Unconventional feed refers to feed that is different in terms of the raw material source or preparation process compared to conventional feed. This kind of feed is usually obtained from diversified raw materials such as agricultural and sideline products, aquatic product by-products, and industrial by-products, which are obtained through special processing or treatment; China possesses rich resources of such materials [
1,
2]. However, the nutrient composition of unconventional feed is complex, and it has shortcomings such as a high content of anti-nutritional factors and poisons, poor palatability, unstable nutrient composition, and significant quality variations [
3]. Therefore, the comprehensive utilization level of unconventional feed is low, resulting in a waste of resources, environmental pollution, and other problems. At present, unconventional feed processed through microbial fermentation technology, crushing, heating, hydrolysis, drying, and other methods, in order to degrade the anti-nutritional factors, toxins, crude fiber, lignin, and other substances present in it and reflect its high nutritional value [
4] in terms of protein, minerals, and trace elements required for livestock supplementation, is called “special feed” or “alternative feed”. Therefore, unconventional feed is often used, in part, to replace conventional feed to reduce feed costs, improve the economic value, and achieve sustainable development in the feed industry. In recent years, the popularity of unconventional feeds has gradually increased.
2. Types and Applications of Unconventional Feed
The sources of unconventional feed are very extensive, including, but not limited to, grain and oil processing by-products, livestock and poultry processing by-products, aquatic product processing by-products, and other industrial processing by-products. Unconventional raw materials are abundant resources, but their application in animal feeding is limited due to their high amounts of anti-nutritional factors and toxins [
21,
22]. Therefore, improving the quality of unconventional raw materials and elevating their utilization rate in animal feeding are important topics of current scientific feed research. Current commonly used unconventional raw materials such as wheat bran, rice bran, bean dregs, distiller’s grains, sweet potatoes, straw, and other processing by-products require physical processing, chemical treatment, or microbial fermentation to decompose crude fiber and increase their feed value. Anti-nutritional factors and toxins in unconventional fermented feed can be reduced in a number of ways. During fermentation, microorganisms and enzymes that digest anti-nutritional factors such as phytic acid and cellulose are produced [
23], while high-temperature treatment helps to destroy the structure of some toxins. In addition, regulating the pH and microbial metabolism during fermentation can also reduce the toxin content in feed [
24]. Physical treatments such as filtration and sedimentation can also be used to reduce toxin levels [
25]. By combining these methods, unconventional fermented feed can be safely provided to animals while improving their nutrient availability and health.
Table 1 shows the positive effects of the fermentation of unconventional feed on animal health, nutrition and performance, and antioxidant aspects.
Table 1. Positive effects of the fermentation of unconventional feed on animal health, nutrition and performance, and antioxidant aspects.
Unconventional Fermented Feed Feeding |
Animal |
Raw Materials |
Probiotics |
Regulated Items |
Antioxidant Substance |
References |
Boer goats |
Pennisetum giganteum |
Bacillus coagulans preparation |
Abundance of Lactobacillus and unidentified Clostridiales ↑ Anaerovibrio and Methanobrevibacter ↓ |
CAT, GSH-Px activities and glutathione ↑ |
Qiu et al. [26] |
Laying hens |
Corn–soybean meal wheat bran |
Bacillus subtilis and Saccharomyces cerevisiae |
In relative Lactobacillus, Megasphaera, and Peptococcus abundance ↑ Campylobacter abundance ↓ |
Immunoglobulin A, immunoglobulin M, and immunoglobulin G ↑ |
Guo et al. [27] |
Broilers |
Corn, soybean meal, corn–gluten meal, and corn dried distillers’ grains |
Lactobacillus plantarum, Bacillus subtilis, and Saccharomyces cerevisiae |
Abundance of Ruminococcaceae, Lactobacillaceae, and unclassified Clostridiales ↑ Abundance of Rikenellaceae, Lachnospiraceae, and Bacteroidaceae ↓ |
Acetic acid, propionic acid, butyric acid, and lactic acid ↑ |
Zhu et al. [28] |
Laying hens |
Astragalus |
Lactobacillus plantarum |
CAT, GSH-Px, superoxide dismutase and total antioxidant capacity in serum ↑ |
CAT ↑ |
Hong et al. [29] |
Cobb male broilers |
Corn–soybean meal |
Lactobacillus acidophilus |
Body weight, ADG, average daily feed intake, and jejunum and ileum V:C ratio at 14 d and 21 d ↑ |
The mRNA expression of inducible nitric oxide synthase, interleukin-8, and interleukin-1β in the jejunum ↓ |
Wu et al. [30] |
Nursery pig |
Corn–soybean meal |
Lactobacillus plantarum and Pediococcus acidilactici |
ADG and significantly increased fecal acetate, butyrate, and total short-chain fatty acid concentrations ↑ |
Short-chain fatty acid ↑ |
Yang et al. [31] |
Berkshire pigs |
Rubus coreanus |
Lactobacillus plantarum |
The mRNA expression of transcription factors and cytokines in Th1 and Treg cells ↑ The mRNA expression of T helper cell 2 and Th17 transcription factors and cytokines ↓ |
The mRNA expression of transcription factors and cytokines in Th1 and Treg cells ↑ |
Yu et al. [32] |
Cyprinus carpio |
Wheat, soybean meal, corn–gluten meal, chicken meal |
C. somerae XMX-1, S. cerevisiae GCC−1, L. rhamnosus GCC-3, and B. subtilis HGcc-1 |
Health and production ↑ |
Liver anti-inflammatory factors transforming growth Factor-β↑ |
Zhang et al. [33] |
Juvenile olive flounder |
Garlic husks, Tuna |
Bacillus licheniformis and Bacillus subtilis |
Weight gain, specific growth rate, and feed efficiency ↑ |
Sucrose reductase↑ |
Fatma et al. [34] |