidosis: Rumen liquor profile and its therapeutic management. Journal of Animal Research. 2018; 8 (4):691-696 - 53.
Mahfuz S, Shang Q , Piao X. Phenolic compounds as natural feed additives in poultry and swine diets: A review. Journal of Animal Science and Biotechnology. 2021; 12 (1):1-18 - 54.
Adjei-Fremah S, Everett A, Franco R, Moultone K, Asiamah E, Ekwemalor K, et al. Health and production benefits of feeding cowpeas to goats. Journal of Animal Science. 2016; 94 :80-81 - 55.
Moringa oleifera polyphenols modulate galectin expression in LPS-induced bovine peripheral blood mononuclear cells. Journal of Dairy Science: Elsevier Science Inc STE 800, 230 Park AVE, New York, NY 10169 USA; 2019. - 56.
Alhidary IA, Abdelrahman MM. Effects of naringin supplementation on productive performance, antioxidant status and immune response in heat-stressed lambs. Small Ruminant Research. 2016; 138 :31-36 - 57.
Mu C, Yang W, Wang P, Zhao J, Hao X, Zhang J. Effects of high-concentrate diet supplemented with grape seed proanthocyanidins on growth performance, liver function, meat quality, and antioxidant activity in finishing lambs. Animal Feed Science and Technology. 2020; 266 :114518 - 58.
Patra AK, Geiger S, Schrapers KT, Braun H, Gehlen H, Starke A, et al. Effects of dietary menthol-rich bioactive lipid compounds on zootechnical traits, blood variables and gastrointestinal function in growing sheep. Journal of Animal Science and Biotechnology. 2019; 10 (1):1-14 - 59.
Worku M, Adjei-Fremah S, Whitley N, Jackai L. Effect of cowpea (Vigna unguiculata) pasture grazing on growth, gastrointestinal parasite infection and immune response biomarkers of goat. The Journal of Agricultural Science. 2017; 10 (1):27 - 60.
Magalhães L, Nitschke M. Antimicrobial activity of rhamnolipids against listeria monocytogenes and their synergistic interaction with nisin. Food Control. 2013; 29 (1):138-142 - 61.
Pashtetsky V, Ostapchuk P, Kuevda T, Zubochenko D, Yemelianov S, Uppe V. Use of phytobiotics in animal husbandry and poultry. In: E3S Web of Conferences 2020. Vol. 215. EDP Sciences, Les Ulis Cedex A, France. p. 02002 - 62.
Hashemzadeh F, Rafeie F, Hadipour A, Rezadoust MH. Supplementing a phytogenic-rich herbal mixture to heat-stressed lambs: Growth performance, carcass yield, and muscle and liver antioxidant status. Small Ruminant Research. 2022; 206 :106596 - 63.
Zhang X, Liu X, Chang S, Zhang C, Du W, Hou F. Effect of Cistanche deserticola on rumen microbiota and rumen function in grazing sheep. Frontiers in Microbiology. 2022; 31 (13):840725 - 64.
Goel G, Makkar HP. Methane mitigation from ruminants using tannins and saponins. Tropical Animal Health and Production. 2012; 44 :729-739 - 65.
Wei-Lian H, Yue-ming W, Jian-xin L, Yan-qiu G, Jun-an Y. Tea saponins affect in vitro fermentation and methanogenesis in faunated and defaunated rumen fluid. Journal of Zhejiang University Science B. 2005; 6 :787-792 - 66.
Wang CJ, Wang SP, Zhou H. Influences of flavomycin, ropadiar, and saponin on nutrient digestibility, rumen fermentation, and methane emission from sheep. Animal Feed Science and Technology. 2009; 148 (2-4):157-166 - 67.
Liu Y, Ma T, Chen D, Zhang N, Si B, Deng K, et al. Effects of tea saponin supplementation on nutrient digestibility, methanogenesis, and ruminal microbial flora in Dorper crossbred ewe. Animals. 2019; 9 (1):29 - 68.
Yaxing Z, Erdene K, Changjin A, Zhibi B, Hongxi D, Zejun F, et al. Effects of Allium mongolicum regel and its extracts supplementation on the growth performance, carcass parameters and meat quality of sheep. Italian Journal of Animal Science. 2021; 20 (1):1899-1908 - 69.
Shrivastav A, Sharma RK, Shrivastav N, Gautam V, Jain SK. Inhibitory effect of herbs on extended spectrum beta lactamase enzyme from Escherichia coli of healthy broilers. Indian Journal of Animal Research. 2021;55 (2):160-166 - 70.
Habibi H, Firouzi S, Nili H, et al. Anticoccidial effects of herbal extracts on Eimeria tenella infection in broiler chickens: In vitro and in vivo study. Journal of Parasitic Diseases. 2016;40 :401-407. DOI: 10.1007/s12639-014-0517-4 - 71.
Mejia-Delgadillo MA, Lee-Rangel HA, Hernandez-Garcia PA, Vazquez-Valladolid A, Mendez-Cortes H, Guerra-Liera JE, et al. Effect of a polyherbal additive on performance and parasite infection of hair creole ewes. Indian Journal of Animal Research. 2021; 1 (1-5) - 72.
Moharam M, El-Far A, Kamal E. Antioxidant and antinematodal effects of Nigella sativa and Zingiber officinale supplementations in ewes. International Journal of Pharmaceutical Sciences Review and Research. 2014; 26 :222-227 - 73.
Mostafa OM, Eid RA, Adly MA. Antischistosomal activity of ginger (Zingiber officinale) against Schistosoma mansoni harbored in C57 mice. Parasitology Research. 2011; 109 :395-403 - 74.
Lin R, Chen C, Lee J, Lu C, Chung L, Yen C. Larvicidal constituents of Zingiber officinale (ginger) against Anisakis simplex. Planta Medica. 2010; 76 (16):1852-1858 - 75.
Pathak AK. Potential of using condensed tannins to control gastrointestinal nematodes and improve small ruminant performance. International Journal of Molecular Veterinary Research. 2013; 3 (8):36-50. DOI: 10.5376/ijmvr.2013.03.0008 - 76.
Saparova E, Zubova T. The effectiveness of phytobiotic additives in the diet of sheep. IOP Conference Series: Earth and Environmental Science. Bristol, United Kingdom: IOP Publishing; 2019; 403 (1):012034 - 77.
Windisch W, Schedle K, Plitzner C, Kroismayr A. Use of phytogenic products as feed additives for swine and poultry. Journal of Animal Science. 2008; 86 (Suppl. 14):E140-E148 - 78.
Steiner T. Managing Gut Health: Natural Growth Promoters as a Key to Animal Performance. Nottingham, England: Nottingham University Press; 2006 - 79.
Kroismayr A, Sehm J, Pfaffl MW, Schedle K, Plitzner C, Windisch W. Effects of avilamycin and essential oils on mRNA expression of apoptotic and inflammatory markers and gut morphology of piglets. Czech Journal of Animal Science. 2008; 53 (9):377-387 - 80.
Sharmeen JB, Mahomoodally FM, Zengin G, Maggi F. Essential oils as natural sources of fragrance compounds for cosmetics and cosmeceuticals. Molecules. 2021; 26 (3):666 - 81.
He S, Ho Row K, Tang W. Deep eutectic solvents based in situ isolation technique for extractive deterpenation of essential oils. Food Chemistry. 2024; 431 :137153 - 82.
Beleckė A, Kupčinskas T, Stadalienė I, Höglund J, Thamsborg SM, Stuen S, et al. Anthelmintic resistance in small ruminants in the Nordic-Baltic region. Acta Veterinaria Scandinavica. 2021; 63 (1):1-7 - 83.
Štrbac F, Krnjajić S, Stojanović D, Ratajac R, Simin N, Orčić D, et al. In: vitro and in vivo anthelmintic efficacy of peppermint (Mentha x piperita L.) essential oil against gastrointestinal nematodes of sheep. Frontiers in Veterinary Science. 2023; 10 :1-11 - 84.
Camurça-Vasconcelos ALF, Bevilaqua CML, Morais SM, Maciel MV, Costa CTC, Macedo ITF, et al. Anthelmintic activity of Lippia sidoides essential oil on sheep gastrointestinal nematodes. Veterinary Parasitology. 2008; 154 (1):167-170 - 85.
da Silva MTSP, de Carvalho MB, Santana DAD, dos Santos SK, Ollhoff RD, Luciano FB, et al. Can orange essential oil reduce the severity of parasitic infection in sheep? Veterinary Parasitology: Regional Studies and Reports. 2021; 26 :100637 - 86.
Lin B, Lu Y, Salem AZM, Wang JH, Liang Q , Liu JX. Effects of essential oil combinations on sheep ruminal fermentation and digestibility of a diet with fumarate included. Animal Feed Science and Technology. 2013; 184 (1):24-32